Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes

被引:28
|
作者
Wulf, Christoph [1 ]
Reckers, Matthias [1 ]
Perechodjuk, Anna [1 ]
Werner, Thomas [1 ]
机构
[1] Leibniz Inst Catalysis LIKAT, Rostock, Germany
来源
关键词
cyclic carbonate; non-isocyanate polyurethane (NIPU); organocatalysis; earth-abundant metal catalysis; homogeneous catalysis; carbon dioxide; Cl building block; CYCLIC CARBONATES; POLYMERIC CARBONATES; EXHAUST CARBON; CO2; FIXATION; DIOXIDE; EPOXIDES; CYCLOADDITION; CAPTURE; AMINES; POLYHYDROXYURETHANES;
D O I
10.1021/acssuschemeng.9b06662
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis of non-isocyanate polyurethanes (NIPUs) has recently gained great attention. In this respect, a bifunctional catalyst and an abundant metal catalyst system were investigated for the conversion of polyfunctional epoxides to gain general access to the corresponding cyclic carbonates as monomers for NIPU synthesis. A Ca-based catalytic system and a bifunctional ammonium salt were established for the synthesis of these monomers. In total, 14 terminal polyfunctional epoxides were converted to the corresponding carbonates in yields up to 99% and high purities. With regard to the one-pot synthesis of NIPUs directly from epoxides and CO2, the influence of the catalyst systems was evaluated. In general, both catalytic systems allowed the synthesis of NIPUs in a sequential one-pot procedure yielding polymers with a molecular mass of up to 19 kg-mol(-1).
引用
收藏
页码:1651 / 1658
页数:15
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