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 electroluminescence devices employing the same are provided. The organic metal compound has a chemical structure represented below: wherein R1, R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-8 alkyl or C1-8alkoxy; L can be acetylacetone ligand, picolinic acid ligand, N,N′-diisopropylbenzamidinate, or N,N′-diisopropyl-diisopropyl-guanidinate.
Abstract:
Organic metal compounds, organic light-emitting devices, and a method for preparing the same are provided. The organic metal compound has a chemical structure represented by Formula (I): wherein one of R1 and R2 is hydrogen, and the other is trialkyl silyl group; and L is an acetylacetone ligand, a picolinate ligand, a 2-(imidazol-2-yl) pyridine ligand, a 2-(4,5-dimethyl-imidazol-2-yl)pyridine ligand, a 3-(trifluoromethyl)-5-(pyridine-2-yl)-1,2,4-triazolate ligand, or a 3-(tert-butyl)-5-(pyridine-2-yl)-1,2,4-triazolate ligand.
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): The definitions of R1-R18 and n are as defined in specification. The organic light-emitting device includes a pair of electrodes; and an organic light-emitting element, disposed between the electrodes, wherein the organic light-emitting element includes the aforementioned organic metal compound.
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): In particular, one of the following two conditions (1) and (2) is met:(1) R1 is deuterium or C1-6 deuterated alkyl group, when R3 and R4 are independently hydrogen, halogen, C1-6 alkyl group, C1-6 fluoroalkyl or C3-12 heteroaryl group; and(2) R1 is hydrogen, deuterium, C1-6 alkyl group, C1-6 deuterated alkyl group, C3-12 heteroaryl group, or C6-12 aryl group, when at least one of R3 and R4 is C6-12 aryl group or C6-12 fluoroaryl group.
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:
Organometallic compounds and organic electroluminescence devices employing the same are provided. The organometallic compound has a chemical structure represented below: In Formula (I), one of R1 and R2 is trimethylsilyl (TMS) and the other is hydrogen, at least one of R3 and R4 is fluorine or C1-6 alkyl, or one of R3 and R4 is fluorine and the other is C1-6 alkyl, n is 2 or 3, and m is 0 or 1, wherein n+m=3.
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:
Organometallic compounds and organic electroluminescence devices employing the same are provided. The organometallic compound has a chemical structure as represented by wherein R1, R2 are hydrogen, phenyl, biphenyl, diisopropyl amino, or derivatives thereof. The organic electroluminescence device includes a pair of electrodes and an electroluminescent element disposed between the pair of electrodes, wherein the electroluminescent element includes the organometallic compound.
Abstract:
A light color conversion layer structure includes a pixel separation layer over a substrate. The pixel separation layer includes several separating components. The receiving region over the substrate is defined by adjacent separating components. The light color conversion layer structure also includes a first isolation layer continuously formed over the substrate and on the sidewalls of the separating components surrounding the receiving region. The first isolation layer continuously covers the top surface of the substrate and the sidewalls of the separating components adjacent to the receiving region. The light color conversion layer structure also includes a light color conversion unit within the receiving region and on the first isolation layer. The light color conversion layer structure further includes a second isolation layer on the first isolation layer and the light color conversion unit. The second isolation layer covers the first isolation layer and the light color conversion unit.