Liquid crystal compound and preparation method thereof, liquid crystal composition and microwave communication device
A technology for liquid crystal compounds and liquid crystal compositions, applied in chemical instruments and methods, liquid crystal materials, etc., can solve the problems of increasing the amount of microwave phase shift, insufficient phase shift amount, large dielectric loss of liquid crystal materials, etc. Effects of electrical loss, large optical anisotropy, and structural stability
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[0058] figure 1 Shown is an example of the preparation method of the liquid crystal compound provided by the present invention. see figure 1 , in this embodiment, the preparation method of the liquid crystal compound comprises the following steps:
[0059] Step S10, under nitrogen protection, the first reactant, 2-ethyl-4-iodoaniline, palladium catalyst, K 2 CO 3 , ethanol, toluene and water were subjected to Suzuki coupling reaction under heating and stirring conditions for 3.5-4.5 hours, and then separated, washed, dried and purified to obtain the first intermediate;
[0060] The separation, washing, drying and purification in step S10 can be carried out according to conventional methods in the field of organic synthesis, such as separating the reaction product by centrifugation or filtration, then extracting with an organic solvent, washing with water, drying with a desiccant, and finally Through chromatography, elution, etc., the purified product is obtained. In this ...
Embodiment 1
[0090] The synthesis of embodiment 1 liquid crystal compound 5PP (2) GIP4, structural formula is:
[0091]
[0092] The preparation process is:
[0093] (1) Add 4-n-pentylphenylboronic acid (0.04mol, 7.68g), 2-ethyl-4-iodoaniline (0.04mol, 9.88g), K 2 CO 3 (0.10mol, 13.8g), ethanol 80mL, toluene 60mL and water 30mL, after nitrogen replacement 4 times, add catalyst tetrakistriphenylphosphine palladium (0.01mol, 0.46g), heat and stir and keep the liquid phase temperature at 70°C , stop stirring after reflux reaction for 4h, the reaction solution is naturally cooled to room temperature, then add hydrochloric acid to neutralize and filter to remove insoluble matter, then add toluene (3 × 50mL) to extract and separate the liquid, wash to neutrality, wash the product with anhydrous Na 2 SO 4 After drying and filtering, the filtrate was evaporated to dryness and loaded into a chromatography column, eluted with petroleum ether, and finally the solvent was removed by rotary evapo...
Embodiment 2
[0101] The synthesis of embodiment 2 liquid crystal compound 5PP (2) GIP5, structural formula is:
[0102]
[0103] The preparation process is:
[0104] (1) Add 4-n-pentylphenylboronic acid (0.08mol, 15.36g), 2-ethyl-4-iodoaniline (0.08mol, 19.76g), K 2 CO 3 (0.24mol, 33.12g), ethanol 100mL, toluene 60mL and water 35mL, nitrogen replacement 4 times, add catalyst tetraphenylphosphine palladium (0.01mol, 1.24g), heat and stir and keep the liquid phase temperature at 70°C , stop stirring after reflux reaction for 4h, the reaction solution is naturally cooled to room temperature, then add hydrochloric acid to neutralize and filter to remove insoluble matter, then add toluene (3 × 50mL) to extract and separate the liquid, wash to neutrality, wash the product with anhydrous Na 2 SO 4 After drying and filtering, the filtrate was evaporated to dryness and loaded into a chromatography column, eluted with petroleum ether, and finally the solvent was removed by rotary evaporation t...
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