ICCAS OpenIR
Synthesis of macrocyclic arylene ketone oligomers containing the phthaloyl moiety by Friedel-crafts acylation reaction
Guo, QZ; Bo, SQ; Chen, TL
2004-04-05
Source PublicationCHEMISTRY LETTERS
ISSN0366-7022
Volume33Issue:4Pages:414-415
AbstractTwo 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.
Indexed BySCI
Language英语
WOS IDWOS:000220913500025
PublisherCHEMICAL SOC JAPAN
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Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/81648
Collection中国科学院化学研究所
Corresponding AuthorChen, TL
AffiliationChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Recommended Citation
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.
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