A spectroelectrochemical study of poly(dithienothiophenes) (Articolo in rivista)

Type
Label
  • A spectroelectrochemical study of poly(dithienothiophenes) (Articolo in rivista) (literal)
Anno
  • 1997-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/S0022-0728(96)04879-6 (literal)
Alternative label
  • Arbizzani, C; Catellani, M; Mastragostino, M; Cerroni, MG (1997)
    A spectroelectrochemical study of poly(dithienothiophenes)
    in Journal of electroanalytical chemistry and interfacial electrochemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Arbizzani, C; Catellani, M; Mastragostino, M; Cerroni, MG (literal)
Pagina inizio
  • 23 (literal)
Pagina fine
  • 28 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.sciencedirect.com/science/article/pii/S0022072896048796 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 423 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 6 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 1-2 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Arbizzani, C; Mastragostino, M; Cerroni, MG UNIV PALERMO,DIPARTIMENTO CHIM FIS,I-90123 PALERMO,ITALY Catellani, M ISMAC-CNR (literal)
Titolo
  • A spectroelectrochemical study of poly(dithienothiophenes) (literal)
Abstract
  • The use of n- and p-dopable conjugated polymers as both the working and counter electrodes in an electrochemical device has always attracted chemists and has stimulated the design of new molecules with a low energy gap that can be p- and n-doped efficiently. The present paper reports the spectroelectrochemical study of polymers obtained from several dithienothiophene isomers, molecules with three thiophene rings fused in different positions. Of the six isomers, poly(dithieno[3,4-b:3',2'-d]thiophene) and poly(dithieno[3,4-b:2',3'-d]thiophene) were tested against poly(dithieno[3,2-b:2',3'-d]thiophene) and poly(dithieno[3,4-b:3',4'-d]thiophene). The differences in their performance, related to the geometry of the starting molecules and to enchainment, are reported and discussed. (literal)
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Autore CNR

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