Hydrogen Atom Transfer Reactions of a Ruthenium Imidazole Complex: Hydrogen Tunneling and the Applicability of the Marcus Cross Relation
- 9 October 2008
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 130 (44) , 14745-14754
- https://doi.org/10.1021/ja805067h
Abstract
The reaction of RuII(acac)2(py-imH) (RuIIimH) with TEMPO• (2,2,6,6-tetramethylpiperidine-1-oxyl radical) in MeCN quantitatively gives RuIII(acac)2(py-im) (RuIIIim) and the hydroxylamine TEMPO-H by transfer of H• (H+ + e−) (acac = 2,4-pentanedionato, py-imH = 2-(2′-pyridyl)imidazole). Kinetic measurements of this reaction by UV−vis stopped-flow techniques indicate a bimolecular rate constant k3H = 1400 ± 100 M−1 s−1 at 298 K. The reaction proceeds via a concerted hydrogen atom transfer (HAT) mechanism, as shown by ruling out the stepwise pathways of initial proton or electron transfer due to their very unfavorable thermochemistry (ΔG°). Deuterium transfer from RuII(acac)2(py-imD) (RuIIimD) to TEMPO• is surprisingly much slower at k3D = 60 ± 7 M−1 s−1, with k3H/k3D = 23 ± 3 at 298 K. Temperature-dependent measurements of this deuterium kinetic isotope effect (KIE) show a large difference between the apparent activation energies, Ea3D − Ea3H = 1.9 ± 0.8 kcal mol−1. The large k3H/k3D and ΔEa values appear to be greater than the semiclassical limits and thus suggest a tunneling mechanism. The self-exchange HAT reaction between RuIIimH and RuIIIim, measured by 1H NMR line broadening, occurs with k4H = (3.2 ± 0.3) × 105 M−1 s−1 at 298 K and k4H/k4D = 1.5 ± 0.2. Despite the small KIE, tunneling is suggested by the ratio of Arrhenius pre-exponential factors, log(A4H/A4D) = −0.5 ± 0.3. These data provide a test of the applicability of the Marcus cross relation for H and D transfers, over a range of temperatures, for a reaction that involves substantial tunneling. The cross relation calculates rate constants for RuIIimH(D) + TEMPO• that are greater than those observed: k3H,calc/k3H = 31 ± 4 and k3D,calc/k3D = 140 ± 20 at 298 K. In these rate constants and in the activation parameters, there is a better agreement with the Marcus cross relation for H than for D transfer, despite the greater prevalence of tunneling for H. The cross relation does not explicitly include tunneling, so close agreement should not be expected. In light of these results, the strengths and weaknesses of applying the cross relation to HAT reactions are discussed.Keywords
This publication has 99 references indexed in Scilit:
- Probing concerted proton–electron transfer in phenol–imidazolesProceedings of the National Academy of Sciences, 2008
- Facile Concerted Proton−Electron Transfers in a Ruthenium Terpyridine-4′-Carboxylate Complex with a Long Distance Between the Redox and Basic SitesJournal of the American Chemical Society, 2008
- Synthesis and Characterization of Ruthenium Bis(β-diketonato) Pyridine-Imidazole Complexes for Hydrogen Atom TransferInorganic Chemistry, 2007
- Proton-Coupled Electron TransferChemical Reviews, 2007
- Theoretical studies of proton-coupled electron transfer: Models and concepts relevant to bioenergeticsCoordination Chemistry Reviews, 2007
- Large Ground-State Entropy Changes for Hydrogen Atom Transfer Reactions of Iron ComplexesJournal of the American Chemical Society, 2007
- Linking protein structure and dynamics to catalysis: the role of hydrogen tunnellingPhilosophical Transactions Of The Royal Society B-Biological Sciences, 2006
- Summarizing lecture: factors influencing enzymatic H-transfers, analysis of nuclear tunnelling isotope effects and thermodynamic versus specific effectsPhilosophical Transactions Of The Royal Society B-Biological Sciences, 2006
- MPW1K Performs Much Better than B3LYP in DFT Calculations on Reactions that Proceed by Proton-Coupled Electron Transfer (PCET)Journal of Chemical Theory and Computation, 2006
- Hydrogen tunneling in the activation of dioxygen by a tris(pyrazolyl)borate cobalt complexJournal of the American Chemical Society, 1994