Electronic tuning effects via cyano substitution of a fused tetrathiafulvalene–benzothiadiazole dyad for ambipolar transport properties
Data(s) |
2014
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Resumo |
Electronic tuning effects of substituents at the 4- and 8-positions of benzothiadiazole (BTD) within the fused tetrathiafulvalene–BTD donor–acceptor dyad have been studied. The electron acceptor strength of BTD is greatly increased by replacing Br with CN groups, extending the optical absorption of the small dyad into the near-IR region and importantly, the charge transport can be switched from p-type to ambipolar behaviour. |
Formato |
application/pdf |
Identificador |
http://boris.unibe.ch/49523/1/c3ra46784h.pdf Amacher, Anneliese; Luo, Hewei; Liu, Zitong; Bircher, Martin; Cascella, Michele; Hauser, Jürg; Decurtins, Silvio; Zhang, Deqing; Liu, Shi-Xia (2014). Electronic tuning effects via cyano substitution of a fused tetrathiafulvalene–benzothiadiazole dyad for ambipolar transport properties. RSC advances, 4(6), pp. 2873-2878. Royal Society of Chemistry 10.1039/c3ra46784h <http://dx.doi.org/10.1039/c3ra46784h> doi:10.7892/boris.49523 info:doi:10.1039/c3ra46784h urn:issn:2046-2069 |
Idioma(s) |
eng |
Publicador |
Royal Society of Chemistry |
Relação |
http://boris.unibe.ch/49523/ |
Direitos |
info:eu-repo/semantics/restrictedAccess |
Fonte |
Amacher, Anneliese; Luo, Hewei; Liu, Zitong; Bircher, Martin; Cascella, Michele; Hauser, Jürg; Decurtins, Silvio; Zhang, Deqing; Liu, Shi-Xia (2014). Electronic tuning effects via cyano substitution of a fused tetrathiafulvalene–benzothiadiazole dyad for ambipolar transport properties. RSC advances, 4(6), pp. 2873-2878. Royal Society of Chemistry 10.1039/c3ra46784h <http://dx.doi.org/10.1039/c3ra46784h> |
Palavras-Chave | #570 Life sciences; biology #540 Chemistry #500 Science |
Tipo |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion PeerReviewed |