A novel bonding of 6,7-dichloroquinoxlaine-2,3-dione, DCQX, to two molybdenum (0) metal centers: Synthesis, characterization, biological activity studies and semiempirical calculations of [(bpy)2Mo(μ2-κ2:η6-DCQX)Mo(CO)3] complex

Attia S. Attia ; Abdel Aziz, Ayman ; Khalifa A. Alfallous ; M.F. El-Shahat 


Abstract


A complex of the general formula Mo2(bpy)2(DCQX)(CO)3, (where DCQX and bpy are 6,7-dichloroquinoxaline-2,3-dione and 2,2′-bipyridine), was synthesized in two steps starting with the reaction of Mo(CO)6with bpy then followed by the addition of DCQX ligand. Initial characterization based on the elemental and mass analyses has suggested three possible structures (1-3). In the three suggested structures the DCQX ligand bonded to two Mo(0) metal centers; to one Mo metal through its C=O functional groups and the other through the aromatic ring forming η6-arene type. In structure 1 the DCQX ligands bonded to (bpy)2Mo and Mo(CO)3moieties, whereas in the other structures the DCQX ligands bonded to Mo(bpy)(CO) and cis-(bpy)(CO)2Mo (2) or trans-(bpy)(CO)2Mo (3) moieties. The IR studies were useful in assigning the coordination modes of the ligands especially in the carbonyl region of the spectrum.1H NMR studies in DMSO-d6displayed typical patterns corresponding to cis-(bpy)2M moiety. The electronic absorption spectrum of the complex revealed two bands assignable to Mo(dπ) → arene(π) and Mo(dπ) → bpy(π) MLCT transitions. The thermogravimetric analysis gave more insight into the composition and the thermal stability of the complex. The structural and vibrational behaviors of the Mo2(bpy)2(DCQX)(CO)3complex have been elucidated using semiempirical parameterized PM3 method. Although, both DCQX ligand and the molybdenum complex showed antimicrobial activities, the complex inhibition to the studied microorganisms was higher. © 2012 Published by Elsevier Ltd. All rights reserved.


Other data

Issue Date 2012
Journal Polyhedron 
URI http://research.asu.edu.eg/handle/123456789/169967
DOI 1
238
244
http://www.scopus.com/inward/record.url?eid=2-s2.0-84864942141&partnerID=MN8TOARS
44
10.1016/j.poly.2012.07.007


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