Microreview
Ligand Redox Non-Innocence in Transition-Metal σ-Alkynyl and Related Complexes
Article first published online: 13 DEC 2011
DOI: 10.1002/ejic.201100995
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

European Journal of Inorganic Chemistry
Special Issue: Coopertive & Redox Non-Innocent Ligands in Directing Organometallic Reactivity (Cluster Issue)
Volume 2012, Issue 3, pages 390–411, January 2012
Additional Information
How to Cite
Schauer, P. A. and Low, P. J. (2012), Ligand Redox Non-Innocence in Transition-Metal σ-Alkynyl and Related Complexes. Eur. J. Inorg. Chem., 2012: 390–411. doi: 10.1002/ejic.201100995
Publication History
- Issue published online: 16 JAN 2012
- Article first published online: 13 DEC 2011
- Manuscript Received: 19 SEP 2011
Funded by
- Engineering and Physical Science Research Council (EPSRC)
- Abstract
- Article
- References
- Cited By
Keywords:
- Redox chemistry;
- Radical reactions;
- Ligand effects;
- Alkyne ligands;
- Ruthenium
Abstract
Transition-metal σ-alkynyl complexes are valuable functional materials that have found application as sructural units in the assembly of polymetallic arrays and large molecular structures, reagents for the transfer, oligomerisation or functionalisation of alkynes, magnetic or optical materials and putative components for use in a future molecular-based electronics platform. Many σ-alkynyl complexes are redox-active, undergoing facile oxidation (reduction) at moderate potentials to generate radical cations (anions) in which the charge and spin density can be tuned from being largely metal-centred to alkynyl ligand-centred by variation of the nature of the metal, supporting ligands and alkynyl substituents. This review summarises the diverse chemical behaviour of metal-supported σ-alkynyl radicals, and some selected closely related systems, which can often be rationalised in terms of the distribution of electron-spin density over the metal–alkynyl scaffold.

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