Why is the ground state of <i>m</i>-benzoquinone a triplet?-Reference-Cited by-同舟云学术

Why is the ground state of m-benzoquinone a triplet?

Published:2023 Issue:36 Volume:47 Page:17066-17071
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Leyva-Parra Luis¹²,Pino-Rios Ricardo³⁴^ORCID

Affiliation:

1. Universidad Andrés Bello, Facultad de Ciencias Exactas, Departamento de Ciencias Químicas, Centro de Química Teórica & Computacional (CQT&C), Avenida República 275, 8370146 Santiago de Chile, Chile

2. Programa de Doctorado en Fisicoquímica Molecular, Facultad de Ciencias Exactas, Universidad Andrés Bello, Avenida República 275, Santiago de Chile 8370146, Chile

3. Instituto de Estudios de la Salud, Universidad Arturo Prat, Iquique, 1100000, Chile

4. Química y Farmacia, Facultad de Ciencias de la Salud, Universidad Arturo Prat, Casilla 121, Iquique, Chile, 1100000

Abstract

The electronic structure, changes in aromatic behavior, and stability of the m-quinone, the least studied member of the benzoquinone family, have been analyzed.

Funder

Fondo Nacional de Desarrollo Científico y Tecnológico

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D3NJ03212D

Reference39 articles.

1. Natural Quinone Dyes: A Review on Structure, Extraction Techniques, Analysis and Application Potential

2. Quinones as Promising Compounds against Respiratory Viruses: A Review

3. Cannabinoid Quinones—A Review and Novel Observations

4. Organic quinones towards advanced electrochemical energy storage: recent advances and challenges

5. Half-Wave Potentials and In Vitro Cytotoxic Evaluation of 3-Acylated 2,5-Bis(phenylamino)-1,4-benzoquinones on Cancer Cells