Efficient green synthesis of bis(cyclic carbonate) poly(dimethylsiloxane) derivative using CO2 addition: a novel precursor for synthesis of urethanes

被引:38
作者
Aguiar, K. R. [1 ]
Santos, V. G. [2 ]
Eberlin, M. N. [2 ]
Rischka, K. [3 ]
Noeske, M. [3 ]
Tremiliosi-Filho, G. [1 ]
Rodrigues-Filho, U. P. [1 ]
机构
[1] Univ Sao Paulo, Inst Chem Sao Carlos, Sao Carlos, SP, Brazil
[2] Univ Estadual Campinas, ThoMSon Mass Spectrometry Lab, Campinas, SP, Brazil
[3] Fraunhofer Inst Fertigungstech & Angew Mat Forsch, Bremen, Germany
基金
巴西圣保罗研究基金会;
关键词
CYCLIC CARBONATE; DIOXIDE; POLYCARBONATES; POLYDIMETHYLSILOXANE; POLYMERIZATION; MEMBRANES; CATALYSTS; EPOXIDES; SOLVENTS; ALKYLENE;
D O I
10.1039/c4ra03846k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Poly(dimethyl siloxane), PDMS, with terminal cyclic carbonate groups was prepared by cycloaddition of carbon dioxide to epoxy rings using tetra alkyl-ammonium bromide as a catalyst under efficient and mild conditions. The process was carried out under a modest pressure of carbon dioxide (i.e., <2 MPa) and temperature (<200 degrees C). The oligomeric species was found to be a non-Newtonian fluid with low molecular weight (MW similar to 1200 g mol(-1)) with n = xx - yy and thermally stable up to 200 degrees C. Its formation was verified by mid infrared spectroscopy (FT-MIR), Matrix-Assisted Laser Desorption Ionization Mass Spectroscopy MALDI-Tof-MS and multinuclear magnetic resonance (C-13 NMR, Si-29 NMR, H-1 NMR). The urethane synthesis was confirmed by FTIR, NMR and X-ray Photoelectron Spectroscopy (XPS) after reacting amines or diamines, in mild reactions conditions, with bis(cyclic carbonate) poly(dimethylsiloxane).
引用
收藏
页码:24334 / 24343
页数:10
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