

FOLLOWUS
School of Materials Science and Engineering and Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin 300072, China
Li-xia Ren, E-mail:lxren@tju.edu.cn
Received:12 August 2016,
Revised:2016-9-9,
Accepted:12 September 2016,
Published:2017-01
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Ji-xing Yang, Li-xia Ren, Yue-sheng Li. Ring-opening Metathesis Polymerization of Cis-5-norbornene-
A series of
cis
-5-norbornene-
endo
-2
3-dicarboxylic anhydride (NDCA
M1) derivatives (M2-M4) with different types of nonpolar substituted groups were synthesized and characterized by
1
H/
13
C-NMR and mass spectrometry (MS). Ring-opening metathesis polymerization (ROMP) of these monomers using the Grubbs third generation catalyst (G3) generated high molecular weight polymers with much improved solubility compared with the NDCA's homopolymer. It was found that the solubility of these polymers increased with increased substituent's steric hindrance. The living polymerization of NDCA derivative containing the bulkiest substituent (M4) catalyzed by G3 in tetrahydrofuran was confirmed by the kinetic studies with low polydispersity indices (PDI) (
<
1.30). By using sequential ROMP
well-defined diblock copolymers containing anhydride groups were synthesized.
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