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Issue 32, 2013
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N-Aryl β-diiminate complexes of the platinum metals

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Abstract

This perspective summarizes the chemistry of platinum metal complexes of β-diiminate ligands bearing aryl groups at the nitrogen atoms. While β-diiminate ligands mostly coordinate in a κ2-N,N′ mode, palladium complexes have a tendency to rearrange to C-bound structures (κ2-N,C or μ-N,N′:C). Diiminate ligands are remarkably effective at stabilizing coordinatively unsaturated metal centers, and the resulting reactive complexes often activate C–H bonds even of relatively unreactive substrates (ethers, alkanes). However, the ligands are not completely innocent: addition of H2, O2, olefins, alkynes and phospha-alkynes across M-Cβ has been observed for several of the platinum metals, and may even be relevant to catalytic activity. A comparison with related ligands (triazapentadienyl, formazanate, bis(phosphinimino)methanate) suggests that the β-diiminate ligand represents a lucky combination of steric rigidity and strong σ (and π?) donor character, making it an ideal platform for mechanistic studies of catalytic reactions.

Graphical abstract: N-Aryl β-diiminate complexes of the platinum metals

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Supplementary files

Article information


Submitted
16 Mar 2013
Accepted
10 Jun 2013
First published
20 Jun 2013

Dalton Trans., 2013,42, 11343-11354
Article type
Perspective

N-Aryl β-diiminate complexes of the platinum metals

D. Zhu and P. H. M. Budzelaar, Dalton Trans., 2013, 42, 11343
DOI: 10.1039/C3DT50715G

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