http://www.cnr.it/ontology/cnr/individuo/prodotto/ID16780
Thiodiacetate and Oxydiacetate Cobalt Complexes: Synthesis, Structure and Stereochemical Features (Articolo in rivista)
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- Thiodiacetate and Oxydiacetate Cobalt Complexes: Synthesis, Structure and Stereochemical Features (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/ejic.200700075 (literal)
- Alternative label
GrirraneAbdessamad; Pastor, Antonio; Álvarez, Eleuterio; Mealli, Carlo; Ienco, Andrea; Rosa, Patrick; Galindo, Agustin (2007)
Thiodiacetate and Oxydiacetate Cobalt Complexes: Synthesis, Structure and Stereochemical Features
in European journal of inorganic chemistry (Print); WILEY-V C H VERLAG GMBH, WEINHEIM (Germania)
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- GrirraneAbdessamad; Pastor, Antonio; Álvarez, Eleuterio; Mealli, Carlo; Ienco, Andrea; Rosa, Patrick; Galindo, Agustin (literal)
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- Univ Seville, Dept Quim Inorgan, E-41071 Seville, Spain
Univ Seville, CSIC, Inst Invest Quim, E-41092 Seville, Spain
CNR, ICCOM, I-50019 Florence, Italy
Univ Florence, Dipartimento Chim, LAMM, Florence, Italy
Univ Bordeaux 1, Inst Chim Mat Condensee Bordeaux, CNRS, Grp Sci Mol, F-33608 Pessac, France (literal)
- Titolo
- Thiodiacetate and Oxydiacetate Cobalt Complexes: Synthesis, Structure and Stereochemical Features (literal)
- Abstract
- A series of cobalt complexes containing the dianionic ligands X(CH,COO)(2) 2- (X = S, tda; or X = O, oda) is reported. The complexes [Co(tda)(bipy)(H2O)center dot-4H(2)O (2), which was characterised by X-ray crystallography, [Co(tda)(phen)(H2O)] (3), [Co(tda){(MeO)(2)bipy}(H2O)]-2H(2)O (4) and [Co(tda)(dpp)(H2O)]center dot 2H(2)O (5) are obtained by reaction of the precursor complex [Co(tda)(H2O)], (1a) with the bidentate N-donor ligands 2,2'-bipyridine (bipy), o-phenanthroline (phen), 4,4'dimethoxy-2,2'-bipyridine [{(MeO)2bipy] and 2,3-bis(2-pyridyl)pyrazine (dpp), respectively. The reaction of la with di(2-pyridyl) ketone unexpectedly displaces tda from the coordination sphere and leads to the Co-III species [Co(OC(OH)(2-pyridyl)2-puridil)(2)}(2)](+)[Htda]center dot 3H(2)O (6), as confirmed by an X-ray analysis. Three new oxydiacetate complexes of cobalt are also synthesised by treating the known complex [(Co(oda)(H2O)2)-H2O], with 4,4'-di-tert-butyl-2,2'-bipyridine (tBu(2)bipy), 2,3-bis(2-pyridyl)pyrazine (dpp) and 4,4'-bipyridine (4,4'-bipy). The complexes [Co(oda)(tBu(2)bipy)(H2O)]center dot l.5H(2)O (7), [Co(oda)(dpp)(H2O)j-2H(2)O (8) and [Co(oda)(H2O)2)2(P4,4'-bipy)]-2H(2)O (9) are structurally characterised (8 as a methanol solvate). Complex 9 is binuclear, in contrast to 7 and 8 (mononuclear), and magnetic susceptibility measurements down to 2 K for this complex show high-spin noncorrelated Con ions with a typical Curie-Weiss behaviour. The Co(oda) fragment in 7-9 adopts a planar (mer) rather than a folded (fac) conformation, the latter of which is common to all the M(tda) complexes but is only occasionally observed in the M(oda) ones. In the final section of the paper, the key geometric parameters that control the stereochemistry of the two ligands are determined from a statistical analysis based on the structurally characterised Co(oda) and Co(tda) complexes. (literal)
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