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Coordination-induced polymerization of P═C bonds leads to regular (P─C)(n) polycarbophosphanes

The replacement of carbon in (C─C)(n) chains of polyolefins by phosphorus leads to polycarbophosphanes (P─C)(n), which may possess unique chemical and physical properties. However, macromolecules with a regular (P─C)(n) chain have never been unambiguously identified. Here, we demonstrate that additi...

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Detalles Bibliográficos
Autores principales: Mei, Yanbo, Gamboa-Carballo, Juan José, Bao, Yinyin, Wu, Na, Le Corre, Grégoire, Grützmacher, Hansjörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946365/
https://www.ncbi.nlm.nih.gov/pubmed/33692112
http://dx.doi.org/10.1126/sciadv.abf4272
Descripción
Sumario:The replacement of carbon in (C─C)(n) chains of polyolefins by phosphorus leads to polycarbophosphanes (P─C)(n), which may possess unique chemical and physical properties. However, macromolecules with a regular (P─C)(n) chain have never been unambiguously identified. Here, we demonstrate that addition polymerization, a general concept to polymerize olefins, can be extended to P═C double bonds. The polymerization of monomeric 2-phosphanaphthalenes is mediated by copper(I) halides and leads to polycarbophosphanes with an M(n) of 14 to 34 kDa. Each phosphorus is coordinated to Cu(I), which can be easily removed. Unlike long-term durable polyolefins, the metal-free polymers depolymerize rapidly back to monomers under sunlight or ultraviolet irradiation at λ = 365 nm. The monomers can be recycled for repolymerization, demonstrating a cradle-to-cradle life cycle for polycarbophosphanes.