Synthesis, structure, solution chemistry and the electronic effect of para substituents on the vanadium center in a family of mixed-ligand [(VO)-O-V(ONO)(ON)] compexes

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Ghosh, T., Mondal, B., Ghosh, T., Sutradhar, M., Mukherjee, G. and Drew, M.G.B. (2007) Synthesis, structure, solution chemistry and the electronic effect of para substituents on the vanadium center in a family of mixed-ligand [(VO)-O-V(ONO)(ON)] compexes. Inorganica Chimica Acta, 360 (5). pp. 1753-1761. ISSN 0020-1693 doi: 10.1016/j.ica.2006.10.003

Abstract/Summary

Four tridentate dibasic ONO donor hydrazone ligands derived from the condensation of benzoylhydrazine with either 2-hydroxyacetophenone or its para substituted derivatives (H2L1-4, general abbreviation H2L) have been used as primary ligands and 8-hydroxyquinoline (Hhq, a bidentate monobasic ON donor species) has been used as auxiliary ligand. The reaction of [(VO)-O-IV(acac)21 with H2L in methanol followed by the addition of Hhq in equimolar ratio under aerobic condition afforded the mixed-ligand oxovanadium(V) complexes of the type [(VO)-O-V(L)(hq)] (1-4) in excellent yield. The X-ray structure of the compound [(VO)-O-V(L-4)(hq)] (4) indicates that the H2L4 ligand is bonded with vanadium meridionally in a tridentate dinegative fashion through its deprotonated phenolic-O, deprotonated enolic-O and imine-N atoms. The V-O bond length order is: oxo < phenolato < enolato. H-1 NMR spectra of 4 in CDCl3 solution indicates that it's solid-state structure is retained in solution. Complexes are diamagnetic and exhibit only ligand to metal charge transfer (LMCT) transition band near 530 nm in CH2Cl2 solution in addition to intra-ligand pi-pi* transition band near 335 rim and they display quasi-reversible one electron reduction peak near -0.10 V versus SCE in CH2Cl2 solution. lambda(max) (for LMCT transition) and the reduction peak potential (E-p(c)) values of the complexes are found to be linearly related with the Hammett (sigma) constants of the substituents in the aryloxy ring of the hydrazone ligands. lambda(max) and E-p(c) values show large dependence d lambda(max)/d sigma = 32.54 nm and dE(p)(c)/d sigma = 0.19 V, respectively, on the Hammett constant. (c) 2006 Elsevier B.V. All rights reserved.

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Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/11273
Identification Number/DOI 10.1016/j.ica.2006.10.003
Refereed Yes
Divisions Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
Uncontrolled Keywords mixed-ligand oxovanadium(V) complexes, hydrazone complexes, crystal structure, solution chemistry , MODELING SUPRAMOLECULAR INTERACTIONS, DONOR HYDRAZONE LIGANDS, OXOVANADIUM(V) COMPLEXES, N-SALICYLIDENEHYDRAZIDES, METAL REDOX, DIOXOVANADIUM(V) COMPLEXES, CRYSTAL-STRUCTURE, ZIEGLER-NATTA, V COMPLEX, HALOPEROXIDASES
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