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Highly Efficient Synthesis of Functionalizable Polymers from a CO2/1,3-Butadiene-Derived Lactone
ACS Macro Letters ( IF 5.1 ) Pub Date : 2017-11-30 00:00:00 , DOI: 10.1021/acsmacrolett.7b00774
Muhua Liu 1, 2, 3 , Yunyan Sun 1 , Yuanqi Liang 1, 2 , Bo-Lin Lin 1, 2, 3, 4
Affiliation  

Making polymers from CO2 and olefins has been long sought and is of particular significance for chemical utilizations of CO2. Herein, high molecular-weight polymers with 29 wt % CO2 were obtained by polymerizing a δ-lactone (L) synthesized from a C–C coupling reaction between CO2 and 1,3-butadiene, an economical large-volume chemical that can also be derived from top biomass platform chemicals. Although L has been known for many years, little was investigated in its polymerization. We found that L’s polymerizability can be vitalized upon simply heating in the presence of O2. The polymerization is additive/solvent-free with abundant preserved olefins and up to full monomer conversion, providing a convenient, economical, and scalable avenue to obtain CO2-derived polymers with potentially tailorable properties via the readily modifiable olefins.

中文翻译:

由 CO2/1,3-丁二烯衍生的内酯高效合成功能化聚合物

长期以来一直在寻找由 CO 2和烯烃制造聚合物,并且对于 CO 2的化学利用具有特别重要的意义。在此,通过聚合由 CO 2和 1,3-丁二烯之间的 C-C 偶联反应合成的 δ-内酯 ( L ) 获得了具有 29 wt % CO 2的高分子量聚合物,这是一种经济的大体积化学品,可以也来源于顶级生物质平台化学品。尽管L已为人所知多年,但对其聚合的研究却很少。我们发现L的聚合性可以通过在 O 2存在下简单加热来激活. 该聚合反应不含添加剂/溶剂,具有丰富的保存烯烃和高达完全的单体转化率,为通过易于改性的烯烃获得具有潜在可定制性能的CO 2衍生聚合物提供了一种方便、经济且可扩展的途径。
更新日期:2017-11-30
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