中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis of macrocyclic arylene ketone oligomers containing the phthaloyl moiety by Friedel-crafts acylation reaction

文献类型:期刊论文

作者Guo QZ ; Bo SQ ; Chen TL
刊名chemistry letters
出版日期2004
卷号33期号:4页码:414-415
关键词RING-OPENING POLYMERIZATION 1 ETHER KETONE) 2-DIBENZOYLBENZENE MOIETY
ISSN号0366-7022
通讯作者chen tl
中文摘要two kinds of macrocyclic arylene ketone oligomers have been synthesized in high yield from phthaloyl dichloride and various bridge-linking electron-rich aromatic hydrocarbons via the modified friedel-crafts acylation reaction. the presence of a lewis base in this reaction is demonstrated to be advantageous for forming macrocycle oligomers. these resultant oligomers can undergo melt ring-opening polymerization to give polymers with high t. and excellent thermal stability.
收录类别SCI
语种英语
WOS记录号WOS:000220913500025
公开日期2010-08-17
源URL[http://202.98.16.49/handle/322003/15419]  
专题长春应用化学研究所_长春应用化学研究所知识产出_期刊论文
推荐引用方式
GB/T 7714
Guo QZ,Bo SQ,Chen TL. Synthesis of macrocyclic arylene ketone oligomers containing the phthaloyl moiety by Friedel-crafts acylation reaction[J]. chemistry letters,2004,33(4):414-415.
APA Guo QZ,Bo SQ,&Chen TL.(2004).Synthesis of macrocyclic arylene ketone oligomers containing the phthaloyl moiety by Friedel-crafts acylation reaction.chemistry letters,33(4),414-415.
MLA Guo QZ,et al."Synthesis of macrocyclic arylene ketone oligomers containing the phthaloyl moiety by Friedel-crafts acylation reaction".chemistry letters 33.4(2004):414-415.

入库方式: OAI收割

来源:长春应用化学研究所

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