Copolymerization of carbon dioxide and oxetane catalyzed by aluminum porphyrin complex system

被引:5
|
作者
Honda, Masayoshi [1 ]
Nakamura, Ryo [1 ]
Sugimoto, Hiroshi [1 ]
机构
[1] Tokyo Univ Sci, Dept Ind Chem, Fac Engn, Tokyo, Japan
关键词
aluminum porphyrin; CO2; conversion; copolymerization; oxetane; polycarbonate; RING-OPENING POLYMERIZATION; ALIPHATIC POLYCARBONATES; ALTERNATING COPOLYMERIZATION; CYCLIC CARBONATES; POLY(TRIMETHYLENE CARBONATE); CO2; POLYMERS; EPOXIDES; SELECTIVITY; DEPOLYMERIZATION;
D O I
10.1002/pol.20210536
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Tetraphenylporphinatoaluminum chloride ([TPP]AlCl) catalyst and tetra-n-butylammonium bromide (TBAB) cocatalyst system is effective for the copolymerization of CO2 and oxetane even under low CO2 pressure (similar to 2 MPa). In the presence of toluene as a solvent, poly(trimethylene carbonate) (PTMC) containing >99% of carbonate linkages with M-n = 8600 and M-w/M-n = 1.70 was synthesized. This is the first report of PTMC formation with excellent ratio of carbonate linkages from oxetane and CO2. According to the kinetic analysis, proton nuclear magnetic resonance (H-1 NMR) and matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/MS) measurements of the products, PTMC was mainly synthesized via (i) the trimethylene carbonate (TMC) formation from CO2 and oxetane and (ii) the successive ring-opening polymerization of TMC.
引用
收藏
页码:3122 / 3130
页数:9
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