Autor según el artículo: Josep Casellas; Gerard Alcover-Fortuny; Coen de Graaf ; Mar Reguero
Departamento: Química Física i Inorgànica
e-ISSN: 1996-1944
Autor/es de la URV: De Graaf, Cornelis / Reguero de la Poza, Maria del Mar
Palabras clave: Thermal relicts Reaction mechanism Photochemistry Phenylazopyridine Pannonian region Mechanism of reaction Holocene thermal maximum Excited states Disjunction Casscf/caspt2 photoisomerization photochromism phenylazopyridine casscf/caspt2
Resumen: Azo compounds are organic photochromic systems that have the possibility of switching between cis and trans isomers under irradiation. The different photochemical properties of these isomers make azo compounds into good light-triggered switches, and their significantly different geometries make them very interesting as components in molecular engines or mechanical switches. For instance, azo ligands are used in coordination complexes to trigger photoresponsive properties. The light-induced trans-to-cis isomerization of phenylazopyridine (PAPy) plays a fundamental role in the room-temperature switchable spin crossover of Ni-porphyrin derivatives. In this work, we present a computational study developed at the SA-CASSCF/CASPT2 level (State Averaged Complete Active Space Self Consistent Field/CAS second order Perturbation Theory) to elucidate the mechanism, up to now unknown, of the cis-trans photoisomerization of 3-PAPy. We have analyzed the possible reaction pathways along its lowest excited states, generated by excitation of one or two electrons from the lone pairs of the N atoms of the azo group (nazo pi*2 and nazo2 pi*2 states), from a pi delocalized molecular orbital (pi pi* state), or from the lone pair of the N atom of the pyridine moiety (npy pi* state). Our results show that the mechanism proceeds mainly along the rotation coordinate in both the nazo pi* and pi pi* excited states, although the nazo2 pi*2 state can also be populated temporarily, whilethe npy pi* does not intervene in the reaction. For rotationally constrained systems, accessible paths to reach the cis minimum along planar geometries have also been located, again on the nazo pi* and pi pi* potential energy surfaces, while the nazo 2 pi*2 and npy pi* states are not involved in the reaction. The relative energies of the different paths differ from those found for azobenzene in a previous work, so our results predict some differences between the reactivities of both compounds.
Áreas temáticas: Química Odontología Medicina veterinaria Medicina i Materials science, multidisciplinary Materiais Interdisciplinar General materials science Engenharias iv Engenharias iii Engenharias ii Engenharias i Condensed matter physics Ciências biológicas ii Ciências biológicas i Ciências agrárias i Ciência de alimentos Ciência da computação Biotecnología Astronomia / física Arquitetura, urbanismo e design
Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
ISSN: 19961944
Direcció de correo del autor: coen.degraaf@urv.cat mar.reguero@urv.cat
Identificador del autor: 0000-0001-8114-6658 0000-0001-9668-8265
Fecha de alta del registro: 2023-02-22
Volumen de revista: 10
Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
Enlace a la fuente original: https://www.mdpi.com/1996-1944/10/12/1342
Referencia al articulo segun fuente origial: Materials. 10 (12): 1342-
Referencia de l'ítem segons les normes APA: Josep Casellas; Gerard Alcover-Fortuny; Coen de Graaf ; Mar Reguero (2017). Phenylazopyridine as switch in photochemical reactions. A detailed computational description of the mechanism of its Photoisomerization. Materials, 10(12), 1342-. DOI: 10.3390/ma10121342
URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
DOI del artículo: 10.3390/ma10121342
Entidad: Universitat Rovira i Virgili
Año de publicación de la revista: 2017
Tipo de publicación: Journal Publications
Repositori URV