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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.
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页码:3122 / 3130
页数:9
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