Norrish Type I Reaction of Diphenyltetrahydrobenzocycloheptenones. Conformational Effects on Biradical Lifetime
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/22/8/22_8_1447/_pdf
Reference15 articles.
1. Effects of chain length on behavior of biradicals generated from Norrish type I reaction of 2,2-diphenylcycloalkanones. Isolation and photochemistry of intermediate methylenecyclohexadienyl ketones
2. Lifetime of a conformationally constrained Norrish II biradical. Photochemistry of cis-1-benzoyl-2-benzhydrylcyclohexane
3. Does intersystem crossing in triplet biradicals generate singlets with conformational memory?
4. Factors distinguishing one-way and two-way photoisomerization of aromatic olefins. Effects of substituents on triplet energy surfaces of 8-fluoranthenylethylenes
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1. Norrish Type I Reaction;Comprehensive Organic Name Reactions and Reagents;2010-09-15
2. Laser Flash Photolysis of [3,n]Paracyclophan-2-ones. Direct Observation and Chemical Behavior of 4,4‘-(1,n-Alkanediyl)bisbenzyl Biradicals;The Journal of Organic Chemistry;2002-07-30
3. Behavior of Biradicals Generated from a Norrish Type-I Reaction of 2,2-Diphenylcycloalkanones. Chain-Length Dependence and Magnetic Field Effects;Bulletin of the Chemical Society of Japan;1999-01
4. 12.1.4 1,6-biradicals;Biradicals, Radicals in Excited States, Carbenes and Related Species
5. References for 12;Biradicals, Radicals in Excited States, Carbenes and Related Species
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