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Expanded-ring and backbone-functionalised N-heterocyclic carbenes

Iglesias, Manuel Alonso, Beetstra, Dirk Johannes, Cavell, Kingsley John, Dervisi, Athanasia, Fallis, Ian Andrew, Kariuki, Benson, Harrington, Ross W., Clegg, William, Horton, Peter N., Coles, Simon J. and Hursthouse, Michael B. 2010. Expanded-ring and backbone-functionalised N-heterocyclic carbenes. European Journal of Inorganic Chemistry 2010 (11) , pp. 1604-1607. 10.1002/ejic.200901182

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Abstract

An unsaturated seven-membered amidinium salt 7 decomposes in the presence of metal salts under basic conditions. However, 7 readily forms a Diels–Alder cycloadduct with CpH from which the RhI complexes may be prepared. Thus, structurally elaborate, sterically crowded carbene ligand complexes bearing peripheral unsaturated functionality are available in a short versatile synthesis.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Cardiff Catalysis Institute (CCI)
Subjects: Q Science > QD Chemistry
Uncontrolled Keywords: Carbene ligands; Cycloaddition; Rhodium; Ligand design; Isomers
Publisher: Wiley
ISSN: 1434-1948
Last Modified: 04 Jun 2017 02:51
URI: http://orca.cf.ac.uk/id/eprint/12849

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Cited 14 times in Web of Science. View in Web of Science.

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