4.8 Article

Electron-Proton Decoupling in Excited-State Hydrogen Atom Transfer in the Gas Phase

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 54, Issue 50, Pages 15089-15093

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201506467

Keywords

hydrogen transfer; IR spectroscopy; photochemistry; reaction mechanisms; time; resolved spectroscopy

Funding

  1. MEXT [2503]
  2. JSPS [15H02157, 22003]
  3. MEXT (Cooperative Research Program of the Network Joint Research Center for Materials and Devices)
  4. Grants-in-Aid for Scientific Research [15H02157, 25104008] Funding Source: KAKEN

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Hydrogen-release by photoexcitation, excited-state-hydrogen- transfer (ESHT), is one of the important photochemical processes that occur in aromatic acids and is responsible for photoprotection of biomolecules. The mechanism is described by conversion of the initial state to a charge-separated state along the O(N)-H bond elongation, leading to dissociation. Thus ESHT is not a simple H-atom transfer in which a proton and a 1s electron move together. Here we show that the electron-transfer and the proton-motion are decoupled in gas-phase ESHT. We monitor electron and proton transfer independently by picosecond time-resolved near-infrared and infrared spectroscopy for isolated phenol-(ammonia) 5, a benchmark molecular cluster. Electron transfer from phenol to ammonia occurred in less than 3 picoseconds, while the overall H-atom transfer took 15 picoseconds. The observed electron-proton decoupling will allow for a deeper understanding and control of of photochemistry in biomolecules.

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