CHINESE JOURNAL OF ENERGETIC MATERIALS
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1,4-对二(2,4,6-三硝基苯乙烯基)苯的合成、结构和性能(英)
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LIU Yan-hong(1976-), female, Ph. D. Research field: Physical Chemistry. e-mail: liuyanhong-2000@163.com

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National Natural Science Foundation of China (No. 20471008) and the Foundation for basic research by the Beijing Institute of Technology.


Crystal Structure and Thermal Analysis of 1,4-Di(2,4,6-trinitro-styryl)benzene
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    摘要:

    为了寻找新的多硝基茋耐热炸药,采用脑文格缩合反应制备得到了1,4-对二(2,4,6-三硝基苯乙烯基)苯,并采用自然挥发溶剂法在N,N-二甲基甲酰胺(DMF)溶液中培养了单晶。用X-射线单晶衍射法测定了它的晶体结构,结果表明:该晶体属于三斜晶系,P-1空间群,有一个对称中心。通过元素分析、FT-IR、 1H NMR、13C NMR、MS对化合物的结构作了进一步的表征,结果表明得到的化合物为目标化合物。采用Gaussian 98程序在DFT-B3LYP/6-31G*,6-311G**水平下对化合物分子进行了几何优化和振动分析。计算结果无虚频,而且计算结果和试验结果一致,证明所得化合物结构相对稳定。通过差示扫描量热法(DSC)和热失重法(TG-DTG),在10 ℃·min-1的升温速率下研究了化合物的热分解性能,此化合物有较高的熔点(302 ℃)和热分解温度(311 ℃),结果表明该化合物有较高的耐热性能。

    Abstract:

    The synthesis, culture of crystal and single-crystal X-ray crystallography of a new kind of polynitrostilbene [1,4-di(2,4,6-trinitro-styryl)benzene, TNT-TTD], which was synthesized through Knoevenagel Condensation by using piperidine as a base catalyst were reported. The crystal belongs to the Triclinic system with space group P-1.The compound was characterized by using FT-IR, 1H NMR, 13C NMR and MS spectroscopy techniques. Density functional theory (DFT) B3LYP was employed to optimize structure and calculate frequencies of TNT-TTD. The calculated geometrical parameters were close to the corresponding experiments ones. The thermal decomposition of the title compound was investigated by DSC and TG-DTG methods at heating rate 10 ℃·min-1. The melting point and initial decomposed temperature of TNT-TTD is 302 ℃ and 311 ℃. The results indicate that TNT-TTD has high heat resistant ability.

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刘艳红,张同来,张建国,等.1,4-对二(2,4,6-三硝基苯乙烯基)苯的合成、结构和性能(英)[J].含能材料, 2006, 14(5):367-373.
LIU Yan-hong, ZHANG Tong-lai, ZHANG Jian-guo, et al. Crystal Structure and Thermal Analysis of 1,4-Di(2,4,6-trinitro-styryl)benzene[J]. Chinese Journal of Energetic Materials, 2006, 14(5):367-373.

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  • 收稿日期: 2006-03-31
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  • 在线发布日期: 2011-11-04
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