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Theoretical studies on a series of nitroaliphatic energetic compounds

Theoretical studies on a series of nitroaliphatic energetic compounds
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摘要 Density functional theory calculations at the B3LYP/6-311G** level are performed to study the geometric and elec- tronic structures of a series of nitroaliphatic compounds. The heats of formation (HOF) are predicted through the designed isodesmic reactions. Thermal stabilities are evaluated via the homolytic bond dissociation energies (BDEs). Further, the correlation is developed between impact sensitivity h50% and the ratio (BDE/E) of the weakest BDE to the total energy E containing zero point energy correction. In addition, the relative stability of the title compounds is evaluated based on the analysis of calculated Mulliken population and the energy gaps between the frontier orbitals. The calculated BDEs, HOFs, and energy gaps consistently indicate that compound 1,1,1,6,6,6-hexanitro-3-hexyne is the most unstable and the compound 3,3,4,4,-tetranitro-hexane is the most stable. These results provide basic information for the molecular design of novel high energetic density materials. Density functional theory calculations at the B3LYP/6-311G** level are performed to study the geometric and elec- tronic structures of a series of nitroaliphatic compounds. The heats of formation (HOF) are predicted through the designed isodesmic reactions. Thermal stabilities are evaluated via the homolytic bond dissociation energies (BDEs). Further, the correlation is developed between impact sensitivity h50% and the ratio (BDE/E) of the weakest BDE to the total energy E containing zero point energy correction. In addition, the relative stability of the title compounds is evaluated based on the analysis of calculated Mulliken population and the energy gaps between the frontier orbitals. The calculated BDEs, HOFs, and energy gaps consistently indicate that compound 1,1,1,6,6,6-hexanitro-3-hexyne is the most unstable and the compound 3,3,4,4,-tetranitro-hexane is the most stable. These results provide basic information for the molecular design of novel high energetic density materials.
作者 曾晖 赵俊
出处 《Chinese Physics B》 SCIE EI CAS CSCD 2014年第6期150-157,共8页 中国物理B(英文版)
基金 supported by the National Natural Science Foundation of China(Grant Nos.11304022 and11347010) the Research Foundation of Education Bureau of Hubei Province,China(Grant Nos.Q20131208,T201204,and XD2014069) the Foundation of Yangtze University for Outstanding Young Teachers,China(Grant Nos.cyq201321 and cyq201322) the Project for Basic Subjects(Grant No.2013cjp10)
关键词 density functional theory heats of formation bond dissociation energy isodesmic reaction density functional theory, heats of formation, bond dissociation energy, isodesmic reaction
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