Synthesis, Crystal Structure and Antimicrobial Activity of a Mixed-Ligand Copper (II) Complex [Cu(pht)2 (phen)H2O]

Article Preview

Abstract:

A novel mixed-ligand copper(II) complex [Cu(pht)2(phen)H2O] (Hpht = 5,5-diphenylimidazolidine-2,4-dione, phen = 1,10-phenanthroline) was has been synthesized solvent-thermally and characterized by elemental analysis, IR and single-crystal X-ray diffraction. The crystal of the copper complex belongs to Triclinic system with space group P1, a = 11.747(14), b = 12.639(15), c = 14.021(17)Å, α= 97.986(18)º, β= 104.958(18) º, γ= 108.485(19) º, V = 1851(4) Å3, Dc = 1.371 g/cm3, Z = 2, F(000) = 790, µ = 0.644mm-1, R1 = 0.0835, wR2 = 0.1436 [I>2σ(I)] and GOF=0.867. The X-ray data showed that the Cu(II) atom adopted a distorted CuN2O3 square pyramidal configuration when coordinated with two phen ligands and one water ligand. The antimicrobial activity of the title complex was evaluated against a series of fungi or bacteria in vitro by agar method and the filter paper method, respectively.The results showed that the title complex was more active against the Fusarim gramine arum, Escherichia coli and Staphylococcus Aureus than its precursor Hpht and Cu(Ac)2×H2O.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 239-242)

Pages:

2132-2136

Citation:

Online since:

May 2011

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2011 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Ray, M. S.; Mukhopadhyay, G. M.; Drew, M. G. B.; Lu, T. H.; Chaudhuri, S.; Ghosh, A. A diphenoxo bridged antiferromagnetically coupled dimer of copper (II) having bridging methanol. Inorg. Chem. Commun., 6(2003), p.961

DOI: 10.1016/s1387-7003(03)00143-6

Google Scholar

[2] Chaviara,A.Th.; Cox P.J.; Repana K.H.; Papi R.M.; Papazisis K.T.; Zambouli,D. ; Kortsaris A.H.; Kyriakidis D.A.; Bolos C.A. Copper(II) Schiff base coordination compounds of dien with heterocyclic aldehydes and 2-amino-5-methyl-thiazole: synthesis, characterization, antiproliferative and antibacterial studies.Crystal structure of CudienOOCl2. J. Inorg. Biochem., 98(2004), p.1271

DOI: 10.1016/j.jinorgbio.2004.05.010

Google Scholar

[3] Akitsu ,T. Komorita, S. Tamura,H. Diastereomers of copper (II) complexes exhibiting difference in coordination geometry by R- or S-1-phenylethylamine ligands in the solid state and structural conversion of crystals into solutions.Inorganica Chimica Acta., 348(2003), p.25

DOI: 10.1016/s0020-1693(03)00002-1

Google Scholar

[4] Hu, X.-L.; Shi, P.-F.; Xu, X.-Y.; Luan, Y.; Chen,J.-P.; Wang, D.-Q. Acta Chim. Sinica 67(2009), p.2517 (in Chinese).

Google Scholar

[5] Hu, XL., Xu, XY., Xu, TT. et al. Acta Cryst. E62(2006), p. m2352.

Google Scholar

[6] Hu, XL., Xu, XY., Xu, TT. et al. Acta Cryst. E62(2006), p. m2974.

Google Scholar

[7] Nokhodchi, A.; Bolourtchian, N.; Dinarvand, R. Int. J. Pharm. 250(2003), p.85.

Google Scholar

[8] Milne, P.; Hô, M.; Weaver, D. F.; J. Mol. Struct., 49(19992), p.19.

Google Scholar

[9] Muhrer, G.; Meier, U.; Fusaro, F.; Albano,S.; Mazzotti, M. Int. J. Pharm. 308(2006), p.69.

Google Scholar

[10] Akitsu,T. Einaga,Y. Acta Cryst., C61(2005), p.183

Google Scholar

[11] Akitsu,T. Komorita,S. and Urushiyama,A. The Chemical Society of Japan., 74(2001), p.851 [12]Hu, X.-L. Xu, X.-Y. Xu, T.-T. Zhang, H.-S. Synth.React.Inorg. Met.-Org.Chem. 36(2006), p.701

Google Scholar

[13] Sheldrick GM SADABS, Version 2, Multi-Scan Absorption Correction Program, University of Göttingen, Germany, 2001.

Google Scholar

[14] Sheldrick GM. SHELX-97, A Computer Program for Crystal Structure Solution and Refinement, University of Göttingen, Göttingen (Germany), 1997.

Google Scholar

[15] Sheldrick G.M. SHELXL-97, Program for X-ray Crystal Structure re- finement; University of Göttingen: Göttingen, Germany, 1997.

Google Scholar

[16] Shen P, Fan X-R, Li G-W, Microbiological Experiment, 3rd edn. Beijing: Higher Education Press. (1999)

Google Scholar