Thiophene/cyclopentadiene regular copolymers from electrochemical oxidation of dithienylcyclopentadienes (Articolo in rivista)

Type
Label
  • Thiophene/cyclopentadiene regular copolymers from electrochemical oxidation of dithienylcyclopentadienes (Articolo in rivista) (literal)
Anno
  • 2002-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/1521-3935(200206)203:9<1228::AID-MACP1228>3.0.CO;2-T (literal)
Alternative label
  • Berlin A.; Zotti G.; Zecchin S.; Schiavon G. (2002)
    Thiophene/cyclopentadiene regular copolymers from electrochemical oxidation of dithienylcyclopentadienes
    in Macromolecular chemistry and physics (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Berlin A.; Zotti G.; Zecchin S.; Schiavon G. (literal)
Pagina inizio
  • 1228 (literal)
Pagina fine
  • 1237 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://onlinelibrary.wiley.com/doi/10.1002/1521-3935%28200206%29203:9%3C1228::AID-MACP1228%3E3.0.CO;2-T/abstract (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 203 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 9 (literal)
Note
  • ISI Web of Science (WOS) (literal)
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • 1 : Istituto CNR di Scienze e Tecnologie Molecolari, via C. Golgi 19, 20133 Milano, Italy / 2-4 : Istituto CNR per l'Energetica e le Interfasi, c.o Stati Uniti 4, 35127 Padova, Italy (literal)
Titolo
  • Thiophene/cyclopentadiene regular copolymers from electrochemical oxidation of dithienylcyclopentadienes (literal)
Abstract
  • Anodic coupling to polymer of some dithienyleyclopentadienes has been performed in acetonitrile. The polymers have been characterized by cyclic voltammetry, UV vis, MALDI mass and FT-IR spectroscopies, and in situ conductivity. Nonsubstituted dithienylcyclopentadiene undergoes coupling both at the thiophene ?-position and at the internal cyclopentadiene sites with the production of an insoluble polymer corresponding to a tetrameric formulation. Protection of the cyclopentadiene 5 position with alkyl chains has allowed the production of regularly ?-coupled polymers. The optical gap of poly(dithienylcyclopentadiene) has been evaluated as 2.2 eV, i.e., close to that of polythiophene (2.3 eV). (literal)
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