Anionic homo- and copolymerization of p-diethynylbenzene in the presence of n-BuLi in polar solvents was carried out. The use of hexamethylphosphortriamide (HMPA) makes it possible to synthesize a completely linear soluble polymer that does not have branching and phenylene fragments. A copolymer of p-diethynylbenzene with diphenyldiacetylene was synthesized. Homo- and copolymers of p-diethynylbenzene have high thermo- and thermo-oxidative stability. By the interaction of side reactive ethynylphenylene groups with various reagents, it is proposed to synthesize clusters along the conducting chain of poly-p-diethynylbenzene. Due to presenting C≡CH side groups, boron, copper, and cobalt derivatives were synthesized. It is shown that not all theoretically possible stereoisomers can be formed as a result of the polymerization. The application of p-diethynylbenzene polymers for the modification of industrial samples of epoxy novolac resin, oligoester acrylates, and carbon fibers has been demonstrated.

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.

Homopolymerization of para‐diethynylbenzene and its copolymerization with 1,4‐diphenylbutadiyne (DPDA) in a boiling solution using carbonyl cobalt‐DPDA complex as a catalyst leads to the formation of weakly branched polymers with high thermal‐oxidative stability.

Polymer composites with high dielectric permittivity (>10) and low dielectric loss are critical for energy storage and microelectronic applications. This study reports on a semi-transparent composite of a PVDF copolymer filled with Cu₇S₄ nanoparticles synthesized via a wet chemical route. Only a small content (6%) of copper sulfide increases the dielectric permittivity of the material from 10.4 to 15.9 (1 kHz), maintaining a low dielectric loss coefficient (less than 0.1). The incorporated nanoparticles affect the morphology of the composite film surface and crystalline phases in the whole volume, which was studied with FTIR spectroscopy, differential scanning calorimetry and scanning probe microscopy.