58400-12-7Relevant academic research and scientific papers
Highly soluble and thermally stable alkyl-free star-shaped D-π-A oligomer with electron-withdrawing phenyldicyanovinyl groups for organic photovoltaics
Luponosov, Yuriy N.,Solodukhin, Alexander N.,Mannanov, Artur L.,Trukhanov, Vasiliy A.,Peregudova, Svetlana M.,Pisarev, Sergey A.,Bakirov, Artem V.,Shcherbina, Maxim A.,Chvalun, Sergei N.,Paraschuk, Dmitry Yu,Ponomarenko, Sergei A.
, p. 180 - 189 (2017)
Synthesis of the first star-shaped donor-acceptor oligomer with phenyldicyanovinyl electron-withdrawing units, namely N(Ph-2T-DCV-Ph)3, is reported. The physical and photovoltaic properties of this molecule were comprehensively studied and comp
Oligothiophenes III: Synthesis of tetra-thienyl-substituted ethylenes including an abnormal Mcmurry coupling result
Halvorsen, Harald,Skramstad, Jan,Hope, Hakon
, p. 1179 - 1187 (2007)
This article describes the synthesis of some selected tetra-thiophenyl- substituted ethenes by McMurry coupling of some selected thienyl ketones, including a surprising coupling product. The products were analyzed by MS, NMR, UV, and x-ray crystallography
Synthesis of functionalized 2-arylthiophenes with triarylbismuths as atom-efficient multicoupling organometallic nucleophiles under palladium catalysis
Rao, Maddali L. N.,Banerjee, Debasis,Dhanorkar, Ritesh J.
supporting information; experimental part, p. 1324 - 1330 (2011/07/07)
Atom-efficient cross-coupling reactions of functionalized 2-bromo- and 2-iodothiophenes have been demonstrated using triarylbismuths as atom-efficient multicoupling organometallic nucleophiles under palladium-catalyzed conditions. These couplings with various functionalized triarylbismuths proceeded smoothly to afford the corresponding functionalized 2-arylthiophenes in high yields. Georg Thieme Verlag Stuttgart · New York.
Absorption, emission and mass spectral characteristics of oligothiophenes and their derivatives
Krishnaswamy, N. R.,Kumar, Ch. Siva Sai Ramana
, p. 766 - 771 (2007/10/02)
Oligothiophenes ranging from bithiophene to pentathiophene (1-5) and a number of alkyl and carbonyl derivatives of 1 and 2 have been prepared and their UV absorption, fluorescence and mass spectra recorded.UV absorption and fluorescence spectra have been
