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Ethylenedithio end-capped oligothiophenes (bEDTnT); dimer, trimer and tetramer.
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Organic Chemistry.
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Organic Chemistry.
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Organic Chemistry.ORCID iD: 0000-0002-8444-181X
1999 (English)In: Synthetic metals, ISSN 0379-6779, E-ISSN 1879-3290, Vol. 101, no 1-3, 107-108 p.Article in journal (Refereed) Published
Abstract [en]

Two new ethylenedithio substituted thiophenes (I; R = H, Br) have been synthesized. Starting from I (R = Br), oligomers II (n = 0, 1, 2) were synthesized. Their cyclic voltammetric behavior and electronic structure (by UV-Vis) have been recorded. Low oxidn. potentials and small differences between first and second oxidn. potential were found. In the UV-Vis spectra large red shifts compared to other end-capped oligomers were obsd. [on SciFinder(R)]

Place, publisher, year, edition, pages
1999. Vol. 101, no 1-3, 107-108 p.
Keyword [en]
ethylenedithio capped oligothiophene prepn oxidn potential, spectra electronic ethylenedithio capped oligothiophene
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-92004DOI: 10.1016/S0379-6779(98)01272-7OAI: oai:DiVA.org:kth-92004DiVA: diva2:511782
Note
CAPLUS AN 1999:459219(Journal) NR 20140805Available from: 2012-03-23 Created: 2012-03-23 Last updated: 2017-12-07Bibliographically approved

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