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Toward Sustainable Organic Semiconductors from a Broad Palette of Green Reactions.
- Source :
- European Journal of Organic Chemistry; 5/18/2017, Vol. 2017 Issue 19, p2707-2714, 8p
- Publication Year :
- 2017
-
Abstract
- New conjugated materials, based on the triphenylamine- thiophene moiety and integrating azomethine bonds with a dibenzofuran unit or a cyanovinyl bond with a phenylthiophene or bithiophene unit, have been synthesized by using a wide range of green reactions such as direct heteroarylation coupling reactions, Knoevenagel and Schiff-base condensations and Stille cross-coupling reactions using ionic-liquid-supported thiophenylstannane. The electronic properties of the new molecules were analyzed by UV/Vis spectroscopy and cyclic voltammetry. The potential use of the molecules as donor materials for photovoltaic conversion were evaluated in simple bilayer solar cells using C<subscript>60</subscript> as the acceptor material. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 1434193X
- Volume :
- 2017
- Issue :
- 19
- Database :
- Complementary Index
- Journal :
- European Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 123238067
- Full Text :
- https://doi.org/10.1002/ejoc.201700317