聚合
双环戊二烯
开环复分解聚合
聚合物
试剂
催化作用
高分子化学
复分解
反应性(心理学)
化学
无环二烯复分解
活化能
化学工程
材料科学
有机化学
医学
替代医学
病理
工程类
作者
Benjamin A. Suslick,Aliza N. Yazdani,Morgan M. Cencer,Justine E. Paul,Nil A. Parikh,Katherine J. Stawiasz,Isabel P. S. Qamar,Nancy R. Sottos,Jeffrey S. Moore
出处
期刊:Macromolecules
[American Chemical Society]
日期:2022-06-16
卷期号:55 (13): 5459-5473
被引量:11
标识
DOI:10.1021/acs.macromol.2c00775
摘要
Frontal ring-opening metathesis polymerization (FROMP) catalyzed by Grubbs-type Ru complexes enables new, rapid, and energy-efficient syntheses of high-performance, structural plastics. Ideal catalysts survive the extended time periods associated with resin preparation, storage, and transportation. Current catalysts, however, induce premature polymerization within hours to days under ambient conditions. In this work, a thermally latent bis-N-heterocyclic carbene complex provides exceedingly robust resins, which are viable for 8 weeks. When mixed with CuI coreagents, precatalyst activation primes the system for rapid reactivity after thermal initiation. In this study, more than 40 dual-component formulations successfully catalyzed FROMP of dicyclopentadiene. The polymerization process parameters (front temperatures and velocities), resin storability, and resultant polymer properties (e.g., Tg) were determined for each composition. Intriguingly, the Cu to Ru ratio dramatically impacts the observed frontal velocity and temperature, as well as the polymer glass-transition temperature; slower, colder reaction fronts result from formulations with large Cu to Ru ratios. The resultant polymers display lower Tg values. Mechanistic analysis of a related model system demonstrated that an excess Cu reagent decreases the activation and polymerization rates.
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