Normal and abnormal N-heterocylic carbene ligands: Similarities and differences of different mesoionic C-donor complexes
Files in This Item:
|AdvOM_carbenes_final.doc||1.39 MB||Microsoft Word||Download|
|Title:||Normal and abnormal N-heterocylic carbene ligands: Similarities and differences of different mesoionic C-donor complexes||Authors:||Albrecht, Martin||Permanent link:||http://hdl.handle.net/10197/6662||Date:||3-Oct-2014||Abstract:||Similarities and differences of normal versus abnormal carbene complexes are highlighted, with an emphasis on effects that can be directly attributed to the different bonding mode and which are thus not imparted by potential stereoelectronic effects such as more or less shielding of the MC bond. While generally, the bonding scheme is similar throughout all classes of carbenes, distinctly different behaviors have been noted in some reactivity patterns, in particular when comparing different bonding modes of imidazolylidenes. This distinction is blurred with triazolylidenes, and the normal/abnormal nomenclature is not particularly meaningful in these cases. With pyridylidenes, structural differences are noted in the ground state, while reactivity patterns are not significantly dependent on the metal binding site. Common denominators for all normal and abnormal heterocyclic carbene complexes include (i) a strongly mesoionic character of both normal and abnormal bonding modes of the ligand, and (ii) a negligibly small carbenic character. Accordingly 'carbene' is a rather debatable name for this class of ligands, and 'mesoionic C-donor' may be more accurate.||Type of material:||Book Chapter||Publisher:||Elsevier||Copyright (published version):||2014 Elsevier||Keywords:||N-Heterocyclic carbene; Mesoionic; Abnormal bonding; Catalysis; Structures; Triazolylidenes; Pyridylidenes; Hydrogenation; Cross-coupling; Donor properties||DOI:||10.1016/B978-0-12-800976-5.00002-3||Language:||en||Status of Item:||Peer reviewed||Is part of:||Pérez, P. J. (ed.). Advances in Organometallic Chemistry, vol. 62|
|Appears in Collections:||Chemistry Research Collection|
Show full item record
Page view(s) 5028
This item is available under the Attribution-NonCommercial-NoDerivs 3.0 Ireland. No item may be reproduced for commercial purposes. For other possible restrictions on use please refer to the publisher's URL where this is made available, or to notes contained in the item itself. Other terms may apply.