Catalyst tuning by changing ligands is a well-established protocol in transition-metal chemistry. N-Heterocyclic carbenes (NHCs) and tertiary phosphines (R(3)P) are the ubiquitous ligand actors. Here we demonstrate that the relative sigma-donor/pi-acceptor ability of the NHC ligand itself can be influenced by a simple substituent-controlled conformational change, thereby directly impacting the reactivity of the transition-metal complex.
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Aktas et al. (2009) studied this question.
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