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Concerted proton-electron transfer reactions in the Marcus inverted region

Parada, Giovanny A. (author)
Yale Univ, Dept Chem, New Haven, CT 06520 USA
Goldsmith, Zachary K. (author)
Yale Univ, Dept Chem, New Haven, CT 06520 USA
Kolmar, Scott (author)
Yale Univ, Dept Chem, New Haven, CT 06520 USA
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Pettersson-Rimgard, Belinda (author)
Uppsala universitet,Fysikalisk kemi
Mercado, Brandon Q. (author)
Yale Univ, Dept Chem, New Haven, CT 06520 USA
Hammarström, Leif, 1964- (author)
Uppsala universitet,Fysikalisk kemi
Hammes-Schiffer, Sharon (author)
Yale Univ, Dept Chem, New Haven, CT 06520 USA
Mayer, James M. (author)
Yale Univ, Dept Chem, New Haven, CT 06520 USA
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 (creator_code:org_t)
American Association for the Advancement of Science (AAAS), 2019
2019
English.
In: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 364:6439, s. 471-475
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Electron transfer reactions slow down when they become very thermodynamically favorable, a counterintuitive interplay of kinetics and thermodynamics termed the inverted region in Marcus theory. Here we report inverted region behavior for proton-coupled electron transfer (PCET). Photochemical studies of anthracene-phenol-pyridine triads give rate constants for PCET charge recombination that are slower for the more thermodynamically favorable reactions. Photoexcitation forms an anthracene excited state that undergoes PCET to create a charge-separated state. The rate constants for return charge recombination show an inverted dependence on the driving force upon changing pyridine substituents and the solvent. Calculations using vibronically nonadiabatic PCET theory yield rate constants for simultaneous tunneling of the electron and proton that account for the results.

Subject headings

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

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