Ionization of Amino-, Thio- and Hydroxy-naphtalenes via Free (Unhindered) Electron Transfer
Author:
Affiliation:
1. Interdisciplinary Group Time-resolved Spectroscopy, University of Leipzig, Permoserstrasse 15, 04303 Leipzig, Germany, and Leibniz Institute of Surface Modification, Permoserstrasse 15, 04303 Leipzig, Germany
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp806711m
Reference22 articles.
1. Femtodynamics Reflected in Nanoseconds: Bimolecular Free Electron Transfer in Nonpolar Media
2. Mehnert, R.InRadical Ionic Systems − Properties in Condensed Phases;Lund, A.; Shiotani, M., Eds.Kluwer Academic Publishers:Dordrecht, The Netherlands,1991; p231.
3. Radical Cations in Radiation Chemistry of Liquid Hydrocarbons.
4. Mechanism of the formation of cationic species in the radiolysis of butyl chlorides. 1
5. Handbook of Chemistry and Physics,73rd ed.Lide, D. R.Ed.CRC Press:Boca Raton,1992; pp10−214.
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1. Oxidation Reactions of 1- and 2-Naphthols: An Experimental and Theoretical Study;The Journal of Physical Chemistry A;2013-10-29
2. Shedding Light into the Detailed Excited-State Relaxation Pathways and Reaction Mechanisms of Thionaphthol Isomers;The Journal of Physical Chemistry A;2010-12-30
3. Reactivity of Radical Cations in Nonpolar Condensed Matter;Charged Particle and Photon Interactions with Matter;2010-12-13
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5. Structure dependence of the photogeneration of thionaphthol triplets;Chemical Physics Letters;2009-08
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