利用 Kumada Coupling 成功合成 α-bithiophene (α-2T)、α-terthiophene (α-3T)、α-quinquethiophene (α-5T) ,藉由 1H-MNR 與 FT-IR 以及熔點測定鑑定結構無誤。用熱蒸鍍方式沉積在TFT上,但是並沒有顯著元件特性表現。 利用Grignard metathesis 合成三種不同側鍵烷基位置規則(3-烷基吩)三嵌段型共聚物分別為 poly(3-hexylthiophene-co-3-thiophene-co-3-dodecylthiophene)(P3HT-co-PT-co-P3DDT), poly(3-octylthiophene- co-3-hexylthiophene-co-3-methylthiophene)(P3MT-co-P3HT-co-P3OT), poly(3-hexylthiophene-co-3-octylthio- phene-co-3-hexylthiophene)(P3HT-co-P3OT-co-P3HT)。以NMR, FTIR, GPC, XRD, UV 和 CV 對合成出的產物進行一系列物性探討比較。將聚(3-烷基吩)共聚物應用作為有機薄膜電晶體之半導體材質,其載子位移率、開關電流比分別為 1.65×10-4 cm2/Vs, 1.85×104 (P3HT-co-P3OT- co-P3HT), 3.19×10-4 cm2/Vs, 8.69×103 (P3HT-co-PT-co-P3DDT),以及 2.88×10-3 cm2/Vs, 2.73×104 (P3MT-co-P3HT-co-P3OT)。除此之外相對比較他們的物性與TFT元件特性,發現三成份的共聚物載子位移率都有較低的趨勢,但是驅動電壓均較聚(3-烷基吩),二嵌段型(3-烷基吩)共聚物更低,而其開關電流比則有隨著分子量增加而提高的趨勢。
The series of oligothiophene, which contains α-bithiophene (α-2T), α-terthiophene (α-3T), and α-quinquethiophene (α-5T), have been synthesized successfully by Kumada Coupling method. The structure of above oligothiophenes has been confirmed by FT-IR, 1H-NMR, and melting point. Unfortunately, the charactaistics of thin-film transitor with oligothiophene by vacuum thermal evaporation cannot exhibit. Three kinds of the 3-alkylthiophene copolymers: poly(3-hexylthiophene-co-3-thiophene-co-3-dodecylthiophene)(P3HT-co-PT-co-P3DDT), poly(3-octylthiophene- co-3-hexylthiophene-co-3-methylthiophene)(P3OT-co-P3HT-co-P3MT), and poly(3-hexylthiophene-co-3-octyl- thiophene-co-3-hexylthiophene)(P3HT-co-P3OT-co-P3HT) have been synthesized successfully by Grignard metathesis. The physical properties of synthesized products were done by NMR, FT-IR, GPC, XRD, UV, and CV. The structure and regioregularity of triblock copolymers were identified by NMR analysis. The characteristics of organic thin-film transistor fabricated with triblock copolymers acted as semiconducting material have been carried out. The charge transport mobility and on/off current ratio of triblock copolymers OTFT are 1.65×10-4 cm2/Vs and 1.85×104 of P3HT-co-P3OT-co-P3HT, 3.19×10-4 cm2/Vs and 8.69×103 of P3HT-co-PT-co-P3DDT, and 2.88×10-3 cm2/Vs and 2.73×104 of P3MT-co-P3HT-co-P3OT, respectively. Besides, compared with the physical properties and characteristics of poly(3-alkylthiophene) and diblock copolymer TFTs have been investigated. It is found that the charge transport mobility of triblock copolymer TFTs is lower than that of poly(3- alkylthiophene) and diblock copolymer TFTs, but the threshold voltage of triblock copolymer TFTs is better than that of poly(3-alkylthiophene) and diblock copolymer TFTs. The on/off ratio increases with increasing molecular weight.