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Concise synthesis of 3-alkylthieno[3,2-b]thiophenes; building blocks for organic electronic and optoelectronic materials

机译:简化合成3-烷基硫氧化物[3,2-B]噻吩;有机电子和光电材料构建块

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Four step synthesis of 3-alkylthieno[3,2- b ]thiophenes in the literature was reduced to two steps in good yields, through the preparation of the mono ketone, i.e. 1-(thiophene-3-ylthio)alkan-2-one, from 3-bromothiophene and ring formation reaction. This convenient method provides an easy access with good yields to the preparation of 3-alkylthieno[3,2- b ]thiophenes, which are important materials for organic electronic and optoelectronic applications. SEM, AFM and contact angle (CA) analyses of their electropolymers on indium tin oxide (ITO) indicated that as the alkyl chains became longer, the polymers provide a more hydrophobic layer with CA up to 107°.
机译:通过制备单酮,即1-(噻吩-3-基硫基)Alkan-2-One ,来自3-溴噻吩和环形反应。这种便利的方法提供了良好的良好收益率,其制备3-烷基噻吩[3,2-B]噻吩,这是有机电子和光电应用的重要材料。 SEM,AFM和接触角(CA)在氧化铟锡(ITO)上的电聚合物分析表明,随着烷基链变长,聚合物提供更疏水层,其Ca高达107°。

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