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Título

TTF–PTM dyads: from switched molecular self assembly in solution to radical conductors in solid state

AutorSouto Salom, Manuel; Rovira, Concepció CSIC ORCID; Ratera, Immaculada; Veciana, Jaume CSIC ORCID CVN
Palabras claveIntramolecular electron-transfer
Donor-acceptor systems
Bond ground-state
Charge delocalization
Mixed-valence
Organic radicals
Room-temperature
Building-blocks
Pi-dimers
Tetrathiafulvalene
Fecha de publicación14-ene-2017
EditorRoyal Society of Chemistry (UK)
CitaciónCrystEngComm 19(2): 197-206 (2017)
ResumenOrganic donor-acceptor (D-A) systems formed by the electron-donor tetrathiafulvalene (TTF) linked to the electron-acceptor polychlorotriphenylmethyl (PTM) radical through different π-conjugated bridges exhibit interesting physical properties such as bistability in solution or conductivity in solid state. Understanding the interplay between intra- and intermolecular charge transfer processes in solution is of high interest in order to rationalize the self-assembling ability and conducting properties of such dyads in solid state. In this Highlight we go over the self-assembling properties of different TTF-π-PTM radical dyads that find potential applications as molecular switches or conductors in the field of molecular electronics.
Versión del editorhttp://dx.doi.org/10.1039/C6CE01660J
URIhttp://hdl.handle.net/10261/150991
DOI10.1039/C6CE01660J
ISSN1466-8033
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