Force Fields for “Ultrafast” Photochemistry: The S2(1Bu) → S1(2Ag) → S0(1Ag) Reaction Path forall-trans-Hexa-1,3,5-triene
- 1 November 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (47) , 11487-11494
- https://doi.org/10.1021/ja971280u
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- Femtochemistry: Recent Progress in Studies of Dynamics and Control of Reactions and Their Transition StatesThe Journal of Physical Chemistry, 1996
- Molecular "Trigger" for the Radiationless Deactivation of Photoexcited Conjugated HydrocarbonsJournal of the American Chemical Society, 1995
- Femtosecond Time-Delayed Photoionization Studies of Ultrafast Internal Conversion in 1,3,5-HexatrieneThe Journal of Physical Chemistry, 1995
- Theoretical study of the electronic spectra ofcis-1,3,5-hexatriene andcis-1,3-butadieneTheoretical Chemistry Accounts, 1994
- Theoretical study of the electronic spectrum of all-trans-1,3,5,7-octatetraeneThe Journal of Physical Chemistry, 1993
- Octatetraene photoisomerizationChemical Reviews, 1993
- Electrostatic properties of zwitterionic micellesThe Journal of Physical Chemistry, 1992
- Fluorescence excitation spectra of the S1 states of isolated trienesThe Journal of Chemical Physics, 1992
- Second-order perturbation theory with a complete active space self-consistent field reference functionThe Journal of Chemical Physics, 1992
- Photochemistry of Vitamin D and its Isomers and of Simple TrienesPublished by Wiley ,1979