Triplet and ground state potential energy surfaces of 1,4-diphenyl-1,3-butadiene: theory and experiment-Reference-Cited by-同舟云学术

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Triplet and ground state potential energy surfaces of 1,4-diphenyl-1,3-butadiene: theory and experiment

Published:2008 Issue:5 Volume:7 Page:566
ISSN:1474-905X
Container-title:Photochemical & Photobiological Sciences
language:en
Short-container-title:Photochem. Photobiol. Sci.

Author:

Saltiel J.,Dmitrenko O.,Pillai Z. S.,Klima R.,Wang S.,Wharton T.,Huang Z.-N.,van de Burgt L. J.,Arranz J.

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2008/PP/B801075G

Reference44 articles.

1. Photoprocesses in diphenylpolyenes. Oxygen and heavy-atom enhancement of triplet yields

2. Role of geometric distortion in the quenching behaviors of all-trans 1,4-diphenyl-1,3-butadiene triplet

3. Photoprocesses in diphenylpolyenes. 3. Efficiency of singlet oxygen generation from oxygen quenching of polyene singlets and triplets

4. Direct and sensitized photoisomerization of 1,4-diphenylbutadienes

5. Unusual case of selectivity in a photochemical reaction. Photoisomerization of unsymmetrical 1,3-dienes

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5. Photoisomerization mechanisms from trans, trans-1,4-diphenyl-1,3-butadiene: CASSCF on-the-fly trajectory surface hopping dynamic simulations;Physical Chemistry Chemical Physics;2016

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