Artigo Revisado por pares

Oxidomolybdenum(VI) complexes with atrane-type [O3N] ligands

2009; Elsevier BV; Volume: 28; Issue: 18 Linguagem: Inglês

10.1016/j.poly.2009.09.033

ISSN

1873-3719

Autores

E. Lauren, Henri Kivelä, Mikko M. Hänninen, Ari Lehtonen,

Tópico(s)

Metal-Catalyzed Oxygenation Mechanisms

Resumo

Dioxomolybdenum(VI) complex [MoO2Cl2(dmso)2] reacts with a series of tetradentate O3N-type aminoalcohol–bisphenol ligands to form oxomolybdenum(VI) complexes of type [MoOCl(Ln)]. The reaction of H3L1 produces [MoOCl(L1)] as two separable isomers, whereas the reaction of H3L2 or H3L3 yields a single product. The X-ray analyses of cis- and trans-[MoOCl(L1)] reveal that the complexes are formed of monomeric molecules. The ligands have tetradentate coordination through three oxygen donors and one nitrogen donor, which is located trans to the terminal oxo group. The sixth coordination site is occupied by a chloro ligand.

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