Autor según el artículo: Castro, Pedro J.; Reguero, Mar;
Departamento: Química Física i Inorgànica
Autor/es de la URV: Reguero de la Poza, Maria del Mar
Palabras clave: Unpaired electrons Topography State Spin orbit coupling Single-crystals Reaction coordinates Quantum chemistry Potential energy Photochromism Paramagnetic resonance Naphthalimides Inter-system crossings Hydrogen abstraction Geometrical differences Excited states Energies Electronic states Electron spin resonance spectroscopy Electron paramagnetic resonances (epr) Density functional theory studies Density functional theory Crystals Computational studies Computation theory Compound
Resumen: Biindenylidenediones (BIDs) are a family of compounds that have been studied for a relatively short time. The crystals of these compounds are yellowish, and become purplish when they are irradiated and return back to their original color slowly in the dark or quickly when they are heated up. BIDs can be classified into different subfamilies depending on the nature of their substituents. BID-II crystals show a thermally dependent electron paramagnetic resonance (EPR) signal that is a characteristic of chemical species with unpaired electrons. These properties make BIDs very attractive for industrial applications but the mechanisms responsible for their photochromism and photomagnetism are still under debate. In this article, a computational study focused on the BID-II subfamily is presented. A variety of multiconfigurational methods (CASSCF, CASPT2 and IDDCI) have been used to study exhaustively the topography of the potential energy surfaces of the lower electronic states of a single BID molecule. Methods based on density functional theory (DFT) were then used to model the most important structures in a periodic crystal system. Our results suggest that delta-hydrogen abstraction could explain the observed experimental phenomena. After the initial excitation to the (1)pi pi* state, non-symmetric n pi* minima are populated, which are adiabatically connected to the photoproduct zone through a barrier along the reaction coordinate. Based on our set of results, we propose that an epoxide constitutes the most stable and accessible photoproduct preceded by the population of a triplet biradical of pi(O)pi* nature which has only small geometrical differences in comparison with the reactant. The spin-orbit coupling indicates that the EPR signal arises due to the population of a low energy triplet through a thermally accessible intersystem crossing in the photoproduct zone.
Áreas temáticas: Química Physics, atomic, molecular & chemical Physics and astronomy (miscellaneous) Physics and astronomy (all) Physical and theoretical chemistry Odontología Medicina ii Medicina i Materiais Matemática / probabilidade e estatística Interdisciplinar Geociências General physics and astronomy General medicine Farmacia Ensino Engenharias iv Engenharias iii Engenharias ii Ciências biológicas ii Ciências biológicas i Ciências ambientais Ciências agrárias i Ciência de alimentos Ciência da computação Chemistry, physical Biotecnología Biodiversidade Astronomia / física
Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
Direcció de correo del autor: mar.reguero@urv.cat
Identificador del autor: 0000-0001-9668-8265
Fecha de alta del registro: 2024-07-27
Versión del articulo depositado: info:eu-repo/semantics/acceptedVersion
Enlace a la fuente original: https://pubs.rsc.org/en/content/articlelanding/2021/cp/d1cp01692j
URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
Referencia al articulo segun fuente origial: Physical Chemistry Chemical Physics. 23 (32): 17453-17465
Referencia de l'ítem segons les normes APA: Castro, Pedro J.; Reguero, Mar; (2021). The mechanism behind the photochromism and photomagnetism of type II biindenylidenediones: multiconfigurational, perturbative and density functional theory studies. Physical Chemistry Chemical Physics, 23(32), 17453-17465. DOI: 10.1039/d1cp01692j
DOI del artículo: 10.1039/d1cp01692j
Entidad: Universitat Rovira i Virgili
Año de publicación de la revista: 2021
Tipo de publicación: Journal Publications
Repositori URV