首页> 外文期刊>Chemistry: A European journal >Syntheses, Phase Behavior, Supramolecular Chirality, and Field-EffectCarrier Mobility of Asymmetrically End-Capped Mesogenic Oligothiophenes
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Syntheses, Phase Behavior, Supramolecular Chirality, and Field-EffectCarrier Mobility of Asymmetrically End-Capped Mesogenic Oligothiophenes

机译:不对称封端的介晶低聚噻吩的合成,相行为,超分子手性和场效应载流子迁移。

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摘要

A novel series of asymmetricallyend-capped mesogenic oligothiophenes,with various oligothiophenecore lengths, alkoxy tail lengths, and molecular polarities through introducingalkylsulfanyl or alkylsulfonyl functionalitiesas the terminal group, havebeen synthesized by palladium-catalyzedSuzuki cross-coupling and Kumada cross-coupling reactions askey steps. For the single end-cappedoligothiophenes, CmO-Ar-OT(4)-H inwhich m=10, 12, 14, 16, and 18, all of these oligomers exhibited a broad temperaturerange of highly ordered smectic E and enantiotropic nematic phases,apart from the one with the longest octadecyloxytail.
机译:通过钯催化的铃木交叉偶联和熊田交叉偶联反应合成了一系列新的不对称封端的介晶低聚噻吩,具有不同的低聚噻吩核长度,烷氧基尾长和分子极性(通过引入烷基硫烷基或烷基磺酰基官能团作为末端基团)。对于单端封端的低聚噻吩CmO-Ar-OT(4)-H(其中m = 10、12、14、16和18),所有这些低聚物均表现出很宽的温度范围,包括高度有序的近晶E相和对映向列相从最长的十八烷氧基尾巴中提取。

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