Polycarbonate and preparation method and application thereof
A polycarbonate, an independent technology, applied in the field of polycarbonate and its preparation, can solve the problems of complex lens composition, large chromatic aberration, etc., and achieve the effect of multi-selectivity, high glass transition temperature, and high refractive index
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[0159]Preparation Example 1
[0160]2,2-bis(2-hydroxyethoxy)-6,6-diphenyl-1,1-dithionaphthalene (BINSL-2EO)
[0161]The synthetic route is as follows:
[0162]
[0163](1) In a four-necked flask equipped with a magnetic stirrer, thermometer, constant pressure dropping funnel and condensing reflux tube, add 223g (1mol) of 6-bromo-2-naphthol (Wuhan Rongcan Biopharmaceutical), toluene and 500mL of ethyl acetate mixed solution (the mass ratio of toluene to ethyl acetate is 3:2), stir to dissolve, under ice bath conditions, slowly add 53g (0.52mol) sulfur dichloride dropwise, and control the temperature of the reaction system at Around 15°C. After dripping, continue to react for 3h. Warm up to 100℃, after distilling out most of the solvent, put it in the refrigerator and freeze for 1h, there is solid precipitation, filter, recrystallize from absolute ethanol, filter and dry to obtain 6,6-dibromo-1,1-dithionaphthalene phenol.
[0164](2) Dissolve 1 mol of 6,6-dibromo-1,1-dithionaphthalene and 2 mol of p...
Example Embodiment
[0167]Preparation Example 2
[0168]2,2-bis(2-hydroxyethoxy)-6,6-bis(naphthalene-1-yl)-1,1-dithionaphthalene (1DNBINSL-2EO)
[0169]The synthetic route is as follows:
[0170]
[0171]The specific preparation method differs from Preparation Example 1 only in that the phenylboronic acid in step (2) is replaced with an equimolar amount of 1-naphthylboronic acid (Puyang Huicheng Technology); other reaction steps are the same as those in Preparation Example 1. The target product 1DNBINSL-2EO was obtained.
[0172]The NMR results of the target product are as follows:1H-NMR(400MHz, CDCl3)δ / ×10-6: 8.55 (t, 2H), 8.42 (t, 2H), 8.08-8.04 (m, 6H), 7.95 (t, 2H), 7.86 (d, 2H), 7.61-7.55 (m, 8H), 6.85 (d , 2H), 4.43 (t, 4H), 3.69 (m, 4H), 3.65 (m, 2H).
Example Embodiment
[0173]Preparation Example 3
[0174]2,2-bis(2-hydroxyethoxy)-1,1-dithionaphthalene (BNSE)
[0175]The synthetic route is as follows:
[0176]
[0177](1) In a four-necked flask equipped with a magnetic stirrer, a thermometer, a constant pressure dropping funnel and a condensing reflux tube, 144g (1mol) of 2-naphthol (Jiangsu Chiral Chemical Industry) and a mixture of toluene and ethyl acetate were sequentially added 500 mL of the mixed solution (the mass ratio of toluene and ethyl acetate is 3:2), stir to dissolve, and slowly add 53 g (0.52 mol) sulfur dichloride dropwise under ice bath conditions, and control the temperature of the reaction system at about 15°C. After dripping, continue to react for 3h. The temperature was raised to 100°C, and most of the solvent was distilled out, and then placed in the refrigerator for 1 hour. A solid precipitated out, filtered, recrystallized with anhydrous ethanol, filtered and dried to obtain dithionaphthol.
[0178](2) In the reactor, the molar ratio of the...
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