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Oxovanadium(IV) complexes of quinoline derivatives

Garribba, Eugenio and Micera, Giovanni and Sanna, Daniele and Lodyga-Chruscinska, Elzbieta (2003) Oxovanadium(IV) complexes of quinoline derivatives. Inorganica Chimica Acta, Vol. 348 , p. 97-106. ISSN 0020-1693. Article.

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DOI: 10.1016/S0020-1693(02)01483-4

Abstract

Complex formation between oxovanadium(IV) and five quinoline derivatives, 8-hydroxyquinoline (8-HQ), 8-hydroxyquinoline-5-sulphonic acid (8-HQS), 2-methyl-8-hydroxyquinoline (8-HQD), 8-hydroxyquinoline-N-oxide (8-HQNO), and 8-quinolinecarboxylic acid (8-QC), was studied in aqueous solution through the combined application of potentiometric and spectroscopic (electronic absorption and EPR) techniques. The results indicate that all the ligands form mono and bis chelated complexes with the VO(IV) ion. The bis chelated complexes are neutral and poorly soluble. In solution 8-HQ and 8-HQS form two cis isomers bearing a water molecule in the equatorial plane. This water molecule deprotonates with a pKa of 8.76 (8-HQ) to give the corresponding EPR-active mono hydroxo species. Four five-coordinated complexes were isolated in the solid state: [VO(8-HQ)2], [VO(8-HQD)2], [VO(8-HQNO)2] and [VO(8-QC)2]. They were characterised by IR spectroscopy and diffuse reflectance electronic absorption, and by solution studies in coordinating (DMSO) or non-coordinating (toluene and CH2Cl2) solvents. Moreover, the corresponding species with Zn2+, GaCl2+ or TiO2+ were doped with different amounts of VO2+. The structures of [VO(8-HQ)2] and [VO(8-HQD)2] show a distortion toward the trigonal bipyramid, whilst those of [VO(8-HQNO)2] and [VO(8-QC)2] are closer to the square pyramid. In coordinating solvents, [VO(8-HQ)2] shows a trans–cis isomerisation and re-originates the structure displayed in aqueous solution. The features of five-coordinated VO(IV) complexes in solution and in solid state are discussed.

Item Type:Article
ID Code:1436
Status:Published
Refereed:Yes
Uncontrolled Keywords:Oxovanadium(IV), EPR, electronic spectroscopy, potentiometry, quinoline
Subjects:Area 03 - Scienze chimiche > CHIM/03 Chimica generale e inorganica
Divisions:001 Università di Sassari > 01 Dipartimenti > Chimica
002 Altri enti e centri di ricerca del Nord Sardegna > CNR-Consiglio Nazionale delle Ricerche > Istituto di chimica biomolecolare, Sassari
Publisher:Elsevier
ISSN:0020-1693
Deposited On:18 Aug 2009 10:05

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