September 12, 2016
Journal Article

Nickel Bis-Diphosphine Complexes: Controlling the Binding and Heterolysis of H2

Abstract

Two new Ni(II) complexes, the homoleptic [Ni-(8PCy2NH)2]2+ complex (8PCy 2NH = 3,7-cyclohexyl-1-amino-3,7-diphosphacyclooctane) containing two pendant amines on adjacent ligands, and the heteroleptic [Ni(8PCy2NH)(dppe)]2+ complex (dppe = bis-(diphenylphosphino)ethane) containing only a single pendant amine, have been synthesized, and their electrochemical properties are reported. The [Ni(8PCy2NH)(dppe)]2+ complex is capable of heterolytically cleaving hydrogen, allowing for the first observation of an endoprotonated nickel hydride related to the [Ni(PR2NR'2)2]2+ family of complexes. The [Ni(8PCy2NH)(dppe)]2+ complex did not exhibit electrocatalytic H2 oxidation activity; however, [Ni(8PCy2NH)2]2+ is an active electrocatalyst for H2 oxidation with a maximum turnover frequency (kobs) of 18 s-1 under 1 atm H2 at Ecat/2 = -0.71 V versus the ferrocenium/ferrocene (Cp2Fe+/0) couple. In addition to an analysis of the effect of the number of pendant amines on the rates of electrocatalytic H2 oxidation of compounds related to the [Ni(PR 2NR'2)2]2+ family, the effect of the secondary pendant amine on intermolecular deprotonation is discussed.

Revised: January 16, 2020 | Published: September 12, 2016

Citation

Stolley R.M., J.M. Darmon, P. Das, and M.L. Helm. 2016. Nickel Bis-Diphosphine Complexes: Controlling the Binding and Heterolysis of H2. Organometallics 35, no. 17:2965-2974. PNNL-SA-121159. doi:10.1021/acs.organomet.6b00486