A1 Refereed original research article in a scientific journal
Oxidomolybdenum(VI) complexes with atrane-type [O3N] ligands
Authors: Lauren E, Kivela H, Hanninen M, Lehtonen A
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Publication year: 2009
Journal:Polyhedron
Journal name in sourcePOLYHEDRON
Journal acronym: POLYHEDRON
Volume: 28
Issue: 18
First page : 4051
Last page: 4055
Number of pages: 5
ISSN: 0277-5387
DOI: https://doi.org/10.1016/j.poly.2009.09.033
Abstract
Dioxomolybdenum(VI) complex [MoO2Cl2(dmso)(2)] reacts with a series of tetradentate O3N-type amino-alcohol-bisphenol ligands to form oxomolybdenum(VI) complexes of type [MoOCl(L-n)]. The reaction of H3L1 produces [MoOCl(L-1)] as two separable isomers, whereas the reaction of H3L2 or H3L3 yields a single product. The X-ray analyses of cis- and trans-[MoOCl(L-1)] 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. (C) 2009 Elsevier Ltd. All rights reserved.
Dioxomolybdenum(VI) complex [MoO2Cl2(dmso)(2)] reacts with a series of tetradentate O3N-type amino-alcohol-bisphenol ligands to form oxomolybdenum(VI) complexes of type [MoOCl(L-n)]. The reaction of H3L1 produces [MoOCl(L-1)] as two separable isomers, whereas the reaction of H3L2 or H3L3 yields a single product. The X-ray analyses of cis- and trans-[MoOCl(L-1)] 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. (C) 2009 Elsevier Ltd. All rights reserved.
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