Cationic Copolymerization of o-Phthalaldehyde and Vinyl Monomers with Various Substituents on the Vinyl Group or in the Pendant: Effects of the Structure and Reactivity of Vinyl Monomers on Copolymerization Behavior
Cationic Copolymerization of o-Phthalaldehyde and Vinyl Monomers with Various Substituents on the Vinyl Group or in the Pendant: Effects of the Structure and Reactivity of Vinyl Monomers on Copolymerization Behavior
复制标题
邻苯二甲醛与乙烯基上或侧链具有不同取代基的乙烯基单体的阳离子共聚:乙烯基单体的结构和反应活性对共聚行为的影响
DOI:
10.1021/acs.macromol.2c00470
复制
发表时间:
2022-04
期刊:
影响因子:
5.5
通讯作者:
Keisuke Hayashi;Arihiro Kanazawa;S. Aoshima
中科院分区:
文献类型:
--
作者:
Keisuke Hayashi;Arihiro Kanazawa;S. Aoshima
Cationic copolymerization ofo-phthalaldehyde with various styrene derivatives and vinyl ethers was investigated, particularly focusing on the relationship between the structure and reactivity of vinyl monomers and the copolymerization behavior. In the case of styrene derivatives, the existence ofα- orβ-substituents (or cyclic structures) on the vinyl group was indispensable for efficient crossover reactions. Styrene derivatives with no substituents on the vinyl group did not undergo copolymerization with OPA. In contrast, various vinyl ethers other thanα-substituted vinyl ethers underwent copolymerization with OPA. To realize alternating-like copolymerization, the use of vinyl monomers that have both large steric hindrance and highly reactiveβ-carbon was effective. In addition, copolymers that are degradable into low-molecular-weight compounds were successfully obtained from styrene derivatives.