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

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.

[MoO2Cl2(dmso)2] reacts with tripodal aminoalcohol-bis(phenol)s to form oxomolybdenum(VI) complexes [MoOCl(L)] as two separable isomers. The ligand has tetradentate coordination through three oxygen donors and one nitrogen donor. The sixth coordination site is occupied by a chloro ligand, which can be further substituted by a methyl group to obtain an air-stable organomolybdenum(VI) derivative.Figure optionsDownload as PowerPoint slide