Recent advances in the polymerization of elemental sulphur, inverse vulcanization and methods to obtain functional Chalcogenide Hybrid Inorganic/Organic Polymers (CHIPs)

被引:208
作者
Zhang, Yueyan [1 ]
Glass, Richard S. [1 ]
Char, Kookheon [2 ]
Pyun, Jeffrey [1 ,2 ]
机构
[1] Univ Arizona, Dept Chem & Biochem, 1306 East Univ Blvd, Tucson, AZ 85721 USA
[2] Natl Creat Res Initiat Ctr Intelligent Hybrids, Sch Chem & Biol Engn, Program Chem Convergence Energy & Environm, Seoul 151744, South Korea
关键词
RING-OPENING POLYMERIZATION; HIGH REFRACTIVE-INDEX; DYNAMIC COVALENT POLYMERS; SELF-HEALING MATERIALS; ONE-POT SYNTHESIS; CATHODE MATERIAL; ANIONIC COPOLYMERIZATION; HIGH-CAPACITY; HYPERBRANCHED POLYMERS; SUSTAINABLE MATERIALS;
D O I
10.1039/c9py00636b
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Recent developments in the polymerization of elemental sulfur and the preparation of functional Chalcogenide Hybrid Inorganic/Organic Polymers (CHIPs) are reviewed. CHIPs represent a class of polymers synthesized from elemental sulfur with the incorporation of inorganic chalcogenide components (S, Se, Te) into the organic polymeric backbones. Novel CHIP materials exhibit interesting optical, electrochemical and mechanical properties that lead to applications in thermal imaging, energy storage, self-healable materials and separation science. The emphasis of this review is on the key advances in the synthetic approaches to prepare functional polymeric sulfur-rich materials, with recent developments in synthesis, characterization, and application milestones being highlighted.
引用
收藏
页码:4078 / 4105
页数:28
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