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Nitrosation and Nitration of Tetraacetyldibenzylhexaazaisowurtzitane 被引量:1
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作者 吕连营 欧育湘 +1 位作者 王建龙 陈博仁 《Defence Technology(防务技术)》 SCIE EI CAS 2005年第1期57-60,共4页
Tetraacetyldibenzylhexaazaisowurtzitane (TADBIW) was subjected to debenzylation by nitrosating with inorganic materials available commercially to synthesize tetraacetyldinitrosohexaazaisowurtzitane (TADNSIW). TADNSIW ... Tetraacetyldibenzylhexaazaisowurtzitane (TADBIW) was subjected to debenzylation by nitrosating with inorganic materials available commercially to synthesize tetraacetyldinitrosohexaazaisowurtzitane (TADNSIW). TADNSIW was purified, and its structure was determined by FTIR, 1H NMR, MS and element analysis. The debenzylation reaction of TADBIW gave quantitative benzaldehyde as a by-product. This indicates that the reaction produces an imine cation as an intermediate. Hexanitrohexaazaisowurtzitane (HNIW) was prepared from unpurified TADNSIW with the yield over 96.0 % and the purity more than 98.0 %. And the mechanism of the reaction from TADNSIW to HNIW is proposed to be oxidation of nitroso and nitration of acetyl on the molecule of TADNSIW. This reaction system involved is simple, and the reaction can complete within a short time and under mild conditions. The product can be easily to separate and the waste disposed readily. 展开更多
关键词 四乙酰二亚苄 基作用 硝基化 硝基置换 炸药原料 六硝基六纤锌
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