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Bisperfluorophenyl-Substituted Thiophene Oligomers. Organic Semiconductors with Complementary-Type Carrier Mobility

机译:双氟苯基 - 取代的噻吩低聚物。具有互补式载流子移动性的有机半导体

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The design, synthesis, and properties of two mixed perfluorophenyl-thiophene oligomers 5,5'"-diperfluorophenyl-2,2':5',2":5",2'":5'",2"":5"",2'""-quaterthiophene (2) and 5,5'-bis{1-[4-(thien-2-yl)-2,3,5,6-tetrafluorophenyl)]}-2,2'-dithiophene (3) are presented. Molecular characterization included the following techniques: multinuclear NMR, DSC and TGA, optical UV-Vis and photoluminescence spectroscopy, and cyclic voltammetry. Thin films can be easily grown by vacuum evaporation and have been characterized by optical UV-Vis and photoluminescence, XRD, and field-effect transistor measurements. Electron and hole mobilities of 0.06-0.08 cm~2/(V s) and 0.001-0.003 cm~2/(V s) were found for 2 and 3, respectively.
机译:两个混合全氟苯基硫代素寡聚蛋白5,5'“ - DIPELFOROPHENYL-2,2':5',2”:5“,2”:5',2“:5”的设计,合成和性质的性质。 “,2'” - Quatterthiophene(2)和5,5'-BIS {1- [4-(噻吩-2-基)-2,3,5,6-四氟苯基)]} - 2,2'-提出了二噻吩(3)。分子表征包括以下技术:多核NMR,DSC和TGA,光学紫外 - VIS和光致发光光谱和循环伏安法。薄膜可以通过真空蒸发容易地生长,并且已经通过光学蒸发而易于生长。 VIS和光致发光,XRD和场效应晶体管测量。分别为0.06-0.08cm〜2 /(v s)和0.001-0.003cm〜2 /(v s)的电子和孔迁移率分别为2和3。

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