Moving Protons with Pendant Amines: Proton Mobility in a Nickel Catalyst for Oxidation of Hydrogen

• Published in: Journal of the American Chemical Society 2011-09, Vol.133 (36), p.14301-14312
• Main Authors: O’Hagan, Molly, Shaw, Wendy J, Raugei, Simone, Chen, Shentan, Yang, Jenny Y, Kilgore, Uriah J, DuBois, Daniel L, Bullock, R. Morris
• Format: Article
• Language: English
• Subjects: 08 HYDROGEN; AMINES; Amines - chemistry; AVAILABILITY; CATALYSIS; CATALYSTS; ELECTROCATALYSTS; Environmental Molecular Sciences Laboratory; FUNCTIONALS; HYDROGEN; Hydrogen - chemistry; HYDROGENASES; ISOMERS; Magnetic Resonance Spectroscopy; NICKEL; Nickel - chemistry; OXIDATION; Oxidation-Reduction; PROTONS
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja201838x

Proton transport is ubiquitous in chemical and biological processes, including the reduction of dioxygen to water, the reduction of CO2 to formate, and the production/oxidation of hydrogen. In this work we describe intramolecular proton transfer between Ni and positioned pendant amines for the hydrogen oxidation electrocatalyst [Ni(PCy 2NBn 2H)2]2+ (PCy 2NBn 2 = 1,5-dibenzyl-3,7-dicyclohexyl-1,5-diaza-3,7-diphosphacyclooctane). Rate constants are determined by variable-temperature one-dimensional NMR techniques and two-dimensional EXSY experiments. Computational studies provide insight into the details of the proton movement and energetics of these complexes. Intramolecular proton exchange processes are observed for two of the three experimentally observable isomers of the doubly protonated Ni(0) complex, [Ni(PCy 2NBn 2H)2]2+, which have N–H bonds but no Ni–H bonds. For these two isomers, with pendant amines positioned endo to the Ni, the rate constants for proton exchange range from 104 to 105 s–1 at 25 °C, depending on isomer and solvent. No exchange is observed for protons on pendant amines positioned exo to the Ni. Analysis of the exchange as a function of temperature provides a barrier for proton exchange of ΔG ⧧ = 11–12 kcal/mol for both isomers, with little dependence on solvent. Density functional theory calculations and molecular dynamics simulations support the experimental observations, suggesting metal-mediated intramolecular proton transfers between nitrogen atoms, with chair-to-boat isomerizations as the rate-limiting steps. Because of the fast rate of proton movement, this catalyst may be considered a metal center surrounded by a cloud of exchanging protons. The high intramolecular proton mobility provides information directly pertinent to the ability of pendant amines to accelerate proton transfers during catalysis of hydrogen oxidation. These results may also have broader implications for proton movement in homogeneous catalysts and enzymes in general, with specific implications for the proton channel in the Ni–Fe hydrogenase enzyme.