Theoretical Study of Benzotriazole UV Photostability: Ultrafast Deactivation through Coupled Proton and Electron Transfer Triggered by a Charge-Transfer State-Reference-Cited by-同舟云学术

Theoretical Study of Benzotriazole UV Photostability: Ultrafast Deactivation through Coupled Proton and Electron Transfer Triggered by a Charge-Transfer State

Published:2004-02-13 Issue:9 Volume:126 Page:2912-2922
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Paterson Martin J.¹,Robb Michael A.¹,Blancafort Lluís¹,DeBellis Anthony D.¹

Affiliation:

1. Contribution from the Department of Chemistry, Imperial College London, London, SW7 2AZ, United Kingdom, Institut de Química Computacional, Departament de Química, Universitat de Girona, Campus de Montilivi, 17071 Girona, Spain, and Ciba Specialty Chemicals, Coating Effects Research Department, 540 White Plains Road, Tarrytown, New York 10591

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0386593

Reference39 articles.

1. Light Stabilisers

2. Twisted Intramolecular Charge Transfer States in 2-Arylbenzotriazoles: Fluorescence Deactivation via Intramolecular Electron Transfer Rather Than Proton Transfer

3. Light-Induced Opening of the Intramolecular Hydrogen Bond of UV Absorbers of the 2-(2-Hydroxyphenyl)-1,3,5-triazine and the 2-(2-Hydroxyphenyl)benzotriazole Type

4. Unexpected electronic effects on benzotriazole UV absorber photostability: Mechanistic implications beyond excited state intramolecular proton transfer

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