A Highly Active Manganese Precatalyst for the Hydrosilylation of Ketones and Esters

Published on 2017-12-07T20:13:50Z (GMT) by
The reduction of (<sup>Ph<sub>2</sub>PPr</sup>PDI)­MnCl<sub>2</sub> allowed the preparation of the formally zerovalent complex, (<sup>Ph<sub>2</sub>PPr</sup>PDI)­Mn, which features a pentadentate bis­(imino)­pyridine chelate. This complex is a highly active precatalyst for the hydrosilylation of ketones, exhibiting TOFs of up to 76,800 h<sup>–1</sup> in the absence of solvent. Loadings as low as 0.01 mol % were employed, and (<sup>Ph<sub>2</sub>PPr</sup>PDI)Mn was found to mediate the atom-efficient utilization of Si–H bonds to form quaternary silane products. (<sup>Ph<sub>2</sub>PPr</sup>PDI)Mn was also shown to catalyze the dihydrosilylation of esters following cleavage of the substrate acyl C–O bond. Electronic structure investigation of (<sup>Ph<sub>2</sub>PPr</sup>PDI)Mn revealed that this complex possesses an unpaired electron on the metal center, rendering it likely that catalysis takes place following electron transfer to the incoming carbonyl substituent.

Cite this collection

Mukhopadhyay, Tufan

K.; Flores, Marco; Groy, Thomas L.; Trovitch, Ryan J. (2017): A Highly

Active Manganese Precatalyst for the Hydrosilylation

of Ketones and Esters. ACS Publications. Collection.