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4'-(4-Pyridyl)-2,2':6',2"-Terpyridine (Pyterpy) as Ligand in the ...

4'-(4-Pyridyl)-2,2':6',2"-Terpyridine (Pyterpy) as Ligand in the ...

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Global J. Pharmacol., 7 (2): 187-191, 2013<br />

Fig 6: [Gd(pyterpy) (NO ) ]morphology<br />

3 3<br />

Thermogravimetric Analyses: The <strong>the</strong>rmal properties of<br />

REFRENCES<br />

[Gd(pyterpy) (NO 3) 3] w<strong>as</strong> <strong>in</strong>vestigated by <strong>the</strong>rmograms<br />

(TG/ DTA). Figure 5 shows TGA and DTA curves for 1. Roesky, H.W. and M. Andruh, 2003. The <strong>in</strong>terplay of<br />

[Gd(pyterpy)(NO 3) 3]. In <strong>the</strong> temperature range 420°C, a coord<strong>in</strong>ative, hydrogen bond<strong>in</strong>g and %- % stack<strong>in</strong>g<br />

weight los<strong>in</strong>g w<strong>as</strong> observed which w<strong>as</strong> related to <strong>the</strong> <strong>in</strong>teractions <strong>in</strong> susta<strong>in</strong><strong>in</strong>g supramolecular solid<br />

degradationand evaporation of pyterpy.<br />

statearchitectures.: A study c<strong>as</strong>e of bis(4-pyridyl)-<br />

and bis(4-pyridyl-Noxide) tectons. Coord. Chem.<br />

SEM Pictures: Scann<strong>in</strong>g Electron Microscope image of Rev., 236: 91-119.<br />

[Gd(pyterpy)(NO 3) 3] with different magnification h<strong>as</strong> been 2. Zaman, M.B., M.D. Smith, D.M. Ciurt<strong>in</strong> and<br />

shown (Fig 6).<br />

H.C. Zur Loye, 2002. New Cd(II), Co(II) and Cu(II)<br />

CONCLUSION<br />

Conta<strong>in</strong><strong>in</strong>g Coord<strong>in</strong>ation Polymers Syn<strong>the</strong>sized<br />

us<strong>in</strong>g <strong>the</strong> Rigid <strong>Ligand</strong> 1,2-bis(3-pyridyl)ethyne<br />

(3,3'-DPA)” Inorg. Chem, 41: 4895-4903.<br />

In summary, <strong>the</strong> syn<strong>the</strong>sis and characterization of 3. Barnett, S.A., N.R. Blake, J.E.B. Champness,<br />

complexes have been described pyterpy and [Gd C. Nicolson and J. Wilson, 2001. Chem. Soc. Dalton<br />

(pyterpy) (NO 3) 3] w<strong>as</strong> syn<strong>the</strong>sized simply. These Trans., pp: 567-573.<br />

1<br />

compounds w<strong>as</strong> Characterized by IR and HNMR, UV-Vis 4. Zaman, M.B., N.R. Smith Champness,<br />

and TG/DTA.<br />

J.E.B.C. Nicolson and J. Wilson, 2001. Chem. Soc.<br />

ACKNOWLEDGMENTS 5.<br />

Dalton Trans, pp: 567.<br />

Dong, Y.B., R.C. Layland and D.N.G. Smith, 1999.<br />

We gratefully acknowledge <strong>the</strong> f<strong>in</strong>ancial support 6.<br />

Inorg. Chem., 38: 3056.<br />

Fujita, M., Y.J. Kwon, O.K. S<strong>as</strong>aki and K. Yamaguchi,<br />

from <strong>the</strong> Research Council of Takestan Islamic Azad 1995. J. Am. Chem. Soc., 117: 7287.<br />

University and many technical supports that provided by 7. Plater, M.J., M.R. Foreman, J. Tst, Gelbrich, S.J. Coles<br />

TarbiatModarres University.<br />

and M.B. Hursthouse, 2000. J. Chem. Soc. Dalton<br />

Trans., pp: 3065.<br />

8. Bujaci, M.T.X. S WangandLiZheng, (2002).Inorg.<br />

Chim. Acta, 333: 152.<br />

9. Khlobystov, A.K., M.T. Brett, A.J. Blake,<br />

N.R. Champness, P.M.W. Gill, D.P. Neill, O.S. Teat,,<br />

J.C. Wilson and M. Schr_oder, 2003. J. Am. Chem.<br />

Soc., 125: 6753.<br />

10. Neels, A. and H. Stoeckli-Evans, 1999. Inorg. Chem.,<br />

38: 6164.<br />

191

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