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Synthesis and properties of cyclic olefin polymers by ring-opening metathesis (co)polymerization of α-methyl-substituted norbornene lactones
Previously, we prepared new cyclic olefin polymers (COPs) by performing a ring-opening metathesis polymerization (ROMP) of endo - and exo -norbornene lactones (NBLs) and then hydrogenation. In this study, we produced new thermally and chemically stable COPs with random, gradient, and block sequences...
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Published in: | Polymer chemistry 2022-10, Vol.13 (41), p.5882-5888 |
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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: | Previously, we prepared new cyclic olefin polymers (COPs) by performing a ring-opening metathesis polymerization (ROMP) of
endo
- and
exo
-norbornene lactones (NBLs) and then hydrogenation. In this study, we produced new thermally and chemically stable COPs with random, gradient, and block sequences by homo- and copolymerizing
endo
- and
exo
-methyl-substituted NBLs (MNBLs) with norbornene (NB), in addition to the COPs obtained by copolymerizing NBLs with
endo
,
anti
-tetracyclododecene (TCD). The rates of ring-opening metathesis copolymerization (ROMCP) between
endo
- and
exo
-MNBLs,
endo
- and
exo
-NBLs, TCD, and NB are compared, and the random copolymers are prepared by dropwise addition of more reactive monomers. The thermal and optical properties, structural analysis, and hydrophobicity of the resultant COPs are investigated. The block and gradient hydrogenated copolymers (H-poly(
endo
-MNBL-
co
-NB)) are crystalline, yet the corresponding random copolymer is amorphous. Notably, the COPs obtained from MNBLs and NBLs show lower birefringence values than a conventional linear-ester-substituted COP, ARTON®.
New cyclic olefin polymers derived from norbornene lactones are prepared, and their thermal, physical, and optical properties are revealed. |
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ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/d2py01020h |