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ISMSC 2007 - Università degli Studi di Pavia

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Novel Copper(II) and Nickel(II) [2×2] Molecular Grids based on a<br />

Polynucleative Oxime-containing Shiff Base Ligand<br />

I. S. Moroz a , M. Haukka b and I. O. Fritsky a<br />

a Department of Chemistry, Kiev National Taras Shevchenko University, 01033 Kiev, Ukraine<br />

b Department of Chemistry, University of Joensuu, 80101 Joensuu, Finland<br />

One of the most succesfull approaches for obtaining polynuclear coor<strong>di</strong>nation compounds is<br />

use of well-designed polynucleative ligand systems. In this work we present copper(II) and<br />

nickel(II) compounds with novel polyfunctional Schiff base ligand 2-(hydroxyimino)-N'-(1-<br />

(pyri<strong>di</strong>n-2-yl)ethylidene)propanehydrazide (pop), which contain several donor functions (oximic,<br />

hydrazide, hydrazone and pyri<strong>di</strong>ne cycle).<br />

The synthesized complexes have been characterized by<br />

a variety of spectral methods; three of them [Cu4(pop-<br />

2H)4(H2O)4] (1), [Cu4(pop-2H)4(HCOOH)4] (2) and<br />

[Ni4(pop-H)4(HCOO)4] (3) were stu<strong>di</strong>ed by X-ray single<br />

crystal analysis. The complexes 1-3 in<strong>di</strong>cate [22]<br />

pop<br />

PSB 15<br />

molecular grid structure and comprise of tetranuclear sixcoor<strong>di</strong>nated<br />

metal arrays. In the nickel complex two types<br />

of chromophors are realized (NiN2O4 and NiN4O2). On the other hand, for the copper complexes<br />

only one type of chromophor (CuN3O3) is observed. The coor<strong>di</strong>nation of pop is realized in a<br />

tetradentate mode via the pyri<strong>di</strong>ne, azomethine and oximic nitrogen atoms and the bridging<br />

amide oxygen atom.<br />

Molecular structure of 3<br />

The average metal-metal separation in all cases is ca. 4 Å, the M--M angles are in the range<br />

137-139 o for 3 and 139-142 o for 1, 2.<br />

4-(4-Thiocarbamoyl-1,2,3-triazol-1-yl)benzoannelated Crown Ethers as<br />

Amino Acid's Receptors.<br />

PSB 16<br />

Yuri Yu. Morzherin, Polina E. Kropotina, Tatiana V. Glukhareva, Nadezhda A. Itsikson, Anatoly<br />

I. Matern<br />

Urals State Technical University, Chemical Technology Faculty, Mira, 19, 620002, Ekaterinburg,<br />

Russia<br />

In the last decade, considerable effort has been devoted to molecular recognition and/or<br />

selforganization within the field of supramolecular chemistry. One of the most noticeable<br />

aspects in this inter<strong>di</strong>sciplinary area is the emergence of the wide range of intriguing<br />

compounds specially designed and created on the basis of complimentary to function as<br />

sensors and receptors for biological and abiotic particles. Extensive stu<strong>di</strong>es of non-covalent<br />

interactions between synthetic receptors and simple species as cations, anions and small and<br />

simple neutral molecules have not only led to various molecular and supramolecular devices<br />

but, more significantly, had a big impact on the development of modern chemistry as well. A<br />

challenging research area in this field is the design and construction of sophisticated artificial<br />

receptors with polytopicity and polyfunctionality that would be highly efficient in complexation<br />

with more complicated molecules. A convenient method for one-step mo<strong>di</strong>fication of crown<br />

ether by nitrogen containing heterocycle based on the methodology of rearrangements of 1,2,3thia<strong>di</strong>azoles.<br />

Now we report the synthesis of amino acid's receptor.<br />

The complexating properties of obtained crown ether toward amino acids have been stu<strong>di</strong>ed by<br />

used various methods. We was shown that benzocrown ether containing the 4-thiocabamoyl-<br />

1,2,3-triazole is receptors for amino acid.<br />

This work was financially supported by the grants Russian Foundation of Basic Researches 05-<br />

03-32094

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