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Hydrogen Atom Transfer Reactions of a Ruthenium Imidazole Complex: Hydrogen Tunneling and the Applicability of the Marcus Cross Relation

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 130, Issue 44, Pages 14745-14754

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja805067h

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Funding

  1. U.S. National Institutes of Health [GM50422]
  2. University of Washington

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The reaction of Ru-11(acac)(2)(py-imH) (Ru(II)imH) with TEMPO* (2,2,6,6-tetramethylpiperidine-1-oxyl radical) in MeCN quantitatively gives Ru-III(acac)(2)(py-im)(Ru(III)im) 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 k(3H) = 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 thermochernistry (Delta G degrees). Deuterium transfer from Ru-II(acac)2(PY-imD) (Ru(II)imD) to TEMPO* is surprisingly much slower at k(3D) = 60 7 M-1 s-1, with k(3H)/k(3D) = 23 3 at 298 K. Temperature-dependent measurements of this deuterium kinetic isotope effect (KIE) show a large difference between the apparent activation energies, E-a3D - E-a3H = 1.9 +/- 0.8 kcal mol(-1). The large k3H/k3D and Delta E-a values appear to be greater than the semiclassical limits and thus suggest a tunneling mechanism. The self-exchange HAT reaction between Ru(II)imH and Ru(III)im, measured by H-1 NMR line broadening, occurs with k(4H) = (3.2 +/- 0.3) x 105 M-1 s(-1) at 298 K and k(4H)/k(4D) = 1.5 +/- 0.2. Despite the small KIE, tunneling is suggested by the ratio of Arrhenius pre-exponential factors, log(A(4H)/A(4D)) = -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 Ru(II)mH(D) + TEMPO* that are greater than those observed: k(3H,calc)/k(3H) = 31 +/- 4 and k(3D,calc)/k(3D) = 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.

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