Application of trans-cucurbiturils iQ[7] and preparation method

A seven-member melon ring and recognition method technology, applied in the field of supramolecular chemistry, can solve the problems of low yield, low yield, difficult separation and purification, etc., and achieve the effect of wide application prospects
CN106932425AActive Publication Date: 2017-07-07GUIZHOU UNIV
7 Cites 2 Cited by

Patent Information

Authority / Receiving Office
CN · China
Current Assignee / Owner
GUIZHOU UNIV
Publication Date
2017-07-07

Smart Images

  • Figure 1
    Figure 1
  • Figure 2
    Figure 2
  • Figure 3
    Figure 3
Patent Text Reader

Abstract

The invention discloses application of trans-cucurbiturils iQ[7] and a preparation method. The trans-cucurbiturils iQ[7] can be used for recognizing lysine, arginine or histidine. The trans-cucurbiturils iQ[7] can effectively recognize lysine, arginine and histidine of 10 amino acids essential for human bodies, has great significances in revealing biological phenomena and process, and has wide application prospects.
Need to check novelty before this filing date? Find Prior Art

Description

technical field

[0001] The invention relates to the field of supramolecular chemistry, in particular to the application and preparation method of a trans seven-membered melon ring iQ[7]. Background technique

[0002] As a class of macrocyclic compounds, cucurbit rings are macrocyclic cage compounds that are bridged by glycoside urea units through methylene groups. Its structure is characterized by a cavity with two ends open. The two ports have the same size and the diameter of the port is smaller than that of the cavity. lumen diameter. The two ports of the melon ring are respectively distributed with carbonyl oxygen atoms with the same number of structural units, forming a cationic bonding site, so it can interact with hydrophilic substances, metal ions, etc.; and its cavity is hydrophobic, not only It can include organic molecules, small inorganic molecules and inorganic anions. Compared with macrocyclic molecules such as crown ethers, cyclodextrins, and calixarenes, th...

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