Misin Vyacheslav M, Maltseva Irina E, Kazakov Mark E, Volkov Vladimir A
N.M. Emanuel Institute of Biochemical Physics, Russian Academy Science, 4 Kosygina Street, 119334 Moscow, Russia.
SPC UVICOM Ltd., 38A Olympic Avenue, 141009 Mytischi, Russia.
Polymers (Basel). 2023 Feb 22;15(5):1105. doi: 10.3390/polym15051105.
In this review, all available publications on the polymerization of all isomers of bifunctional diethynylarenes due to the opening of C≡C bonds were considered and analyzed. It has been shown that with the use of polymers of diethynylbenzene, heat-resistant and ablative materials, catalysts, sorbents, humidity sensors, and other materials can be obtained. Various catalytic systems and conditions of polymer synthesis are considered. For the convenience of comparison, the publications considered are grouped according to common features, including the types of initiating systems. Critical consideration is given to the features of the intramolecular structure of the synthesized polymers since it determines the entire complex of properties of this material and subsequent materials. Branched and/or insoluble polymers are formed as a result of solid-phase and liquid-phase homopolymerization. It is shown that the synthesis of a completely linear polymer was carried out for the first time by anionic polymerization. The review considers in sufficient detail publications from hard-to-reach sources, as well as publications that required a more thorough critical examination. The review does not consider the polymerization of diethynylarenes with substituted aromatic rings because of their steric restrictions; the diethynylarenes copolymers with complex intramolecular structure; and diethynylarenes polymers obtained by oxidative polycondensation.
在本综述中,对所有因碳碳三键打开而引发的双官能二乙炔基芳烃异构体聚合的现有出版物进行了考量和分析。结果表明,使用二乙炔基苯聚合物可制得耐热材料、烧蚀材料、催化剂、吸附剂、湿度传感器及其他材料。文中还探讨了各种催化体系及聚合物合成条件。为便于比较,所考量的出版物按共同特征进行了分组,包括引发体系类型。由于合成聚合物的分子内结构特征决定了该材料及后续材料的所有性能,因此对其进行了重点考量。通过固相和液相均聚会形成支化和/或不溶性聚合物。研究表明,首次通过阴离子聚合实现了完全线性聚合物的合成。本综述充分详细地考量了来自难以获取来源的出版物,以及需要更深入严格审查的出版物。由于空间位阻限制,本综述未涉及带有取代芳环的二乙炔基芳烃的聚合反应;未涉及具有复杂分子内结构的二乙炔基芳烃共聚物;也未涉及通过氧化缩聚获得的二乙炔基芳烃聚合物。