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