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Hyperbranched pyridylphenylene polymers based on the first-generation dendrimer as a multifunctional monomer
An A 6 + B 2 approach was applied for the first time to synthesize novel hyperbranched pyridylphenylene polymers by Diels–Alder cyclocondensation reaction. For this, the first-generation pyridylphenylene dendrimer with six ethynyl functionalities (A 6 ) was used as a branching core for the molecule...
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Published in: | RSC advances 2015-01, Vol.5 (120), p.99510-99516 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | An A
6
+ B
2
approach was applied for the first time to synthesize novel hyperbranched pyridylphenylene polymers by Diels–Alder cyclocondensation reaction. For this, the first-generation pyridylphenylene dendrimer with six ethynyl functionalities (A
6
) was used as a branching core for the molecule growth. The phenyl-substituted bis(cyclopentadienone)s (B
2
) of different structures were used as co-monomer in the reaction. A careful choice of reaction conditions allowed us to obtain high molecular weight polymers without undesirable gelation. The molecular weight of the polymers varied in the range of 10 800–80 100 with a polydispersity degree of 1.69 to 4.07 according to SEC analysis. The
1
H and inverse-gated decoupling
13
C NMR combined with heteronuclear single quantum correlation and heteronuclear multiple bond correlation measurements were used to estimate the branching degree of the polymers synthesized. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C5RA16847C |