Mechanisms of C–H bond activation: rich synergy between computation and experiment | Zendy

Y. Boutadla | Zendy; David L. Davies | Zendy; Stuart A. Macgregor | Zendy; Amalia I. PobladorBahamonde | Zendy

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Mechanisms of C–H bond activation: rich synergy between computation and experiment

Author(s) -

Y. Boutadla,

David L. Davies,

Stuart A. Macgregor,

Amalia I. PobladorBahamonde

Publication year - 2009

Publication title -

dalton transactions

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.98

H-Index - 184

eISSN - 1477-9234

pISSN - 1477-9226

DOI - 10.1039/b904967c

Subject(s) - heteroatom , ligand (biochemistry) , chemistry , lone pair , bond , metal , stereochemistry , transition metal , molecule , catalysis , organic chemistry , business , ring (chemistry) , receptor , biochemistry , finance

Recent computational studies of C-H bond activation at late transition metal systems are discussed and processes where lone pair assistance via heteroatom co-ligands or carboxylates are highlighted as a particularly promising means of cleaving C-H bonds. The term 'ambiphilic metal ligand activation' (AMLA) is introduced to describe such reactions.

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