A comparative analysis of isomerization pathways in 3- and 4-styrylpyridines

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Authors: Derreck W Nongspung, Aditya Narayan Panda
Cited by: 0
References: 90

Abstract

side, with 3-C2 → 3-CI1 and 4-C1 → 4-CI1 identified as the most favorable pathways for 3-STPY and 4-STPY, respectively. Additionally, relaxation toward the cyclized MECIs proceeds with little to no energy barriers in both systems. The findings offer mechanistic insight into the excited-state processes in styrylpyridine derivatives and suggest isomer-specific pathways for photoinduced isomerization and cyclization of the two molecules.

Fields of Study & Subjects

Chemical Reactions and Mechanisms Photochemistry and Electron Transfer Studies Advanced Chemical Physics Studies

Publication details

Journal / source
Physical Chemistry Chemical Physics
Volume
28
Issue
10
Pages
6457–6469
Publication date
1 January 2026
Language
EN