期刊
POLYMER CHEMISTRY
卷 12, 期 43, 页码 6355-6362出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1py01039e
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资金
- Russian Science Foundation [21-73-20246, 20-13-00428]
- Ministry of Science and Higher Education of the Russian Federation
- Russian Science Foundation [21-73-20246, 20-13-00428] Funding Source: Russian Science Foundation
The research examines the influence of precatalyst and cocatalyst on the vinyl-addition polymerization of norbornenes with polar groups, finding the proper combination of the two components is crucial for successful polymerization. The resulting polymers' catalytic activity and molecular weights can be efficiently tuned by the nature of both pre- and cocatalyst, with cocatalyst impacting differently based on the nature of the monomer groups. These findings provide insights and opportunities for further exploration in obtaining new high-performance polymers.
Polymers derived from norbornenes with polar groups are of interest as modular templates and materials for membrane processes and microelectronic applications due to the attractive combination of their properties. However, the synthesis of high-molecular weight homopolymers from norbornenes containing polar groups is still a challenge. Herein, we report our examination of the precatalyst and cocatalyst influence on vinyl-addition polymerization of two types of norbornene monomers with bulky and polar groups (substituted nadimides and norbornenes with cellosolve motif). The key to successful vinyl addition polymerization of these monomers is the proper combination of a cocatalyst and a Pd precatalyst. Both components of a catalytic system seem to play equal roles. The catalytic activity and molecular weights of the resulting polymers are efficiently tuned by the nature of both pre- and cocatalyst. Moreover, the impact of the cocatalyst depends on the monomer nature and can be different for norbornenes with nonpolar and polar groups. As a result, a set of glassy and amorphous vinyl-addition homopolymers from norbornenes with polar groups is prepared with yields up to 98% and M-w <= 3 x 10(6) over Pd complexes with N-heterocyclic carbene ligands. The polymers exhibit excellent film-forming properties. These results provide an insight and opportunity for further work expansion in order to obtain new high-performance polymers based on strained cycloalkenes with polar groups, which are not currently available.
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