Incorporating peptides in the outer-coordination sphere of bioinspired electrocatalysts for hydrogen production

Inorg Chem. 2011 May 2;50(9):4073-85. doi: 10.1021/ic1025872. Epub 2011 Apr 1.

Abstract

Four new cyclic 1,5-diaza-3,7-diphosphacyclooctane ligands have been prepared and used to synthesize [Ni(P(Ph)(2)N(R)(2))(2)](2+) complexes in which R is a mono- or dipeptide. These complexes represent a first step in the development of an outer-coordination sphere for this class of complexes that can mimic the outer-coordination sphere of the active sites of hydrogenase enzymes. Importantly, these complexes retain the electrocatalytic activity of the parent [Ni(P(Ph)(2)N(Ph)(2))(2)](2+) complex in an acetonitrile solution with turnover frequencies for hydrogen production ranging from 14 to 25 s(-1) in the presence of p-cyanoanilinium trifluoromethanesulfonate and from 135 to 1000 s(-1) in the presence of protonated dimethylformamide, with moderately low overpotentials, ∼0.3 V. The addition of small amounts of water results in rate increases of 2-7 times. Unlike the parent complex, these complexes demonstrate dynamic structural transformations in solution. These results establish a building block from which larger peptide scaffolding can be added to allow the [Ni(P(R)(2)N(R')(2))(2)](2+) molecular catalytic core to begin to mimic the multifunctional outer-coordination sphere of enzymes.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acids / chemistry
  • Biomimetic Materials / chemical synthesis
  • Biomimetic Materials / chemistry*
  • Catalysis
  • Dipeptides / chemistry
  • Electrochemistry
  • Hydrogen / chemistry*
  • Hydrogenase / chemistry
  • Hydrogenase / metabolism
  • Ligands
  • Models, Molecular
  • Molecular Conformation
  • Nitrogen / chemistry
  • Peptides / chemistry*
  • Spectrum Analysis
  • Water / chemistry

Substances

  • Amino Acids
  • Dipeptides
  • Ligands
  • Peptides
  • Water
  • Hydrogen
  • Hydrogenase
  • Nitrogen