On the mechanism of visible‐light sensitized photosulfoxidation of toluidine blue O

Author:

Otero‐González Jennifer1,Querini‐Sanguillén Whitney1,Torres‐Mendoza Daniel234ORCID,Yevdayev Ikhil5,Yunayev Sharon5,Nahar Kamrun56ORCID,Yoo Barney7,Greer Alexander56ORCID,Fuentealba Denis8ORCID,Robinson‐Duggon José19ORCID

Affiliation:

1. Universidad de Panamá, Facultad de Ciencias Naturales, Exactas y Tecnología, Departamento de Bioquímica Panamá Panama

2. Universidad de Panamá, Facultad de Ciencias Naturales, Exactas y Tecnología, Laboratorio de Bioorgánica Tropical Panamá Panama

3. Universidad de Panamá, Facultad de Ciencias Naturales, Exactas y Tecnología, Departamento de Química Orgánica Panamá Panama

4. Universidad de Panamá, Vicerrectoría de Investigación y Postgrado Panamá Panama

5. Department of Chemistry, Brooklyn College City University of New York Brooklyn New York USA

6. Ph.D. Program in Chemistry The Graduate Center of the City University of New York New York New York USA

7. Department of Chemistry, Hunter College City University of New York New York USA

8. Laboratorio de Química Supramolecular y Fotobiología Escuela de Química Facultad de Química y de Farmacia Pontificia Universidad Catolica de Chile Santiago Chile

9. Sistema Nacional de Investigación (SNI) Secretaría Nacional de Ciencia Tecnología e Innovación (SENACYT) Panamá Panama

Abstract

AbstractWe report on the formation of toluidine blue O (TBO) sulfoxide by a self‐sensitized photooxidation of TBO. Here, the photosulfoxidation process was studied by mass spectrometry (MS) and discussed in the context of photodemethylation processes which both contribute to TBO consumption over time. Analysis of solvent effects with D2O, H2O, and CH3CN along with product yields and MS fragmentation patterns provided mechanistic insight into TBO sulfoxide's formation. The formation of TBO sulfoxide is minor and detectable up to 12% after irradiation of 3 h. The photosulfoxidation process is dependent on oxygen wherein instead of a type II (singlet oxygen, 1O2) reaction, a type I reaction involving TBO to reach the TBO sulfoxide is consistent with the results. Density functional theory results point to the formation of the TBO sulfoxide by the oxidation of TBO via transiently formed peroxyl radical or thiadioxirane intermediates. We discover that the TBO photosulfoxidation arises competitively with TBO photodemethylation with the latter leading to formaldehyde formation.

Funder

Division of Advanced Cyberinfrastructure

Fondo Nacional de Desarrollo Científico y Tecnológico

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,General Medicine,Biochemistry

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