Novel macrocyclic precursors of poly{aryl ether ketone (sulfone)} containing hexafluoroisopropylidene units: Synthesis, characterization, and polymerization


Autoria(s): Qi YH; Song NH; Chen TL; Bo SQ; Xu JP
Data(s)

2000

Resumo

Cyclic oligomers containing hexafluoroiso-propylidene(HFIP) units were prepared in excellent yields by a nucleophilic aromatic substitution reaction of 4,4(7)- (hexafluoroisopropylidene) diphenol with difluoro-monomers in the presence of anhydrous potassium carbonate under pseudo high dilution conditions. A combination of GPC, MALDI-TOF MS and NMR analysis confirmed the structure of the cyclic oligomers. All macrocyclic oligomers are crystalline and undergo facile melt polymerization to give high molecular weight fluorinated polyethers.

Identificador

http://202.98.16.49/handle/322003/19703

http://www.irgrid.ac.cn/handle/1471x/154586

Idioma(s)

英语

Fonte

Qi YH;Song NH;Chen TL;Bo SQ;Xu JP.Novel macrocyclic precursors of poly{aryl ether ketone (sulfone)} containing hexafluoroisopropylidene units: Synthesis, characterization, and polymerization,MACROMOLECULAR CHEMISTRY AND PHYSICS,2000,201(8):840-845

Palavras-Chave #RING-OPENING POLYMERIZATION #OLIGOMERS #MOIETY #COPOLYMERS #ROUTE
Tipo

期刊论文