2001
DOI: 10.1002/1616-3028(200108)11:4<305::aid-adfm305>3.0.co;2-y
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Synthesis and Electrochemical Properties of Novel 1,3,5-Tris(oligothienyl)benzenes: A New Generation of 3D Reticulating Agents

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Cited by 79 publications
(59 citation statements)
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“…The final product, purified by column chromotagraphy, was a dark orange solid and its 1 The synthesis of BT-azine was a two step process. First, 2,2 0 -bithiophene was acetylated by treating it with n-BuLi in Et 2 O and then adding dimethyl-acetylamide to produce 5-acetyl-2,2 0 -bithiophene as a yellow solid in 41% purified yield [30]. This was then mixed with hydrazine hydrate in a 2:1 ratio in ethanol with 0.5% acetic acid and refluxed overnight.…”
Section: Monomers and Chemicalsmentioning
confidence: 99%
“…The final product, purified by column chromotagraphy, was a dark orange solid and its 1 The synthesis of BT-azine was a two step process. First, 2,2 0 -bithiophene was acetylated by treating it with n-BuLi in Et 2 O and then adding dimethyl-acetylamide to produce 5-acetyl-2,2 0 -bithiophene as a yellow solid in 41% purified yield [30]. This was then mixed with hydrazine hydrate in a 2:1 ratio in ethanol with 0.5% acetic acid and refluxed overnight.…”
Section: Monomers and Chemicalsmentioning
confidence: 99%
“…In addition, we incorporated thiophenyl and bithiophenyl groups to increase the compatibility with conventional donor polymer, such as P3HT. The mono-ketone compounds having thiophenyl group were easily synthesized from the method in the literature [7][8]. Compound 1, 2, 3, and 4 were produced as similar procedure at literature through Hirch-Bingel reaction under mild condition [9][10].…”
Section: Design and Synthesis Of Methanofullerene Derivatives With Vamentioning
confidence: 99%
“…P3HT [Poly(3-hexylthiophene)] was purchased from Rieke Metals.Synthesis of Mono-ketone Modified Methanofullerene DerivativesGeneral Procedure 2-Hexylthiophene, 2-hexyl-5-5 0 -bithiophene, 1-(thiophen-2-yl)octan-1-one, 1-(2,2 0 -bithiophen-5-yl)octan-1-one, 1-(5-hexylthiophen-2-yl)hexan-1-one, 0 -hexyl-2,2 0 -bithiophen-5-yl)hexan-1-one were synthesized in the similar methods described in the literature[7][8]. Fullerene C 60 (1.0 mmol) was stirred overnight in o-dichlorobenzene solution.…”
mentioning
confidence: 99%
“…Thiophenes with well-defined chemical structures have recently attracted great attention not only as an example of model compounds for conducting materials, but also as a new class of functional π-electron systems [5][6][7][8][9][10][11]. Branched oligothiophenes based on central phenyl core have come to the fore over the last several years, acting both as monomers in cross-linked semiconducting polymers [12][13][14][15] and as components of conjugated dendrimers [16][17][18].…”
Section: Introductionmentioning
confidence: 99%