Synthesis and free-radical ring opening polymerization of macrocyclic aryl thioether ether ketone (sulfone) oligomers


Autoria(s): Qi YH; Chen TL; Liu SZ; Xu JP
Data(s)

2000

Resumo

Two kinds of novel macrocyclic aryl thioether ether oligomers were synthesized by nucleophilic condensation reaction in high yields under pseudo-high-dilution condition. A combination of H-1 NMR, GPC and MALDI-TOF MS analyses unambiguously confirmed the cyclic nature and their distributions, Macrocyclic thioether ether ketone oligomers can undergo facile melt ring opening polymerization(ROP) initiated by thiyl radical to give a high molecular weight polymer.

Identificador

http://202.98.16.49/handle/322003/19843

http://www.irgrid.ac.cn/handle/1471x/154656

Idioma(s)

中文

Fonte

Qi YH;Chen TL;Liu SZ;Xu JP.Synthesis and free-radical ring opening polymerization of macrocyclic aryl thioether ether ketone (sulfone) oligomers,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,2000,21(3):480-483

Palavras-Chave #DISULFIDE OLIGOMERS
Tipo

期刊论文