Premium
Oligothienylenevinylene Polarons and Bipolarons Confined between Electron‐Accepting Perchlorotriphenylmethyl Radicals
Author(s) -
Mayorga Burrezo Paula,
Franco Carlos,
Caballero Rubén,
MasTorrent Marta,
Langa Fernando,
López Navarrete Juan T.,
Rovira Concepció,
Veciana Jaume,
Casado Juan
Publication year - 2018
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201705080
Subject(s) - unpaired electron , chemistry , radical , polaron , valence (chemistry) , ion , electron , counterintuitive , electron transfer , radical ion , photochemistry , crystallography , chemical physics , physics , organic chemistry , quantum mechanics
A detailed analysis is undertaken of positively charged species generated on a series of thienylenevinylene ( n TV) wires terminally substituted with two perchlorotriphenylmethyl ( . PTM) radical acceptor groups, . PTM‐ n TV‐PTM . ( n =2–7). Motivated by the counterintuitive key role played by holes in the n TV 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 n TV 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.