Abstract: Disclosed is a liquid crystal compound with negative dielectric anisotropy, having a general formula as Formula 1. In Formula 1, each of L1, L2, L3, and L4, being same or different, is hydrogen, halogen, or cyano group. Each of R1 and R2, being same or different, is hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 haloalkyl group, C2-12 alkenyl group, C2-12 ether group, or C2-12 alkynyl group. Each of A1 and A2, being same or different, is benzene, cyclohexane, or cyclohexene. Z1 is —CF2O—, or —OCF2—, and Z2 is —CF2O—, or —OCF2—.

Abstract: Organic metal compounds, organic light-emitting devices, and lighting devices employing the same are provided. The organic metal compound has a chemical structure represented by Formula (I): , wherein M is Ir, Pt, Ru, Os, Cu, Au, or Pd; n is 1, 2, or 3; m is 0, 1, or 2, and the sum of m and n is equal to a valence of M; L is a bidentate ligand; R1 is hydrogen, C1-9 alkyl group, C5-10 cycloalkyl group, or C5-12 aromatic group; each of R2 is independent and can be hydrogen, halogen, cyano group, C1-9 alkyl group, C1-6 fluoroalkyl group, C5-10 cycloalkyl group, or C5-12 aromatic group; R3 is halogen; and, R4 and R5 are independently the same or different hydrogen, hydroxyl group, amine group, alkyl amine group, halogen, cyano group, C1-9 alkyl group, C1-6 fluoroalkyl group, C5-10 cycloalkyl group, or C5-12 aromatic group.

Abstract: Disclosed is a liquid crystal compound with negative dielectric anisotropy, having a general formula as Formula 1. In Formula 1, each of L1, L2, L3, and L4, being same or different, is hydrogen, halogen, or cyano group. Each of R1 and R2, being same or different, is hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 haloalkyl group, C2-12 alkenyl group, C2-12 ether group, or C2-12 alkynyl group. Each of A1 and A2, being same or different, is benzene, cyclohexane, or cyclohexene. Z1 is —CF2O—, or —OCF2—, and Z2 is —CF2O—, or —OCF2—.

Abstract: Disclosed is a liquid-crystal compound with negative dielectric anisotropy, having the chemical formula: wherein A1, A2, and A3 are independently selected from cyclohexyl group, cyclohexenyl group, or phenyl group; L1 and L2 are independently selected from H or F; R is selected from H, F, Cl, C1-10 alkyl group, C1-10 alkenyl group, C1-10 alkoxy group, or C1-10 ether group; Y is fluorinated methyl group; m and n are independently selected from an integer of 0-2; and 1?m+n?3.

Abstract: A method for maintaining a file system of a computer system is disclosed. An operating system is loaded to the computer system when the computer system is booted, such that the file system of the computer system is monitored in real time after the computer system is booted. When occurrence of an error in the file system is detected, a number of times the error has occurred is accumulated. When the number of times the error has occurred reaches a predetermined threshold, a notification message is generated and displayed on an electronic apparatus. Accordingly, a manager of the computer system may be notified immediately when the occurrence of the error in the file system is detected.

Abstract: In an embodiment of the present disclosure, a liquid crystal display is provided. The liquid crystal display includes an upper substrate, a lower substrate opposite to the upper substrate, and a liquid crystal layer disposed between the upper substrate and the lower substrate, wherein the liquid crystal layer includes a first chiral compound and a second chiral compound, and the first chiral compound and the second chiral compound are enantiomeric and separated from each other.

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: Disclosed is a liquid-crystal compound with negative dielectric anisotropy, having the chemical formula: wherein A1, A2, and A3 are independently selected from cyclohexyl group, cyclohexenyl group, or phenyl group; L1 and L2 are independently selected from H or F; R is selected from H, F, Cl, C1-10 alkyl group, C1-10 alkenyl group, C1-10 alkoxy group, or C1-10 ether group; Y is fluorinated methyl group; m and n are independently selected from an integer of 0-2; and 1?m+n?3.

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 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: 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 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 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 data recovery device including an analog to digital converter (ADC), a filtering-equalizing unit, a zero crossing detector, a data phase locked loop, a data mapping unit and an estimation unit is provided. The ADC converts a radio frequency signal to a plurality of sampling data points. The sampling data points are converted to a plurality of retiming data points and a clock signal by the filtering-equalizing unit, the zero crossing detector and the data phase locked loop. The data mapping unit selects a plurality of maximum data points and minimum data points from the returning data points, and determines whether to map the maximum data points and the minimum data points to other levels for partially reconstructing the retiming data points. The estimation unit recovers the reconstructed retiming data points to a modulation signal.

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.