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Dennis H. Evans, Department of Chemistry, The University of Arizona
Photo of Dennis H. Evans

Dennis H. Evans


Professor of Chemistry
dhevans@email.arizona.edu
Carl S. Marvel Laboratories 436
Phone: (520) 626-0318
Fax: (520) 621-8407

Honors


  • Manuel M. Baizer Award of the Division of Organic and Biological Electrochemistry, 2004
  • Fellow of the Electrochemical Society, 1998
  • University of Delaware Faculty Award: Outstanding Scholar in the College of Arts and Science, 1995
  • C. N. Reilley Award, Society for Electroanalytical Chemistry, 1993

Education and Appointments


  • B.S. 1960, Ottawa University
  • M.S. 1961, Harvard University
  • Ph.D. 1964, Harvard University

Research Interests


  • Analytical
  • Catalysis and Reaction Dynamics
  • Instrumentation
  • Organometallic and Coordination Chemistry
  • Surface Science

Research Summary

Elucidation of the Mechanisms of Complex, Multi-step Electrode Reactions of Organic and Organometallic Compounds including the Evaluation of the Catalytic Efficiency of Synthetic Diiron Hydrogenase Mimics

The principal objective of research in this group is the elucidation of the mechanisms of complex, multi-step electrode reactions of organic and organometallic compounds. The results of this research are relevant not only in the areas of organic and inorganic chemistry, but also find applications in chemical analysis, electroorganic synthesis, pollution control, electrocatalysis, batteries and fuel cells.

A full understanding of an electrode reaction must include a complete description of its component steps. Thus, our work includes studies of the factors controlling the rates of simple electron-transfer reactions occurring at electrode surfaces as well as the electron-transfer reactions in solution near the electrode that involve the various species in the overall mechanism (reactants, intermediates, products).

Other component reactions are of a more chemical nature. They may be as simple as an isomerization or conformational change of the reactant or an intermediate. However, bonds may also be formed (dimerization, protonation) or broken (loss of an atom or functional group) and these steps combine with the electron-transfer reactions to make up the overall process.

We have recently initiated studies of the electrocatalysis of the reduction of weak acids to produce dihydrogen. These synthetic catalysts are mimics of the active sites of diiron hydrogenase enzymes. The mechanisms of the electrocatalysis have not been fully elucidated and such studies are underway in order to obtain mechanistic understanding that will guide the synthesis of new catalysts.

The techniques that are employed include all of the methods of electroanalytical chemistry with particular emphasis on the use of microelectrodes to facilitate fast measurements. The group is especially well known for the application of fast scan cyclic voltammetry to electroanalytical problems. New capabilities recently acquired include instrumentation for electrochemical impedance spectroscopy and the electrochemical quartz crystal microbalance. The standard chromatographic and spectroscopic methods are employed for the characterization of the starting materials and products of electrode reactions.

Selected Publications

  • "Reduction of Diesters of 1,2-Diols. Regioselective C-O Bond Cleavage in the Anionic Forms", N. A. Macías-Ruvalcaba, C. L. Moy, Z.-R. Zheng and D. H. Evans, J. Org. Chem. 2006, 71, 4829-4834.

  • "Studies of Potential Inversion in an Extended Tetrathiafulvalene", N. E. Gruhn, N. A. Macías-Ruvalcaba and D. H. Evans, Langmuir 2006, 22, 10683-10688.

  • "Iron-only Hydrogenase Mimics. Thermodynamic Aspects of the Use of Electrochemistry to Evaluate Catalytic Efficiency for Hydrogen Generation", G. A. N. Felton, R. S. Glass, D. L. Lichtenberger and D. H. Evans, Inorg. Chem. 2006, 45, 9181-9184. Correction: Inorg. Chem. 2007, 46, 5126.

  • "Change in Reaction Pathway in the Reduction of 3,5-Di-tert-butyl-1,2-benzoquinone with Increasing Concentrations of 2,2,2-Trifluoroethanol", N. A. Macías-Ruvalcaba, N. Okumura and D. H. Evans, J. Phys. Chem. B 2006, 110, 22043-22047.

  • "Studies of the Electrochemical Reduction of Some Dinitroaromatics", N. A. Macías-Ruvalcaba, João P. Telo, and D. H. Evans, J. Electroanal. Chem. 2007, 600, 294-302.

  • "Electron-transfer Reactions with Significant Changes in Structure. Unsymmetrical Crowded Ethylenes", N. A. Macías-Ruvalcaba and D. H. Evans, J. Phys. Chem. B 2006, 110, 24786-24795.

  • "Quantitative Evaluation of the Mechanism of Electroreduction of Benzoyl Cyanides", N. A. Macías-Ruvalcaba and D. H. Evans, J. Org. Chem. 2007, 72, 589-594.

  • "Mechanism Involving a Preceding Structural Change in Homogeneous Redox Catalysis", N. A. Macías-Ruvalcaba and D. H. Evans, J. Electroanal. Chem. 2007, 602, 77-81.

  • "Oxidation Reactions of a Series of Benzidines. Electrochemical Detection of Dimerization of Cation Radicals and Examples of Potential Inversion Caused by Very Small Steric Effects", N. A. Macías-Ruvalcaba and D. H. Evans, J. Phys. Chem. C 2007, 111, 5805-5811.

  • "Electron Transfer and Structural Change: Distinguishing Concerted and Two-Step Processes", N. A. Macías-Ruvalcaba and D. H. Evans, Chem. Eur. J. 2007, 13, 4386-4395.