ãAmbipolar organic field-effect transistors based on N-Unsubstituted thienoisoindigo derivativesã?was published in Dyes and Pigments in 2020. These research results belong to Yoo, Dongho; Hasegawa, Tsukasa; Kohara, Akihiro; Sugiyama, Haruki; Ashizawa, Minoru; Kawamoto, Tadashi; Masunaga, Hiroyasu; Hikima, Takaaki; Ohta, Noboru; Uekusa, Hidehiro; Matsumoto, Hidetoshi; Mori, Takehiko. Name: Oxetan-3-ol The article mentions the following:
To investigate a hybrid of isoindigo and thienoisoindigo (TIIG), a new series of unsym. TIIG analogs, in which one of the outer thiophene rings of TIIG is replaced by benzene (CS) or pyridine (NS) are prepared In addition, the π-skeleton extension effects are studied by examining α-substituted TIIG derivatives with thienyl (Dth-TIIG), furyl (Dfu-TIIG), and 1-phenyl-5-pyrazolyl groups (Bis(1-ph-5-py)-TIIG). These materials exhibit ambipolar transistor properties as expected from the energy levels. Dth-TIIG and Dfu-TIIG show hole mobilities exceeding 0.05 cm2 V-1 s-1, and electron mobilities about 0.04 cm2 V-1 s-1, which are close to those of the di-Ph derivative These mols. are arranged nearly perpendicularly to the substrates in the thin films, and Dth-TIIG has a brickwork-like structure, whereas Dfu-TIIG has uniform columns. CS and Bis(1-ph-5-py)-TIIG have uniform stacking structures, but NS has a dimerized stacking structure due to the slightly bent mol. plane that results from largely unbalanced electron d. In the experimental materials used by the author, we found Oxetan-3-ol(cas: 7748-36-9Name: Oxetan-3-ol)
Oxetan-3-ol(cas: 7748-36-9) is used as a reagent in the synthesis of 5-fluoro-4,6-dialkoxypyrimidine GPR119 agonists. It is also used as a reagent in the synthesis of cyclic sulfone hydroxyethylamines as potent and selective β-site APP-cleaving enzyme 1 (BACE1) inhibitors.Name: Oxetan-3-ol
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