Inhibition of Light-Induced Tautomerization of 7-Azaindole by Phenol: Indications of Proton-Coupled Electron/Energy Transfer Quenching
Author:
Affiliation:
1. Department of Physical Chemistry and Raman Centre for Atomic Molecular and Optical Sciences, Indian Association for the Cultivation of Science, Jadavpur, Calcutta 700032, India
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp1084422
Reference45 articles.
1. EXCITED-STATE TWO-PROTON TAUTOMERISM IN HYDROGEN-BONDED N-HETEROCYCLIC BASE PAIRS
2. Photoinduced double proton transfer in a model hydrogen bonded base pair. Effects of temperature and deuterium substitution
3. Femtosecond molecular dynamics of tautomerization in model base pairs
4. Photophysics of 7-Azaindole, Its Doubly-H-Bonded Base-Pair, and Corresponding Proton-Transfer-Tautomer Dimeric Species, via Defining Experimental and Theoretical Results
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1. Competing Excited‐State Hydrogen and Proton‐Transfer Processes in 6‐Azaindole‐S3,4 and 2,6‐Diazaindole‐S3,4 Clusters (S=H2O, NH3);ChemPhysChem;2023-10-04
2. Hydrogen Bonding Effects on Vibrational Dynamics and Photochemistry in Selected Binary Molecular Complexes;Journal of the Indian Institute of Science;2019-12-30
3. pH-Driven Mechanistic Switching from Electron Transfer to Energy Transfer between [Ru(bpy)3]2+ and Ferrocene Derivatives;Journal of the American Chemical Society;2018-08-02
4. Fast excited state dynamics in the isolated 7-azaindole-phenol H-bonded complex;The Journal of Chemical Physics;2013-02-07
5. Ultraviolet and infrared spectroscopy of matrix-isolated 7-azaindole dimer: Matrix effect on excited state tautomerization;Chemical Physics Letters;2012-09
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