SYNTHESIS AND POLYMERIZATION OF 2-OXO-3-METHYLENE-5, 6-DIPHENYL-1,4-DIOXAN*

FENG Pinzhen; LU Jiantao

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SYNTHESIS AND POLYMERIZATION OF 2-OXO-3-METHYLENE-5, 6-DIPHENYL-1,4-DIOXAN*

Papers | Updated：2021-06-21

- SYNTHESIS AND POLYMERIZATION OF 2-OXO-3-METHYLENE-5, 6-DIPHENYL-1,4-DIOXAN*
- SYNTHESIS AND POLYMERIZATION OF 2-OXO-3-METHYLENE-5, 6-DIPHENYL-1,4-DIOXAN*
- 高分子科学（英文版） 1994年12卷第3期页码：284-288
- Affiliations：
  
  1.   Chemistry Departmemt
  2.   Graduate School
  3.   Academia Sinica
  4.   Beijing
  5.   100039
- Author bio：
- Funds：
- DOI：
  中图分类号： TQ317
- 纸质出版：1994-09-20
- Accepted：
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[1]冯品珍,鲁剑涛.SYNTHESIS AND POLYMERIZATION OF 2-OXO-3-METHYLENE-5, 6-DIPHENYL-1,4-DIOXAN[J].Chinese Journal of Polymer Science,1994,{4}(03):284-289.

FENG Pinzhen, LU Jiantao. SYNTHESIS AND POLYMERIZATION OF 2-OXO-3-METHYLENE-5, 6-DIPHENYL-1,4-DIOXAN*[J]. 1994, 12(3): 284-288.
[1]冯品珍,鲁剑涛.SYNTHESIS AND POLYMERIZATION OF 2-OXO-3-METHYLENE-5, 6-DIPHENYL-1,4-DIOXAN[J].Chinese Journal of Polymer Science,1994,{4}(03):284-289. DOI：

FENG Pinzhen, LU Jiantao. SYNTHESIS AND POLYMERIZATION OF 2-OXO-3-METHYLENE-5, 6-DIPHENYL-1,4-DIOXAN*[J]. 1994, 12(3): 284-288. DOI：

摘要

正

A new cyclic monomer

2-oxo-3-methylene-5

6-diphenyl-1

4-dioxan

was synthesized. Thestructure of the intermediates and the monomer were determined by IR

H NMR

C NMR andelemental analysis. This new monomer is different from other cyclic monomers in this series

it isa solid （mp 108--109℃）and not very reactive

but still can undergo free radical ring-openingpolymerization. The free radical polymerization was carried out at 130℃. The structure of theresulting polymer was discussed and charaterized by IR

H NMR

C NMR and elementalanalysis. The molecular weight of the polymer was estimated by viscosity determination.

Abstract

A new cyclic monomer

2-oxo-3-methylene-5

6-diphenyl-1

4-dioxan

was synthesized. Thestructure of the intermediates and the monomer were determined by IR

H NMR

C NMR andelemental analysis. This new monomer is different from other cyclic monomers in this series

it isa solid （mp 108--109℃）and not very reactive

but still can undergo free radical ring-openingpolymerization. The free radical polymerization was carried out at 130℃. The structure of theresulting polymer was discussed and charaterized by IR

H NMR

C NMR and elementalanalysis. The molecular weight of the polymer was estimated by viscosity determination.

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