One Photon Yields Two Isomerizations: Large Atomic Displacements during Electronic Excited-State Dynamics in Ruthenium Sulfoxide Complexes
Author:
Affiliation:
1. Nanoscale and Quantum Phenomena Institute, Department of Chemistry and Biochemistry, Ohio University, Athens, Ohio 45701, United States
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja409262r
Reference66 articles.
1. Excited States of Conjugated Hydrocarbons Using the Molecular Mechanics - Valence Bond (MMVB) Method: Conical Intersections and Dynamics
2. Adiabatic Versus Nonadiabatic Photoisomerization in Photochromic Ruthenium Sulfoxide Complexes: A Mechanistic Picture from Density Functional Theory Calculations.
3. Triplet Pathways in Diarylethene Photochromism: Photophysical and Computational Study of Dyads Containing Ruthenium(II) Polypyridine and 1,2-Bis(2-methylbenzothiophene-3-yl)maleimide Units
4. Dihydroazulene/Vinylheptafulvene Photochromism: A Model for One-Way Photochemistry via a Conical Intersection
5. Toward a Mechanistic Understanding of the Photochromism of Dimethyldihydropyrenes
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