Toggle Main Menu Toggle Search

Open Access padlockePrints

Synthesis of Copper(I) Complexes of N-Heterocyclic Carbene-Phenoxyimine/amine Ligands: Structures of Mononuclear Copper(II), Mixed-Valence Copper(I)/(II), and Copper(II) Cluster Complexes

Lookup NU author(s): Professor William Clegg, Dr Ross Harrington, Lucinda Male

Downloads

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


Abstract

Copper(I) bromide complexes (2a and 2b) of NHC-phenolimine ligand precursors {3-[(1R,2R)-2-{[1-(3,5-di-tert-butyl-2-hydroxyphenyl)meth-(E)-ylidene]amino}cyclohexyl]-1-isopropyl-4-phenyl-3H-imidazol-1-ium bromide (1a) and 3-(1R,2R)-2-{[1-(2-hydroxyphenyl)meth-(E)-ylidene]amino}- cyclohexyl]-1-isopropyl-4-phenyl-3H-imidazol-1-ium bromide (1b), respectively} have been prepared. Complexes 2a and 2b exhibit copper coordination only through the carbene carbon atom (C) and do not spontaneously eliminate HBr to give additional phenoxyimine (NO) bonds, which is attributed to intramolecular hydrogen bonding. Crystallisation of 2a and 2b gives 2a' and 2b', respectively, that contain (C) copper(I) bromide and (NO)(2) copper(II) coordination. Complex 2b' also exhibits intermolecular CuIBr interactions giving a Cu2Br2 bridge that links two molecules of 2b' resulting in an ellipse motif. Reduction of the hgand precursor imine group of la allows synthesis of silver(I) and copper(I) NHCphenolamine complexes 6 and 7, respectively, that also retain the phenol hydrogen atom. Attempts to selectively prepare 2a' gave a copper(II) complex 9 that exhibits an (NO)(2)Cu-II structure with pendant in-ddazolium salt groups. Reaction between the silver(I) bromide derivative of la and CuCl2 center dot 2H(2)O gives a complex derived from a Cu-6(O)(OH)(4)Cl-3 core and two (NO) and one (CNO) ligands, respectively. The use of 2a and 7 as precatalysts for 1,4-conjugate addition to enones and aziridination of alkenes was studied, showing that, whilst both catalysts are active, enantioselectivities are low, which is attributed to the lack of Cu-(NO) coordination. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheirn, Germany, 2009)


Publication metadata

Author(s): Simonovic S, Whitwood AC, Clegg W, Harrington RW, Hursthouse MB, Male L, Douthwaite RE

Publication type: Review

Publication status: Published

Journal: European Journal of Inorganic Chemistry

Year: 2009

Issue: 13

Pages: 1786-1795

ISSN (print): 1434-1948

ISSN (electronic): 1099-0682

Publisher: WILEY-V C H VERLAG GMBH

URL: http://dx.doi.org/10.1002/ejic.200801152

DOI: 10.1002/ejic.200801152


Share