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57results about How to "Optically active" patented technology

Method for splitting 2-heterocycle substituted dihydropyrimidine racemic compound

The invention provides a method for splitting 2-heterocycle substituted dihydro pyrimidine racemic body, which comprises the following steps: (1) putting the 2-heterocycle substituted dihydro pyrimidine racemic body and 1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate resolving agent with optical activity in a reactor, and adding a solvent; (2) stirring the mixture; (3) filtering the mixture, concentrating a mother solution and standing the mother solution; (4) filtering and concentrating the mother solution to be dry; and (5) refining. The single chiral 2-heterocycle substituted dihydro pyrimidine compounds prepared by the splitting method has the product yield about 20 percent and the optical purity above 98 percent; and the splitting method has the advantages of stability, high yield, high optical purity, simple and convenient operation, strong practicability and easy industrialization.
Owner:SUNSHINE LAKE PHARM CO LTD

Liquid crystal display panel and liquid crystal display device

The invention discloses a liquid crystal display panel and a liquid crystal display device. A display area of the liquid crystal display panel comprises a pixel layer, a liquid crystal layer, a firstpolaroid and an optical sensor which are arranged in sequence. The first polaroid comprises a first polarizing unit and a second polarizing unit, wherein the polarizing directions of the first polarizing unit and the second polarizing unit are perpendicular and adjacent. The liquid crystal layer comprises a first liquid crystal unit corresponding to the first polarization unit and a second liquidcrystal unit corresponding to the second polarization unit, the polarization direction of polarized light passing through the first liquid crystal unit is kept unchanged, and the polarization direction of polarized light passing through the second liquid crystal unit rotates by 90 degrees; the pixel layer comprises a transparent area corresponding to the first liquid crystal unit and a pixel areacorresponding to the second liquid crystal unit; and the optical sensor is arranged corresponding to the first polarizing unit. According to the optical sensor, a collimation light path is provided for the optical sensor through the transparent area, the first liquid crystal unit and the first polarization unit which are correspondingly arranged, the optical crosstalk is avoided, and the LCD under-screen sensing technology is achieved.
Owner:WUHAN CHINA STAR OPTOELECTRONICS TECH CO LTD

Preparation and application of phenylalanine dipeptide-graphene quantum dot composite material

The invention relates to preparation and application of a phenylalanine dipeptide-graphene quantum dot composite material. The preparation includes the following steps: preparation of graphene quantum dots, preparation of the phenylalanine dipeptide-graphene quantum dot composite material, preparation of a phenylalanine dipeptide-graphene quantum dot composite material modified electrode, and electrochemical method identification of tryptophan enantiomers. The beneficial effects are that the preparation method of the phenylalanine dipeptide-graphene quantum dot composite material modified electrode is simple and environment-friendly, and the phenylalanine dipeptide-graphene quantum dot composite material modified electrode has better tryptophan enantiomer recognition ability because of some optical rotation of the phenylalanine dipeptide.
Owner:CHANGZHOU UNIV

Chiral geminal disilicide alkane compound containing four silicon-hydrogen bonds as well as synthesis method and application thereof

The invention discloses a chiral geminal disilicide alkane compound containing four silicon-hydrogen bonds, shown as a formula VI, and discloses a synthesis method of the chiral geminal disilicide alkane compound. For the first method, in inert gas, a vinyl silane type compound shown as a formula V and silane trihydride shown as a formula IV are used as raw materials; a chiral CoX2-IIP complex compound is used as a catalyst; under the existence of reducing agents, reaction is performed to prepare VI. For the second method, in the inert gas, alkyne shown as a formula I, silane trihydride shownas a formula II and silane trihydride shown as a formula IV are used as raw materials; CoY2, bi(2-diphenyl phosphenyl) ether and a chiral CoX2-IIP complex compound are used as catalysts; under the existence of reducing agents, reaction is performed to prepare a formula VI. The method has the advantages of mild reaction conditions, operation simplicity and convenience, high atom economy, excellentproductive rate (57 to 84 percent), high regioselectivity (greater than 19:1) and high enantioselectivity (91.6 to 98.8 percent ee). The formulas are shown in description.
Owner:ZHEJIANG UNIV

Method for preparing thioalkyl/alkenyl cysteine sulfoxide by fractional crystallization

The invention discloses a method for preparing thioalkyl / alkenyl cysteine sulfoxide by fractional crystallization, belonging to the technical field of compound preparation. The method comprises the following steps: adding cysteine or cysteine salts, a sodium hydroxide solution and an R group (alkyl or alkenyl)-derived material into absolute ethanol in sequence for reaction to synthesize coarse ACSs, re-crystallizing ACSs, purifying, oxidizing to form ACSOs, and fractionally crystallizing to obtain natural dextrorotatory ACSOs, wherein the R group-derived material is replaced to synthesize different types of ACSOs in allium; enantiomers in racemes are separated by adopting the fractional crystallization method to obtain natural dextrorotatory ACSOs with optical activity. Compared with a conventional extraction method, the method has the characteristics that the yield and the purity are high, a conventional complicated extraction process is avoided, the product has the optical activity, and the physical property is close to that of natural extract; the product is used in the fields of health products, pharmaceuticals and the like, the effects of resisting bacteria and cancers, reducing blood fat and the like of ACSOs are brought into play, or the product serves as an intermediate such as an active ingredient-diallyl thiosulfinate for synthesizing allium.
Owner:JIANGNAN UNIV

Azo-like liquid crystal monomer with reaction character and preparation method thereof

The invention discloses an azo liquid crystal monomer with reaction properties and a preparation method thereof. The structural formula of the compound is listed, wherein, the n1 is an integer between 6 and 14, n2 is an integer between 1 and 7 and n3 is an integer between 1 and 5; the substitute position of the dilute oxygen is the adjacent position or contraposition of alkoxy; a synthesis method of the compound is that: the substituted dilute oxygen pairs by alkoxy benzoic acid is adopted as raw material to obtain aniline compounds by processes of amidation and hoffman degradation reaction; then low temperature diazotization coupling is carried out to obtain the new liquid crystal compound. A central bridge bond of the liquid crystal monomer of the invention is the azo group and has optical activity and a side chain of the invention is double bonds with reactivity; at last, novel waist connected type macromolecule liquid crystal and liquid crystal elastomer are made by polymerization or graft the double bonds to macromolecule main chain. The invention has easy obtained raw material, simple and safe operation and being applied to such fields as non-linear optical materials, optical information storage, optical switch, display, artificial muscles, shape memory and biomedicine.
Owner:NORTHWESTERN POLYTECHNICAL UNIV

Method for constructing tartaric acid coating layer with corrosion protection function on surface of magnesium metal

The invention discloses a method for constructing a tartaric acid coating layer with a corrosion protection function on the surface of magnesium metal. The method comprises the following steps: A. polishing and carrying out ultrasonic cleaning on a pickling solution; B. soaking the magnesium metal obtained in the step A in NaOH solution with a concentration of 3mol/L, placing the NaOH solution in a water bath environment at 50-70 DEG C, standing for 11-14h, carrying out alkaline activation pre-treatment, then thoroughly washing the magnesium metal, and then drying the magnesium metal; C. preparing a tartaric acid solution with a concentration of 5-25g/L, and adjusting the pH value of the tartaric acid solution to achieve 5-9 by virtue of NaOH with a concentration of 1mol/L; and D. soaking the magnesium metal obtained in the step B in the tartaric acid solution prepared in the step C, placing the tartaric acid solution in a water bath environment at 30-80 DEG C, standing for 3-12h, then taking out the magnesium metal and thoroughly washing the magnesium metal by virtue of deionized water, and carrying out vacuum drying; and the tartaric acid coating layer with the corrosion protection function is successfully constructed on the surface of the magnesium metal. After the surface of the magnesium metal is modified through the method, the corrosion speed of a corrosive environment for the magnesium metal can be much effectively controlled, so that the corrosion-degradation period of the magnesium metal is matched with the treatment-recovery period of organisms when the magnesium metal is used as a biodegradable medical material.
Owner:SOUTHWEST JIAOTONG UNIV

Preparation method of optically active AIE fluorescent material and water-based polymer thereof

The invention discloses a preparation method of an optically active AIE fluorescent material water-based polymer. The preparation method comprises the following steps: A, synthesizing an aldehyde group AIE fluorescent compound by utilizing a Suzuki coupling reaction between phenylboronic acid and bromobenzene; B, synthesizing a methoxy fluorescent compound by utilizing a condensation reaction between an aldehyde group and phenyl acetonitrile, and further demethylating methoxy through BBr3 to generate hydroxyl; C, introducing tertiary hydroxyl into the fluorescent compound through a nucleophilic substitution reaction between benzene hydroxyl and fatty chlorine to generate a corresponding tertiary hydroxyl AIE fluorescent compound; D, introducing an acrylic acid element into the fluorescentcompound through a selective ester exchange reaction under the catalysis of lipase B to obtain an AIE fluorescent monomer with optical activity; and E, preparing the AIE fluorescent polymer with optical activity through RAFT active polymerization. The fluorescent dye and polymer have optical activity.
Owner:UNIV OF ELECTRONICS SCI & TECH OF CHINA ZHONGSHAN INST
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