Amphiphilic macrocyclic polymer and preparation method

An amphiphilic and polymer technology, which is applied in the field of amphiphilic macrocyclic polymers and their preparation, can solve the problems of single chemical structure of side chains, limited number of side chains, no polymers found, etc., and achieve clear synthesis routes, The method is simple and the effect of high yield

Inactive Publication Date: 2009-06-24
FUDAN UNIV
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  • Abstract
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  • Application Information

AI Technical Summary

Problems solved by technology

A large number of cyclic complexes with various structures have been synthesized successively: 1) At present, the ring size of these crown ethers with lipophilic side chains is limited to 20 to 30 atoms, and most of the lipophilic chains were obtained later by chemical The reaction is connected to the nitrogen atom of the ring or the benzene ring, the number of side chains is limited, and the chemical structure of the side chains is relatively simple, and the chain length is generally within 20 atoms
2) The use of linear polyethylene glycol (PEG) for cyclization to obtain macrocyclic crown ethers has also become a research hotspot, but the ion complexation behavior of macrocyclic crown ethers with more than 50 atoms on the ring has been less studied. and no sidechains
However, this type of polymer has not been found so far, and there is no clear and easily feasible method for preparing this polymer

Method used

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  • Amphiphilic macrocyclic polymer and preparation method
  • Amphiphilic macrocyclic polymer and preparation method
  • Amphiphilic macrocyclic polymer and preparation method

Examples

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Embodiment 1

[0041] c-PEO-g-PS

[0042] 1. Preparation of 4-glycidyl-2,2,6,6-tetramethylpiperidine nitroxide radical (GTEMPO)

[0043] Add 340mL 50% (v / v) sodium hydroxide solution to a 1000mL three-necked flask, add 7g tetra-n-butylammonium hydrogensulfate (TBAHS) into the flask, keep an ice-water bath, so that the reaction temperature does not exceed 25°C. While stirring mechanically, 210mL of epichlorohydrin was added through the dropping funnel within 30min. After keeping the reaction in the ice-water bath for 2 hours, 86 g of 4-hydroxy-2,2,6,6-tetramethylpiperidine nitroxide was added in batches within 1 hour. After the reaction was carried out for 24 hours, the reaction mixture was poured into an ice-water mixture (1.5 L), and the aqueous phase was repeatedly extracted with ether until the aqueous layer turned pale yellow. The ether solutions extracted several times were combined and washed with anhydrous MgSO 4 After drying for 3 h, CaH 2 Let dry overnight. After diethyl ether ...

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Abstract

The present invention provides a polymer with new structure, its molecular structure and synthesis method have unique features. Said polymer is an amphiphilic macrocyclic polymer containing hydrophilic ring chain and oleophilic side chain. It is characterized by that said invention utilies the synthesis of a new type monomer GTEMPO containing epoxy unit to make anionic polymerization, and can introduce the functional group for regulating and controlling free radical polymerization onto cyclopolyether polymer chain to obtain cyclopolyether whose chain side has TEMOP, then utilizes active free radical polymerization to introduce the oleophilic side chain onto polyether ring, so that it can utilize ring side TEMPO to initiate styrene monomer to make controllable free radical polymerization. Said method can obtain new polymer with special structure.

Description

technical field [0001] The invention relates to an amphiphilic macrocyclic polymer containing a hydrophilic ring chain and an lipophilic side chain and a preparation method thereof. Background technique [0002] Since Pedersen et al. won the Nobel Prize in Chemistry in 1987 for their discovery of the cyclic ligand compound crown ether, the synthesis and application of macrocyclic ligand compounds have developed rapidly. A large number of cyclic complexes with various structures have been synthesized successively: 1) At present, the ring size of these crown ethers with lipophilic side chains is limited to 20 to 30 atoms, and most of the lipophilic chains were obtained later by chemical The reaction is connected to the nitrogen atom of the ring or the benzene ring, the number of side chains is limited, and the chemical structure of the side chains is relatively simple, and the chain length is generally within 20 atoms. 2) The use of linear polyethylene glycol (PEG) for cycliz...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08G65/00C08F2/38C08F290/14
Inventor 黄骏廉贾中凡
Owner FUDAN UNIV
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