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Title: The role of solvent and the outer coordination sphere on H 2 oxidation using [Ni(P Cy 2N Pyz 2) 2] 2+

Abstract

Hydrogenase enzymes are reversible catalysts for H 2 production/oxidation, operating with fast rates and minimal overpotentials in water. Many synthetic catalyst mimics of hydrogenase operate in organic solvents. However, recent work has demonstrated the importance of water in the performance of some model complexes. In this work, the H 2oxidation activity of [Ni(P Cy 2N (3–pyridazyl)methyl 2) 2] 2+ (CyPyz) was compared as a function of acetonitrile, methanol, and water. The reactivity was compared under neutral and acidic conditions in all three solvents and improvement in catalytic activity, from 2 to 40 s -1, was observed with increasing hydrogen bonding ability of the solvent. In addition, the overpotential for catalysis drops significantly in the presence of acid in all solvents, from as high as 600 mV to as low as 70 mV, primarily due to the shift in the equilibrium potential under these conditions. Finally, H 2 production was also observed in the same solution, demonstrating bidirectional (irreversible) homogeneous H 2 production/oxidation. A structurally and electronically similar complex with a benzyl instead of a pyridazyl group was not stable under these conditions, limiting the evaluation of the contributions of the outer coordination sphere. Collectively, we show that by tuning conditionsmore » we can promote fast, efficient H 2 oxidation and bidirectional catalysis.« less

Authors:
; ; ; ;
Publication Date:
Research Org.:
Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)
Sponsoring Org.:
USDOE
OSTI Identifier:
1233766
Report Number(s):
PNNL-SA-105208
Journal ID: ISSN 1099-0682; 44681; KC0302010
DOE Contract Number:  
AC05-76RL01830
Resource Type:
Journal Article
Journal Name:
European Journal of Inorganic Chemistry (Online)
Additional Journal Information:
Journal Volume: 2015; Journal Issue: 31; Journal ID: ISSN 1099-0682
Publisher:
ChemPubSoc Europe
Country of Publication:
United States
Language:
English
Subject:
Bidirectional catalysis; Outer coordination sphere; H2 oxidation/production; Catalytic directionality; Bioinspired catalyst design; Environmental Molecular Sciences Laboratory

Citation Formats

Dutta, Arnab, Lense, Sheri J., Roberts, John A., Helm, Monte L., and Shaw, Wendy J. The role of solvent and the outer coordination sphere on H2 oxidation using [Ni(PCy2NPyz2)2]2+. United States: N. p., 2015. Web. doi:10.1002/ejic.201500732.
Dutta, Arnab, Lense, Sheri J., Roberts, John A., Helm, Monte L., & Shaw, Wendy J. The role of solvent and the outer coordination sphere on H2 oxidation using [Ni(PCy2NPyz2)2]2+. United States. doi:10.1002/ejic.201500732.
Dutta, Arnab, Lense, Sheri J., Roberts, John A., Helm, Monte L., and Shaw, Wendy J. Fri . "The role of solvent and the outer coordination sphere on H2 oxidation using [Ni(PCy2NPyz2)2]2+". United States. doi:10.1002/ejic.201500732.
@article{osti_1233766,
title = {The role of solvent and the outer coordination sphere on H2 oxidation using [Ni(PCy2NPyz2)2]2+},
author = {Dutta, Arnab and Lense, Sheri J. and Roberts, John A. and Helm, Monte L. and Shaw, Wendy J.},
abstractNote = {Hydrogenase enzymes are reversible catalysts for H2 production/oxidation, operating with fast rates and minimal overpotentials in water. Many synthetic catalyst mimics of hydrogenase operate in organic solvents. However, recent work has demonstrated the importance of water in the performance of some model complexes. In this work, the H2oxidation activity of [Ni(PCy2N(3–pyridazyl)methyl2)2]2+ (CyPyz) was compared as a function of acetonitrile, methanol, and water. The reactivity was compared under neutral and acidic conditions in all three solvents and improvement in catalytic activity, from 2 to 40 s-1, was observed with increasing hydrogen bonding ability of the solvent. In addition, the overpotential for catalysis drops significantly in the presence of acid in all solvents, from as high as 600 mV to as low as 70 mV, primarily due to the shift in the equilibrium potential under these conditions. Finally, H2 production was also observed in the same solution, demonstrating bidirectional (irreversible) homogeneous H2 production/oxidation. A structurally and electronically similar complex with a benzyl instead of a pyridazyl group was not stable under these conditions, limiting the evaluation of the contributions of the outer coordination sphere. Collectively, we show that by tuning conditions we can promote fast, efficient H2 oxidation and bidirectional catalysis.},
doi = {10.1002/ejic.201500732},
journal = {European Journal of Inorganic Chemistry (Online)},
issn = {1099-0682},
number = 31,
volume = 2015,
place = {United States},
year = {2015},
month = {5}
}