Issue 2, 2013

Carbazole functionalized luminescent silver(i), gold(i) and gold(iii)–N-heterocyclic carbene complexes: a new synthetic disproportionation approach towards Au(i)–NHC to provide Au(iii)–NHC

Abstract

Synthetic, structural and photophysical properties of carbazole functionalized novel procarbenic species 1-(methyl/picolyl)-3-(N-ethylcarbazolyl)-1H benzimidazoliumhexaflurophosphate (1 and 2) and their N-heterocyclic carbene (NHC) complexes of Ag(I) (3 and 4), Au(I) (5 and 6) and Au(III) (7 and 8) are described. According to the solid-state structures, a linear coordination geometry of Ag(I)–NHC (4) and Au(I)–NHC (6) has been established by X-ray diffraction studies; whereas the Au(III)–NHC complex (7) adopts the square planar geometry. The Au(III)–NHC (7 and 8) complexes have been synthesized from Au(I)–NHC (5 and 6) by capitalizing on a novel disproportionation protocol. Furthermore, the Au–Ccarbene bonds in complexes 7 and 8 are inert towards changes in the oxidation state of the metal atom. All the proligands (1 and 2) and complexes (3–8) are luminescent at room temperature.

Graphical abstract: Carbazole functionalized luminescent silver(i), gold(i) and gold(iii)–N-heterocyclic carbene complexes: a new synthetic disproportionation approach towards Au(i)–NHC to provide Au(iii)–NHC

Supplementary files

Article information

Article type
Paper
Submitted
19 Aug 2012
Accepted
24 Oct 2012
First published
26 Oct 2012

New J. Chem., 2013,37, 431-438

Carbazole functionalized luminescent silver(I), gold(I) and gold(III)–N-heterocyclic carbene complexes: a new synthetic disproportionation approach towards Au(I)–NHC to provide Au(III)–NHC

J. Dinda, S. D. Adhikary, S. K. Seth and A. Mahapatra, New J. Chem., 2013, 37, 431 DOI: 10.1039/C2NJ40740J

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