Electronic devices
An electronic device and device technology, applied in the field of electronic devices, can solve the problems of large disconnection current, increased electric rate, and low current on/off ratio of the device
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Embodiment I
[0061] Add 1 g of 2,6-dibromo-4,8-dodedecylbenzo[1,2-b:4,5; b']dithiophene to a 100 ml 3-necked reaction flask (according to H.Pan , prepared by Y.Li, Y.Wu, P.Liu, B.S.Ong, S.Zhu, G.Xu, Chem.Mater., Vol.18, P.3237 (2006), the disclosure of which is hereby incorporated in its entirety as reference), 0.37 g of 3-methylthiophene-2-boronic acid pinacol ester, and 25 ml of toluene. The resulting mixture was stirred well and purged with argon. Then 0.04 g of tetrakis(triphenylphosphine palladium(O))(Pd(Ph 3 P) 4 ), 0.3 g Aliquat in 5 mL toluene, and 3.5 mL 2M aqueous Na 2 CO 3 . The resulting reaction mixture was stirred at 105°C for 26 hours. After cooling to room temperature, about 23 °C to about 26 °C, 100 mL of toluene was added, and the organic layer was washed 3 times with deionized water in a separatory funnel, washed over anhydrous MgSO 4 Dry and filter. After removal of the solvent, the residual solid was purified by column chromatography on silica gel (eluent: hexa...
Embodiment II
1) Synthesis of poly(4,8-dihexyl-2,6-bis-(3-hexyl-thiophen-2-yl)-benzo[1,2-b:4,5-b']dithiophene) ( 23) (reaction process 1)
(a) Preparation of benzo[1,2-b:4,5-b']dithiophene-4,8 according to Beimling, P.; Koβmehl, G.Chem.Ber.Vol.119, P.3198 (1986) - diketones, the disclosure of which is hereby incorporated by reference in its entirety.
(b) 4,8-dihexynyl (dihexynyl) benzo [1, 2-b: 4, 5-b'] dithiophene
[0067] To a solution of hexyne (6.71 g, 81.7 mmol) in THF (20 mL) in a 100 mL flask equipped with a condenser under an argon atmosphere was added dropwise 36 mL (72 mmol) of 2M chloride in THF at room temperature. isopropylmagnesium solution. An exothermic reaction occurred upon addition. After the addition, the reaction mixture was heated at 50° C. for 95 minutes and cooled to room temperature. Benzo[1,2-b:4,5-b']dithiophene-4,8-dione (3 g, 13.6 mmol) was added and the mixture was heated at 50°C for 1 hour before cooling to room temperature. Subsequently, 20 g of SnCl wa...
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