Coinage metal amido and thiolate SNS complexes: consequences of catalyst speciation in Cu(I)-catalysed carbonyl hydroboration
Saeed Ataie1, Maxwell Lohoar2, Loïc P Mangin1
1Department of Chemistry and Biomolecular Sciences and Centre for Catalysis Research and Innovation, University of Ottawa, Ottawa, Ontario, K1N 6N5, Canada. rbaker@uottawa.ca.
Abstract:
Three new IPr-Ag- and -Au-SNS amido and thiolate complexes were synthesized and compared to their previously reported Cu analogues as carbonyl hydroboration catalysts (IPr = bis(2,6-diisopropylphenyl)imidazol-2-ylidene). Although these complexes showed no catalytic activity, treatment of the IPr-Ag-SNS amido complex with pinacolborane released the N-borylated ligand, SMeNBpinSMe, (L1-Bpin). This finding led us to reinvestigate the IPr-Cu-SNS amido precatalyst, revealing that immediate loss of L1-Bpin converts our catalyst system to [CuH(IPr)]2.
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