高等学校化学学报
高等學校化學學報
고등학교화학학보
CHEMICAL JOURNAL OF CHINESE UNIVERSITIES
2015年
1期
142-148
,共7页
申程%王鹏程%赵国政%陆明
申程%王鵬程%趙國政%陸明
신정%왕붕정%조국정%륙명
1,3,4,5,7,8-六硝基八氢化二咪唑4,5-b:4ˊ,5ˊ-e吡嗪-2,6-(1H,3H)-N,Nˊ-二亚硝胺%硝基取代的中间产物%密度泛函理论%爆轰性能
1,3,4,5,7,8-六硝基八氫化二咪唑4,5-b:4ˊ,5ˊ-e吡嗪-2,6-(1H,3H)-N,Nˊ-二亞硝胺%硝基取代的中間產物%密度汎函理論%爆轟性能
1,3,4,5,7,8-륙초기팔경화이미서4,5-b:4ˊ,5ˊ-e필진-2,6-(1H,3H)-N,Nˊ-이아초알%초기취대적중간산물%밀도범함이론%폭굉성능
N,Nˊ-(1,3,4,5,7,8-hexanitrooctahydro-diimidazo[4,5-b:4ˊ,5ˊ-e]pyrazine-2,6(1H,3H)- diylidene) dinitramide%Intermediate with nitro group%Density functional theory%Detonation property
应用密度泛函理论,在B3PW91/6-31G++(d,p)水平下,分析了合成1,3,4,5,7,8-六硝基八氢化二咪唑[4,5-b:4ˊ,5ˊ-e]吡嗪-2,6-(1H,3H)-N,Nˊ-二亚硝胺(ONIP)时可能产生的不同数量硝基取代的中间产物,并分析了在相同数量的硝基取代时,中间产物可能具有的同分异构体的热力学选择性,确认了热力学选择下的反应历程。比较了4~8个硝基取代中间产物的结构性能数据,计算结果表明,超过四硝基取代后,特别是六硝基中间产物,具有良好的爆轰性能,同时稳定性远超ONIP,并且更易于合成。
應用密度汎函理論,在B3PW91/6-31G++(d,p)水平下,分析瞭閤成1,3,4,5,7,8-六硝基八氫化二咪唑[4,5-b:4ˊ,5ˊ-e]吡嗪-2,6-(1H,3H)-N,Nˊ-二亞硝胺(ONIP)時可能產生的不同數量硝基取代的中間產物,併分析瞭在相同數量的硝基取代時,中間產物可能具有的同分異構體的熱力學選擇性,確認瞭熱力學選擇下的反應歷程。比較瞭4~8箇硝基取代中間產物的結構性能數據,計算結果錶明,超過四硝基取代後,特彆是六硝基中間產物,具有良好的爆轟性能,同時穩定性遠超ONIP,併且更易于閤成。
응용밀도범함이론,재B3PW91/6-31G++(d,p)수평하,분석료합성1,3,4,5,7,8-륙초기팔경화이미서[4,5-b:4ˊ,5ˊ-e]필진-2,6-(1H,3H)-N,Nˊ-이아초알(ONIP)시가능산생적불동수량초기취대적중간산물,병분석료재상동수량적초기취대시,중간산물가능구유적동분이구체적열역학선택성,학인료열역학선택하적반응역정。비교료4~8개초기취대중간산물적결구성능수거,계산결과표명,초과사초기취대후,특별시륙초기중간산물,구유량호적폭굉성능,동시은정성원초ONIP,병차경역우합성。
The intermediate products of N,Nˊ-(1,3,4,5,7,8-hexanitrooctahydro-diimidazo[4,5-b:4ˊ,5ˊ-e] pyrazine-2,6(1H,3H)-diylidene)dinitramide(ONIP) were studied via quantum chemistry method. When the ONIP is not nitrified completely, several intermediate products under different degree of nitrification are obtained. And what’ s more, each intermediate has several isomers. We used the Gaussian 03 software to research these isomers. The thermodynamic selective products could be identified. Then the structures, density and some other important properties were calculated under B3PW91 level and 6-31G++(d,p)basis set with density functional theory. The results showed that the intermediate with six nitro groups owns very good detonation performance. It may be easier to be synthetized than ONIP, and more inactive than ONIP.