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首页> 外文期刊>Designed Monomers and Polymers: An International Journal on Monomer and Macromolecular Synthesis >Chemoselective epoxidation of hydroxyl-terminated polybutadiene (HTPB) using in-situ generated dimethyl dioxirane (DMD)
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Chemoselective epoxidation of hydroxyl-terminated polybutadiene (HTPB) using in-situ generated dimethyl dioxirane (DMD)

机译:使用原位生成的二甲基二环氧乙烷(DMD)对羟基封端的聚丁二烯(HTPB)进行化学选择性环氧化

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In this report hydroxyl-terminated polybutadiene (HTPB) was functionalized to epoxi-dized HTPBs containing various epoxide group moieties by using in situ-generated dimethyl dioxirane (DMD) as oxidant and tetra-n-butyl ammonium bromide as a phase-transfer catalyst (PTC) in convenient,simple and mild conditions.The system shows to be sensetive to electronic,steric and chain microstracture factors and reveals the high reactivity of cis in comparison with trans and vinyl double bonds.1H-NMR,13C-NMR and FT-IR spectra analysis of the products reveal that no significant side reactions take place in this system even at high epoxidation levels.Influences of various factors,i.e.,reaction time and the PTC concentration were investigated in detail.Also,it was found that double bonds oxidized chemoselectively in comparision with terminal hydroxyl groups.
机译:在此报告中,通过使用原位生成的二甲基二环氧乙烷(DMD)作为氧化剂和四正丁基溴化铵作为相转移催化剂,将羟基封端的聚丁二烯(HTPB)功能化为环氧化的HTPB,这些环氧化合物包含多个环氧基团( PTC)在方便,简单和温和的条件下显示。该系统显示出对电子,空间和链微结构因子的感应,并且与顺式和乙烯基双键相比,揭示了顺式的高反应活性.1H-NMR,13C-NMR和FT-产物的红外光谱分析表明,即使在高环氧化水平下,该体系也不会发生明显的副反应。详细研究了反应时间和PTC浓度等各种因素的影响。此外,还发现双键被氧化与末端羟基相比具有化学选择性。

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