CHINESE JOURNAL OF ENERGETIC MATERIALS
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2,2,4,4,6,6-六硝基金刚烷的合成、表征及晶体结构
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(南京理工大学化工学院, 江苏 南京 210094)

作者简介:

张萍萍(1989-),女,硕士研究生,主要从事精细合成研究。e-mail: zhangpingping1016@163.com 通信联系人: 罗军(1975-),男,副研究员,主要从事有机合成化学研究。e-mail: luojun@njust.edu.cn

通讯作者:

罗军(1975-),男,副研究员,主要从事有机合成化学研究。e-mail: luojun@njust.edu.cn

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Synthesis, Characterization and Crystal Structure of 2,2,4,4,6,6-Hexanitroadamantane
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(Nanjing University of Science and Technology, Nanjing 210094, China)

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    摘要:

    以丙二酸二乙酯和多聚甲醛为起始原料, 经环合、脱羧、缩酮化、臭氧化、肟化、偕硝化等步骤, 合成了2, 2, 4, 4, 6, 6-六硝基金刚烷(HNA)。优化了Meerwein′s酯的合成、臭氧化反应和酮肟偕硝化的反应条件, HNA的总收率提高到3%。用五氧化二氮作酮肟偕硝化反应的硝化剂, 考察了物料配比、反应温度、反应时间、溶剂对酮肟偕硝化反应的影响。确定的最佳反应条件为:物料比n(2, 2, 6, 6-二乙撑二氧基-4-金刚烷酮肟):n(N2O5)=1:3, 反应温度为50 ℃, 反应时间为30 min, 反应溶剂为二氯甲烷, 偕二硝基化合物的收率为65%。用1H NMR, 13C NMR, IR及元素分析表征了中间体与目标化合物的结构。培养了HNA单晶, 用X射线四圆衍射仪测定了它的单晶结构。用热重分析(TG)和差示扫描量热法(DSC)研究了HNA的热性能。结果表明: HNA晶体属单斜晶系, P2(1)/n空间群, 晶胞参数为a=1.2011(2) nm, b=2.1129(4) nm, c=1.1967(2) nm, α=90°, β=90.59(3)°, γ=90°, V=3.0368(11) nm3, Z=8, Dc=1.777 g·cm-3, μ=0.166 mm-1, F(000)=1664。HNA的热分解过程可分为三个阶段, 从分解反应开始到结束的总失重为94%。DSC曲线在256.21 ℃处有一个明显的放热峰, 显示加热时HNA在该温度有剧烈的放热分解反应发生。

    Abstract:

    2, 2, 4, 4, 6, 6-Hexanitroadamantane (HNA) was synthesized via cyclization, decarboxylation, ketalization, ozonation, oximation, and oxidative nitration etc. steps, using diethyl malonate and paraformaldehyde as raw materials. The reaction conditions of the preparation of Meerwein′s ester, ozonation and nitration were optimized, and the overall yield of HNA was promoted to 3%. The effects of substrates ratio, reaction temperature, reaction time and solvent on the gem-nitration reaction were investigated using nitrogen pentoxide as nitrating agent of gem-nitration reaction of ketoxime.The optimum reaction conditions were determined as with the yield of gem-dinitro compound being 65%: n(compound 7):n(N2O5)=1:3, reaction temperature 50 ℃, reaction time 30 min and methylene chloride as solvent. The structures of intermediates and target compound were characterized by 1H NMR, 13C NMR, IR and elemental analyses. The single crystal of HNA was cultivated and its single crystal structure was determined by a four-circle X-ray diffractometer. The thermal decomposition properties of HNA were studied by thermogravimetry(TG) and differential scanning calorimetry(DSC). Results show that the crystal belongs to monoclinic system, space group P2(1)/n with crystal parameters of a=1.2011(2) nm, b=2.1129(4) nm, c=1.1967(2) nm, α=90°, β=90.59(3)°, γ=90°, V=3.0368(11) nm3, Z=8, Dc=1.777 g·cm-3, μ=0.166 mm-1, F(000)=1664. The thermal decomposition process of HNA can be divided into three stages and the total mass loss from start to the end of decomposition reaction is 94%. There is an obvious exothermic peak at 256.21 ℃ on DSC curve of HNA, revealing that an intense exothermic decomposition reaction of HNA would occur on heating.

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引用本文

张萍萍,凌亦飞,孙露,等.2,2,4,4,6,6-六硝基金刚烷的合成、表征及晶体结构[J].含能材料, 2014, 22(5):646-653. DOI:10.3969/j. issn.1006-9941.2014.05.013.
ZHANG Ping-ping, LING Yi-fei, SUN Lu, et al. Synthesis, Characterization and Crystal Structure of 2,2,4,4,6,6-Hexanitroadamantane[J]. Chinese Journal of Energetic Materials, 2014, 22(5):646-653. DOI:10.3969/j. issn.1006-9941.2014.05.013.

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  • 收稿日期: 2013-09-26
  • 最后修改日期: 2014-02-22
  • 录用日期: 2014-03-04
  • 在线发布日期: 2014-10-29
  • 出版日期: