Decomposition of triazole and 3-nitrotriazole upon low-energy electron attachment-Reference-Cited by-同舟云学术

Decomposition of triazole and 3-nitrotriazole upon low-energy electron attachment

Published:2023 Issue:20 Volume:25 Page:13892-13901
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Saqib Muhammad¹²,Izadi Farhad¹²,Isierhienrhien Leon U.¹,Ončák Milan¹^ORCID,Denifl Stephan¹²^ORCID

Affiliation:

1. Institut für Ionenphysik und Angewandte Physik, Universität Innsbruck, Technikerstraße 25, A-6020 Innsbruck, Austria

2. Center for Biomolecular Sciences Innsbruck, Universität Innsbruck, Technikerstraße 25, A-6020 Innsbruck, Austria

Abstract

The addition of the NO2 group to the triazole ring promotes the efficiency of electron attachment. Low-energy electrons decompose the molecule at sub-excitation energies.

Funder

Austrian Science Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CP/D3CP01162C

Reference58 articles.

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2. Quantum Computational Investigation of (E)-1-(4-methoxyphenyl)-5-methyl-N′-(3-phenoxybenzylidene)-1H-1,2,3-triazole-4-carbohydrazide

3. Triazole analogues as potential pharmacological agents: a brief review

4. Triazoles and Their Derivatives: Chemistry, Synthesis, and Therapeutic Applications

5. Triazole antifungals: A review

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