Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Research Article

A New Photoisomerization of 1,2,4-Oxadiazoles. A Computational Study

Author(s): Maurizio D'Auria*

Volume 15, Issue 12, 2018

Page: [1021 - 1024] Pages: 4

DOI: 10.2174/1570178615666171219164920

Price: $65

conference banner
Abstract

The photochemical isomerization of 1,2,4-oxadiazole derivatives to 1,2,4-triazoles has been studied at B3LYP/6-311G+(d,p) level of theory. The reaction occurred in the presence of Ru(bpy)2Cl2. The irradiation of the Ru complex allowed the substitution of chlorine with the substrate. The irradiation at 760 nm of this new complex led to an electron transfer process that favors the transfer of a hydrogen atom from the hydrazonic NH group to the N atom at the fourth position in the 1,2,4-oxadiazole ring. The resulting radical cation cyclized to give a reaction product through Dewar isomer structure.

Keywords: 1, 2, 4-oxadiazole, photoisomerization, Ruthenium, 1, 2, 4-triazole, DFT, isomer.

Graphical Abstract

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy