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On charge transfer-assisted polynucleation reactions. A trinuclear carbonyl-tungsten complex of ambident 4,4'-bipyrimidine

, und . Inorganica Chimica Acta 144 (2): 223--226 (1988)

Zusammenfassung

Coordinative satn. of 4,4'-bipyrimidine (L) was achieved in W(CO)52-m4-LW(CO)4. Electrochem. and spectroscopic studies of the compd. and its anion radical exhibit a metal-to-ligand charge-transfer absorption max. at unexpected high energy, despite a small HOMO/LUMO gap. Inspection of band widths shows that large Franck-Condon contributions from the structurally flexible W(CO)5 fragments are responsible for the hypsochromic shift relative to the mononuclear chelate system. The propensity of polyfunctional p acceptor ligands towards complete coordinative satn. with electron-rich metal fragments is discussed. on SciFinder(R)

Links und Ressourcen

DOI:
10.1016/S0020-1693(00)86290-8
BibTeX-Schlüssel:
Ernst.1988
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