Oligothienylenevinylene Polarons and Bipolarons Confined between Electron‐Accepting Perchlorotriphenylmethyl Radicals

A detailed analysis is undertaken of positively charged species generated on a series of thienylenevinylene (nTV) wires terminally substituted with two perchlorotriphenylmethyl (.PTM) radical acceptor groups, .PTM‐nTV‐PTM. (n=2–7). Motivated by the counterintuitive key role played by holes in the nT...

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Detalles Bibliográficos
Autores: Mayorga-Burrezo, Paula, Franco, Carlos, Caballero, Rubén, Mas Torrent, Marta, Langa, Fernando, López Navarrete, Juan Teodomiro, Rovira, Concepció, Veciana, Jaume, Casado, Juan
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2018
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/164412
Acceso en línea:http://hdl.handle.net/10261/164412
Access Level:acceso abierto
Palabra clave:Electron transfer
Mixed-valent compounds
Molecular wires
Radical ions
Thienylenevinylene
Descripción
Sumario:A detailed analysis is undertaken of positively charged species generated on a series of thienylenevinylene (nTV) wires terminally substituted with two perchlorotriphenylmethyl (.PTM) radical acceptor groups, .PTM‐nTV‐PTM. (n=2–7). Motivated by the counterintuitive key role played by holes in the nTV bridges on the operating mechanism of electron transfer in their radical anion mixed‐valence derivatives, a wide combination of experimental and theoretical techniques is used, with the aim of gaining further insights into their structural location. Consequently, contributions of the .PTM units for the stabilization of the radical cations and hole localization, particularly in the case of the shortest molecular wire, are probed. In this sense, the formation of quinoidal ring segments, resulting from the coupling of the unpaired electron of the .PTM radical site with those generated along the nTV chains is found. Additionally, open‐shell dications, described by the recovery of the central aromaticity and two terminal quinoidal segments, assisted by the .PTM units, are detected.