Unlock instant, AI-driven research and patent intelligence for your innovation.
Tripodia pseudorotaxane supramolecular gel based on trimesoyl chloride and preparation and application of metal gel
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 trimesoyl chloride and supramolecular gel, which is applied in gel preparation, analytical materials, colloid chemistry, etc., and can solve the problems of complicated operation, expensive equipment, and unsuitable
Inactive Publication Date: 2019-03-29
NORTHWEST NORMAL UNIVERSITY
View PDF3 Cites 11 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
However, these methods are more complicated to operate, and the equipment is expensive, so it is not suitable to be put into practical application in large quantities.
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
Embodiment 1、 3
[0052] Embodiment 1, the synthesis of tripod pseudorotaxane supramolecular organogel TP-Q
[0053] (1) Synthesis of pillar[5]arene TP: see T. Ogoshi, S. Kanai, S. Fujinami, T.Yamagishi and Y. Nakamoto, J. Am. Chem. Soc., 2008, 130, 5022 for details;
[0054] (2) Synthesis of 4-aminopyridine-functionalized trimesoyl chloride gelling factor Q: see X.Z. Luo, X. J. Jia, J. H. Deng, J. L. Zhong, H. J. Liu, K. J. Wang, and D. C.Zhong, J. Am. Chem. Soc., 2013, 135, 11684-11687;
[0055] (3) Synthesis of tripod pseudorotaxane supramolecular organogel (TP-Q): Weigh 4-aminopyridine-functionalized trimesoyl chloride gel factor Q (4.1mg, 0.0093mmol) and put it on the column[5] Aromatic TP (20.2 mg, 0.027 mmol), added to 0.5 mL DMSO-HO 2 O (0.3 mL DMSO, 0.2 mL H 2 O), fully dissolved under heating to obtain a transparent solution; cooled to room temperature, the transparent solution formed a stable supramolecular organogel TP-Q.
Embodiment 2
[0056] Embodiment 2, TP-Q fluorescent recognition Fe 3+
[0057] Take 13 small amounts (about 0.02g) of organogel TP-Q on a white drip plate, and add 20 μL of different cations (C=0.1moL / L, Mg 2+ , Ca 2+ , Cr 3+ , Fe 3+ ,Co 2+ , Ni 2+ , Cu 2+ , Zn 2+ , Ag + , Cd 2+ , Hg 2+ , Pb 2+ ) in aqueous solution. Observe the fluorescence color change under the ultraviolet light. If the fluorescence color of organogel TP-Q changes from blue-white to black, it means that Fe is added. 3+ Solution, if the fluorescent color of TP-Q does not change, it means that the aqueous solution of other cations is added.
Embodiment 3
[0058] Embodiment 3, supramolecular metal gel TP-Q+Fe 3+ preparation of
[0059] Weigh column [5] arene TP (20.2 mg, 0.027 mmol), 4-aminopyridine functionalized trimesoyl chloride gelling factor Q (4.1 mg, 0.0093 mmol) and ferricperchlorate hexahydrate (4.6 mg, 0.010 mmol), added together to 0.5mL DMSO-H 2 O (0.3 mL DMSO, 0.2 mL H 2 O), heated to dissolve it, and cooled to room temperature to form a supramolecular organogel based on tripod quasirotaxane (TP-Q+Fe 3+ ).
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 tripodia pseudorotaxane supramolecular organic gel based on trimesoyl chloride. According to the tripodia pseudorotaxane supramolecular gel based on the trimesoyl chloride, thepillar[5]arene and 4-aminopyridine functionalized trimesoyl chloride is fully dissolved into DMSO-H2O under the heating condition so as to obtain a transparent solution; cooling is carried out to reach room temperature so as to form the stable supramolecular organic gel TP-Q with blue and white aggregation-state fluorescence; a series of cationic solutions are added into the TP-Q, and fluorescencequenching can be realized only by adding Fe3+>, so that the TP-Q can specifically and selectively recognize the Fe3+>; and the tripodia pseudorotaxane supramolecular organic gel and ferricperchlorate hexahydrate are heated and dissolved in the DMSO-H2O, then cooling is carried out so as to obtain metal organic gel, when a series of anions are added into the metal gel separately, the fluorescence of the metal gel can be opened only by adding F<->, the fluorescence is changed into blue and white from black, and therefore high-sensitivity detection of the F<-> is realized.
Description
technical field [0001] The invention relates to a tripod quasirotaxane supramolecular gel based on trimesoyl chloride and the selective fluorescence recognition of the supramolecular organogel. 3+ application in; the present invention also relates to a metal organic gel based on the tripod quasirotaxane supramolecular gel and the metal gel in the selective fluorescence recognition F - The application of the invention belongs to the technical field of supramolecular organogel and the technical field of ion detection. Background technique [0002] Supramolecular organogels are low-molecular-weight organic compounds (gelling factors) that undergo multiple hydrogen bonds, van der Waals forces, π-π Supramolecular (soft) materials formed by self-assembly of weak interactions between molecules such as stacking and hydrophilic-hydrophobic interactions. This kind of material has the unique advantages of both solid materials and liquid materials: supramolecular organogel molecules m...
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.