Two different mechanisms of stabilization of regular pi-stacks of radicals in switchable dithiazolyl-based materials

Materials based on regular π-stacks of planar organic radicals are intensively pursued by virtue of their technologically relevant properties. Yet, these π-stacks are commonly unstable against π-dimerization. In this computational study, we reveal that regular π-stacks of planar dithiazolyl radicals...

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Detalles Bibliográficos
Autores: Francese, Tommaso, Vela Llausí, Sergi, Deumal i Solé, Mercè, Mota Valeri, Fernando, Novoa Vide, Juan J., Camellone, Matteo Farnesi, Fabris, Stefano, Havenith, Remco W. A., Broer, Ria, Ribas Ariño, Jordi
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2020
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/175839
Acceso en línea:https://hdl.handle.net/2445/175839
Access Level:acceso abierto
Palabra clave:Anàlisi tèrmica
Pi (Nombre)
Radicals (Química)
Thermal analysis
Pi (Number)
Radicals (Chemistry)
Descripción
Sumario:Materials based on regular π-stacks of planar organic radicals are intensively pursued by virtue of their technologically relevant properties. Yet, these π-stacks are commonly unstable against π-dimerization. In this computational study, we reveal that regular π-stacks of planar dithiazolyl radicals can be rendered stable, in some range of temperatures, via two different mechanisms. When the radicals of a π-stack are both longitudinally and latitudinally slipped with respect to each other, the corresponding regular π-stacked configuration is associated with a locally stable minimum in the potential energy surface of the system. Conversely, those regular π-stacks in which radicals are latitudinally slipped with respect to each other are stable as a result of a dynamic interconversion between two degenerate dimerized configurations. The existence of two stabilization mechanisms, which can be traced back to the bonding properties of isolated π-dimers, translates into two different ways of exploiting spin-Peierls-like transitions in switchable dithiazolyl-based materials.