Stereoelectronics of the Hydrogen-Bond-Induced Fluorescence Quenching of 3-Aminofluorenones with Alcohols
Author:
Affiliation:
1. Department of Chemistry, College of William and Mary, Williamsburg, Virginia 23185, United States
Funder
American Chemical Society Petroleum Research Fund
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.7b02142
Reference15 articles.
1. Solution photophysics of 1- and 3-aminofluorenone: the role of inter- and intramolecular hydrogen bonding in radiationless deactivation
2. Photophysical Properties of Intramolecular Charge-Transfer Excited Singlet State of Aminofluorenone Derivatives
3. Molecular Mechanism for the Radiationless Deactivation of the Intramolecular Charge-Transfer Excited Singlet State of Aminofluorenones through Hydrogen Bonds with Alcohols
4. Effects of Molecular Structure and Hydrogen Bonding on the Radiationless Deactivation of Singlet Excited Fluorenone Derivatives
5. The role of intersystem crossing in the deactivation of the singlet excited aminofluorenones
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