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<strong>Re</strong> s e <strong>arch</strong> <strong>De</strong> <strong>gre</strong> e s <strong>in</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

<strong>Ne</strong> w cas tle Unive rs ity, UK


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong> th e <strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Introduction...............................................................................................1<br />

Facilitie s ....................................................................................................2<br />

Applications ..............................................................................................3<br />

Staff re s e <strong>arch</strong> <strong>in</strong>te re s ts .......................................................................4-25<br />

<strong>Ch</strong> e m <strong>is</strong> <strong>try</strong> laboratorie s at <strong>Ne</strong> w cas tle .<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong>


1<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Th e <strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong> at <strong>Ne</strong> w cas tle <strong>is</strong> a vibrant ce ntre <strong>of</strong> re s e <strong>arch</strong> <strong>in</strong><br />

ch e m <strong>is</strong> <strong>try</strong> w ith an <strong>in</strong>te rnational re putation <strong>in</strong> a w ide range <strong>of</strong> fie lds from<br />

catalys <strong>is</strong> to anticance r drug de s ign and m ole cular ph otonics to<br />

nanote ch nology. W e als o h ave s trong <strong>in</strong>dus trial l<strong>in</strong>k s w ith m ajor com panie s<br />

<strong>in</strong>clud<strong>in</strong>g GlaxoSm ith Kl<strong>in</strong>e , Joh ns on-Matth e y, Proctor and Gam ble ,<br />

Am e rs h am , Davy Proce s s Te ch nology, BAE Sys te m s , Inte l, Du Pont and<br />

Pfiz e r.<br />

Co laborative e ngage m e nt and m ulti-d<strong>is</strong> cipl<strong>in</strong>arity are e ncourage d, as are<br />

l<strong>in</strong>k s w ith oth e r <strong>Sch</strong> <strong>ool</strong>s <strong>in</strong> th e Unive rs ity and th e cros s -Faculty <strong>Re</strong> s e <strong>arch</strong><br />

Ins titute s . Th riv<strong>in</strong>g co laborations e x<strong>is</strong> t w ith co le ague s <strong>in</strong> Biology, Me dic<strong>in</strong>e ,<br />

<strong>Ch</strong> e m ical Eng<strong>in</strong>e e r<strong>in</strong>g and Mate rials , Ce l and Mole cular Biology, Ele ctrical<br />

Eng<strong>in</strong>e e r<strong>in</strong>g, and Civil Eng<strong>in</strong>e e r<strong>in</strong>g. Se ve ral s taff are as s ociate d w ith th e<br />

Ins titute for Nanos cale Scie nce and Te ch nology<br />

(h ttp://w w w .ncl.ac.uk /<strong>in</strong>s at/), th e North e rn Ins titute for Cance r <strong>Re</strong> s e <strong>arch</strong><br />

(h ttp://w w w .ncl.ac.uk /nicr/), th e <strong>Re</strong> s e <strong>arch</strong> Ce ntre for Catalys <strong>is</strong> and<br />

Inte ns ifie d Proce s s <strong>in</strong>g (h ttp://w w w .ncl.ac.uk /catalys <strong>is</strong> /), and th e Ins titute for<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong> Environm e nt and Sus ta<strong>in</strong>ability<br />

(h ttp://w w w .ncl.ac.uk /e nvironm e nt/). <strong>Re</strong> s e <strong>arch</strong> opportunitie s are available <strong>in</strong><br />

a l th e s e are as .<br />

Th e <strong>Sch</strong> <strong>ool</strong> <strong>of</strong>fe rs a varie ty <strong>of</strong> opportunitie s for pos tgraduate re s e <strong>arch</strong> for<br />

th e <strong>De</strong> <strong>gre</strong> e s <strong>of</strong> Mas te r <strong>of</strong> Ph ilos oph y (MPh il) and Doctor <strong>of</strong> Ph ilos oph y<br />

(Ph D). Th e MPh il tak e s one ye ar fu l-tim e , and th e Ph D tak e s a m <strong>in</strong>im um <strong>of</strong><br />

th re e ye ars fu l-tim e or five ye ars part-tim e . Th e <strong>Sch</strong> <strong>ool</strong> als o <strong>of</strong>fe rs a<br />

num be r <strong>of</strong> taugh t MSc program m e s <strong>in</strong> applie d and drug ch e m <strong>is</strong> <strong>try</strong>. W e<br />

w e lcom e e nq uirie s and applications at any tim e .<br />

Dr Be n H orrock s<br />

Dire ctor <strong>of</strong> Pos tgraduate Studie s (b.r.h orrock s @ ncl.ac.uk )


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Facilitie s<br />

Much <strong>of</strong> th e s pe cial<strong>is</strong> t s cie ntific e q uipm e nt for ch e m <strong>is</strong> <strong>try</strong> <strong>is</strong> locate d <strong>in</strong><br />

<strong>in</strong>dividual re s e <strong>arch</strong> laboratorie s (e .g., <strong>in</strong> Mole cular Ph otonics and <strong>Ch</strong> e m ical<br />

Nanos cie nce ).<br />

Synth e s <strong>is</strong><br />

Th e re <strong>is</strong> a s tate -<strong>of</strong>-th e -art laboratory for s ynth e tic w ork and a fu l s uite <strong>of</strong><br />

analytical e q uipm e nt<br />

(h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong>/pos tgrad/facilitie s /facilitie s .h tm ).<br />

X-ray crys ta lograph y<br />

W e h ave tw o m ode rn are a-de te ctor diffractom e te rs capable <strong>of</strong> co le ct<strong>in</strong>g a<br />

fu l s e t <strong>of</strong> X-ray diffraction data <strong>in</strong> a fe w h ours , e nabl<strong>in</strong>g rapid de te rm <strong>in</strong>ation<br />

<strong>of</strong> crys tal s tructure s for organic, organom e ta lic and <strong>in</strong>organic com pounds .<br />

For m ore de m and<strong>in</strong>g s am ple s s uch as ve ry s m a l crys tals , acce s s to th e<br />

national s ynch rotron radiation facilitie s <strong>is</strong> available .<br />

NMR<br />

Th e <strong>Sch</strong> <strong>ool</strong>’s W olfs on NMR s uite <strong>is</strong> h ous e d <strong>in</strong> purpos e -built accom m odation<br />

and <strong>is</strong> e q uippe d w ith th re e h igh re s olution m ult<strong>in</strong>ucle ar puls e d Fourie r<br />

trans form NMR s pe ctrom e te rs ope rat<strong>in</strong>g at proton fre q ue ncie s <strong>of</strong> 300 to 500<br />

MH z . Alm os t a l m agne tic nucle i can be s tudie d ove r a te m pe rature range <strong>of</strong><br />

173 to 39 3 K. A ve ry w ide range <strong>of</strong> one - and tw o-dim e ns ional e xpe rim e nts<br />

<strong>is</strong> available and m any <strong>in</strong>ve rs e de te ction proce dure s for ach ie v<strong>in</strong>g h igh<br />

s e ns itivity.<br />

Com put<strong>in</strong>g<br />

<strong>De</strong> dicate d s e rve rs and clus te rs for q uantum ch e m ical and m ole cular<br />

dynam ics s im ulations are available <strong>in</strong> th e <strong>Sch</strong> <strong>ool</strong> and th e re <strong>is</strong> e xce le nt<br />

acce s s to h igh pe rform ance com put<strong>in</strong>g.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

2


3<br />

Applications<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

A l pos tgraduate applications s h ould be m ade via th e Unive rs ity's onl<strong>in</strong>e<br />

application form<br />

h ttp://w w w .ncl.ac.uk /pos tgraduate /apply/applicationform s /<br />

Ple as e do not pr<strong>in</strong>t th e form and pos t it: s ubm it onl<strong>in</strong>e . Afte r s ubm itt<strong>in</strong>g th e<br />

form , you s h ould as k your re fe re e s to s e nd th e ir le tte rs <strong>of</strong> re com m e ndation<br />

to th e adm <strong>is</strong> s ions tutor, Dr Be n H orrock s (b.r.h orrock s @ ncl.ac.uk ).<br />

Pos tgraduate <strong>Re</strong> s e <strong>arch</strong> <strong>De</strong> <strong>gre</strong> e s , Ph D/ MPh il<br />

Your application w i l be cons ide re d on its acade m ic m e rit s e parate ly from<br />

q ue s tions <strong>of</strong> fund<strong>in</strong>g and w e are <strong>in</strong>te re s te d prim arily <strong>in</strong> th e fo low <strong>in</strong>g<br />

<strong>in</strong>form ation:<br />

* Your unive rs ity q ualifications , e .g., BSc - s ubje ct, clas s or GPA, trans cript.<br />

* <strong>Re</strong> le vant w ork e xpe rie nce , e .g., w ith a ch e m ical com pany.<br />

* A brie f s tate m e nt <strong>of</strong> your re s e <strong>arch</strong> <strong>in</strong>te re s ts - 50 w ords <strong>is</strong> s ufficie nt. Ple as e<br />

type th <strong>is</strong> <strong>in</strong>to th e w e b form .<br />

* W h ich s upe rv<strong>is</strong> ors you w ould pre fe r to w ork w ith . Ple as e fe e l fre e to<br />

cons ult th e s taff page s and contact pote ntial s upe rv<strong>is</strong> ors by e m ail to as k<br />

about th e ir re s e <strong>arch</strong> <strong>in</strong>te re s ts , facilitie s and pos s ible proje cts .<br />

Inte rnational s tude nts<br />

Applications are ve ry w e lcom e from <strong>in</strong>te rnational s tude nts . You w i l ne e d to<br />

provide e vide nce <strong>of</strong> your Engl<strong>is</strong> h language ability be fore be g<strong>in</strong>n<strong>in</strong>g your<br />

program m e , h ow e ve r th e Unive rs ity can als o <strong>of</strong>fe r language tra<strong>in</strong><strong>in</strong>g and<br />

s upport dur<strong>in</strong>g your program m e <strong>of</strong> s tudy.<br />

Furth e r <strong>in</strong>form ation, <strong>in</strong>clud<strong>in</strong>g fund<strong>in</strong>g, for ove rs e as pos tgraduate s <strong>is</strong><br />

available at h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong>/pos tgrad/<strong>in</strong>te rnational.h tm


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

My <strong>in</strong>te re s ts lie <strong>in</strong> th e fie ld <strong>of</strong><br />

ch e m ical X-ray crys ta lograph y and<br />

crys tal e ng<strong>in</strong>e e r<strong>in</strong>g at th e <strong>in</strong>te rface<br />

be tw e e n <strong>in</strong>organic coord<strong>in</strong>ation<br />

ch e m <strong>is</strong> <strong>try</strong> and m ate rials s cie nce <strong>of</strong><br />

crys ta l<strong>in</strong>e rare e arth com pounds .<br />

<strong>Ne</strong> w s olve nt-poor s ynth e tic path w ays<br />

for crys ta l<strong>in</strong>e m ole cular ne tw ork s are<br />

e xplore d, com b<strong>in</strong><strong>in</strong>g ionic rare e arth<br />

com ple xe s w ith carboxylato and<br />

am <strong>in</strong>o functional<strong>is</strong> e d organic and<br />

<strong>in</strong>organic te ctons .<br />

Furth e rm ore , crys ta l<strong>in</strong>e m ate rial <strong>is</strong><br />

te s te d aga<strong>in</strong>s t th e e x<strong>is</strong> te nce <strong>of</strong> oth e r<br />

crys ta l<strong>in</strong>e ph as e s <strong>of</strong> th e s am e<br />

com pound (polym orph <strong>is</strong> m ), e .g. by<br />

Dr Ulrich Ba<strong>is</strong> ch<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

4<br />

Dipl.-<strong>Ch</strong> e m ., Unive rs ity <strong>of</strong> Tüb<strong>in</strong>ge n, 2001<br />

Dr. re r. nat., Unive rs ity <strong>of</strong> Munich , 2006<br />

Pos tdoctoral fe low , CNRS LCC, Toulous e ,<br />

2006-7<br />

Pos tdoctoral fe low , Unive rs ity <strong>of</strong> Bologna,<br />

2007-8<br />

EC Marie -Curie Fe low (IEF), Unive rs ity <strong>of</strong><br />

Br<strong>is</strong> tol 2008-9<br />

Le cture r, <strong>Ne</strong> w cas tle Unive rs ity, 2009 -pre s e nt<br />

e m ail: ulrich .ba<strong>is</strong> ch @ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Crys tal e ng<strong>in</strong>e e r<strong>in</strong>g, lanth anide ch e m <strong>is</strong> <strong>try</strong><br />

Se le cte d Publications<br />

[1] [Yb(C 2 O 4 ) 4 ] 5- – a ve rs atile m e tal– organic<br />

build<strong>in</strong>g block for laye re d coord<strong>in</strong>ation<br />

polym e rs . U. Ba<strong>is</strong> ch , D. Braga,<br />

Crys tEngCom m , 2009 , 11, 40.<br />

[2] <strong>Re</strong> m ark able s tructural s im ilaritie s be tw e e n<br />

organic co-crys tals and a m e tal– organic<br />

coord<strong>in</strong>ation ne tw ork – <strong>in</strong>s igh ts <strong>in</strong>to h ydroge n<br />

bonde d aliph atic am m onium ch loride s . U.<br />

Ba<strong>is</strong> ch , K. Rub<strong>in</strong>i, D. Braga, Crys tEngCom m ,<br />

2008, 10, 19 39 .<br />

us <strong>in</strong>g oth e r re action conditions or<br />

e xpos <strong>in</strong>g th e m ate rial to diffe re nt<br />

te m pe rature and pre s s ure . In th <strong>is</strong><br />

m anne r, <strong>of</strong>te n ne w <strong>gre</strong> e n ch e m <strong>is</strong> <strong>try</strong><br />

m e th ods are d<strong>is</strong> cove re d for th e<br />

s ynth e s <strong>is</strong> <strong>of</strong> nove l crys ta l<strong>in</strong>e and<br />

nanocrys ta l<strong>in</strong>e m ate rials .<br />

Crys tal e ng<strong>in</strong>e e r<strong>in</strong>g <strong>is</strong> th e de libe rate<br />

de s ign <strong>of</strong> crys ta l<strong>in</strong>e com pounds<br />

w h e re build<strong>in</strong>g block s are conne cte d<br />

by <strong>in</strong>te rm ole cular <strong>in</strong>te ractions (e .g.<br />

h ydroge n bond<strong>in</strong>g).Th <strong>is</strong> m ole cular<br />

approach <strong>of</strong>fe rs h igh -yie ld, low -<br />

e ne rgy s ynth e tic alte rnative s for<br />

crys ta l<strong>in</strong>e com pou<strong>in</strong>ds .<br />

[3] Nanocrys ta l<strong>in</strong>e lanth anide nitride m ate rials<br />

s ynth e s <strong>is</strong> e d by th e rm al tre atm e nt <strong>of</strong> am ido and<br />

am m <strong>in</strong>e m e ta loce ne s : X-ray s tudie s and DFT<br />

calculations . U. Ba<strong>is</strong> ch , M. Z e une r, N. Barros ,<br />

L. Maron, W . <strong>Sch</strong> nick , <strong>Ch</strong> e m . Eur. J., 2006, 12,<br />

4785.<br />

[4] H om olytic bond s tre ngth s and form ation<br />

rate s <strong>in</strong> h alf-s andw ich ch rom ium alk yl<br />

com ple xe s : re le vance for contro le d radical<br />

polym e riz ation. Y. <strong>Ch</strong> am poure t, U. Ba<strong>is</strong> ch , R.<br />

Poli, L. Tang, J. L. Conw ay, K. M. Sm ith ,<br />

Ange w . <strong>Ch</strong> e m . Int. Ed. 2008, 47, 6069 .


5<br />

Se le cte d Publications<br />

[1] A Donor-Acce ptor Mole cular Dyad Sh ow <strong>in</strong>g<br />

Multiple Ele ctronic Ene rgy-Trans fe r Proce s s e s<br />

<strong>in</strong> Crys ta l<strong>in</strong>e and Am orph ous State s , A. C.<br />

Be nn<strong>is</strong> ton, G. Cople y, A. H arrim an, D. B.<br />

<strong>Re</strong> w <strong>in</strong>s k a, R. W . H arr<strong>in</strong>gton, W . Cle gg, J. Am .<br />

<strong>Ch</strong> e m . Soc. 2008, 130, 7174.<br />

[2] <strong>Re</strong> dox Contro le d Fluore s ce nce Modulation<br />

<strong>in</strong> a BODIPY-q u<strong>in</strong>one Dyad, A. C. Be nn<strong>is</strong> ton,<br />

G. Cople y, K. J. E liott, R. W . H arr<strong>in</strong>gton, W .<br />

Cle gg, Eur. J. Org. <strong>Ch</strong> e m . 2008, 16, 2705.<br />

Dr Andre w C. Be nn<strong>is</strong> ton<br />

Ph D W arw ick Unive rs ity 19 9 1<br />

Pos tdoctoral fe low , Unive rs ity <strong>of</strong> Stras bourg<br />

19 9 1-19 9 2; Unive rs ity <strong>of</strong> Te xas at Aus t<strong>in</strong><br />

19 9 2-9 4<br />

Unive rs ity <strong>of</strong> Glas gow 19 9 4-2001<br />

<strong>Ne</strong> w cas tle Unive rs ity 2001-pre s e nt<br />

Dr Be nn<strong>is</strong> ton co-founde d th e Mole cular<br />

Ph otonics Laboratory (MPL) at <strong>Ne</strong> w cas tle .<br />

te l: 44(0)19 1 222 5706<br />

e m ail: a.c.be nn<strong>is</strong> ton@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Mole cular ph otonics<br />

Dr Be nn<strong>is</strong> ton's re s e <strong>arch</strong> <strong>is</strong> prim arily i lum <strong>in</strong>ation <strong>of</strong> th e s piropyran <strong>is</strong> not<br />

conce rne d w ith th e de s ign and ne ce s s ary, and s e cond-ge ne ration<br />

s ynth e s <strong>is</strong> <strong>of</strong> m ulti-com pone nt s ys te m s are <strong>in</strong> th e pipe l<strong>in</strong>e bas e d on<br />

s upe rm ole cule s for fundam e ntal s e le nos piropyrans .<br />

s tudie s <strong>in</strong> e ne rgy and/or e le ctron A re curr<strong>in</strong>g th e m e <strong>is</strong> th e de ve lopm e nt<br />

trans fe r. Applications <strong>in</strong>clude re al- <strong>of</strong> donor-s pace r-acce ptor as s e m blie s<br />

tim e m onitor<strong>in</strong>g <strong>of</strong> nano-<br />

conta<strong>in</strong><strong>in</strong>g s e ve ral ch rom oph ore s .<br />

e nvironm e nts , pre s s ure -s e ns itive Atte ntion h as turne d to organic-bas e d<br />

m ate rials , ph otoch rom ic m ate rials for m ate rials s uch as th e boron<br />

data re cord<strong>in</strong>g, and biological dipyrrom e th e ne - oligoth ioph e ne<br />

im ag<strong>in</strong>g.<br />

dyad w h ich d<strong>is</strong> plays s <strong>in</strong>gle t-s <strong>in</strong>gle t,<br />

Multi-com pone nt s piropyran-bas e d s <strong>in</strong>gle t-triple t and triple t-triple t e ne rgy<br />

s ys te m s h ave be e n s ynth e s iz e d trans fe r, and als o unde rgoe s ligh t-<br />

w h ich function as ph otoch rom ic <strong>in</strong>duce d e le ctron trans fe r.<br />

s w itch e s th at are ope ne d via an <strong>Re</strong> m ark ably, fas t e le ctron e xch ange<br />

e xciple x <strong>in</strong>te rm e diate . In th e s e , dire ct tak e s place w ith <strong>in</strong> th e crys tal lattice .<br />

[3] Ele ctron Exch ange <strong>in</strong> Conform ationa ly<br />

<strong>Re</strong> s tricte d Donor-Space r-Acce ptor Dyads :<br />

Angle <strong>De</strong> pe nde nce and Involve m e nt <strong>of</strong> Uppe rly<strong>in</strong>g<br />

Excite d State s , A. C. Be nn<strong>is</strong> ton, A.<br />

H arrim an, P. Li, P. V. Pate l, C. A. Sam s , <strong>Ch</strong> e m .<br />

Eur. J., 2008, 14, 1710.<br />

[4] Ele ctron-trans fe r <strong>Re</strong> actions <strong>in</strong> th e 9 -m e s ityl-<br />

10-m e th ylacrid<strong>in</strong>ium ion: Im puritie s , Triple t<br />

State s and Inf<strong>in</strong>ite ly Long-live d <strong>Ch</strong> arge -s h ift<br />

State s ? A. C. Be nn<strong>is</strong> ton, A. H arrim an, J. W .<br />

Ve rh oe ve n, Ph ys . <strong>Ch</strong> e m . <strong>Ch</strong> e m . Ph ys . 2008,<br />

10, 5156.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Dr Cél<strong>in</strong>e Cano<br />

BSc Unive rs ity <strong>of</strong> Poitie rs , France 19 9 9<br />

Ph D Unive rs ity <strong>of</strong> Poitie rs , France 2004<br />

Pos tdoctoral fe low , Unive rs ity <strong>of</strong> Manch e s te r<br />

<strong>Ne</strong> w cas tle Unive rs ity 2005-pre s e nt.<br />

Dr Cano <strong>is</strong> curre ntly Le cture r <strong>in</strong> Me dic<strong>in</strong>al<br />

<strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>.<br />

te l: 44(0) 19 1 222 7060<br />

e m ail: ce l<strong>in</strong>e .cano@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : organic ch e m <strong>is</strong> <strong>try</strong> and drug d<strong>is</strong> cove ry<br />

Drug D<strong>is</strong> cove ry Program m e :<br />

North e rn Ins titute <strong>of</strong> Cance r<br />

<strong>Re</strong> s e <strong>arch</strong><br />

Th e North e rn Ins titute <strong>of</strong> Cance r<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>is</strong> a cros s -faculty Ins titute<br />

w ith <strong>in</strong> th e Unive rs ity bas e d <strong>in</strong> th e<br />

ne w Paul O’Gorm an build<strong>in</strong>g and th e<br />

Be ds on Build<strong>in</strong>g. Our re s e <strong>arch</strong> <strong>is</strong><br />

focus s e d on th e d<strong>is</strong> cove ry <strong>of</strong><br />

<strong>in</strong>h ibitors <strong>of</strong> nove l m ole cular targe ts ,<br />

<strong>in</strong>clud<strong>in</strong>g k e y e nz ym e s l<strong>in</strong>k e d w ith<br />

re s <strong>is</strong> tance to conve ntional radiation<br />

and ch e m oth e rapy. In co laboration<br />

w ith Agouron/Pfiz e r, w e d<strong>is</strong> cove re d<br />

pote nt <strong>in</strong>h ibitors <strong>of</strong> th e e nz ym e<br />

poly(ADPribos e ) polym e ras e 1, for<br />

Se le cte d publications<br />

[1] M. <strong>De</strong> s age -El Murr, C. Cano-Soum i lac, B.<br />

T. Gold<strong>in</strong>g, I. R. H ardcas tle , M. G.<br />

H um m e rs om e , M. Frige rio, N. J. Curt<strong>in</strong>, K. A.<br />

Me ne ar, C. J. Rich ards on, G. C. M. Sm ith , R.<br />

J. Griff<strong>in</strong>. Bioorg. Me d. <strong>Ch</strong> e m . Le tt. 2008, 185,<br />

489 0.<br />

us e w ith DNA-dam ag<strong>in</strong>g anticance r<br />

th e rapie s . Ph as e II cl<strong>in</strong>ical trials are<br />

curre ntly unde rw ay.<br />

Th e m e dic<strong>in</strong>al ch e m <strong>is</strong> <strong>try</strong> group w ork s<br />

<strong>in</strong> co laboration w ith groups <strong>in</strong><br />

<strong>in</strong>dus <strong>try</strong> (As tra Z e ne ca) and<br />

acade m ia (Oxford), to d<strong>is</strong> cove r s m a lm<br />

ole cule <strong>in</strong>h ibitors <strong>of</strong> cance r targe ts .<br />

Curre nt targe ts <strong>in</strong>clude DNAde<br />

pe nde nt prote <strong>in</strong> k <strong>in</strong>as e , oth e r PIKK<br />

fam ily m e m be rs , th e MDM2-p53 and<br />

MDMX-p53 prote <strong>in</strong> prote <strong>in</strong><br />

<strong>in</strong>te ractions , th e cycl<strong>in</strong> de pe nde nt<br />

k <strong>in</strong>as e s , m itotic k <strong>in</strong>as e s , and nove l<br />

targe ts <strong>in</strong> pros tate cance r.<br />

Aus t<strong>in</strong>, B. W . Durk acz Cl<strong>in</strong>. Cance r <strong>Re</strong> s . 2008,<br />

14, 39 84.<br />

[3] C. Cano-Soum i lac. In: Com pre h e ns ive<br />

H e te rocyclic <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong> III, volum e 4, e d. A. R.<br />

Katritz k y. Oxford: Els e vie r, 2008, pp. 1243-<br />

1270; pp. 1271-1304.<br />

[4] J. J. H o lick , L. J. M. Rigore au, C. Cano-<br />

[2] E. W i lm ore , S. L. E liot, T. Ma<strong>in</strong>ou-Fow le r, Soum i lac, X. Cock cr<strong>of</strong>t, N. J. Curt<strong>in</strong>, M.<br />

G. Sum m e rfie ld, G. H . Jack s on, F. O'<strong>Ne</strong> il, C. Frige rio, B. T. Gold<strong>in</strong>g, S. Guiard, I. R.<br />

Low e , A. Carte r, R. H arr<strong>is</strong> , A. R. Pe ttit, C. H ardcas tle , I. H ick s on, M. G. H um m e rs om e e t<br />

Cano-Soum i lac, R. J. Griff<strong>in</strong>, I. G. Cow e l, C. A. al. J. Me d. <strong>Ch</strong> e m . 2007, 50, 19 58.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

6


7<br />

Se le cte d Publications<br />

[1] M. A. Carro l, J. Nairne , G. Sm ith , D. A.<br />

W iddow s on, Radical s cave nge rs : A practical<br />

s olution to th e re producibility <strong>is</strong> s ue <strong>in</strong> th e<br />

fluoridation <strong>of</strong> diaryliodonium s alts , J. Fluor<strong>in</strong>e<br />

<strong>Ch</strong> e m ., 2007, 128, 127.<br />

[2] M. A. Carro l, R. A. W ood, Arylation <strong>of</strong><br />

anil<strong>in</strong>e s : Form ation <strong>of</strong> diarylam <strong>in</strong>e s us <strong>in</strong>g<br />

diaryliodonium s alts , Te trah e dron, 2007, 63,<br />

11349 .<br />

Dr Mich ae l Carro l<br />

Ph D Im pe rial Co le ge , London 19 9 4<br />

Pos tdoctoral fe low , Unive rs ity <strong>of</strong><br />

South am pton 19 9 4-9 5;<br />

BP <strong>Ch</strong> e m icals 19 9 6-9 7<br />

Unive rs ity <strong>of</strong> Cam bridge 19 9 7-9 8<br />

Im pe rial Co le ge 19 9 8-2001<br />

<strong>Ne</strong> w cas tle Unive rs ity 2001-pre s e nt<br />

Dr Carro l <strong>is</strong> th e founde r <strong>of</strong> <strong>Ne</strong> w Im ag<strong>in</strong>g Ltd.<br />

te l: 44(0)19 1 222 7074<br />

e m ail: m .a.carro l@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : s ynth e tic ch e m <strong>is</strong> <strong>try</strong> and radioph arm ace uticals<br />

A m ajor goal <strong>is</strong> th e s ynth e s <strong>is</strong> <strong>of</strong> Th e <strong>in</strong>clus ion <strong>of</strong> s table or<br />

natural products , <strong>in</strong> particular radio<strong>is</strong> otope s a low s th e m ole cule to<br />

e nz ym e <strong>in</strong>h ibitors and re late d be de te cte d w ith a h igh de <strong>gre</strong> e <strong>of</strong><br />

com pounds . H ype rvale nt iod<strong>in</strong>e accuracy, ye t re ta<strong>in</strong> th e activity pr<strong>of</strong>ile<br />

re age nts and <strong>in</strong>te rm e diate s h ave <strong>of</strong> th e ‘natural’ com pound. Th e<br />

provide d a rapid, ve rs atile approach curre nt focus <strong>of</strong> our re s e <strong>arch</strong> <strong>is</strong> th e<br />

to com ple x bioactive s tructure s . W e de ve lopm e nt and com m e rcializ ation<br />

are als o purs u<strong>in</strong>g th e s e le ctive <strong>of</strong> nove l radioph arm ace uticals (e .g. 6-<br />

<strong>in</strong>corporation, <strong>in</strong>to dive rs e organic [<br />

fram e w ork s , <strong>of</strong> e le m e nts not us ua ly<br />

as s ociate d w ith biological s ys te m s -<br />

typica ly fl uor<strong>in</strong>e and s ilicon. A nove l<br />

s ilicon-bas e d clas s <strong>of</strong> antim icrobial<br />

age nts , de rive d from bioactive<br />

ch alcone s , h as be e n de m ons trate d.<br />

18F]FluoroDOPA) for Pos itron<br />

Em <strong>is</strong> s ion Tom ograph y (PET).<br />

Innovative e xpe rim e ntal proce dure s<br />

<strong>in</strong> both batch and flow ch e m <strong>is</strong> <strong>try</strong> us e<br />

autom ate d s ynth e tic ch e m <strong>is</strong> <strong>try</strong><br />

platform s , m icr<strong>of</strong>luidic s ys te m s and<br />

m ultiple advance d analytical<br />

te ch niq ue s .<br />

[3] R. Yan, M. A. Carro l, Th e firs t pre paration<br />

<strong>of</strong> a l re gio<strong>is</strong> om e rs <strong>of</strong> e th yl[ 18 F]fluorobe nz oate s ,<br />

J. Labe l. Com pd. Radioph arm ., 2008, 51, 259 .<br />

[4] M. A. Carro l, R. Yan, L. Brich ard, D.<br />

Solovie v, F. I. Aigbirh io, S<strong>in</strong>gle -s te p s ynth e s <strong>is</strong><br />

<strong>of</strong> N-s ucc<strong>in</strong>im idyl-4-[ 18 F]fluorobe nz oate , J.<br />

Nucl. Me d., 2008, 49 S, 29 8P.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Pr<strong>of</strong>e s s or W i liam Cle gg<br />

Ph D, ScD Unive rs ity <strong>of</strong> Cam bridge<br />

Pos tdoctoral fe low , Gött<strong>in</strong>ge n, Ge rm any<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 84-pre s e nt.<br />

Pr<strong>of</strong>e s s or Cle gg <strong>is</strong> als o re s pons ible for th e<br />

ope ration <strong>of</strong> th e EPSRC National<br />

Crys ta lograph y Se rvice at th e Diam ond<br />

Ligh t Source <strong>in</strong> Oxfords h ire .<br />

te l: 44(0) 19 1 222 6649<br />

e m ail: w .cle gg@ ncl.ac.uk<br />

My m a<strong>in</strong> re s e <strong>arch</strong> activity <strong>is</strong> X-ray<br />

crys ta lograph y, us <strong>in</strong>g m ode rn CCDbas<br />

e d are a-de te ctor e q uipm e nt both<br />

<strong>in</strong> th e local laboratory (late s t<br />

e q uipm e nt <strong>in</strong>s ta le d <strong>in</strong> 2008) and th e<br />

Diam ond Ligh t Source <strong>in</strong> Oxfords h ire .<br />

W e provide facilitie s for crys tal<br />

s tructure de te rm <strong>in</strong>ation to co le ague s<br />

<strong>in</strong> <strong>Ne</strong> w cas tle , <strong>in</strong> oth e r Unive rs itie s <strong>in</strong><br />

th e UK and abroad, and <strong>in</strong> <strong>in</strong>dus <strong>try</strong>.<br />

My re s e <strong>arch</strong> group are als o e ngage d<br />

<strong>in</strong> th e pre paration and<br />

ch aracte r<strong>is</strong> ation <strong>of</strong> a varie ty <strong>of</strong> s -<br />

block (alk ali and alk al<strong>in</strong>e e arth ) m e tal<br />

com ple xe s w ith nitroge n and oxyge n<br />

Se le cte d publications<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : X-ray crys ta lograph y<br />

[1] Synch rotron <strong>Ch</strong> e m ical Crys ta lograph y. J.<br />

<strong>Ch</strong> e m . Soc. Dalton Trans ., 2000, 3223.<br />

[2] <strong>Re</strong> gios e le ctive Te tram e talation <strong>of</strong> Fe rroce ne<br />

<strong>in</strong> a S<strong>in</strong>gle <strong>Re</strong> action: Exte ns ion <strong>of</strong> s -Block<br />

Inve rs e Crow n <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong> to th e d-Block .<br />

donor ligands , particularly organic<br />

am <strong>in</strong>e s , pyridone s , cyanuric acid and<br />

de rivative s ; th e s e range from<br />

m ononucle ar m ole cular com ple xe s to<br />

ne tw ork polym e ric s tructure s .<br />

Anoth e r re s e <strong>arch</strong> th e m e conce rns<br />

s upram ole cular coord<strong>in</strong>ation<br />

ch e m <strong>is</strong> <strong>try</strong>, particularly <strong>of</strong><br />

polycarboxylic acids , w ith both m a<strong>in</strong>group<br />

and trans ition m e tals . One -,<br />

tw o- and th re e -dim e ns ional polym e ric<br />

ne tw ork s h ave be e n ge ne rate d, and<br />

s om e <strong>of</strong> th e m are m icroporous .<br />

<strong>of</strong> th e e ffe ct <strong>of</strong> re action s toich iom e <strong>try</strong> on th e<br />

crys ta l<strong>in</strong>e products form e d <strong>in</strong> th e<br />

potas s ium – cyanurate s ys te m . Acta Crys t.<br />

2006, B62, 79 8.<br />

[4] Synth e s <strong>is</strong> and s tructure s <strong>of</strong> alk ali m e tal<br />

Ange w . <strong>Ch</strong> e m . Int. Ed., 2001, 40, 39 02 (journal com ple xe s <strong>of</strong> <strong>is</strong> oph th alic acid: th e <strong>in</strong>te rplay <strong>of</strong><br />

front cove r).<br />

organic s upram ole cular <strong>in</strong>te ractions and<br />

fle xible m e tal coord<strong>in</strong>ation as s tructure -<br />

[3] Stoich iom e <strong>try</strong>-de pe nde nt s tructure s : an X- dire ct<strong>in</strong>g factors . Crys t. Grow th <strong>De</strong> s ., 2009 , 9 ,<br />

ray and ne utron s <strong>in</strong>gle -crys tal dffraction s tudy 1158.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

8


9<br />

Se le cte d Publications<br />

[1] Synth e s <strong>is</strong> <strong>of</strong> Biaryl Diph os ph <strong>in</strong>e s via a<br />

<strong>Re</strong> gios e le ctive Double Die ls -Alde r<br />

Cycloaddition Elim <strong>in</strong>ation Se q ue nce : Efficie nt<br />

Ligands for th e Pa ladium -Catalyz e d Am <strong>in</strong>ation<br />

<strong>of</strong> Arom atic Brom ide s . S. Doh e rty, C. H .<br />

Sm yth , R. W . H arr<strong>in</strong>gton and W . Cle gg,<br />

Organom e ta lics , 2009 , 28, 5273.<br />

[2] Rh odium Com ple xe s <strong>of</strong> (S)-Me -CATPH OS<br />

and (R)-(S)-JOSIPH OS: H igh ly<br />

Enantios e le ctive Catalys ts for th e As ym m e tric<br />

Dr Sim on Doh e rty<br />

Ph D Unive rs ity Co le ge , London 19 9 0<br />

Pos tdoctoral fe low , Unive rs ity <strong>of</strong> W ate rloo,<br />

Canada 19 9 0-19 9 2; Indiana Unive rs ity 19 9 2-<br />

9 4;<br />

Unive rs ity <strong>of</strong> W ale s , Sw ans e a 19 9 4-19 9 5<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 9 5-2001<br />

Que e n’s Unive rs ity <strong>of</strong> Be lfas t 2001-2004<br />

<strong>Ne</strong> w cas tle Unive rs ity 2004-pre s e nt<br />

te l: 44(0)19 1 222 6537<br />

e m ail: s im on.doh e rty@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : organom e ta lic ch e m <strong>is</strong> <strong>try</strong> and catalys <strong>is</strong><br />

Synth e s <strong>is</strong><br />

Our re s e <strong>arch</strong> <strong>is</strong> bas e d <strong>in</strong> th e are a <strong>of</strong><br />

plat<strong>in</strong>um group m e tal catalys <strong>is</strong> w ith<br />

an e m ph as <strong>is</strong> on de ve lop<strong>in</strong>g<br />

<strong>in</strong>novative route s to ne w fam ilie s <strong>of</strong><br />

ph os ph <strong>in</strong>e s , particularly th os e bas e d<br />

on a biaryl or biaryl-lik e <strong>arch</strong> ite cture .<br />

W e are particularly <strong>in</strong>te re s te d <strong>in</strong><br />

de ve lop<strong>in</strong>g ne w approach e s th at us e<br />

<strong>in</strong>e xpe ns ive build<strong>in</strong>g block s , th at are<br />

ope rationa ly s traigh tforw ard, h igh ly<br />

m odular and th at can be us e d to<br />

cons truct <strong>arch</strong> ite ctura ly uniq ue<br />

ligand fram e w ork s . <strong>Re</strong> ce nt<br />

de ve lopm e nts from our group <strong>in</strong>clude<br />

NUPH OS, NU-BIPH EP, KITPH OS<br />

and CATPH OS, a l <strong>of</strong> w h ich are<br />

com m e rcia ly available from Stre m<br />

<strong>Ch</strong> e m ical Co.<br />

Catalys <strong>is</strong><br />

W e h ave a com pre h e ns ive catalys t<br />

te s t<strong>in</strong>g program m e to e valuate th e<br />

ne w ph os ph <strong>in</strong>e s <strong>in</strong> a range <strong>of</strong><br />

plat<strong>in</strong>um group m e tal catalyz e d<br />

trans form ation. An e xcit<strong>in</strong>g<br />

de ve lopm e nt <strong>in</strong>volve s th e s ynth e s <strong>is</strong><br />

and re s olution <strong>of</strong> atropos CATPH OS<br />

diph os ph <strong>in</strong>e s , a nove l clas s <strong>of</strong> biaryllik<br />

e diph os ph <strong>in</strong>e th at give s e e ’s <strong>in</strong><br />

e xce s s <strong>of</strong> 9 9 % <strong>in</strong> rh odium catalyz e d<br />

as ym m e tric h ydroge nation.<br />

H ydroge nation <strong>of</strong> (E)- and (Z )-β-Aryl-β-<br />

(Acylam <strong>in</strong>o)-v<strong>in</strong>ylph os ph onate s . S. Doh e rty, J.<br />

G. Knigh t, A. L. Be l, S. El-Me nabaw e y, C. M.<br />

Voge ls , A. <strong>De</strong> ck e n, and S. A. W e s tcott,<br />

Te trah e dron: As ym m e <strong>try</strong>, 2009 , 20, 1437.<br />

[3] Can a 1,3-Butadie ne Arch ite cture Com pe te<br />

w ith its Biaryl Counte rpart <strong>in</strong> As ym m e tric<br />

Catalys <strong>is</strong> ? Enantiopure Me -CATPH OS, A<br />

<strong>Re</strong> m ark ably Efficie nt Ligand for As ym m e tric<br />

H ydroge nation. S. Doh e rty, C. H . Sm yth , A.<br />

H arrim an, R. W . H arr<strong>in</strong>gton and W . Cle gg,<br />

Organom e ta lics , 2009 , 28, 888.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Dr Joh n Err<strong>in</strong>gton<br />

BSc Unive rs ity <strong>of</strong> Le e ds 19 77<br />

Ph D Unive rs ity <strong>of</strong> Le e ds 19 80<br />

Pos tdoctral fe low , Indiana Unive rs ity, 19 80-<br />

19 81; QMC, London, 19 82-19 84<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 84-pre s e nt.<br />

Dr Err<strong>in</strong>gton w as H e ad <strong>of</strong> <strong>Sch</strong> <strong>ool</strong> (2002-<br />

2006) and <strong>is</strong> de puty dire ctor <strong>of</strong> th e ce ntre for<br />

catalys <strong>is</strong> and <strong>in</strong>te ns ifie d proce s s <strong>in</strong>g.<br />

te l: 44(0) 19 1 222 6643<br />

e m ail: joh n.e rr<strong>in</strong>gton@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Inorganic and m e talorganic s ynth e s <strong>is</strong><br />

My re s e <strong>arch</strong> <strong>in</strong>volve s<br />

<strong>in</strong>organic/m e talorganic s ynth e s <strong>is</strong> and<br />

re activity at th e boundary be tw e e n<br />

th e m ole cular s cale and th e s olid<br />

s tate , w h e re e ffe cts ar<strong>is</strong> <strong>in</strong>g from th e<br />

trans ition from s m a l m ole cule s to<br />

e xte nde d s olid s ys te m s provide<br />

opportunitie s for advance s <strong>in</strong><br />

catalys <strong>is</strong> and m ate rials s cie nce .<br />

Me tal Alk oxide s<br />

W e h ave an <strong>in</strong>te re s t <strong>in</strong> h e te rom e ta lic<br />

alk oxide s as s <strong>in</strong>gle -s ource<br />

pre curs ors to fe rroe le ctric, non-l<strong>in</strong>e ar<br />

optical and catalytic m ate rials .<br />

Se le cte d publications<br />

[1] R. J. Err<strong>in</strong>gton, S. S. Pe tk ar, P. S.<br />

Middle ton, W . McFarlane , W . Cle gg, R. W .<br />

H arr<strong>in</strong>gton, Dalton Trans ., 2007, 5211<br />

Mole cular m e tal oxide ch e m <strong>is</strong> <strong>try</strong><br />

Polyoxom e talate s are nanos cale<br />

m ole cular oxide s w ith a varie ty <strong>of</strong><br />

s h ape s , s iz e s and e le ctronic<br />

prope rtie s . W e s tudy fundam e ntal<br />

ag<strong>gre</strong> gation and dynam ic s olution<br />

proce s s e s us <strong>in</strong>g m ult<strong>in</strong>ucle ar NMR<br />

and m as s s pe ctrom e <strong>try</strong>.<br />

Catalys t de ve lopm e nt<br />

W e are e xplor<strong>in</strong>g w ays <strong>of</strong> trans fe rr<strong>in</strong>g<br />

catalytic re actions <strong>of</strong> h e te roge ne ous<br />

m e tal oxide s <strong>in</strong>to th e s olution ph as e .<br />

Co laborators <strong>in</strong>clude Joh ns on-<br />

Matth e y, Davy Proce s s Te ch nology<br />

and ACAL Ene rgy.<br />

A. H oulton, L. H . Lie , S. N. Patole , Ange w .<br />

<strong>Ch</strong> e m . Int. Ed. Eng, 2005, 44, 1254<br />

[4] S. Doh e rty, R. J. Err<strong>in</strong>gton, N. H ous le y, W .<br />

Cle gg, Organom e ta lics , 2004, 23, 2382<br />

[2] R. J. Err<strong>in</strong>gton, S. S. Pe tk ar, P. S.<br />

[5] Ge ne ral Strate gie s for Non-Aq ue ous<br />

Middle ton, W . McFarlane , W . Cle gg, R. A. Polyoxom e talate Synth e s <strong>is</strong> . R. J. Err<strong>in</strong>gton, <strong>in</strong><br />

Coxa l, R. W . H arr<strong>in</strong>gton, J. Am . <strong>Ch</strong> e m . Soc. Polyoxom e talate Mole cular Scie nce , J. J.<br />

2007, 129 , 12181<br />

[3] R. J. Err<strong>in</strong>gton, S. S. Pe tk ar, B. R. H orrock s ,<br />

Borrás -Alm e nar, E. Coronado, A. Mü le r, M. T.<br />

Pope Eds ., Kluw e r Dordre ch t, 2003, pp 55-77.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

10


11<br />

Se le cte d Publications<br />

[1] Dynam ic Com b<strong>in</strong>atorial Librarie s<br />

Cons tructe d on Polym e r Scaffolds , D. A.<br />

Fulton, Org. Le tt. 2008, 10, 329 1.<br />

[2] Glycoconjugate s <strong>of</strong> gadol<strong>in</strong>ium com ple xe s<br />

for MRI applications , D. A. Fulton, E. M.<br />

Ele m e nto, S. Aim e , L. <strong>Ch</strong> aabane , M. Botta, D.<br />

Park e r, <strong>Ch</strong> e m . Com m un. 2006, 1064.<br />

[3] Efficie nt <strong>Re</strong> laxivity Ench ance m e nt <strong>in</strong><br />

<strong>De</strong> ndritic Gadol<strong>in</strong>ium Conjugate s : Effe ctive<br />

Dr David Fulton<br />

BSc Strath clyde Unive rs ity, 19 9 6<br />

Ph D Unive rs ity <strong>of</strong> California Los Ange le s ,<br />

2001<br />

Qu<strong>in</strong>tile s 2002<br />

Pos tdoctoral fe low , Unive rs ity <strong>of</strong> Durh am ,<br />

2003-2005<br />

<strong>Ne</strong> w cas tle Unive rs ity 2006-pre s e nt<br />

Dr Fulton <strong>is</strong> an RCUK Acade m ic Fe low <strong>in</strong><br />

Nanos cie nce .<br />

te l: 44(0)19 1 222 7065<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Organic s upram ole cular and polym e r ch e m <strong>is</strong> <strong>try</strong><br />

W e are organic ch e m <strong>is</strong> ts w ith<br />

<strong>in</strong>te re s ts <strong>in</strong> s upram ole cular and<br />

polym e r ch e m <strong>is</strong> <strong>try</strong>.<br />

Polym e r-Scaffolde d Dynam ic<br />

Com b<strong>in</strong>atorial Librarie s<br />

Can w h o ly s ynth e tic m acrom ole cule s<br />

m im ic th e m ole cular re cognition and<br />

catalytic prope rtie s <strong>of</strong> natural<br />

prote <strong>in</strong>s ? W e are apply<strong>in</strong>g ide as from<br />

th e fie ld <strong>of</strong> dynam ic com b<strong>in</strong>atorial<br />

ch e m <strong>is</strong> <strong>try</strong> to addre s s th <strong>is</strong> ch a le nge .<br />

Dynam ic Covale nt Polym e r-Bas e d<br />

Nanos tructure s<br />

Synth e tic organic and polym e r<br />

ch e m <strong>is</strong> trie s are be <strong>in</strong>g us e d to<br />

pre pare nove l polym e r build<strong>in</strong>g<br />

block s w ith th e ability to s e lfas<br />

s e m ble <strong>in</strong>to s tructure s , w h ich<br />

pos s e s s re s pons ive and adaptive<br />

prope rtie s . W e are us <strong>in</strong>g dynam ic<br />

covale nt bonds to facilitate th e s e lfas<br />

s e m bly proce s s .<br />

Dynam ic Covale nt Se lf-As s e m bly<br />

W e are apply<strong>in</strong>g dynam ic covale nt<br />

ch e m <strong>is</strong> <strong>try</strong>, w h ich us e s re ve rs ible<br />

covale nt bond-form <strong>in</strong>g re actions , to<br />

as s e m ble de s igne d organic build<strong>in</strong>g<br />

block s , to form e xotic m ole cule s w ith<br />

unus ual <strong>arch</strong> ite cture s .<br />

Motional Coupl<strong>in</strong>g <strong>in</strong> Me dium Mole cular W e igh t<br />

Conjugate s , D. A. Fulton, M. O'H a loran, D.<br />

Park e r, K. Se nanayak e , M. Botta, S. Aim e ,<br />

<strong>Ch</strong> e m . Com m un. 2005, 474.<br />

[4] Prob<strong>in</strong>g polyvale ncy <strong>in</strong> artificial s ys te m s<br />

e xh ibit<strong>in</strong>g m ole cular re cognition, D. A. Fulton,<br />

S. J. Cantri l, J. F. Stoddart, J. Org. <strong>Ch</strong> e m .<br />

2002, 67, 79 68.<br />

[5] <strong>Ne</strong> oglycoconjugate s bas e d on cyclode xtr<strong>in</strong>s<br />

and calixare ne s , D. A. Fulton, J. F. Stoddart,<br />

Bioconjug. <strong>Ch</strong> e m . 2001, 12, 655.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Pr<strong>of</strong>e s s or Be rnard Gold<strong>in</strong>g<br />

BSc Unive rs ity <strong>of</strong> Manch e s te r, 19 62<br />

Ph D Unive rs ity <strong>of</strong> Manch e s te r, 19 65<br />

Pos tdoctoral fe low , ETH 19 65-67<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 83-pre s e nt.<br />

Pr<strong>of</strong>e s s or Gold<strong>in</strong>g <strong>is</strong> a s e nior re s e <strong>arch</strong><br />

<strong>in</strong>ve s tigator and <strong>is</strong> s cie ntific dire ctor <strong>of</strong> th e<br />

com pany <strong>Ne</strong> w <strong>Ch</strong> e m Te ch nologie s .<br />

te l: 44(0) 19 1 222 6647<br />

e m ail: b.t.gold<strong>in</strong>g@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Organic, m e dic<strong>in</strong>al and biological ch e m <strong>is</strong> <strong>try</strong><br />

Enz ym e Me ch an<strong>is</strong> m s<br />

Es pe cia ly unus ual or ‘im pos s ible ’<br />

re actions <strong>in</strong>clud<strong>in</strong>g th os e for w h ich<br />

radicals are <strong>in</strong>te rm e diate s (e .g.<br />

coe nz ym e B12-de pe nde nt re actions ,<br />

flav<strong>in</strong>-de pe nde nt de h ydratas e s ,<br />

h ydroge nas e s ).<br />

Mole cular Toxicology<br />

Us e <strong>of</strong> cob(I)alam <strong>in</strong> as an analytical<br />

t<strong>ool</strong> <strong>in</strong> toxicology; pos s ible role for<br />

vitam <strong>in</strong> B12 as a de fe nce m e ch an<strong>is</strong> m<br />

aga<strong>in</strong>s t e le ctroph ilic xe nobiotics ;<br />

m ole cular m e ch an<strong>is</strong> m s <strong>in</strong><br />

carc<strong>in</strong>oge ne s <strong>is</strong> (e s pe cia ly be nz e ne ,<br />

<strong>is</strong> opre ne and ch loropre ne ).<br />

Se le cte d publications<br />

[1] P. Frie drich , D. J. Darle y, B. T. Gold<strong>in</strong>g, W .<br />

Buck e l, Th e com ple te s te re och e m <strong>is</strong> <strong>try</strong> <strong>of</strong> th e<br />

e nz ym atic de h ydration <strong>of</strong> 4-h ydroxybutyryl<br />

coe nz ym e A to crotonyl coe nz ym e A. Ange w .<br />

<strong>Ch</strong> e m . Int. Ed. 2008, 47, 3254.<br />

[2] W . Buck e l, C. Kratk y, B. T. Gold<strong>in</strong>g,<br />

Stabil<strong>is</strong> ation <strong>of</strong> m e th yle ne radicals by<br />

cob(II)alam <strong>in</strong> <strong>in</strong> coe nz ym e B12 de pe nde nt<br />

m utas e s , <strong>Ch</strong> e m . Eur. J., 2006, 12, 352.<br />

Anticance r Drug <strong>De</strong> s ign<br />

Rational de s ign <strong>of</strong> ne w anticance r<br />

age nts bas e d on th e m ole cular<br />

path ology <strong>of</strong> cance r; prote <strong>in</strong> targe ts<br />

<strong>in</strong>clude DNA-prote <strong>in</strong> k <strong>in</strong>as e , cycl<strong>in</strong><br />

de pe nde nt k <strong>in</strong>as e s and m dm 2/p53.<br />

Synth e tic Organic <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Synth e s <strong>is</strong> <strong>of</strong> biologica ly active<br />

m ole cule s <strong>in</strong>clud<strong>in</strong>g nove l am <strong>in</strong>o<br />

acids and polyam <strong>in</strong>e s ; ne w<br />

m e th odology <strong>in</strong>clud<strong>in</strong>g prote ct<strong>in</strong>g<br />

groups ; us e <strong>of</strong> trifluoroe th anol as a<br />

m agic s olve nt <strong>in</strong> s ynth e s <strong>is</strong> .<br />

h ttp://w w w .ne w ch e m te ch nologie s .com<br />

[3] R. J. Griff<strong>in</strong>, A. H e nde rs on, N. J. Curt<strong>in</strong>, A.<br />

Ech alie r, J. A. Endicott, I. R. H ardcas tle , D. R.<br />

<strong>Ne</strong> w e l, M. E. Noble , L. Z . W ang, B. T. Gold<strong>in</strong>g.<br />

Se <strong>arch</strong> <strong>in</strong>g for cycl<strong>in</strong>-de pe nde nt k <strong>in</strong>as e<br />

<strong>in</strong>h ibitors us <strong>in</strong>g a ne w variant <strong>of</strong> th e Cope<br />

e lim <strong>in</strong>ation. J. Am . <strong>Ch</strong> e m . Soc. 2006, 128,<br />

6012.<br />

[4] A. J. Pie rik , T. Graf, L. Pe m be rton, B. T.<br />

Gold<strong>in</strong>g, J. <strong>Re</strong> te y. But-3-e ne -1,2-diol: A<br />

m e ch an<strong>is</strong> m -bas e d active s ite <strong>in</strong>h ibitor for<br />

coe nz ym e B-12-de pe nde nt glyce rol<br />

de h ydratas e , <strong>Ch</strong> e m Bio<strong>Ch</strong> e m , 2008, 9 , 2268.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

12


13<br />

Se le cte d Publications<br />

[1] C. Rie d<strong>in</strong>ge r, J. A. Endicott, S. J. Ke m p, L.<br />

A. Sm yth , A. W ats on, E. Vale ur, R. J. Griff<strong>in</strong>, B.<br />

T. Gold<strong>in</strong>g, I. R. H ardcas tle , M. E. M. Noble , J.<br />

M. McDonne l. Analys <strong>is</strong> <strong>of</strong> <strong>Ch</strong> e m ical Sh ift<br />

<strong>Ch</strong> ange s <strong>Re</strong> ve als th e B<strong>in</strong>d<strong>in</strong>g-m ode s <strong>of</strong><br />

Is o<strong>in</strong>dol<strong>in</strong>one Inh ibitors <strong>of</strong> th e MDM2-p53<br />

Inte raction. J. Am . <strong>Ch</strong> e m . Soc. 2008, 130,<br />

16038.<br />

[2] E. W i lm ore , S. L. E liott, T. Ma<strong>in</strong>ou-Fow le r,<br />

G. P. Sum m e rfie ld, G. H . Jack s on, C. Low e , N.<br />

Pr<strong>of</strong>e s s or Roge r Griff<strong>in</strong><br />

BSc Ph arm acy, Unive rs ity <strong>of</strong> Ports m outh ,<br />

19 81<br />

Ph D, As ton Unive rs ity, 19 85<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 9 0-pre s e nt<br />

Pr<strong>of</strong>e s s or Griff<strong>in</strong> <strong>is</strong> a m e m be r <strong>of</strong> th e<br />

North e rn Ins titute for Cance r <strong>Re</strong> s e <strong>arch</strong><br />

(NICR)<br />

te l: 44(0)19 1 222 859 1<br />

e m ail: r.j.griff<strong>in</strong>@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Me dic<strong>in</strong>al ch e m <strong>is</strong> <strong>try</strong> & anticance r drug d<strong>is</strong> cove ry<br />

Th e de s ign, s ynth e s <strong>is</strong> and biological<br />

e valuation <strong>of</strong> antitum our drugs act<strong>in</strong>g<br />

on nove l targe ts as s ociate d w ith th e<br />

m ole cular path ology <strong>of</strong> cance r. Th e<br />

de ve lopm e nt <strong>of</strong> age nts w ith th e<br />

pote ntial to s yne rg<strong>is</strong> e th e antitum our<br />

activity <strong>of</strong> e s tabl<strong>is</strong> h e d drugs by<br />

m odulat<strong>in</strong>g re s <strong>is</strong> tance proce s s e s<br />

(re s <strong>is</strong> tance m odify<strong>in</strong>g age nts ).<br />

Anticance r Drug D<strong>is</strong> cove ry<br />

Th e Me dic<strong>in</strong>al <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong> Group <strong>is</strong> a<br />

core div<strong>is</strong> ion <strong>of</strong> th e Cance r <strong>Re</strong> s e <strong>arch</strong><br />

UK Drug D<strong>is</strong> cove ry Program m e <strong>of</strong><br />

th e North e rn Ins titute for Cance r<br />

<strong>Re</strong> s e <strong>arch</strong> (NICR) at <strong>Ne</strong> w cas tle<br />

Unive rs ity. Th e ove ra l obje ctive s <strong>of</strong><br />

th e Group are th e de s ign, s ynth e s <strong>is</strong><br />

and biological e valuation <strong>of</strong> ne w<br />

antitum our age nts . In addition to th e<br />

de s ign <strong>of</strong> com pounds dire cte d at<br />

targe ts ide ntifie d from an<br />

unde rs tand<strong>in</strong>g <strong>of</strong> th e m ole cular<br />

path ology <strong>of</strong> cance r, th e de ve lopm e nt<br />

<strong>of</strong> age nts (re s <strong>is</strong> tance -m odifie rs ) th at<br />

pote ntiate th e antitum our activity <strong>of</strong><br />

e x<strong>is</strong> t<strong>in</strong>g drugs by m odulat<strong>in</strong>g a<br />

re s <strong>is</strong> tance m e ch an<strong>is</strong> m <strong>is</strong> a m ajor<br />

re s e <strong>arch</strong> th e m e . Th e NICR Me dic<strong>in</strong>al<br />

<strong>Ch</strong> e m <strong>is</strong> <strong>try</strong> Group h as e xte ns ive<br />

co laborations w ith co le ague s w ith <strong>in</strong><br />

th e <strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>.<br />

Bow n, A. Carte r, A. Pe ttitt, C. Cano-Soum i lac,<br />

R. J. Griff<strong>in</strong>, I. Cow e l, C. A. Aus t<strong>in</strong>, B. W .<br />

Durk acz . DNA-de pe nde nt prote <strong>in</strong> k <strong>in</strong>as e <strong>is</strong> a<br />

th e rape utic targe t and an <strong>in</strong>dicator <strong>of</strong> poor<br />

prognos <strong>is</strong> <strong>in</strong> B-ce l ch ronic lym ph ocytic<br />

le uk ae m ia. Cl<strong>in</strong>. Cance r <strong>Re</strong> s . 2008, 14, 39 84.<br />

[3] O. R. Barbe au, R. J. Griff<strong>in</strong>, I. R.<br />

H ardcas tle , G. C. M. Sm ith , C. Rich ards on, W .<br />

Cle gg, R. W . H arr<strong>in</strong>gton, B. T. Gold<strong>in</strong>g.<br />

Qu<strong>in</strong>ol<strong>in</strong>one and pyridopyrim id<strong>in</strong>one <strong>in</strong>h ibitors<br />

<strong>of</strong> th e DNA-de pe nde nt prote <strong>in</strong> k <strong>in</strong>as e (DNA-<br />

PK). Org. Biom ol. <strong>Ch</strong> e m . 2007, 5, 2670.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Dr Mich ae l H a l<br />

M<strong>Ch</strong> e m , Unive rs ity <strong>of</strong> Oxford, 19 9 9<br />

DPh il, Unive rs ity <strong>of</strong> Oxford, 2003<br />

Pos tdoctoral fe low , Unive rs ity Co le ge<br />

Dubl<strong>in</strong>, Ire land, 2004-5;<br />

École Supérie ure de Ph ys iq ue e t de <strong>Ch</strong> im ie<br />

Indus trie le s , Par<strong>is</strong> , 2006.<br />

<strong>Ne</strong> w cas tle Unive rs ity 2007-pre s e nt.<br />

Dr H a l als o runs our MSc <strong>in</strong> Drug <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>.<br />

te l: 44(0) 19 1 222 7321<br />

e m ail: m .h a l@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Organic Synth e s <strong>is</strong> and Mar<strong>in</strong>e Natural Products<br />

Synth e s <strong>is</strong> <strong>of</strong> Natural Products<br />

Curre nt total s ynth e s <strong>is</strong> targe ts are<br />

bas e d on th e pyrrole -im idaz ole<br />

alk aloids , a large fam ily <strong>of</strong> com ple x<br />

natural products found <strong>in</strong> m ar<strong>in</strong>e<br />

s ponge s . W e are <strong>in</strong>ve s tigat<strong>in</strong>g nove l<br />

Die ls -Alde r <strong>in</strong>itiate d cas cade<br />

re actions as fle xible route s for th e<br />

s te re os e le ctive s ynth e s <strong>is</strong> <strong>of</strong> th e core<br />

s tructure s <strong>of</strong> th e s e com pounds .<br />

Synth e tic Me th odology via<br />

Organoe le m e nt <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

W e are curre ntly de ve lop<strong>in</strong>g a ne w<br />

m e th od for th e rapid s ynth e s <strong>is</strong> <strong>of</strong> α,βuns<br />

aturate d δ lactone s (a com m on<br />

Se le cte d publications<br />

[1] V. Drua<strong>is</strong> , M. J. H a l, C. Cors i, S. V.<br />

W e nde born, C. Me ye r, J. Cos s y. A Conve rge nt<br />

Approach tow ards th e C 1 – C 11 Subunit <strong>of</strong><br />

Ph os lactom yc<strong>in</strong>s and Form al Synth e s <strong>is</strong> <strong>of</strong><br />

Ph os lactom yc<strong>in</strong> B. Org. Le tt. 2009 , 11(4), 9 35.<br />

[2] J. Robe rts on, M. J. H a l, S. P. Gre e n.<br />

Ste re os pe cific α-(m e th yl)a lylation <strong>of</strong><br />

h ydroxyalde h yde s by s ilatropic e ne cycl<strong>is</strong> ation.<br />

Te trah e dron 2009 , 65(28), 5541.<br />

cons titue nt <strong>of</strong> polyk e tide natural<br />

products ) us <strong>in</strong>g e nantios e le ctive<br />

Mannich re actions com b<strong>in</strong>e d w ith<br />

cum m ulate d ph os ph orous ylide<br />

ch e m <strong>is</strong> <strong>try</strong>.<br />

Is olation <strong>of</strong> <strong>Ne</strong> w Bioactive Natural<br />

Products<br />

W e are w ork <strong>in</strong>g w ith s taff from th e<br />

<strong>Sch</strong> <strong>ool</strong>s <strong>of</strong> Biology and Mar<strong>in</strong>e<br />

Scie nce and Te ch nology to ide ntify<br />

ne w bioactive (antibacte rial and<br />

anticance r) natural products de rive d<br />

from bacte ria <strong>is</strong> olate d from de e p s e a<br />

s e dim e nts and tropical m ar<strong>in</strong>e<br />

s ponge s .<br />

[3] A. Loude t, R. Bandich h or, K. Burge s s , A.<br />

Palm a, S. O. McDonne l, M. J. H a l, D.<br />

O'Sh e a, B,O-<strong>Ch</strong> e late d Az adipyrrom e th e ne s<br />

as <strong>Ne</strong> ar-IR Probe s . Org. Le tt. 2008, 10, 4771.<br />

[4] J. Robe rts on, S. P. Gre e n, M. J. H a l, A. J.<br />

Tyrre l, W . P. Uns w orth , Furth e r s tudie s on<br />

s ilatropic carbonyl e ne cycl<strong>is</strong> ations : βcrotyl(diph<br />

e nyl)s ilyloxy alde h yde s ubs trate s ;<br />

s ynth e s <strong>is</strong> <strong>of</strong> 2-de oxy-2-C-ph e nylh e xos e s . Org.<br />

Biom ol. <strong>Ch</strong> e m . 2008, 6, 2628.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

14


15<br />

Th e North e rn Ins titute <strong>of</strong> Cance r<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>is</strong> a cros s -faculty Ins titute<br />

w ith <strong>in</strong> th e Unive rs ity bas e d <strong>in</strong> th e<br />

ne w Paul O’Gorm an build<strong>in</strong>g and th e<br />

Be ds on Build<strong>in</strong>g. Synth e tic organic<br />

and m e dic<strong>in</strong>al ch e m <strong>is</strong> <strong>try</strong> form th e<br />

back bone <strong>of</strong> th e drug d<strong>is</strong> cove ry<br />

proje cts w ith <strong>in</strong> th e NICR. Our<br />

re s e <strong>arch</strong> <strong>is</strong> focus s e d on th e<br />

d<strong>is</strong> cove ry <strong>of</strong> <strong>in</strong>h ibitors <strong>of</strong> nove l<br />

m ole cular targe ts w ith <strong>in</strong> cance r,<br />

<strong>in</strong>clud<strong>in</strong>g k e y e nz ym e s l<strong>in</strong>k e d w ith<br />

re s <strong>is</strong> tance to conve ntional radiation<br />

and ch e m oth e rapy. One proje ct, <strong>in</strong><br />

co laboration w ith Agouron/Pfiz e r, le d<br />

Se le cte d Publications<br />

[1] F. M<strong>arch</strong> e tti, K. L. Sayle , J. Be ntle y, A. H .<br />

Calve rt, W . Cle gg, N. J. Curt<strong>in</strong>, J. A. Endicott,<br />

B. T. Gold<strong>in</strong>g, R. J. Griff<strong>in</strong>, K. H agge rty, R. W .<br />

H arr<strong>in</strong>gton, V. Me s guich e , D. R. <strong>Ne</strong> w e l, M. E.<br />

M. Noble , R. J. Pars ons , D. J. Pratt, L. Z .<br />

W ang, I. R. H ardcas tle , Org. Biom ol. <strong>Ch</strong> e m .<br />

2007, 1577.<br />

[2] J. J. H o lick , Laure nt J. M. Rigore au, Ce l<strong>in</strong>e<br />

Cano-Soum i lac, X. Cock cr<strong>of</strong>t, N. J. Curt<strong>in</strong>,<br />

Mark Frige rio, Be rnard T. Gold<strong>in</strong>g, S. Guiard,<br />

Dr Ian H ardcas tle<br />

BSc Br<strong>is</strong> tol Unive rs ity, 19 87<br />

Ph D Manch e s te r Unive rs ity, 19 9 0<br />

Pos tdoctoral fe low , Ins titute <strong>of</strong> Cance r<br />

<strong>Re</strong> s e <strong>arch</strong> , 19 9 0-19 9 9<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 9 9 -pre s e nt<br />

Dr H ardcas tle <strong>is</strong> a m e m be r <strong>of</strong> th e North e rn<br />

Ins titute for Cance r <strong>Re</strong> s e <strong>arch</strong> (NICR)<br />

te l: 44(0)19 1 222 59 34<br />

e m ail: i.r.h ardcas tle @ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Me dic<strong>in</strong>al ch e m <strong>is</strong> <strong>try</strong> and drug d<strong>is</strong> cove ry<br />

th e e nz ym e poly(ADPribos e )<br />

polym e ras e 1 (PARP 1), for us e w ith<br />

DNA-dam ag<strong>in</strong>g anticance r th e rapie s .<br />

Ph as e II cl<strong>in</strong>ical trials are curre ntly<br />

unde rw ay w ith a PARP 1 <strong>in</strong>h ibitor<br />

from th <strong>is</strong> program m e .<br />

Th e m e dic<strong>in</strong>al ch e m <strong>is</strong> <strong>try</strong> group w ork s<br />

<strong>in</strong> co laboration w ith groups <strong>in</strong><br />

<strong>in</strong>dus <strong>try</strong> and acade m ia, to d<strong>is</strong> cove r<br />

s m a l-m ole cule <strong>in</strong>h ibitors <strong>of</strong> cance r<br />

targe ts and to f<strong>in</strong>d th e rapie s for<br />

cance r w h ich can be us e d to tre at<br />

patie nts .<br />

h ttp://w w w .ncl.ac.uk /nicr<br />

to th e d<strong>is</strong> cove ry <strong>of</strong> pote nt <strong>in</strong>h ibitors <strong>of</strong><br />

Ian R. H ardcas tle , Ian H ick s on, Marc G.<br />

H um m e rs one , Ke ith A. Me ne ar, N. M. B.<br />

Mart<strong>in</strong>, Ian Matth e w s , David R. <strong>Ne</strong> w e l, Rach e l<br />

Ord, Carol<strong>in</strong>e J. Rich ards on, G. C. M. Sm ith ,<br />

R. J. Griff<strong>in</strong> J. Me d. <strong>Ch</strong> e m . 2007, 50, 19 58.<br />

[3] I. R. H ardcas tle , S. U. Ah m e d, H . Atk <strong>in</strong>s , G.<br />

Farnie , B. T. Gold<strong>in</strong>g, R. J. Griff<strong>in</strong>, S. Guye nne ,<br />

C. H utton, P. Kä lblad, S. J. Ke m p, M. S.<br />

Kitch <strong>in</strong>g, D. R. <strong>Ne</strong> w e l, S. Norbe do, J. S.<br />

North e n, R. J. <strong>Re</strong> id, K. Saravanan, H . M. G.<br />

W i le m s , J. Lune c, J. Me d. <strong>Ch</strong> e m . 2006, 49 ,<br />

6209 .<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong> 16<br />

Pr<strong>of</strong>e s s or Anth ony H arrim an<br />

As s <strong>is</strong> tant Dire ctor, Royal Ins titution <strong>of</strong> Gre at<br />

Brita<strong>in</strong> (London) 19 78-88<br />

Dire ctor, Ce nte r for Fas t K<strong>in</strong>e tics <strong>Re</strong> s e <strong>arch</strong> ,<br />

Th e Unive rs ity <strong>of</strong> Te xas at Aus t<strong>in</strong>, 19 88-19 9 5<br />

Unive rs ité Lou<strong>is</strong> Pas te ur de Stras bourg 19 9 5-<br />

2000<br />

<strong>Ne</strong> w cas tle Unive rs ity 2000-pre s e nt<br />

Co-founde r, Mole cular Ph otonics Laboratory<br />

Te l: + 44 (0)19 1 222 8660<br />

E-m ail: Anth ony.h arrim an@ ncl.ac.uk<br />

Se le cte d publications<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Mole cular ph otoph ys ics<br />

Ene rgy Trans fe r<br />

Th e Förs te r th e ory w ork s w e l<br />

provide d th e s e paration d<strong>is</strong> tance<br />

<strong>gre</strong> atly e xce e ds th e s um <strong>of</strong> th e<br />

m ole cular radii for donor and<br />

acce ptor. W h e n th e re actants are<br />

clos e ly s pace d and l<strong>in</strong>k e d via an<br />

organic conne ctor, it <strong>is</strong> com m on to<br />

f<strong>in</strong>d th at <strong>De</strong> xte r-type e le ctron<br />

e xch ange com ple m e nts Förs te r-type<br />

e ne rgy trans fe r and Förs te r th e ory<br />

cannot be applie d. W e de s ign and<br />

s tudy clos e ly-s pace d m ole cular<br />

dyads pos s e s s <strong>in</strong>g rigid and w e lde<br />

f<strong>in</strong>e d ge om e trie s w h e re Förs te r<br />

th e ory can be te s te d.<br />

[1] R. Z ie s s e l, M. A. H . Alam iry, K. J. E liott, A.<br />

H arrim an, Ange w . <strong>Ch</strong> e m . Int. Ed., 2009 , 48,<br />

2772.<br />

[2] F. Odobe l, M. Se ve rac, Y. Pe le gr<strong>in</strong>, E.<br />

Blart, C. Fos s e , C. Canniz z o, C. R. Maye r, K.<br />

J. Eliott, A. H arrim an, <strong>Ch</strong> e m . Eur. J. 2009 , 15,<br />

3130.<br />

[3] A. H arrim an, L. J. Ma lon, R. Z ie s s e l, <strong>Ch</strong> e m .<br />

Eur. J. 2008, 14, 11461.<br />

Ph otoch rom ic m ate rials<br />

Our w ork <strong>in</strong> th <strong>is</strong> are a <strong>is</strong> bas e d on th e<br />

de s ign <strong>of</strong> ne w ph otoch rom ic s ys te m s<br />

th at unde rgo an ultrafas t ge om e <strong>try</strong><br />

ch ange unde r puls e d ligh t e xcitation.<br />

Com putational ch e m <strong>is</strong> <strong>try</strong><br />

Our w ork s e e k s an im prove d<br />

unde rs tand<strong>in</strong>g <strong>of</strong> h ow pote ntial<br />

e ne rgy lands cape s e volve as k e y<br />

parts <strong>of</strong> a m ole cule unde rgo<br />

trans lational m otion. Such m ole cular<br />

(or fluore s ce nt) rotors can be us e d to<br />

m onitor frictional force s be tw e e n th e<br />

rotor and th e s urround<strong>in</strong>g<br />

e nvironm e nt.<br />

[4] A. C. Be nn<strong>is</strong> ton, A. H arrim an, P. Y. Li, P. V.<br />

Pate l, C. A. Sam s , <strong>Ch</strong> e m . Eur. J. 2008, 14,<br />

1710.<br />

[5] H . J. Van Ram e s donk , B. H . Bak k e r, M. M.<br />

Groe ne ve ld, J. W . Ve rh oe ve n, B. D. A le n, J.<br />

P. Ros tron, A. H arrim an, J. Ph ys . <strong>Ch</strong> e m . A<br />

2006, 110, 13145.<br />

[6] A. H arrim an, G. Iz z e t, R. Z ie s s e l, J. Am .<br />

<strong>Ch</strong> e m . Soc. 2006, 128, 10868.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong>


17<br />

Iron-Sulfur-Bas e d Clus te rs<br />

Fe -S-bas e d clus te rs are found <strong>in</strong><br />

m any m e ta loe nz ym e s , w h e re th e y<br />

play role s as dive rs e as : e le ctrontrans<br />

fe r m e diators ; iron s e ns ors and<br />

th e s ubs trate b<strong>in</strong>d<strong>in</strong>g s ite s <strong>in</strong> re dox<br />

and non-re dox e nz ym atic re actions .<br />

W e are <strong>in</strong>ve s tigat<strong>in</strong>g th e re action<br />

m e ch an<strong>is</strong> m s <strong>of</strong> s ynth e tic Fe -S-bas e d<br />

clus te rs . Th e b<strong>in</strong>d<strong>in</strong>g <strong>of</strong> acid<br />

ch loride s to th e clus te r can be<br />

de te cte d and th e w ay <strong>in</strong> w h ich th e<br />

acid ch loride b<strong>in</strong>ds s h ow s s om e<br />

unus ual ch aracte r<strong>is</strong> tics w h ich could<br />

Se le cte d Publications<br />

[1] As s e m bly <strong>of</strong> H e te rom e ta lic Clus te rs and<br />

Coord<strong>in</strong>ation Polym e rs by Com b<strong>in</strong><strong>in</strong>g Mo-S-<br />

Bas e d Clus te rs w ith Mn 2+ , P. L<strong>in</strong>, W . Cle gg, R.<br />

W . H arr<strong>in</strong>gton, R. A. H e nde rs on, A. J. Fle tch e r,<br />

J. Be l, K. M. Th om as , Inorg. <strong>Ch</strong> e m ., 2006, 45,<br />

4284.<br />

[2] Me ch an<strong>is</strong> m <strong>of</strong> th e <strong>Re</strong> actions <strong>of</strong> Synth e tic<br />

Fe -S-Bas e d Clus te rs w ith Ph COCl: Para le l<br />

Path w ays Involv<strong>in</strong>g Fre e and Coord<strong>in</strong>ate d<br />

Th iolate as Nucle oph ile s . K. Bate s , L. Joh ns on<br />

Pr<strong>of</strong>e s s or Rich ard H e nde rs on<br />

BSc Unive rs ity Co le ge London, 19 73<br />

Ph D Unive rs ity Co le ge London, 19 76<br />

Proje ct Le ade r, Nitroge n Fixation Laboratory,<br />

19 79 -19 9 9<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 9 9 -pre s e nt<br />

Pr<strong>of</strong>e s s or H e nde rs on w as th e firs t re cipie nt<br />

<strong>of</strong> th e RSC Aw ard <strong>in</strong> Inorganic <strong>Re</strong> action<br />

Me ch an<strong>is</strong> m s .<br />

te l: 44(0)19 1 222 6636<br />

e m ail: r.a.h e nde rs on@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Inorganic m e ch an<strong>is</strong> m s and biom im e tic ch e m <strong>is</strong> <strong>try</strong><br />

<strong>in</strong>te ractions <strong>of</strong> s ubs trate s w ith<br />

clus te rs .<br />

Activation <strong>of</strong> Sm a l Mole cule s<br />

B<strong>in</strong>d<strong>in</strong>g and activation <strong>of</strong> s m a l<br />

m ole cule s at e le ctron-rich m e tal s ite s<br />

h as be e n a long-te rm re s e <strong>arch</strong><br />

<strong>in</strong>te re s t, e s pe cia ly th e protonation<br />

ch e m <strong>is</strong> <strong>try</strong> <strong>of</strong> coord<strong>in</strong>ate d N2 , RNC,<br />

RCN, N -<br />

3 , CN- , uns aturate d<br />

h ydrocarbons and h ydride s . Curre nt<br />

s tudie s are focus s <strong>in</strong>g on th e<br />

protonation <strong>of</strong> coord<strong>in</strong>ate d th iolate<br />

de rivative s bound to a {Ni(triph os )}<br />

h ave broade r ram ifications <strong>in</strong> te rm s <strong>of</strong><br />

2+<br />

s ite , w ith an aim to m e diate and<br />

control long range proton trans fe rs .<br />

and R. A. H e nde rs on. Inorg. <strong>Ch</strong> e m ., 2006, 45,<br />

9 423.<br />

[3] Rate s <strong>of</strong> Proton trans fe r to Fe -S-Bas e d<br />

Clus te rs : Com par<strong>is</strong> on <strong>of</strong> Clus te rs conta<strong>in</strong><strong>in</strong>g<br />

{MFe (µ 2 -S) 2 } n+ and {MFe 3 (µ 3 -S) 4 } n+ (M =<br />

Fe , Mo or W ) Core s . K. Bate s , B. Garre tt, R. A.<br />

H e nde rs on, Inorg. <strong>Ch</strong> e m ., 2007, 46, 11145.<br />

[4] Me ch an<strong>is</strong> m <strong>of</strong> S<strong>in</strong>gle Me tal Exch ange <strong>in</strong><br />

<strong>Re</strong> actions <strong>of</strong> [M 4 (SPh ) 10 ] 2- (M=Z n or Fe ) w ith<br />

CoX 2 (X=Cl or NO 3 ) or Fe Cl 2 . V. Aut<strong>is</strong> s ie r, R.<br />

A. H e nde rs on, Inorg. <strong>Ch</strong> e m ., 2008, 47, 639 3.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Dr Le e H igh am<br />

Ph D Unive rs ity <strong>of</strong> Eas t Anglia, 2000<br />

Pos tdoctoral fe low , BP & Unive rs ity <strong>of</strong><br />

Br<strong>is</strong> tol, 2000-2002; Rh odia & UoB 2002-2003<br />

Marie Curie <strong>Re</strong> s e <strong>arch</strong> Fe low , UCD 2003-<br />

2006<br />

<strong>Ne</strong> w cas tle Unive rs ity 2006-pre s e nt<br />

Dr H igh am <strong>is</strong> an EPSRC Care e r<br />

Acce le ration Fe low 2009 -2014.<br />

te l: 44(0) 19 1 222 5542<br />

e m ail: le e .h igh am @ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Organoph os ph orus ch e m <strong>is</strong> <strong>try</strong><br />

Ph os ph orus com pounds play k e y<br />

role s <strong>in</strong> are as s uch as bioch e m <strong>is</strong> <strong>try</strong>,<br />

catalys <strong>is</strong> , s e m iconductors and<br />

m ilitary te ch nology.<br />

Me dic<strong>in</strong>al <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

W e co laborate w ith Oxford to de s ign<br />

fluore s ce nt, cance r ce l-s pe cific<br />

radioph arm ace uticals and w ith our<br />

Me dical <strong>Sch</strong> <strong>ool</strong> to s tudy bone -m ak <strong>in</strong>g<br />

ce ls by s ta<strong>in</strong><strong>in</strong>g th e ir organe le s .<br />

As ym m e tric Catalys <strong>is</strong><br />

W e pre pare ligands <strong>in</strong>corporat<strong>in</strong>g<br />

planar, axial or P-s te re oge nic ch irality<br />

and be nch m ark th e m .<br />

Se le cte d publications<br />

[3] P-ch iroge nic ph os ph <strong>in</strong>e s . MOP/diPAMP<br />

[1] A re -e valuation <strong>of</strong> th e e le ctroph ilic h ybrids , th e ir oxide crys tal s tructure s , re duction<br />

s ubs titution re actions <strong>of</strong> th e Ram ire z ylide , L. J. s tudie s and alte rnative s ynth e s e s , L. J.<br />

H igh am , J. Muldoon, P. G. Ke ly, D. M. Corr, H . H igh am , E. F. Clark e , H . Mue le r-Bunz , D. G.<br />

Mue le r-Bunz , D. G. Gilh e any, J. Org. <strong>Ch</strong> e m ., Gilh e any, J. Organom e t. <strong>Ch</strong> e m ., 2005, 69 0,<br />

2007, 72, 8780.<br />

211.<br />

[2] Tam <strong>in</strong>g a functional group: Cre at<strong>in</strong>g air-<br />

s table , ch iral prim ary ph os ph ane s , R. M. H <strong>in</strong>e y,<br />

L. J. H igh am , H . Mue le r-Bunz , D. G. Gilh e any,<br />

Ange w . <strong>Ch</strong> e m . Intl. Ed., 2006, 45, 7248.<br />

Organoph os ph orus <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Our pione e r<strong>in</strong>g w ork h as found ch iral<br />

prim ary ph os ph <strong>in</strong>e s th at are air<br />

s table , th e ram ifications m e an<strong>in</strong>g<br />

m ole cular de s ign could re nde r<br />

im portant <strong>in</strong>dus trial proce s s e s m uch<br />

s afe r.<br />

Mate rials & Surface Te ch nology<br />

W ith Im pe rial Co le ge and our<br />

ch e m ical e ng<strong>in</strong>e e rs w e h ave grafte d<br />

ph os ph orus onto Si ch ips ,<br />

s ynth e s <strong>is</strong> e d h igh ly conjugate d<br />

ph os ph ole s for optoe le ctronics and<br />

ph os ph <strong>in</strong>o am <strong>in</strong>o acids w h ich <strong>in</strong>te ract<br />

w ith biom <strong>in</strong>e ral s urface s .<br />

[4] W ate r-s oluble h ydroxyalk ylate d ph os ph <strong>in</strong>e s :<br />

e xam ple s <strong>of</strong> th e ir diffe r<strong>in</strong>g be h aviour tow ard<br />

ruth e nium and rh odium , L. J. H igh am , M. K.<br />

W h ittle s e y, P. T. W ood, Dalton Trans ., 2004,<br />

4202.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

18


19<br />

Se le cte d Publications<br />

[1] S. Prune anu, S. A. Farh a Al-Said, L. Dong,<br />

T. A. H o l<strong>is</strong> , M. A. Gal<strong>in</strong>do, N. G. W righ t, A.<br />

H oulton, and B. R. H orrock s , Adv. Func. Mat.<br />

2008, 18, 2444.<br />

[2] Y. <strong>Ch</strong> ao, L. Si le r, S. Kr<strong>is</strong> h nam urth y, P. R.<br />

Coxon, U. Bange rt, M. Gas s , L. Kje ldgaard, S.<br />

N. Patole , L. H . Lie , N. O’Farre l, T. A. Als op, A.<br />

H oulton and B. R. H orrock s , Nature Nanote ch .<br />

2007, 2, 486.<br />

Dr Be njam <strong>in</strong> H orrock s<br />

BSc Im pe rial Co le ge , London 19 88<br />

Ph D Im pe rial Co le ge , London 19 9 2<br />

Pos tdoctoral fe low , Unive rs ity <strong>of</strong> Te xas at<br />

Aus t<strong>in</strong> 19 9 2-9 4<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 9 4-pre s e nt<br />

Dr H orrock s <strong>is</strong> th e Pos tgraduate Adm <strong>is</strong> s ions<br />

Tutor and th e Dire ctor <strong>of</strong> Pos tgraduate<br />

Studie s for <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>.<br />

te l: 44(0)19 1 222 5619<br />

e m ail: b.r.h orrock s @ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Nanos cie nce and nanote ch nology<br />

Curre nt proje cts focus on DNAte<br />

m plate d nanow ire s , s ilicon<br />

q uantum dots , organic m onolaye rs<br />

on s ilicon and various type s <strong>of</strong> probe<br />

m icros copy (AFM, EFM, SECM).<br />

DNA-te m plate d nanow ire s<br />

W e are us <strong>in</strong>g DNA as a te m plate on<br />

w h ich to de pos it conductive m ate rials<br />

(m e tals , s e m iconductors , conductive<br />

polym e rs ) to pre pare nanom e tre -<br />

th ick ne s s w ire s (nanow ire s ) [1].<br />

Silicon q uantum dots<br />

Stable s ilicon nanocrys tals can be<br />

pre pare d by a route th at com b<strong>in</strong>e s<br />

e le ctroch e m ical e tch <strong>in</strong>g <strong>of</strong> s ilicon<br />

w afe r w ith h ydros ilation <strong>of</strong> alk e ne s<br />

[2]. W e are <strong>in</strong>ve s tigat<strong>in</strong>g th e ir us e as<br />

<strong>in</strong>trace lular s pe ctros copic probe s [3].<br />

Monolaye rs on s ilicon s urface s<br />

W e h ave be e n co laborat<strong>in</strong>g w ith<br />

Pr<strong>of</strong>e s s or Andre w H oulton’s group to<br />

de ve lop m e th ods for th e form ation <strong>of</strong><br />

organic m onolaye rs at s ilicon w afe rs<br />

and porous s ilicon. Curre nt activitie s<br />

<strong>in</strong>clude th e ge ne ration <strong>of</strong> prote <strong>in</strong> and<br />

DNA-bas e d s tructure s and<br />

<strong>in</strong>ve s tigations <strong>of</strong> th e m onolaye r<br />

s tructure , prope rtie s and form ation<br />

m e ch an<strong>is</strong> m [4,5].<br />

[3] N. H . Als h arif, C. E. M. Be rge r, S. S.<br />

Varanas i, Y. <strong>Ch</strong> ao, B. R. H orrock s , H . K. Datta,<br />

Sm a l, 2009 , 5, 221.<br />

[4] C. Roge ro, B. T. <strong>Ch</strong> affe y, E. Mate o-Marti, J.<br />

M. Sobrado, B. R. H orrock s , A. H oulton, J. H .<br />

Lak e y, C. Brione s and J. A. Mart<strong>in</strong>-Gago, J.<br />

Ph ys . <strong>Ch</strong> e m . C 2008, 112, 9 308.<br />

[5] M. W oods , S. Carls s on, Q. H ong, S. N.<br />

Patole , L. H . Lie , A. H oulton, and B. R.<br />

H orrock s , J. Ph ys . <strong>Ch</strong> e m . B 2005, 109 , 24035.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Pr<strong>of</strong>e s s or Andre w H oulton<br />

BSc Unive rs ity <strong>of</strong> Es s e x, 19 85<br />

Ph D Unive rs ity <strong>of</strong> Es s e x, 19 89<br />

Pos tdoctoral fe low , Im pe rial Co le ge<br />

London, 19 9 2-19 9 4<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 9 4-pre s e nt.<br />

Pr<strong>of</strong>e s s or H oulton <strong>is</strong> dire ctor <strong>of</strong> th e ch e m ical<br />

nanos cie nce laboratory.<br />

te l: 44(0) 19 1 222 6262<br />

e m ail: andre w .h oulton@ ncl.ac.uk<br />

Bottom -up and s e lf-as s e m bly<br />

m e th ods <strong>of</strong> s ynth e s <strong>is</strong><br />

W e are e xplor<strong>in</strong>g m e th ods for th e<br />

fabrication <strong>of</strong> functional s ys te m s<br />

us <strong>in</strong>g, s o-ca le d, bottom -up m e th ods .<br />

Th <strong>is</strong> <strong>in</strong>clude s de ve lop<strong>in</strong>g s ynth e tic<br />

ch e m <strong>is</strong> <strong>try</strong> for th e m ole cular<br />

functional<strong>is</strong> ation <strong>of</strong> s ilicon s urface s<br />

and m ole cular com ple xe s capable <strong>of</strong><br />

s e lf-organ<strong>is</strong> ation and s e le ctive<br />

b<strong>in</strong>d<strong>in</strong>g.<br />

Nanom ate rials pre paration and<br />

ch aracte r<strong>is</strong> ation<br />

Conf<strong>in</strong><strong>in</strong>g m ate rials to th e nanom e tre<br />

s cale can h ave pr<strong>of</strong>ound e ffe cts on<br />

Se le cte d publications<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : <strong>Ch</strong> e m ical as pe cts <strong>of</strong> nanos cie nce<br />

[1] DNA-bas e d route s to s e m iconduct<strong>in</strong>g<br />

nanom ate rials , A. H oulton, A. R. Pik e , M. A.<br />

Gal<strong>in</strong>do, B. R. H orrock s . <strong>Ch</strong> e m . Com m un.,<br />

2009 , 179 7-1806.<br />

[2] Fe rroce nyl-Modifie d DNA: Synth e s <strong>is</strong> ,<br />

<strong>Ch</strong> aracte riz ation and Inte gration w ith<br />

Se m iconductor Ele ctrode s , A. R. Pik e , L. C.<br />

Ryde r, B. R. H orrock s , W . Cle gg, B. A.<br />

Conno ly, A. H oulton, <strong>Ch</strong> e m . Eur. J. 2004, 11,<br />

344.<br />

th e ir be h aviour <strong>in</strong>clud<strong>in</strong>g ch ange s to<br />

th e ir ph ys ical and ch e m ical<br />

prope rtie s . W e <strong>in</strong>ve s tigate a range <strong>of</strong><br />

nano-laye rs , -w ire s and -particle s<br />

w ith particular <strong>in</strong>te re s t <strong>in</strong> th e<br />

e le ctronic and e le ctrical prope rtie s .<br />

Mate rials ch e m <strong>is</strong> <strong>try</strong> w ith DNA<br />

W e h ave m ajor <strong>in</strong>te re s ts <strong>in</strong> th e us e <strong>of</strong><br />

DNA, and its com pone nts , as a bas <strong>is</strong><br />

for ne w m ate rials . Th e s e range from<br />

s m a l m ole cule com ple xe s w h ich<br />

provide <strong>in</strong>form ation about<br />

fundam e ntal as pe cts <strong>of</strong> m e tal<br />

ion… DNA <strong>in</strong>te ractions to DNA-bas e d<br />

m ole cular w ire s .<br />

[3] Synth e s <strong>is</strong> , Manipulation and Conductivity <strong>of</strong><br />

Supram ole cular Polym e r Nanow ire s , L. Dong,<br />

T. H o l<strong>is</strong> , Ste ve n F<strong>is</strong> h w ick B. A. Conno ly N. G.<br />

W righ t, B. R. H orrock s , A. H oulton. <strong>Ch</strong> e m . Eur.<br />

J. 2007, 13, 822.<br />

[4] DNA On Silicon <strong>De</strong> vice s : On-<strong>Ch</strong> ip<br />

Synth e s <strong>is</strong> , H ybridiz ation, and <strong>Ch</strong> arge Trans fe r,<br />

A. R. Pik e , L. H . Lie , R. A. Eagl<strong>in</strong>g, L. C.<br />

Ryde r, S. N. Patole , B. A. Conno ly, B. R.<br />

H orrock s , A. H oulton, Ange w . <strong>Ch</strong> e m ie Intl. Ed.<br />

2002, 41(4), 617.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

20


21<br />

Se le cte d Publications<br />

[1] An <strong>in</strong>tram ole cularly bas e -s tabiliz e d<br />

diph os ph age rm yle ne and tw o unus ual<br />

ge rm anium (II) ate com ple xe s : a s tructural,<br />

NMR and DFT s tudy. K. Iz od, W . McFarlane , B.<br />

A le n, W . Cle gg, R. W . H arr<strong>in</strong>gton,<br />

Organom e ta lics 2005, 24, 2157.<br />

[2] H e avie r alk ali m e tal com ple xe s <strong>of</strong> a<br />

ph os ph <strong>in</strong>e -borane -s tabiliz e d carbanion. K.<br />

Iz od, C. W i ls , W . Cle gg, R. W . H arr<strong>in</strong>gton,<br />

Organom e ta lics 2006, 25, 5326.<br />

Dr Ke ith Izod<br />

BSc Que e n Mary Co le ge , London 19 87<br />

Ph D Que e n Mary Co le ge , London 19 9 1<br />

Pos tdoctoral fe low , Unive rs ity <strong>of</strong> Sus s e x<br />

19 9 3-9 5<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 9 6-pre s e nt<br />

Dr Iz od w as a Royal Socie ty <strong>Re</strong> s e <strong>arch</strong><br />

Fe low and <strong>is</strong> curre ntly <strong>Re</strong> ade r <strong>in</strong> Ma<strong>in</strong><br />

Group <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>.<br />

te l: 44(0)19 1 222 7101<br />

e m ail: k .j.iz od@ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Ma<strong>in</strong> group ch e m <strong>is</strong> <strong>try</strong><br />

Lanth anide <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Our <strong>in</strong>te re s t lie s <strong>in</strong> tw o are as (i) th e<br />

ch e m <strong>is</strong> <strong>try</strong> <strong>of</strong> low oxidation s tate<br />

lanth anide com ple xe s (<strong>in</strong>clud<strong>in</strong>g<br />

“nonclas s ical” s ys te m s conta<strong>in</strong><strong>in</strong>g<br />

Tm (II) or Nd(II)) w ith s <strong>of</strong>t C-or Pdonor<br />

ligands , and (ii) lanth anide (III)<br />

alk yl and h ydride com ple xe s<br />

s upporte d by s <strong>of</strong>t donor ligand<br />

s caffolds as catalys ts for ole f<strong>in</strong><br />

trans form ation s uch as<br />

polym e r<strong>is</strong> ation, h ydros ilylation and<br />

h ydroam <strong>in</strong>ation.<br />

H e te roatom -Stabil<strong>is</strong> e d Carbanions<br />

Carbanions s tabil<strong>is</strong> e d by h e te roatom s<br />

s uch as P or Si play a m ajor role <strong>in</strong><br />

conte m porary organic s ynth e s <strong>is</strong> . W e<br />

are <strong>in</strong>te re s te d <strong>in</strong> (i) s tructure -<br />

re activity re lations h ips , (ii) th e<br />

<strong>in</strong>flue nce <strong>of</strong> pe riph e ral<br />

functional<strong>is</strong> ation on ligand b<strong>in</strong>d<strong>in</strong>g<br />

pre fe re nce s , and (iii) th e s tabil<strong>is</strong> ation<br />

<strong>of</strong> carbanions by h e avie r h e te roatom s<br />

s uch as As and Bi.<br />

Ma<strong>in</strong> Group Organom e ta lics<br />

W e are <strong>in</strong>te re s te d <strong>in</strong> th e s tabil<strong>is</strong> ation<br />

<strong>of</strong> unus ual organom e ta lic de rivative s<br />

<strong>of</strong> th e m a<strong>in</strong> group e le m e nts ,<br />

e s pe cia ly <strong>of</strong> th e h e avie r e le m e nts<br />

from groups 1 and 2 and group 14.<br />

[3] Synth e s <strong>is</strong> and s tructure s <strong>of</strong> Ln(II) and Ln(III)<br />

dialk yls de rive d from LnI 2 (Ln = Nd, Tm , Yb).<br />

L. J. Bow m an, K. Iz od, W . Cle gg, R. W .<br />

H arr<strong>in</strong>gton, Organom e ta lics , 2007, 26, 2646.<br />

[4] Agos tic-type B-H … Pb <strong>in</strong>te ractions s tabiliz e<br />

a dialk ylplum byle ne . Structure <strong>of</strong> and bond<strong>in</strong>g<br />

<strong>in</strong> [{nPr 2 P(BH 3 )}(Me 3 Si)C(CH 2 )] 2 Pb. K. Iz od,<br />

W . McFarlane , C. W i ls , W . Cle gg, R. W .<br />

H arr<strong>in</strong>gton, Organom e ta lics 2008, 27, 4386.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Dr Julian Knigh t<br />

BSc, Unive rs ity <strong>of</strong> Cam bridge , 19 85<br />

Ph D Unive rs ity <strong>of</strong> Cam bridge , 19 89<br />

Pos tdoctoral fe low , Im pe rial Co le ge<br />

London, 19 89 -19 9 1<br />

<strong>Ne</strong> w cas tle Unive rs ity 19 9 1-pre s e nt.<br />

Dr Knigh t <strong>is</strong> s e nior le cture r <strong>in</strong> organic<br />

ch e m <strong>is</strong> <strong>try</strong>.<br />

te l: 44(0) 19 1 222 7068<br />

e m ail: j.g.k nigh t@ ncl.ac.uk<br />

Synth e s <strong>is</strong><br />

Us <strong>in</strong>g pa ladium catalys e d<br />

carbonylations , de ve lope d w ith <strong>in</strong> th e<br />

group, w e h ave com ple te d th e<br />

s ynth e s <strong>is</strong> <strong>of</strong> th e natural product<br />

de oxym annojirim yc<strong>in</strong> and are<br />

e xte nd<strong>in</strong>g th <strong>is</strong> to m ore com ple x<br />

alk aloid targe ts .<br />

<strong>Ne</strong> w Ligands for Catalys <strong>is</strong><br />

Oxaz ol<strong>in</strong>e s . W e h ave de s igne d a<br />

num be r <strong>of</strong> ne w ch iral oxaz ol<strong>in</strong>e<br />

ligands for e nantios e le ctive<br />

organocatalys <strong>is</strong> .<br />

Ph os ph <strong>in</strong>e s . W e are <strong>in</strong>te re s te d <strong>in</strong><br />

de s ign<strong>in</strong>g s traigh tforw ard route s to<br />

Se le cte d publications<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Organic s ynth e s <strong>is</strong> and catalys <strong>is</strong><br />

[1] Enantios e le ctive Synth e s <strong>is</strong> <strong>of</strong> 3,6-Dih ydro-<br />

1H -pyrid<strong>in</strong>-2-one s : Une xpe cte d<br />

<strong>Re</strong> gios e le ctivity <strong>in</strong> th e Pa ladium Catalyz e d<br />

<strong>De</strong> carboxylative Carbonylation <strong>of</strong> 5-<br />

V<strong>in</strong>yloxaz olid<strong>in</strong>-2-one s . J. Am . <strong>Ch</strong> e m . Soc.,<br />

2000, 122, 29 44.<br />

[2] Total Synth e s <strong>is</strong> <strong>of</strong> <strong>De</strong> oxym annojirim yc<strong>in</strong> and<br />

D-Mannolactam via Carbonylation <strong>of</strong> 5-<br />

V<strong>in</strong>yloxaz olid<strong>in</strong>-2-one s . Te trah e dron, 2003, 59 ,<br />

281.<br />

ne w ph os ph <strong>in</strong>e ligands for catalys <strong>is</strong> .<br />

Th e s e <strong>in</strong>clude : a z irconium -m e diate d<br />

one -pot s ynth e s <strong>is</strong> <strong>of</strong> a ne w range <strong>of</strong><br />

1,4-diph os ph <strong>in</strong>e s (NUPH OS), and a<br />

Die ls -Alde r bas e d s ynth e s <strong>is</strong> <strong>of</strong> bulk y<br />

e le ctron rich biaryl-lik e<br />

m onoph os ph <strong>in</strong>e s (KITPH OS).<br />

Polym e rs & Ionic Liq uids<br />

W e are <strong>in</strong>te re s te d <strong>in</strong> th e de s ign <strong>of</strong><br />

im m obil<strong>is</strong> e d ligands s uch as<br />

ph os ph <strong>in</strong>e s and oxaz ol<strong>in</strong>e s . W e are<br />

<strong>in</strong>ve s tigat<strong>in</strong>g covale nt im m obil<strong>is</strong> ation<br />

<strong>in</strong>to polym e ric fram e w ork s and<br />

'ph as e -tagg<strong>in</strong>g' <strong>in</strong> s pe cific ionic<br />

liq uids .<br />

[3] Synth e s <strong>is</strong> <strong>of</strong> a <strong>Ne</strong> w Clas s <strong>of</strong> 1,4-<br />

B<strong>is</strong> (diph e nylph os ph <strong>in</strong>o)-1,3-Butadie ne Bridge d<br />

Diph os ph <strong>in</strong>e , NUPH OS, via Z irconium -<br />

Me diate d <strong>Re</strong> ductive Coupl<strong>in</strong>g <strong>of</strong> Alk yne s and<br />

Diyne s : Applications <strong>in</strong> Pa ladium -Catalyz e d<br />

Cros s -Coupl<strong>in</strong>g <strong>Re</strong> actions . Organom e ta lics ,<br />

2002, 21, 1383.<br />

[4] Biaryl-Lik e CATPH OS Diph os ph <strong>in</strong>e s via<br />

Double Die ls – Alde r Cycloaddition be tw e e n 1,4-<br />

B<strong>is</strong> (diph e nylph os ph <strong>in</strong>oyl)buta-1,3-diyne and<br />

Anth race ne s ...Organom e ta lics , 2008, 27, 1679 .<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

22


23<br />

As ym m e tric catalys <strong>is</strong><br />

Th e th e m e <strong>of</strong> our w ork <strong>is</strong> th e de s ign<br />

<strong>of</strong> ch iral Le w <strong>is</strong> acids as catalys ts for<br />

carbon-carbon bond form <strong>in</strong>g<br />

re actions . Th us , w e h ave de ve lope d<br />

s ale n com ple xe s <strong>of</strong> titanium and<br />

vanadium as catalys ts for as ym m e tric<br />

cyanoh ydr<strong>in</strong> s ynth e s <strong>is</strong> by th e addition<br />

<strong>of</strong> a cyanide s ource to an alde h yde or<br />

k e tone . Unlik e oth e r catalys ts for th <strong>is</strong><br />

re action, our com ple xe s are active at<br />

room te m pe rature and at<br />

s ubs trate :catalys t ratios <strong>of</strong> 1000:1. As<br />

a re s ult, our w ork h as be e n lice ns e d,<br />

s cale d-up and com m e rcializ e d by<br />

NPil Ph arm ace uticals .<br />

Se le cte d Publications<br />

[1] Me ch an<strong>is</strong> m -guide d de ve lopm e nt <strong>of</strong><br />

VO(s ale n)X com ple xe s as catalys ts for th e<br />

as ym m e tric s ynth e s <strong>is</strong> <strong>of</strong> cyanoh ydr<strong>in</strong><br />

trim e th yls ilyl e th e rs . <strong>Ch</strong> e m . Eur. J. 2009 , 15,<br />

2148.<br />

[2] Synth e s <strong>is</strong> <strong>of</strong> cyclic carbonate s from<br />

atm os ph e ric pre s s ure carbon dioxide us <strong>in</strong>g<br />

e xce ptiona ly active alum <strong>in</strong>ium (s ale n)<br />

com ple xe s as catalys ts . Eur. J. Inorg. <strong>Ch</strong> e m .<br />

2007, 3323.<br />

Pr<strong>of</strong>e s s or Mich ae l North<br />

DPh il Unive rs ity <strong>of</strong> Oxford 19 88<br />

Pos tdoctoral fe low , Nott<strong>in</strong>gh am 19 89 -19 9 0<br />

Unive rs ity <strong>of</strong> W ale s , Bangor 19 9 0-19 9 5<br />

K<strong>in</strong>gs Co le ge , London 19 9 5-2004<br />

<strong>Ne</strong> w cas tle Unive rs ity 2004-pre s e nt<br />

Pr<strong>of</strong>e s s or North <strong>is</strong> co-Dire ctor <strong>of</strong> th e<br />

<strong>Re</strong> s e <strong>arch</strong> Ce ntre <strong>in</strong> Catalys <strong>is</strong> and Inte ns ifie d<br />

Proce s s <strong>in</strong>g.<br />

te l: 44(0)19 1 222 7128<br />

e m ail: m ich ae l.north @ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Organic s ynth e s <strong>is</strong> , m e ch an<strong>is</strong> m s & catalys <strong>is</strong><br />

Catalys ts to conve rt w as te CO 2 <strong>in</strong>to<br />

us e ful ch e m icals<br />

Tw o <strong>of</strong> th e m ajor ch a le nge s <strong>in</strong> th e<br />

21s t ce ntury are : com bat<strong>in</strong>g clim ate<br />

ch ange and f<strong>in</strong>d<strong>in</strong>g re ne w able<br />

s ource s for bas ic organic<br />

com pounds . W e are w ork <strong>in</strong>g on th e<br />

de ve lopm e nt <strong>of</strong> catalys ts w h ich w i l<br />

conve rt w as te CO2 at atm os ph e ric<br />

pre s s ure and am bie nt te m pe rature<br />

<strong>in</strong>to us e ful ch e m icals . W e h ave<br />

re ce ntly pate nte d and publ<strong>is</strong> h e d a<br />

uniq ue clas s <strong>of</strong> bim e ta lic catalys ts<br />

w h ich w i l conve rt w as te CO2 <strong>in</strong>to<br />

cyclic carbonate s .<br />

[3] Me ch an<strong>is</strong> m <strong>of</strong> cyclic carbonate s ynth e s <strong>is</strong><br />

from e poxide s and CO 2 , Ange w . <strong>Ch</strong> e m . Int.<br />

Ed. 2009 , 48, 29 46.<br />

[4] One -com pone nt catalys ts for cyclic<br />

carbonate s ynth e s <strong>is</strong> , <strong>Ch</strong> e m . Com m un. 2009 ,<br />

2577-2579 .<br />

[5] In s itu form ation <strong>of</strong> h e te robim e ta lic s ale n<br />

com ple xe s conta<strong>in</strong><strong>in</strong>g titanium and/or<br />

vanadium ions . Inorg. <strong>Ch</strong> e m . 2008, 47, 3801.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong>


<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong> 24<br />

Dr Andre w Pik e<br />

BSc, <strong>Ne</strong> w cas tle Unive rs ity, 19 9 4<br />

MSc H ok k aido Unive rs ity, Japan 19 9 8<br />

Ph D <strong>Ne</strong> w cas tle Unive rs ity, 2001<br />

INEX 2004-2005<br />

<strong>Ne</strong> w cas tle Unive rs ity 2005-pre s e nt.<br />

Dr Pik e <strong>is</strong> an RCUK acade m ic fe low <strong>in</strong><br />

nanos cie nce .<br />

te l: 44(0) 19 1 222 7061<br />

e m ail: a.r.pik e @ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Nanom ate rials and s ynth e tic biology<br />

Nanos cale m ate rials<br />

I am <strong>in</strong>te re s te d <strong>in</strong> th e DNA-dire cte d<br />

as s e m bly <strong>of</strong> conductive m ate rials for<br />

e le ctronic applications and <strong>in</strong><br />

particular 1D nanow ire s . DNA can be<br />

m odifie d <strong>in</strong> s e ve ral w ays <strong>in</strong>clud<strong>in</strong>g (i)<br />

covale nt attach m e nt <strong>of</strong> groups to th e<br />

nucle obas e s th rough s ynth e tic<br />

organic ch e m <strong>is</strong> <strong>try</strong>, (ii) as s ociation <strong>of</strong> a<br />

cationic group to th e double h e lix<br />

th rough e le ctros tatic <strong>in</strong>te ractions w ith<br />

th e ph os ph ate back bone , and (iii) th e<br />

non-covale nt <strong>in</strong>te gration <strong>of</strong><br />

<strong>in</strong>te rcalat<strong>in</strong>g and groove -b<strong>in</strong>d<strong>in</strong>g<br />

m ole cule s . W e aim to e xploit th e s e<br />

th re e m ode s <strong>of</strong> DNA m odification to<br />

Se le cte d publications<br />

[1] Tow ards DNA bas e d m ole cular e le ctronics<br />

on s ilicon, A. R. Pik e , B. R. H orrock s , B. A.<br />

Conno ly, A. H oulton, Aus . J. <strong>Ch</strong> e m ., 2002, 55,<br />

19 1.<br />

[2] DNA on s ilicon de vice s : On-ch ip s ynth e s <strong>is</strong> ,<br />

h ybridiz ation, and ch arge trans fe r, A. R. Pik e ,<br />

L. H . Lie , R. A. Eagl<strong>in</strong>g, L. C. Ryde r, S. N.<br />

Patole , B. A. Conno ly, B. R. H orrock s , A.<br />

H oulton Ange w . <strong>Ch</strong> e m . Int. Ed., 2002, 41, 615.<br />

as s e m ble conductive polym e rs , m e tal<br />

nanoparticle s and re dox groups <strong>in</strong>to<br />

nove l nanos cale m ate rials .<br />

Synth e tic biology<br />

One de f<strong>in</strong>ition <strong>is</strong> "th e re -de s ign <strong>of</strong><br />

natural biological s ys te m s for anoth e r<br />

us e ful purpos e ". 2D-ne tw ork s and 3Ds<br />

tructure s can be cons tructe d us <strong>in</strong>g<br />

com ple m e ntary s e q ue nce s <strong>of</strong> DNA.<br />

W e are de ve lop<strong>in</strong>g e nz ym atic<br />

m e th ods th at can be us e d not only to<br />

fabricate DNA-bas e d s ys te m s , but<br />

w i l als o a low for th e de s ign <strong>of</strong> nove l<br />

functionalitie s th at are not natura ly<br />

as s ociate d w ith DNA.<br />

[3] Covale nt and non-covale nt attach m e nt and<br />

patte rn<strong>in</strong>g <strong>of</strong> polypyrrole at s ilicon s urface s , A.<br />

R. Pik e , S. N. Patole , N. C. Murray, T. Ilyas , B.<br />

A. Conno ly, B. R.H orrock s , A.H oulton, Adv.<br />

Mat., 2003, 15, 254.<br />

[4] Fe rroce nyl-Modifie d DNA: Synth e s <strong>is</strong> ,<br />

<strong>Ch</strong> aracte riz ation and Inte gration w ith<br />

Se m iconductor Ele ctrode s , A. R. Pik e , L. C.<br />

Ryde r, B. R. H orrock s , W . Cle gg, B. A.<br />

Conno ly, A. H oulton, <strong>Ch</strong> e m . Eur. J. 2004, 11,<br />

344.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong>


25<br />

DNA <strong>Re</strong> cognition<br />

Targe t<strong>in</strong>g s pe cific s e q ue nce s or<br />

s tructure s <strong>in</strong> nucle ic acids <strong>is</strong> a<br />

prom <strong>is</strong> <strong>in</strong>g s trate gy for th e<br />

de ve lopm e nt <strong>of</strong> drugs to de te ct and<br />

de fe at d<strong>is</strong> e as e at th e m os t<br />

fundam e ntal le ve l.<br />

Se le cte d Publications<br />

[1] D<strong>is</strong> pe rs ions Of Alk yl-Cappe d Silicon<br />

Nanocrys tals In Aq ue ous Me dia:<br />

Ph otolum <strong>in</strong>e s ce nce And Age <strong>in</strong>g. Analys t,<br />

2008, 133, 1573.<br />

[2] Me ch anical and Ele ctroconductive<br />

Prope rtie s <strong>of</strong> Spatia ly D<strong>is</strong> tribute d Double -<br />

Strande d DNA Arrays on Au(111). Th <strong>in</strong> Solid<br />

Film s , 2008, 516, 89 69 .<br />

Dr Eim e r Tuite<br />

BSc Tr<strong>in</strong>ity Co le ge , Dubl<strong>in</strong> 19 89<br />

Ph D Tr<strong>in</strong>ity Co le ge , Dubl<strong>in</strong> 19 9 2<br />

Pos tdoctoral fe low , As s ociate Pr<strong>of</strong>e s s or<br />

<strong>Ch</strong> alm e rs Te k n<strong>is</strong> k a H ögs k ola (CTH ) <strong>in</strong><br />

Göte borg, Sw e de n 19 9 2-2000<br />

<strong>Ne</strong> w cas tle Unive rs ity 2000-pre s e nt<br />

Dr Tuite <strong>is</strong> a m e m be r <strong>of</strong> th e <strong>Ch</strong> e m ical<br />

Nanos cie nce Laboratory.<br />

te l: 44(0)19 1 222 5523<br />

e m ail: e .m .tuite @ ncl.ac.uk<br />

<strong>Re</strong> s e <strong>arch</strong> <strong>in</strong>te re s ts : Bioph ys ical ch e m <strong>is</strong> <strong>try</strong> & nanos cie nce<br />

Oxidative DNA Dam age<br />

Our s tudie s look at th e m e ch an<strong>is</strong> m s<br />

<strong>of</strong> oxidative dam age and h ow to<br />

pre ve nt it, and contro le d <strong>in</strong>duction <strong>of</strong><br />

DNA dam age for various applications<br />

(e .g. de s troy<strong>in</strong>g bacte ria and virus e s ).<br />

Mole cular Ele ctronics<br />

Bioanalytical <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

W e are particularly <strong>in</strong>te re s te d <strong>in</strong><br />

W e s tudy h ow dye s , q uantum dots , ch arge trans fe r and m igration <strong>in</strong> DNA-<br />

and m e tal nanoparticle s can be us e d bas e d as s e m blie s . Th e s e are s tudie d<br />

to analys e biom ole cule s and at th e s <strong>in</strong>gle m ole cule le ve l us <strong>in</strong>g<br />

biom ark e rs , us <strong>in</strong>g fluore s ce nce and STM and AFM, and <strong>in</strong> bulk us <strong>in</strong>g<br />

Ram an s pe ctros copy and m icros copy. ph otoph ys ical m e th ods .<br />

[3] Spatial and Me ch anical Prope rtie s <strong>of</strong> Dilute<br />

DNA Monolaye rs on Gold Im age d by AFM. J.<br />

Ph ys . <strong>Ch</strong> e m . B, 2003, 107, 359 1.<br />

[4] Ph otoble ach <strong>in</strong>g <strong>of</strong> As ym m e tric Cyan<strong>in</strong>e s<br />

Us e d for Fluore s ce nce Im ag<strong>in</strong>g <strong>of</strong> S<strong>in</strong>gle DNA<br />

Mole cule s . J. Am . <strong>Ch</strong> e m . Soc., 2001, 123,<br />

79 85.<br />

[5] Picos e cond Tim e -<strong>Re</strong> s olve d <strong>Re</strong> s onance<br />

Ram an Prob<strong>in</strong>g <strong>of</strong> th e Ligh t Sw itch State s <strong>of</strong><br />

[Ru(ph e n) 2 dppz ] 2+ . J. Ph ys . <strong>Ch</strong> e m . B, 2001,<br />

105, 12653.<br />

h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong><br />

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<strong>Sch</strong> <strong>ool</strong> <strong>of</strong> <strong>Ch</strong> e m <strong>is</strong> <strong>try</strong><br />

Be ds on Build<strong>in</strong>g<br />

<strong>Ne</strong> w cas tle Unive rs ity<br />

<strong>Ne</strong> w cas tle upon Tyne<br />

NE1 7RU<br />

UK<br />

te l: 44 (0)19 1 222 7102<br />

fax: 44 (0)19 1 222 69 29<br />

pg.ch e m <strong>is</strong> <strong>try</strong>@ ncl.ac.uk<br />

Application form :<br />

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h ttp://w w w .ncl.ac.uk /ch e m <strong>is</strong> <strong>try</strong>

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