Photodehydroxylation of methoxybenzyl alcohols: rate constants for solvent and hydronium ion catalyzed photodehydroxylation and applicability of Förster cycle calculations
Author:
Publisher
Elsevier BV
Subject
General Physics and Astronomy,General Chemical Engineering,General Chemistry
Reference14 articles.
1. Fluorescence quenching of methoxybenzyl alcohols by the hydronium ion in aqueous solution: acid-catalyzed formation of methoxybenzyl cations from the singlet excited state
2. Acid-catalyzed photochemical generation of benzyl cations as a probe of the electron-donating abilities of benzene substituents in the singlet excited state
3. Adiabatic photodehydroxylation of 9-phenylxanthen-9-ol. Observation of carbocation fluorescence in neutral aqueous solution
4. Evidence for the generation of aromatic cationic systems in the excited state. Photochemical solvolysis of fluoren-9-ol
5. Structure–reactivity studies and catalytic effects in the photosolvolysis of methoxy-substituted benzyl alcohols
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3. The photochemistry of indenyl alcohols and esters: Substituent effects on the competition between ion- and radical-derived products;Canadian Journal of Chemistry;2003-10-01
4. Photochemistry of Aryl tert-Butyl Ethers in Methanol: The Effect of Substituents on an Excited State Cleavage Reaction;The Journal of Organic Chemistry;2000-06-01
5. 1995 Merck Frosst Award Lecture Quinone methides: relevant intermediates in organic chemistry;Canadian Journal of Chemistry;1996-04-01
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