Photosolvolysis of 5-substituted dibenzosuberol derivatives: a stereoelectronic requirements for carbocation photogeneration
Author:
Publisher
Elsevier BV
Subject
General Physics and Astronomy,General Chemical Engineering,General Chemistry
Reference19 articles.
1. Contrasting photosolvolytic reactivities of 9-fluorenol vs. 5-suberenol derivatives. Enhanced rate of formation of cyclically conjugated four .pi. carbocations in the excited state
2. Photosolvolysis of 11H-benzo[b]fluoren-11-ol in aqueous solution
3. Picosecond spectroscopic characterization of the 9-fluorenyl cation in solution
4. Laser flash photolysis of 9-fluorenol. Production and reactivities of the 9-fluorenol radical cation and the 9-fluorenyl cation
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1. [Co2(CO)6(Alkynyl)] Complexes of Dibenzosuberyl and Dibenzosuberenyl Carbocations: Dibenzotropylium or Dibenzoheptafulvene?;ChemPlusChem;2016-01-06
2. Intramolecular [4+2] cycloaddition of a photogenerated o-quinone methide in aqueous solution;Journal of Photochemistry and Photobiology A: Chemistry;1997-04
3. Excited state carbon acids. Photodeprotonation and photoreduction of suberenes by amines;Journal of Photochemistry and Photobiology A: Chemistry;1996-08
4. 1995 Merck Frosst Award Lecture Quinone methides: relevant intermediates in organic chemistry;Canadian Journal of Chemistry;1996-04-01
5. Photosolvolysis of 2-aminobenzl alcohol in aqueous solution;Journal of Photochemistry and Photobiology A: Chemistry;1994-05
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