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首页> 外文期刊>Polimery >Selective epoxidation of hydroxyl terminated polybutadiene using in situ generated dimethyl dioxirane in the presence of MoO3
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Selective epoxidation of hydroxyl terminated polybutadiene using in situ generated dimethyl dioxirane in the presence of MoO3

机译:在MoO3存在下使用原位生成的二甲基二环氧乙烷对羟基封端的聚丁二烯进行选择性环氧化

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摘要

Hydroxyl terminated polybutadiene (HTPB) was epoxidized using in situ generated dimethyl dioxirane (DMD) as an oxidant and M0O3 as a catalyst at 25 °C.Different reaction factors such as reaction time and catalyst concentration were examined.The ability of different C=C geometries toward epoxidation was evaluated in detail at various reaction times and the products were characterized by H NMR,C NMR and FT-IR techniques and no side reaction were detected.It was found that hydroxyl group of the polymer chain was preserved in the oxidation reaction without using any conditional control and relative reactivity depended on chain microstructure in the following way:1,4-ris > 1,4-irans > 1,2-vinyl.This method is easy,environmentally friendly,convenient and the reaction conditions are straightforward.
机译:以原位生成的二甲基二环氧乙烷(DMD)为氧化剂,以M0O3为催化剂,于25°C对羟基封端的聚丁二烯(HTPB)进行环氧化,研究了不同的反应因素,如反应时间和催化剂浓度,不同C = C的能力在不同的反应时间对环氧化的几何形状进行了详细评估,并通过1 H NMR,C NMR和FT-IR技术对产物进行了表征,未发现副反应。发现在氧化反应中聚合物链的羟基得以保留在不使用任何条件控制的情况下,相对反应性通过以下方式取决于链的微结构:1,4-ris> 1,4-irans> 1,2-乙烯基。该方法简便,环保,方便且反应条件简单。

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