Toggle Main Menu Toggle Search

Open Access padlockePrints

'Electronic bending' of imido ligands and the effect on the coordination mode of a tridentate ancillary ligand

Lookup NU author(s): Emeritus Professor Bill Clegg, Dr Mark Elsegood

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Abstract

The five-coordinate mixed-imido complex [Mo(Nt-Bu)(NC6F5)(L)] (1) can be prepared in high yield via treatment of [Mo(Nt-Bu)(NC6F5)(Ot-Bu)2] with LH2, where LH2 is 2,6-bis(2-hydroxy-2,2-diphenylethyl)pyridine. Contrastingly, the reaction of [Mo(NAd)(NC6F5)(Ot-Bu)2] (Ad = adamantyl, C6H10) with LH2 gave [Mo(NAd)2(L)] (2) via an imido-exchange reaction. Complex 2 can also be synthesised via treatment of in situ generated [Mo(NAd)2(Ot-Bu)2] with LH2; the latter method also results in trace amounts of the five-coordinate complex [MoCl(NAd)2(Ldehyd)] (3) (Ldehyd = 2-(2-hydroxy-2,2-diphenylethenyl)pyridine). The structures of 1-3 have been determined by X-ray crystallographic study. In each complex, the geometry at the metal is distorted trigonal bipyramidal with the pyridinediolate ligand adopting an 'aea' bonding arrangement in 1 and an 'eee' arrangement in 2. The angle associated with the imido moiety also varies, with the greatest deviations found in 1 and 3, indeed, the pentafluoroimido ligand in 1 has one of the largest deviations from linearity for an M-N-C angle recorded to-date [135.98(16)°]. This has been rationalised on the basis of an electronic effect rather than intramolecular steric interactions or crystal packing forces. © 2007 Elsevier Ltd. All rights reserved.


Publication metadata

Author(s): Gibson VC, Redshaw C, Clegg W, Elsegood MRJ

Publication type: Article

Publication status: Published

Journal: Polyhedron

Year: 2007

Volume: 26

Issue: 13

Pages: 3161-3167

ISSN (print): 0277-5387

ISSN (electronic): 1873-3719

Publisher: Pergamon

URL: http://dx.doi.org/10.1016/j.poly.2007.02.008

DOI: 10.1016/j.poly.2007.02.008


Altmetrics

Altmetrics provided by Altmetric


Actions

Find at Newcastle University icon    Link to this publication


Share