US2020140467A1PendingUtilityA1
Phosphine precursor for preparing quantum dot and quantum dot prepared therefrom
Est. expiryMay 18, 2037(~10.8 yrs left)· nominal 20-yr term from priority
Inventors:Jeong-Ho ParkHee-Il ChaeKyung Sil YoonJu-Sik KangYu-Mi ChangNam-Choul YangJae-Kyun ParkSong Lee
C09K 11/70C07F 19/00C07F 9/06Y02E60/10C09K 11/02Y02E10/549C09K 11/565
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Claims
Abstract
The present invention relates to a phosphine precursor for the preparation of a quantum dot, and a quantum dot prepared therefrom. Using the phosphine precursor for the preparation of a quantum dot of the present invention, a quantum dot with improved luminous efficiency and higher luminous color purity can be provided.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A phospine precursor for the preparation of a quantum dot, represented by the following Chemical Formula 1:
in the Chemical Formula 1,
Q 1 is
Q 2 is
Q 3 is
wherein R1 to R9 are identical to or different from each other, and each independently, C1-20 linear or branched alkyl, C6-30 aryl, C7-30 alkylaryl, or C7-30 arylalkyl,
provided that all Q 1 to Q 3 are not the same structure.
2 . The phospine precursor according to claim 1 , wherein R 1 to R 9 are each independently, C1-6 linear alkyl, C3-6 branched alkyl, or C6-12 aryl.
3 . The phospine precursor according to claim 1 , wherein R1 to R9 are each independently, methyl, ethyl, n-propyl, iso-propyl, n-butyl, tert-butyl, iso-butyl, or phenyl.
4 . The phospine precursor according to claim 1 , wherein the compound of the Chemical Formula 1 is selected form the group consisting of the following Structural Formulas:
5 . The phospine precursor according to claim 1 , wherein the compound of the Chemical Formula 1 is represented by the following Chemical Formula 1-1:
in the Chemical Formula 1-1,
R 1 ′ to R 6 ′ are identical to or different from each other, and each independently, C1-20 linear or branched alkyl, C6-30 aryl, C7-30 alkylaryl, or C7-30 arylalkyl, provided that all R 1 ′ to R 6 ′ are not methyl.
6 . The phospine precursor according to claim 1 , wherein the compound of the Chemical Formula 1 is represented by the following Chemical Formula 1-2:
in the Chemical Formula 1-2,
R 1 ″ to R 3 ″ are identical to or different from each other, and each independently, C1-20 linear or branched alkyl, C6-30 aryl, C7-30 alkylaryl, or C7-30 arylalkyl, provided that all R 1 ″ to R 3 ″ are not methyl.
7 . A method for preparing the phosphine precursor of claim 1 , comprising the steps of:
preparing a mixture of a primary or secondary phosphine compound, halogenated hydrocarbon, and tertiary amine; and adding a silyl triflate compound to the mixture.
8 . The method for preparing the phosphine precursor according to claim 7 , wherein the halogenated hydrocarbon is dichloromethane, and the tertiary amine is trimethylamine.
9 . A method for preparing the phosphine precursor of claim 1 , comprising the steps of:
preparing a mixture of a primary or secondary phosphine compound, an ether solvent, and alkyl lithium; and adding a silyl halide compound to the mixture.
10 . The method for preparing a phosphine precursor according to claim 9 , wherein the ether solvent is tetrahydrofuran, and the alkyl lithium is butyl lithium.
11 . A precursor composition for the preparation of a quantum dot, comprising the phosphine precursor of claim 1 .
12 . The precursor composition for the preparation of a quantum dot according to claim 11 , further comprising tris(trimethylsilyl)phosphine.
13 . A quantum dot prepared from the phosphine precursor of claim 1 .
14 . The quantum dot according to claim 13 , wherein the quantum dot comprises InP as a core.
15 . A method for preparing a quantum dot using one or more phosphine precursors of claim 1 .
16 . The method for preparing a quantum dot according to claim 15 , wherein the method comprises the steps of:
heating a mixture of an indium precursor, a zinc precursor, myristic acid and 1-octadecene; cooling the mixture to room temperature; introducing one or more of the phosphine precursors, a gallium precursor, and 1-octadecene into the cooled mixture, and heating and reacting; and introducing dodecanethiol into the reactant, and cooling.
17 . The method for preparing a quantum dot according to claim 16 , wherein the one or more of the phosphine precursors are additionally mixed with tris(trimethylsilyl)phosphine.Join the waitlist — get patent alerts
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