Abstract
The [Pd(SIPr)(PCy3)] complex efficiently promotes a tandem process involving dehydrogenation of formic acid and hydrogenation of C-C multiple bonds using H2 formed in situ. The isolation of a key catalytic hydridoformatopalladium species, [Pd{OC(O)H}(H)(IPr)(PCy 3)], is reported. The complex plays a key role in the Pd(0)-mediated formation of hydrogen from formic acid. Mechanistic and computational studies delineate the operational role of the palladium complex in this efficient tandem sequence. © 2013 American Chemical Society.
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CITATION STYLE
Broggi, J., Jurčík, V., Songis, O., Poater, A., Cavallo, L., Slawin, A. M. Z., & Cazin, C. S. J. (2013). The isolation of [Pd{OC(O)H}(H)(NHC)(PR3)] (NHC = N-heterocyclic carbene) and its role in alkene and alkyne reductions using formic acid. Journal of the American Chemical Society, 135(12), 4588–4591. https://doi.org/10.1021/ja311087c
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