Abstract: A probe card device and a transmission structure are provided. The transmission structure includes a supporting layer, a plurality of metal conductors spaced apart from each other and slantingly inserted into the supporting layer, and an insulating resilient layer formed on the supporting layer. Each of the metal conductors includes a positioning segment held in the supporting layer, a connecting segment and an embedded segment respectively extending from two ends of the positioning segment, and an exposed segment extending from the embedded segment. Each of the embedded segments is embedded and fixed in the insulating resilient layer, and each of the exposed segments protrudes from the insulating resilient layer. When any one of the exposed segments is pressed by an external force, the insulating resilient layer is configured to absorb the external force through the corresponding embedded segment so as to have a deformation providing a stroke distance.

Abstract: A probe card device and a transmission structure are provided. The transmission structure includes a supporting layer, a plurality of metal conductors spaced apart from each other and slantingly inserted into the supporting layer, and an insulating resilient layer formed on the supporting layer. Each of the metal conductors includes a positioning segment held in the supporting layer, a connecting segment and an embedded segment respectively extending from two ends of the positioning segment, and an exposed segment extending from the embedded segment. Each of the embedded segments is embedded and fixed in the insulating resilient layer, and each of the exposed segments protrudes from the insulating resilient layer. When any one of the exposed segments is pressed by an external force, the insulating resilient layer is configured to absorb the external force through the corresponding embedded segment so as to have a deformation providing a stroke distance.

Abstract: Organic metal compounds and organic light-emitting devices employing the same are provided. The organic metal compound has a chemical structure of Formula (I) or Formula (II): wherein X is O or S; L is R12 is and, n is 0, 1, or 2.

Abstract: Organic metal compounds, and organic light-emitting devices employing the same are provided. The organic metal compound has a chemical structure represented by Formula (I) or Formula (II): wherein, R1 is hydrogen, C1-12 alkyl, C1-12 alkoxy, amine, C2-6 alkenyl, C2-6 alkynyl, C5-10 cycloalkyl, C3-12 heteroaryl, or C6-12 aryl; R2, R3, R4, and R5 can be hydrogen, halogen, C1-12 alkyl, C1-12 alkoxy, C1-12 fluoroalkyl; R6 and R7 are independent and can be C1-6 alkyl, or phenyl; R8, R9, R10, R11, R12, R13, R14, and R15 can be hydrogen, halogen, C1-12 alkyl, C1-12 fluoroalkyl, or two adjacent groups of R2, R3, R4, R5, R8, R9, R10, R11, R12, R13, R14 and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl; m is 1 or 2; and, n is 0 or 1.

Abstract: Organic metal compounds, and organic light-emitting devices employing the same, are provided. The organic metal compound has a chemical structure represented by formula (I): wherein each R1 can be independently hydrogen, C1-12 alkyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2 can be independently hydrogen, halogen, C1-12 alkyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group.

Abstract: An organic metal complex is provided. The organic metal complex has the following formula (I): wherein R1 can be hydrogen, halogen, C1-12alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently of each other and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6-R13 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent R6-R13 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group and n is 1 or 2.

Abstract: Organic metal compounds, and organic light-emitting devices employing the same are provided. The organic metal compound has a chemical structure represented by formula (I): wherein each R1 is independent and can be hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6 and R7 are independent and can be C1-6 alkyl group, or phenyl group; and, n is 0 or 1.

Abstract: Organic metal compounds, and organic light-emitting devices employing the same are provided. The organic metal compound has a chemical structure represented by Formula (I) or Formula (II): wherein, R1 is hydrogen, C1-12 alkyl, C1-12 alkoxy, amine, C2-6 alkenyl, C2-6 alkynyl, C5-10 cycloalkyl, C3-12 heteroaryl, or C6-12 aryl; R2, R3, R4, and R5 can be hydrogen, halogen, C1-12 alkyl, C1-12 alkoxy, C1-12 fluoroalkyl; R6 and R7 are independent and can be C1-6 alkyl, or phenyl; R8, R9, R10, R11, R12, R13, R14, and R15 can be hydrogen, halogen, C1-12 alkyl, C1-12 fluoroalkyl, or two adjacent groups of R2, R3, R4, R5, R8, R9, R10, R11, R12, R13, R14 and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl; m is 1 or 2; and, n is 0 or 1.

Abstract: Organic metal compounds, and organic light-emitting devices employing the same, are provided. The organic metal compound has a chemical structure represented by formula (I): wherein each R1 can be independently hydrogen, C1-12 alkyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2 can be independently hydrogen, halogen, C1-12 alkyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group.

Abstract: A method for synthesis of secondary alcohols is provided for pharmaceutical secondary alcohol by addition of organoboronic acids with aldehydes in presence of the cobalt ion and bidentate ligands as the catalyst. In addition, an enantioselective synthesis method for secondary alcohols is also herein provided in the present invention. The present invention has advantages in using less expensive cobalt ion and commercially available chiral ligands as the catalyst, wide scope of organoboronic acids and aldehydes compatible with this catalytic reaction and achieving excellent yields and/or enantiomeric excess.

Abstract: A method for synthesis of secondary alcohols is provided for pharmaceutical secondary alcohol by addition of organoboronic acids with aldehydes in presence of the cobalt ion and bidentate ligands as the catalyst. In addition, an enantioselective synthesis method for secondary alcohols is also herein provided in the present invention. The present invention has advantages in using less expensive cobalt ion and commercially available chiral ligands as the catalyst, wide scope of organoboronic acids and aldehydes compatible with this catalytic reaction and achieving excellent yields and/or enantiomeric excess.