A study of the photochemical behaviour and relaxation mechanisms of anti–syn isomerisation around quinazolinone –N–N[double bond, length as m-dash] bonds

High-resolution NMR experiments revealed that differently substituted quinazolinone-based Schiff bases undergo anti to syn isomerisation on exposure to ultraviolet light in DMSO solution. The degree anti to syn conversion varied significantly upon substitution (between 5% and 100%) and also showed t...

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Detalles Bibliográficos
Autores principales: Hricovíni, Michal, Asher, James R., Hricovíni, Miloš
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524441/
https://www.ncbi.nlm.nih.gov/pubmed/36321162
http://dx.doi.org/10.1039/d2ra04529j

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524441/
https://www.ncbi.nlm.nih.gov/pubmed/36321162
http://dx.doi.org/10.1039/d2ra04529j

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