http://www.cnr.it/ontology/cnr/individuo/prodotto/ID15408
Oxovanadium(IV) Complexes with Pyrazinecarboxylic Acids: The Coordinating Properties of Ligands with the (Naromatic, COO) Donor Set. (Articolo in rivista)
- Type
- Label
- Oxovanadium(IV) Complexes with Pyrazinecarboxylic Acids: The Coordinating Properties of Ligands with the (Naromatic, COO) Donor Set. (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/ejic.200600230 (literal)
- Alternative label
E. Garribba, G. Micera, E. Lodyga-Chruscinska, D. Sanna (2006)
Oxovanadium(IV) Complexes with Pyrazinecarboxylic Acids: The Coordinating Properties of Ligands with the (Naromatic, COO) Donor Set.
in European journal of inorganic chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- E. Garribba, G. Micera, E. Lodyga-Chruscinska, D. Sanna (literal)
- Pagina inizio
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://onlinelibrary.wiley.com/doi/10.1002/ejic.200600230/abstract (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Department of Chemistry, University of Sassari, Via Vienna 2, 07100 Sassari, Italy
Institute of General Food Chemistry, Technical University of Lodz, ul. Stefanowskiego 4/10, 90924 Lodz, Poland
Istituto C.N.R. di Chimica Biomolecolare, Trav. La Crucca 3, 07040 Li Punti, Sassari, Italy (literal)
- Titolo
- Oxovanadium(IV) Complexes with Pyrazinecarboxylic Acids: The Coordinating Properties of Ligands with the (Naromatic, COO) Donor Set. (literal)
- Abstract
- Complex formation between the VIVO ion and four pyrazine
derivatives, 2-pyrazinecarboxylic acid (pzc), 5-methyl-2-pyrazinecarboxylic
acid (5-Mepzc), 2,3-pyrazinedicarboxylic
acid (3-COOHpzc) and 5-hydroxy-2-pyrazinecarboxylic acid
(5-OHpzc), was studied in aqueous solution and in the solid
state through the combined application of potentiometric and
spectroscopic (EPR and FT-IR) techniques. The results indicate
that in acidic and neutral aqueous solution all the
ligands form mono(chelated), bis(chelated) and dinuclear
species of composition VOL, VOL2 and (VO)2L2H2. Hexacoordinated VOL2 complexes are characterised by a cis/trans isomerism, where cis and trans are the species with a water molecule bound in the cis or trans position with respect to the V=O group. The trans arrangement is favoured over the cis arrangement. Three solid derivatives, [VO(5-Mepzc)2] (1), cis-[VO(pzc)2(H2O)] (2) and cis-[VO(3-COOHpzc)2(H2O)] (3), were isolated and characterised. Based on the experimental results and on the data in the literature, the stability of cis and trans isomers in aqueous solution and in the solid state has been discussed, showing that with ligands of comparable basicity and size of the chelate ring the hydrophilicity favours the cis species and determines the relative amount of the two isomers. The analysis of the magnetic properties of the hydroxo-bridged VIVO dimers suggests that for the (VO)2L2H2 species the anti-coplanar arrangement is realised. (literal)
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