Polyvinyl thioether ester as well as preparation method and application thereof

A technology of polyvinyl sulfide ester and polyvinyl sulfide, applied in the field of polyvinyl sulfide ester and its preparation, can solve problems such as limiting the application range of luminescent materials, achieve wide substrate applicability, eliminate influence, The effect of good functional group compatibility

Active Publication Date: 2019-11-22
SUZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The quenching effect caused by this concentration or aggregation limits the application range of this type of luminescent material

Method used

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  • Polyvinyl thioether ester as well as preparation method and application thereof
  • Polyvinyl thioether ester as well as preparation method and application thereof
  • Polyvinyl thioether ester as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051]

[0052] Synthesis of the first monomer dibasic butynolate monomer: add 2.3 g (10 mmol) bisphenol A, 6.2 g (30 mmol) N,N-dicyclohexylcarbonyl in a 250 mL two-necked flask Amine (DCC), 0.5 g (4 mmol) 4-dimethylaminopyridine (DMAP), 0.8 g (4 mmol) p-toluenesulfonic acid hydrate, vacuum three times with nitrogen, add 80 mL of dry dichloromethane and stir to dissolve , to get the reaction system. Then, at 0°C, 2.0 g (25 mmol) butynoic acid was dissolved in 20 mL of dry dichloromethane, and dropped into the above reaction system through a constant pressure dropping funnel, stirred overnight, filtered, and dichloromethane Washing with methane, spinning the filtrate to get the crude product, which was separated and purified by column chromatography, and dried in vacuum to constant weight to obtain 2.6 g of white solid (72% yield), which is the first monomer dibasic butynoic acid phenol ester monomer. 1 H NMR (400 MHz, CDCl 3 ) δ7.24 (t, J = 9.6 Hz, 4H), 7.04 (t, J = 11.3...

Embodiment 2

[0057] The dibasic butynolate monomer and the dibasic thiophenol monomer are the same as in Example 1. Add 36.0 mg (0.1 mmol) of the first monomer and 25.0 mg (0.1 mmol) of the second monomer into a 10 mL polymerization tube, vacuumize the system and fill it with nitrogen, repeat three times, then add 2 mL of dry DMF, and wait for a single After the body was completely dissolved, it was reacted at 60 °C for 24 hours. After cooling to room temperature, dilute with 5 mL of chloroform, and drop the solution into 250 mL of vigorously stirred n-hexane through a dropper plugged with cotton, let it stand, filter, and dry to constant weight to obtain a polymer, the product The rate is 82%. GPC results show: M w = 13800, PDI = 2.2. The polymer also has good solubility and thermal stability, and the 5% thermal weight loss temperature is 298 ℃.

Embodiment 3

[0059] The dibasic butynolate monomer and the dibasic thiophenol monomer are the same as in Example 1. Add 36.0 mg (0.1 mmol) of the first monomer and 25.0 mg (0.1 mmol) of the second monomer into a 10 mL polymerization tube, vacuumize the system and fill it with nitrogen, repeat three times, then add 1 mL of dry DMF, and wait for a single After the body was completely dissolved, react at 60 °C for 24 hours. After cooling to room temperature, dilute with 5 mL of chloroform, and drop the solution into 250 mL of vigorously stirred n-hexane through a dropper plugged with cotton, let it stand, filter, and dry to constant weight to obtain a polymer, the product The rate is 77%. GPC results show: M w = 18600, PDI = 2.3. The polymer also has good solubility and thermal stability.

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Abstract

The invention discloses polyvinyl thioether ester as well as a preparation method and application thereof. The polyvinyl thioether ester is obtained through solution polymerization reaction by takinga binary acetylene acid ester internal alkyne monomer and a binary sulfydryl monomer as raw materials. The reaction raw materials are easy to obtain, no by-product is generated in the polymerization reaction process, and the atom economy is met; the polymerization reaction has wide substrate applicability and good functional group compatibility, and various functional groups can be conveniently introduced; no catalyst is used in the polymerization reaction, so that the influence of catalyst residues on photoelectric and biological properties of the polymer material can be eliminated. The polyvinyl thioether ester prepared by the invention has good processability, high thermal stability and aggregation-induced emission performance, and has application value in the aspects of optical plastics, biomedical materials, fluorescence sensing and the like.

Description

technical field [0001] The invention belongs to the fields of polymer chemistry and material science, and in particular relates to a polyvinyl sulfide ester and a preparation method and application thereof. Background technique [0002] The preparation of polymers with new structures based on new polymerization reactions has important research significance and application value. Among them, the polymerization of alkyne monomers to construct functional polymers has become a research hotspot in recent years. The reaction of alkynes with thiols was reported as early as the early 19th century, but did not attract much attention at the time. In 2009, Bowman and others in the United States used ultraviolet light to trigger the reaction of terminal alkyne and sulfhydryl group, that is, one alkyne group added two mercapto groups, and prepared a cross-linked polysulfide; in 2010, the Tang research group of Hong Kong University of Science and Technology used organic Base-catalyzed p...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08G75/045G01N21/64
CPCC08G75/045G01N21/64G01N2021/6417C08G75/0204C08G75/0227C08G75/024C08L81/02
Inventor 李红坤杜军李永舫
Owner SUZHOU UNIV
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