Halder D, Roy A, Paul A (2026)
Publication Type: Journal article
Publication year: 2026
DOI: 10.1039/d5cp04622j
Photochemical activation enables selective control over specific bond dissociation pathways by tuning the excitation wavelength. Here, we investigate the photochemical activation of 2-aryl-5-carboxytetrazole (ACT), a highly efficient genetically encoded photo-cross-linker, whose reactivity arises from a coupled interplay of charge transfer, bond cleavage, and excited-state aromaticity modulation. Using CASSCF multireference electronic structure theory combined with semiclassical surface-hopping dynamics, we elucidate the complete reaction mechanism. Our CASSCF based nonadiabatic dynamics simulations reveal that upon photoexcitation, electron density migrates from the pyrrole π-system to the tetrazole π*, initiating N–N bond activation and N
APA:
Halder, D., Roy, A., & Paul, A. (2026). Mechanistic investigations into the role of excited state aromaticity during a photochemical ring opening reaction. Physical Chemistry Chemical Physics. https://doi.org/10.1039/d5cp04622j
MLA:
Halder, Debabrata, Arnab Roy, and Ankan Paul. "Mechanistic investigations into the role of excited state aromaticity during a photochemical ring opening reaction." Physical Chemistry Chemical Physics (2026).
BibTeX: Download