http://www.cnr.it/ontology/cnr/individuo/prodotto/ID16460
Synthesis, molecular structure and properties of oxo-vanadium(IV) complexes containing the oxydiacetate ligand (Articolo in rivista)
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- Label
- Synthesis, molecular structure and properties of oxo-vanadium(IV) complexes containing the oxydiacetate ligand (Articolo in rivista) (literal)
- Anno
- 2003-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/b300914a (literal)
- Alternative label
del Río, Diego; Galindo, Agustin; Vicente, Ricardo; Mealli, Carlo; Ienco, Andrea; Masi, Dante (2003)
Synthesis, molecular structure and properties of oxo-vanadium(IV) complexes containing the oxydiacetate ligand
in Dalton transactions (2003. Print); ROYAL SOC CHEMISTRY, THOMAS GRAHAM HOUSE,, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND (Regno Unito)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- del Río, Diego; Galindo, Agustin; Vicente, Ricardo; Mealli, Carlo; Ienco, Andrea; Masi, Dante (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Univ Sevilla, Dept Quim Inorgan, Seville 41071, Spain
Univ Barcelona, Dept Quim Inorgan, E-08028 Barcelona, Spain
CNR, ICCOM, I-50132 Florence, Italy (literal)
- Titolo
- Synthesis, molecular structure and properties of oxo-vanadium(IV) complexes containing the oxydiacetate ligand (literal)
- Abstract
- The complex [V(O)(oda)(H2O)2] 1 [oda = O(CH2COO)2] has been obtained by reaction of aqueous solutions of [V(O)(acac)2] with oxydiacetic acid. The coordination geometry around the vanadium in 1 is distorted octahedral with mutually trans water ligands and a planar conformation of the oda ligand (mer). The relative stability of the experimentally determined structure and that of the alternative isomer with a puckered oda conformation (fac) has been investigated by DFT calculations. The latter con rms that the mer geometry is more stable by 35.6 kJ mol 1. The complex [V(O)(oda)(µ-OMe)]2[Na(H2O)]2 2a is obtained by reaction of 1 with NaOH in methanol. The anions feature two V(O)(oda) units symmetrically bridged by methoxy groups in a syn-orthogonal arrangement, while the oda ligands have the fac conformation. Similar complexes [V(O)(oda)(µ-OMe)]2[K(H2O)]2 2b and [V(O)(oda)- (µ-OMe)]2[HL]2 2c 2g are obtained from reaction with KOH or with selected N-donor bases (L), respectively. An excess of pyridine, however, causes the simple substitution of the water molecules in 1 and generates the monomer [V(O)(oda)(py)2] 3. Antiferromagnetic behaviour of binuclear compounds 2a, 2d and 2e is suggested by a variabletemperature study. Finally, the reaction of 1 with bidentate N-donor ligands allows the synthesis of the complexes [V(O)(oda)(N N)] H2O (N N = 2,2 -bipyridine, 4; o-phenanthroline, 5). X-Ray characterization of 4 shows that the conformation of oda has changed from mer (as in the reactant 1) to fac. (literal)
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