Unlock instant, AI-driven research and patent intelligence for your innovation.
A chiral blue material 3d indium-potassium heterometallic organic framework and its template synthesis method and application
What is Al technical title?
Al technical title is built by PatSnap Al team. It summarizes the technical point description of the patent document.
A technology of blue-light materials and organic frameworks, applied in 3/13 group organic compounds without C-metal bonds, luminescent materials, organic chemistry, etc., can solve the problems of high synthesis cost and low product yield, and achieve low synthesis cost , The preparation method is simple, and the effect of improving the luminescence life
Inactive Publication Date: 2016-09-14
HARBIN INST OF TECH
View PDF2 Cites 0 Cited by
Summary
Abstract
Description
Claims
Application Information
AI Technical Summary
This helps you quickly interpret patents by identifying the three key elements:
Problems solved by technology
Method used
Benefits of technology
Problems solved by technology
[0003] The present invention aims to solve the technical problems that the existing blue fluorescent organic light-emitting materials are difficult to synthesize high-dimensional novel structures, the synthesis cost is high, and the product yield is low, and a chiral blue light material 3D indium-potassium heterometal Organic frameworks and their template synthesis methods and applications
Method used
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more
Image
Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
Click on the blue label to locate the original text in one second.
Reading with bidirectional positioning of images and text.
Smart Image
Examples
Experimental program
Comparison scheme
Effect test
specific Embodiment approach 1
[0026] Embodiment 1: A chiral blue light material 3D indium-potassium heterometallic organic framework described in this embodiment, the molecular formula of a chiral blue light material 3D indium-potassium heterometallic organic framework is [InK 2 C 20 h 14 Cl 3 N 2 o 5 ] n , n is a positive integer, containing a metal indium ion, two potassium ions, two 3-quinoline carboxylic acid ligands, three chloride ions, and a coordinated water molecule in the basic structural unit; metal indium ions and two The oxygen atom of the 3-quinolinecarboxylic acid ligand coordinates with three chloride ions to form a bond, showing a seven-coordination slightly distorted pentagonal bipyramidal configuration; metal potassium ions and the oxygen atoms of the four 3-quinolinecarboxylic acid ligands Atom and nitrogen atom, two chloride ions and a water molecule coordinate to form a bond, forming a seven-coordinated single-cap octahedral configuration; adjacent indium ions and potassium ions ...
specific Embodiment approach 2
[0034] Specific embodiment two: a template synthesis method of a chiral blue light material 3D indium-potassium heterometallic organic framework is carried out according to the following steps:
[0035] Put achiral 2,3-quinoline dicarboxylic acid, potassium hydroxide and indium chloride in distilled water, stir at room temperature until evenly mixed to obtain a mixed solution, and then place the mixed solution in a liner of polytetrafluoroethylene In a stainless steel reaction kettle, react at a temperature of 100°C to 130°C for 4 days to 6 days, and then cool down to room temperature to obtain a colorless and transparent octahedral crystal, which is the chiral blue light material 3D indium-potassium iso metal organic frameworks;
[0036] The molar ratio of the described achiral 2,3-quinoline dicarboxylic acid to potassium hydroxide is 1:(0.2~2); the described achiral 2,3-quinoline dicarboxylic acid and indium chloride The molar ratio of the achiral 2,3-quinoline dicarboxylic...
specific Embodiment approach 3
[0037] Embodiment 3: The difference between this embodiment and Embodiment 2 is that the molar ratio of the achiral 2,3-quinoline dicarboxylic acid to potassium hydroxide is 1:0.5. Others are the same as in the second embodiment.
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More
PUM
Login to View More
Abstract
The invention discloses a chiral blue-light emitting material 3D (three-dimensional) indium-potassium dissimilar-metal organic framework and a template synthetic method and application thereof. The invention relates to a 3D indium-potassium dissimilar-metal organic framework and a template synthetic method and application thereof. The chiral blue-light emitting material 3D indium-potassium dissimilar-metal organic framework and the template synthetic method and the application thereof aim at solving the technical problems that a high-dimension novel structure is quite difficultly synthesized by using an existing blue-fluorescence organic light-emitting material, the synthetic cost is high, and the productivity of products is low. The molecular formula of the chiral blue-light emitting material 3D indium-potassium dissimilar-metal organic framework is [InK2C20H14Cl3N2O5]n. The template synthetic method comprises the following steps of putting achiral 2, 3-quinoline dioctyl phthalate, potassium hydroxide and indium chloride into distilled water, agitating an obtained mixture at a room temperature until the obtained mixture is mixed uniformly, and then putting mixed liquor into a stainless steel reaction kettle of which the liner is made of polytetrafluoroethylene, carrying out reaction at a certain temperature, and finally cooling to the room temperature. The application is that the chiral blue-light emitting material 3D indium-potassium dissimilar-metal organic framework is used as a metal organic blue light-emitting material.
Description
technical field [0001] The invention relates to a 3D indium-potassium heterometallic organic framework and a template synthesis method and application thereof. Background technique [0002] Chiral solid materials have attracted more and more attention because of their great potential applications in enantioselective separation, heterogeneous asymmetric synthesis, nonlinear optics and magnetism. In recent years, relatively mature metal-organic framework materials or coordination polymers containing inorganic and organic units have shown their potential in the preparation of chiral materials. The usual way to prepare chiral compounds is to use a chiral molecule as a basic linking unit or as an auxiliary ligand, which is the most effective way to synthesize chiral compounds. However, the synthesis of chiral compounds from achiral precursors has been highly favored due to the limitation of chiral sources and the cost of chiral ligands. On the other hand, since 8-hydroxyquinoli...
Claims
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More
Application Information
Patent Timeline
Application Date:The date an application was filed.
Publication Date:The date a patent or application was officially published.
First Publication Date:The earliest publication date of a patent with the same application number.
Issue Date:Publication date of the patent grant document.
PCT Entry Date:The Entry date of PCT National Phase.
Estimated Expiry Date:The statutory expiry date of a patent right according to the Patent Law, and it is the longest term of protection that the patent right can achieve without the termination of the patent right due to other reasons(Term extension factor has been taken into account ).
Invalid Date:Actual expiry date is based on effective date or publication date of legal transaction data of invalid patent.
Login to View More 
Login to View More