Achiral side methyl alkyl quaterphenyl liquid crystal compound and preparation method, liquid crystal composition and microwave communication device
A technology of methyl alkyl tetrabiphenyls and liquid crystal compositions, which is applied in the preparation of amino compounds, waveguide type devices, hydrocarbon compounds and the like from amines, can solve the problem that liquid crystal materials for microwaves cannot be satisfied, and the low temperature properties of liquid crystal materials are affected. The problem of large dielectric loss of liquid crystal materials can achieve the effect of increasing optical anisotropy, large sum of optical anisotropy, and reducing dielectric loss.
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[0062] figure 1 The process is schematic flow diagram of the preparation method of the non-haired side methyl alkyl tetraplenzene liquid crystal compound (I-1) provided by the present invention, at this time, Y is an F atom, including the following steps:
[0063] Step S10: Under nitrogen protection, bromobear is dissolved in tetrahydrofuran, followed by mixing to magnesium powder, tetrahydrofuran, and iodine monomi, sufficiently reacted, and the Grid reagent, adding the grace reagent to copper chloride, DL-1-iodo-2-methylbutane and mixture of tetrahydrofuran, reflow reaction, then dilute hydrochloric acid, stir, then separated, washing and purification, the first intermediate;
[0064] In this step, the separation, washing, and purification treatment can be carried out in accordance with the conventional method in the art of organic synthesis, for example, separation can be extracted, washing water to the product is neutral, purified with recrystallization, and the like. The fol...
Embodiment 1
[0123] Example 1 Synthesis of PGPUS, Structure of PGPUS:
[0124]
[0125] The preparation process is:
[0126] (1) Titanium (0.285 mol), 10 ml of anhydrous tetrahydrofuran and 1-2 iodine monohydrate, then dissolved in 100 ml of anhydrous tetrahydrofuran (0.28 mol) 43.6 g (0.28 mol) (0.28 mol) (0.28 mol) (0.28 mol) (0.28 mol) (0.28 mol) (0.28 mol) dissolved in 100 ml of water tetrahydrofuran (0.28 mol) ) The bromobenzene solution was added to a 250 mL constant pressure drop funnel. Nitrogen protection, dripping a little brodipate into a three-bottle from a constant pressure drip funnel, micro-heat. After the reaction is initiated, heating is stopped. Slowly stir, and pixab bromobenzene is mixed into a three-bottle to make it reflow. After the measuring, the temperature was refluxed for about 30 min until the magnesium was close to completely reacted, stop heating, naturally cooled to room temperature, and the reaction liquid was a gray liquid (Ghr's agent).
[0127] Anhydrous co...
Embodiment 2
[0136] Example 2 Synthesis of PWPUS, Structure:
[0137]
[0138] The step is the same as that of Example 1, in which the inverted fluorine boric acid in step (3) is replaced with michlorobree boric acid; the temperature is raised to 110 ° C in step (2), step (4) cooling to -75 At ° C, stirring 2 h then rose to 20 ° C, third intermediate, n-butyllithium, boric acid trimethylate and hydrochloric acid in the fourth intermediate, third reactant in the fourth intermediate, third reactant in step (5) K 2 CO 3 The molar ratio of the palladium catalyst is 1: 2: 5: 0.001, the molar ratio of the fifth intermediate, calcium carbonate and chloride sulfide in step (6) is 1: 2: 2, and the ice bath is cooled to 5 ° C, then Naturally heated to 25 ° C, and finally warmed to 50 ° C.
[0139] The structure of the target compound produced by the hydrogen magnetic resonance spectroscopy and fluorine-nuclear magnetic resonance spectroscopy is demonstrated to the structure of the above-described stru...
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