Synthesis of Polyphenylenes through Bergman Cyclization of Enediynes with Long Chain Alkyl Groups
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Synthesis of Polyphenylenes through Bergman Cyclization of Enediynes with Long Chain Alkyl Groups
Synthesis of Polyphenylenes through Bergman Cyclization of Enediynes with Long Chain Alkyl Groups
Chinese Journal of Polymer Science2015年33卷第1期 页码:184-191
Affiliations:
Shanghai Key Laboratory of Advanced Polymeric Materials, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China
Author bio:
**Aiguo Hu (胡爱国), E-mail: hagmhsn@ecust.edu.cn
Funds:
National Natural Science Foundation of China(20874026;91023008);Ph. D. Programs Foundation of Ministry of Education of China(20100074110002);Fundamental Research Funds for the Central Universities, Shanghai Leading Academic Discipline Project(B502)
Shiyuan Sun, Luhua Dong, Depeng Song, 等. Synthesis of Polyphenylenes through Bergman Cyclization of Enediynes with Long Chain Alkyl Groups[J]. Chinese Journal of Polymer Science, 2015,33(1):184-191.
Shiyuan Sun, Luhua Dong, Depeng Song, et al. Synthesis of Polyphenylenes through Bergman Cyclization of Enediynes with Long Chain Alkyl Groups[J]. Chinese Journal of Polymer Science, 2015, 33(1): 184-191.
Shiyuan Sun, Luhua Dong, Depeng Song, 等. Synthesis of Polyphenylenes through Bergman Cyclization of Enediynes with Long Chain Alkyl Groups[J]. Chinese Journal of Polymer Science, 2015,33(1):184-191.DOI: 10.1007/s10118-015-1566-6.
Shiyuan Sun, Luhua Dong, Depeng Song, et al. Synthesis of Polyphenylenes through Bergman Cyclization of Enediynes with Long Chain Alkyl Groups[J]. Chinese Journal of Polymer Science, 2015, 33(1): 184-191.DOI: 10.1007/s10118-015-1566-6.
Synthesis of Polyphenylenes through Bergman Cyclization of Enediynes with Long Chain Alkyl Groups
Several new enediynes with long chain alkyl groups were synthesized through Sonogashira coupling reactions between long chain alkynes and (Z)-1
2-dichloroethene. These enediynes (1) were then subjected to thermal Bergman cyclization in a refluxing diphenyl ether bath under vacuum to obtain conjugated polyphenylenes with the weight-average molecular weights up to 4.9 × 10
3
g·mol
-1
. The occurrence of Bergman cyclization was confirmed by
1
H-NMR
13
C-NMR
and IR spectroscopic analysis. These polyphenylenes are fully soluble in common organic solvents and exhibit good thermal stability. The optical properties of the polyphenylenes were investigated by UV-Vis absorption and photoluminescence (PL) spectroscopies. A blue emission was observed for all these polyphenylenes.
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