Abstract: An embodiment of the disclosure provides a liquid crystal compound having the following formula: wherein A1, A2, and A3 are independently hydrogen, halogen, cyano, thiocyanato, or —OCF3; R1 is hydrogen, halogen, C1-C12 alkyl, C1-C12 alkoxy, C1-C12 haloalkly, C2-C12 alkenyl, or C2-C12 alkynyl; R2 and R3 are independently hydrogen, halogen, C1-C6 alkyl, C1-C6 haloalkly, cyano, thiocyanato, or —OCF3; and Z is a single bond, —O—, —CH2O—, —C(O)O—, —OCO—, —C(O)NH—, or —CH?CH—. In another embodiment, a liquid crystal display including the liquid crystal compound is also provided.

Abstract: An embodiment of the invention provides a liquid crystal compound having the following formula: wherein A1, A2, and A3 are independently hydrogen, halogen, cyano, thiocyanato, or —OCF3; R1 is hydrogen, halogen, C1-C12 alkyl, C1-C12 alkoxy, C1-C12 haloalkyl, C2-C12 alkenyl, or C2-C12 alkynyl; R2 is hydrogen, halogen, C1-C6 alkyl, C1-C6 haloalkyl, cyano, or —OCF3; and Z is —O—, —CH2O—, —C(O)O—, —OCO—, —C(O)NH—, —CH?CH—, or —C?C—. In another embodiment, a liquid crystal display including the liquid crystal compound is also provided.

Abstract: A liquid crystal compound of Formula (I) is provided. In Formula (I), A is benzene, naphthalene, pyridine, furan, thiophene or a single bond, D is benzene, naphthalene, pyridine, furan, thiophene or a single bond, R1 and R2 are C1-10 alkyl, C1-10 alkoxy, fluoro or trifluoro methyl, E is benzene, naphthalene, pyridine, furan, thiophene or a single bond, W is —CO—O—, —O—CO—, —O—, —CH2—CH2—, —CH?CH—, —CH2—O— or a single bond, Z is benzene, naphthalene, pyridine, furan, thiophene or a single bond, Y is hydrogen, methyl, ethyl or propyl, m is 0, 1 or 2, p is 0, 1 or 2, r is 0, 1 or 2, q is 0, 1 or 2, and n is 0, 1, 2 or 3. The invention also provides a liquid crystal display and photochromic material including the compound.

Abstract: A method of reusing micro-encapsulated cholesteric liquid crystals is provided. The method includes providing a display medium material containing a micro-encapsulated cholesteric liquid crystal and a dispersant. The display medium material is mixed with a solvent to form a mixture having a temperature of between 40° C. and 60° C. A centrifugal process is performed to the mixture for separating the micro-encapsulated cholesteric liquid crystal and the dispersant. Then, the dispersant and the solvent are removed to obtain the micro-encapsulated cholesteric liquid crystal.

Abstract: A method of recycling a cholesteric liquid crystal is provided. The method includes providing a display medium material containing a micro-encapsulated cholesteric liquid crystal. The display medium material is mixed with a hydrophilic solvent to form a mixture having a temperature of between 70° C. and 100° C. Then, a hydrophobic solvent is added to mix with the hydrophilic solvent. The display medium material, the hydrophobic solvent and the hydrophilic solvent are mixed to form a mixture having a hydrophobic layer and a hydrophilic layer. The hydrophobic layer and the hydrophilic layer of the mixture are separated, wherein the hydrophobic layer contains a cholesteric liquid crystal and the hydrophobic solvent. Then, the hydrophobic solvent is removed from the hydrophobic layer to obtain the cholesteric liquid crystal.

Abstract: A liquid crystal compound of Formula (1) is provided below: wherein R is hydrogen, linear or branching C1-15 alkyl, linear or branching C1-15 alkyl (wherein any one of —CH2— is replaced by —O—, —S—, —CO—, —CO—O—, or —O—CO—), linear or branching C2-15 alkenyl, or linear or branching C2-15 alkenyl (wherein any one of —CH2— is replaced by —O—, —S—, —CO—, —CO—O—, or —O—CO—), A and B are, independently, cyclohexane, cyclohexane (wherein any one of —CH2— is replaced by —O— or —NH—), benzene, or benzene (wherein any one of —CH2? is replaced by —N?), X is a single bond, —CO—O—, —O—CO—, —CH2O—, —OCH2—, —CH2CH2—, —C?C—, —C?C—, —CF2O—, or —OCF2—, Q is oxygen or CH2, Y is CF3, CF2H, or CFH2, L1, L2, and L3 are, independently, hydrogen or fluorine, and m is 0, 1, or 2.

Abstract: A liquid crystal compound of Formula (I) is provided. In Formula (I), A is benzene, naphthalene, pyridine, furan, thiophene or a single bond, D is benzene, naphthalene, pyridine, furan, thiophene or a single bond, R1 and R2 are C1-10 alkyl, C1-10 alkoxy, fluoro or trifluoro methyl, E is benzene, naphthalene, pyridine, furan, thiophene or a single bond, W is —CO—O—, —O—CO—, —O—, —CH2—CH2—, —CH?CH—, —CH2—O— or a single bond, Z is benzene, naphthalene, pyridine, furan, thiophene or a single bond, Y is hydrogen, methyl, ethyl or propyl, m is 0, 1 or 2, p is 0, 1 or 2, r is 0, 1 or 2, q is 0, 1 or 2, and n is 0, 1, 2 or 3. The invention also provides a liquid crystal display and photochromic material including the compound.

Abstract: An embodiment of the invention provides a chiral dopant having the following formula: wherein X1 and X2 are independently wherein F is fluorine, m is a positive integer from 1 to 8, and n is a positive integer from 1 to 4; Y1 and Y2 are independently —O—, —CH2CH2—, —CH?CH—, —C(O)O—, or —CH2O—; and R1, R2 are independently substituted or non-substituted C1-C10 linear alkyl, wherein substituents of the substituted C1-C10 linear alkyl are independently —F, —Cl, —OCF3, —NCS, or —CN, wherein a number of backbone carbon atoms in each of —Y1R1 and —Y2R2 is larger than 3.

Abstract: An embodiment of the invention provides a liquid crystal compound having the following formula: wherein A1, A2, and A3 are independently hydrogen, halogen, cyano, thiocyanato, or —OCF3; R1 is hydrogen, halogen, C1-C12 alkyl, C1-C12 alkoxy, C1-C12 haloalkly, C2-C12 alkenyl, or C2-C12 alkynyl; R2 is hydrogen, halogen, C1-C6 alkyl, C1-C6 haloalkly, cyano, or —OCF3; and Z is —O—, —CH2O—, —C(O)O—, —OCO—, —C(O)NH—, —CH?CH—, or —C?C—. In another embodiment, a liquid crystal display including the liquid crystal compound is also provided.

Abstract: An embodiment of the invention provides a chiral dopant having the following formula: wherein X1 and X2 are independently wherein F is fluorine, m is a positive integer from 1 to 8, and n is a positive integer from 1 to 4; Y1 and Y2 are independently —O—, —CH2CH2—, —CH?CH—, —C(O)O—, or —CH2O—; and R1, R2 are independently substituted or non-substituted C1-C10 linear alkyl, wherein substituents of the substituted C1-C10 linear alkyl are independently —F, —Cl, —OCF3, —NCS, or —CN, wherein a number of backbone carbon atoms in each of —Y1R1 and —Y2R2 is larger than 3.

Abstract: A liquid crystal composition and a liquid crystal display employing the same are provided. The liquid crystal composition includes: 100 parts by weight of at least one nematic liquid crystal; 1-20 parts by weight of at least one photosensitive chiral compound; and 1-20 parts by weight of at least one non-photosensitive chiral compound.

Abstract: An isosorbide derivative of Formula (I) is provided. In Formula (I), Z is —CH2—CH2—, —CH?CH—, —C?C—, —CH2—O—, —CH2—S—, —CH?N—O—, —CO—O—, —CO—S—, single bond, -ph-, —CO—O-ph- or —CO—O-ph-CO—O—, and ph represents benzene, R1 and R2 are, independently, C1-25 alkyl, —CN, —NCS, —CX3 or —OCX3, and X represents halogen, and m and n are, independently, 0, 1 or 2. The invention also provides a liquid crystal display including the isosorbide derivative.

Abstract: The present invention relates to chiral binaphthyl compounds having good solubility and high helical twisting power. The chiral binaphthyl compounds as dopants in the liquid crystal compositions can help enhance the display quality of the liquid crystal panels.

Abstract: The present invention relates to chiral binaphthyl compounds having good solubility and high helical twisting power. The chiral binaphthyl compounds as dopants in the liquid crystal compositions can help enhance the display quality of the liquid crystal panels.

Abstract: A liquid crystal compound of Formula (1) is provided. In Formula (1), R is hydrogen, linear or branching C1-15 alkyl, linear or branching C1-15 alkyl (wherein any one of —CH2— is replaced by —O—, —S—, —CO—, —CO—O—, or —O—CO—), linear or branching C2-15 alkenyl, or linear or branching C2-15 alkenyl (wherein any one of —CH2— is replaced by —O—, —S—, —CO—, —CO—O—, or —O—CO—), A and B are, independently, cyclohexane, cyclohexane (wherein any one of —CH2— is replaced by —O— or —NH—), benzene, or benzene (wherein any one of —CH2? is replaced by —N?), X is a single bond, —CO—O—, —O—CO—, —CH2O—, —OCH2—, —CH2CH2—, —C?C—, —C?C—, —CF2O—, or —OCF2—, Q is oxygen or CH2, Y is CF3, CF2H, or CFH2, L1, L2, and L3 are, independently, hydrogen or fluorine, and m is 0, 1, or 2.

Abstract: A liquid crystal composition and a liquid crystal display employing the same are provided. The liquid crystal composition includes: 100 parts by weight of at least one nematic liquid crystal; 1-20 parts by weight of at least one photosensitive chiral compound; and 1-20 parts by weight of at least one non-photosensitive chiral compound.

Abstract: An isosorbide derivative of Formula (I) is provided. In Formula (I), Z is —CH2—CH2—, —CH?CH—, —CH2—O—, —CH2—S—, —CH?N—O—, —CO—O—, —CO—S—, single bond, -ph-, —CO—O-ph- or —CO—O-ph-CO—O—, and ph represents benzene, R1 and R2 are, independently, C1-25 alkyl, —CN, —NCS, —CX3 or —OCX3, and X represents halogen, and m and n are, independently, 0, 1 or 2. The invention also provides a liquid crystal display including the isosorbide derivative.

Abstract: The invention discloses a reflective liquid crystal material formulation, wherein a liquid crystal component of high dielectric anisotropy is employed to lower the driving voltage. By modulating the addition ratio of the high dielectric anisotropy components, reflective liquid crystal compositions of different reflective colors can be driven by a single driving voltage. The invention also provides a reflective bistable display using the above formulation.

Abstract: A liquid crystal display (LCD) and a fabrication method thereof are provided. The LCD includes a first substrate and a second substrate opposite to the first substrate. At least two layers of cholesteric liquid crystal layers are disposed between the first and the second substrates, wherein chiral dopants with different optical activities are respectively added in the cholesteric liquid crystal layers, and the chiral dopants have the same chemical structure. The fabrication method includes providing a first substrate and a second substrate opposite to the first substrate. A plurality of chiral dopants with different optical activities and having the same chemical structure are mixed into the same liquid crystal host respectively to form at least two kinds of cholesteric liquid crystal materials. Then, the cholesteric liquid crystal materials are disposed between the first and the second substrates to form at least two layers of cholesteric liquid crystal layers.

Abstract: A chiral compound of formula (I) or (II) is provided, wherein each of R1 and R2 independently, is hydrogen, hydroxyl, halogen, amino, nitrile, C1-10 alkyl, or C1-10 alkoxyl. A liquid crystal composition comprising 80-99.5 parts by weight of a liquid crystal host; and 0.5-20 parts by weight of the chiral compound as described above is also provided.