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Controllable synthesis method for stereotactic polymethylmethacrylate

A technology of polymethyl methacrylate and methyl methacrylate, which is applied in the field of polymer science, can solve the problems of uncontrollable chain transfer and side reactions, high reactivity and low stability of the growth group, and achieve a synthetic route Clear and actionable, simple to operate, and easy-to-control effects

Active Publication Date: 2019-08-23
HARBIN ENG UNIV
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

At present, there are many reports on the use of ionic polymerization or coordination polymerization to realize the stereo control of polymers, but there are few related studies on the behavior of free radical polymerization and its stereo control of polymers.
Furthermore, in the radical polymerization of methyl methacrylate, due to the lack of conjugated substituents in vinyl esters, its propagating group has high reactivity and low stability, leading to uncontrollable chain transfer and side reactions, regulating The stereochemical configuration of polymers is a huge challenge in synthetic polymer chemistry, and most of the current research is about free radical polymerization reaction systems that improve the syndiotacticity of polymers. There are relatively few reports on how to improve the isotacticity of polymers. few

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  • Controllable synthesis method for stereotactic polymethylmethacrylate
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Embodiment Construction

[0027] The present invention will be further described in detail below in conjunction with the accompanying drawings and specific embodiments.

[0028] The controllable synthesis method of a kind of stereoregular polymethyl methacrylate of the present invention, concrete steps are as follows:

[0029] 1) Take microcrystalline cellulose and vacuum-dry it at high temperature for 4 hours, then stir and reflux in anhydrous N,N-dimethylacetamide for 12 hours; add an appropriate amount of lithium chloride after cooling to room temperature; continue to stir for 2 hours, then heat up again , add anhydrous pyridine, reflux for 6 hours, add excess 3,5-dimethylphenylisocyanate, react for 13 hours, stop the reaction; cool to room temperature, add methanol to settle, filter and wash, vacuum dry at 60°C to constant weight, and produce The rate is 95%.

[0030] 2), weigh the corresponding mass of the product obtained in 1) according to the 17 groups of different ratios set with the methyl m...

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Abstract

The invention provides a controllable synthesis method for stereotactic polymethylmethacrylate. The controllable synthesis method comprises the following steps: step 1: taking microcrystalline cellulose as a matrix raw material and 3,5-dimethylphenylisocyanate as a derivatization reagent and synthesizing a helical polymer cellulose-tri(3,5-dimethylphenylcarbamate) through a traditional esterification method; and step 2: taking the cellulose-tri(3,5-dimethylphenylcarbamate) synthesized in step 1 as a chiral inducing agent and adding into methyl methacrylate free radical polymerization reactionto finally prepare the stereotactic polymethylmethacrylate. The controllable synthesis method provided by the invention has a clear and feasible synthesis route and a mature technology, is simple to operate, has a few conditions needing to be controlled and is easy to realize, so that the controllable synthesis method can be used for large-scale batch production; the cellulose, methyl methacrylateand azobisisobutyronitrile, which are used in the controllable synthesis method, have a wide source and are cheap and easy to obtain; and a whole controllable process is simple, mature and easy to control.

Description

technical field [0001] The invention relates to a controllable synthesis method of polymethyl methacrylate, in particular to a controllable synthesis method of stereoregular polymethyl methacrylate, which belongs to the field of polymer science. Background technique [0002] Cellulose is a natural high molecular polymer with a regular helical structure. After proper derivatization, cellulose derivatives with regular three-dimensional structure and excellent chiral recognition performance can be obtained. Among them, cellulose phenyl carbamate derivatives are currently the most widely used chiral stationary phase materials with the highest recognition performance. Its efficient chiral recognition performance comes from its unique main chain regular helical structure. In addition, the main chain of microcrystalline cellulose has strong rigidity, which makes this type of polymer have better stability and rigid helical structure, and can ensure the stability of its regular heli...

Claims

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Application Information

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IPC IPC(8): C08F120/14C08F2/38C08B15/06
CPCC08B15/06C08F2/38C08F120/14
Inventor 沈军孙梦尘毕婉莹孙悦
Owner HARBIN ENG UNIV
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