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Theoretical Study on the Excited-state Intramolecular Hydrogen Abstraction Reactions of Butanal 被引量:1

Theoretical Study on the Excited-state Intramolecular Hydrogen Abstraction Reactions of Butanal
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摘要 The excited-state intramolecular hydrogen abstraction reactions of butanal have been investigated using the CAS-MP2/6-311+G^*//CASSCF/6-31G^* methods. Calculated results show that the hydrogen transfer induced fluorescence quenching of the n,π^*-excited state of covalent butanal with three paths: (1) The first path corresponds to direct S0-react reconstitution, which involves the first S1 decay by partial hydrogen atom transfer. (2) The second stepwise mechanism can be viewed as a full hydrogen atom transfer followed by a partial hydrogen atom back transfer, electron transfer (near S1/S0 or S0-TS) and finally a proton transfer to S0-react. (3) On the triplet surface, the surface crossing to the singlet state would be clearly much efficient at the T1/S0 region due to the large SOC value of 8.3 cm^-1. The S0-react decay route from T1/S0 was studied with an intrinsic reaction coordinate (IRC) calculation at the CASSCF level, resulting in the S0-React minimum. The excited-state intramolecular hydrogen abstraction reactions of butanal have been investigated using the CAS-MP2/6-311+G^*//CASSCF/6-31G^* methods. Calculated results show that the hydrogen transfer induced fluorescence quenching of the n,π^*-excited state of covalent butanal with three paths: (1) The first path corresponds to direct S0-react reconstitution, which involves the first S1 decay by partial hydrogen atom transfer. (2) The second stepwise mechanism can be viewed as a full hydrogen atom transfer followed by a partial hydrogen atom back transfer, electron transfer (near S1/S0 or S0-TS) and finally a proton transfer to S0-react. (3) On the triplet surface, the surface crossing to the singlet state would be clearly much efficient at the T1/S0 region due to the large SOC value of 8.3 cm^-1. The S0-react decay route from T1/S0 was studied with an intrinsic reaction coordinate (IRC) calculation at the CASSCF level, resulting in the S0-React minimum.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第10期1226-1235,共10页 结构化学(英文)
基金 supported by ‘Qinglan’ Talent Engineering Funds and Key Subject of Inorganic Chemistry by Tianshui Normal University
关键词 butanal valence bond theory (VB) state correlation diagram hydrogen abstraction mechanism butanal, valence bond theory (VB), state correlation diagram, hydrogen abstraction mechanism
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