Anjali Sharma, Dhruba Kshetrimayum, Usman Muhammad Aliyu, Mridula Guin
{"title":"富氮棱镜基笼型化合物:戊唑取代对爆轰和爆炸性能的影响。","authors":"Anjali Sharma, Dhruba Kshetrimayum, Usman Muhammad Aliyu, Mridula Guin","doi":"10.1007/s00894-025-06494-6","DOIUrl":null,"url":null,"abstract":"<div><h3>Context</h3><p>This research explores the impact of systematic addition of pentazole group on the explosive properties of prismane-based compounds on hexanitroprismane and hexaminoprismane. Replacing the NO<sub>2</sub> and NH<sub>2</sub> groups with N<sub>5</sub> in prismane cage-based molecules enhances the material’s energy density and stability, leading to more powerful and stable explosives. The structure-property relationship of the designed molecules is studied using DFT approach. These cage-based compounds exhibit potential as high-energy density explosive compounds reaching up to the level of CL20. Systematic addition of pentazole ring in the prismane cage improves stability and heat of formation. Functionalizing prismane with one pentazole ring can improve the HOF by 300 to 400 kJmol<sup>−1</sup>. The impact of the number of pentazole rings on density is opposite in nature in -NO<sub>2</sub> and -NH<sub>2</sub> containing sets of molecules. The same trend is observed in the values of D, P, and Q of both sets of molecules as the number of pentazole group increased in the prismane. Insertion of a single pentazole ring in prismane for the nitro group substituted molecules has a better impact on improving the impact sensitivity. Pentazole group substitution enhances the energetic properties of prismane-based high energy density compounds, offering a promising avenue for the development of novel, high-performance explosives with tailored detonation characteristics.</p><h3>Methods</h3><p>Density functional theory (DFT) using Gaussian 16 software was used for all quantum chemical calculations. The optimization of the geometry of the designed compounds is performed at two different levels, e.g., B3LYP/6–311 + + G(d,p) and B3PW91/6-31G(d,p). Molecular surface and other properties are visualized using GaussView 6.0 software. The heat of formation (HOF) of the molecules is estimated using isodesmic reactions. The multiwfn program was used for the calculation of molecular surface properties.\n</p></div>","PeriodicalId":651,"journal":{"name":"Journal of Molecular Modeling","volume":"31 10","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nitrogen-rich prismane-based cage compounds: impact of pentazole substitution on detonation and explosive performance\",\"authors\":\"Anjali Sharma, Dhruba Kshetrimayum, Usman Muhammad Aliyu, Mridula Guin\",\"doi\":\"10.1007/s00894-025-06494-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Context</h3><p>This research explores the impact of systematic addition of pentazole group on the explosive properties of prismane-based compounds on hexanitroprismane and hexaminoprismane. Replacing the NO<sub>2</sub> and NH<sub>2</sub> groups with N<sub>5</sub> in prismane cage-based molecules enhances the material’s energy density and stability, leading to more powerful and stable explosives. The structure-property relationship of the designed molecules is studied using DFT approach. These cage-based compounds exhibit potential as high-energy density explosive compounds reaching up to the level of CL20. Systematic addition of pentazole ring in the prismane cage improves stability and heat of formation. Functionalizing prismane with one pentazole ring can improve the HOF by 300 to 400 kJmol<sup>−1</sup>. The impact of the number of pentazole rings on density is opposite in nature in -NO<sub>2</sub> and -NH<sub>2</sub> containing sets of molecules. The same trend is observed in the values of D, P, and Q of both sets of molecules as the number of pentazole group increased in the prismane. Insertion of a single pentazole ring in prismane for the nitro group substituted molecules has a better impact on improving the impact sensitivity. Pentazole group substitution enhances the energetic properties of prismane-based high energy density compounds, offering a promising avenue for the development of novel, high-performance explosives with tailored detonation characteristics.</p><h3>Methods</h3><p>Density functional theory (DFT) using Gaussian 16 software was used for all quantum chemical calculations. The optimization of the geometry of the designed compounds is performed at two different levels, e.g., B3LYP/6–311 + + G(d,p) and B3PW91/6-31G(d,p). Molecular surface and other properties are visualized using GaussView 6.0 software. The heat of formation (HOF) of the molecules is estimated using isodesmic reactions. 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Nitrogen-rich prismane-based cage compounds: impact of pentazole substitution on detonation and explosive performance
Context
This research explores the impact of systematic addition of pentazole group on the explosive properties of prismane-based compounds on hexanitroprismane and hexaminoprismane. Replacing the NO2 and NH2 groups with N5 in prismane cage-based molecules enhances the material’s energy density and stability, leading to more powerful and stable explosives. The structure-property relationship of the designed molecules is studied using DFT approach. These cage-based compounds exhibit potential as high-energy density explosive compounds reaching up to the level of CL20. Systematic addition of pentazole ring in the prismane cage improves stability and heat of formation. Functionalizing prismane with one pentazole ring can improve the HOF by 300 to 400 kJmol−1. The impact of the number of pentazole rings on density is opposite in nature in -NO2 and -NH2 containing sets of molecules. The same trend is observed in the values of D, P, and Q of both sets of molecules as the number of pentazole group increased in the prismane. Insertion of a single pentazole ring in prismane for the nitro group substituted molecules has a better impact on improving the impact sensitivity. Pentazole group substitution enhances the energetic properties of prismane-based high energy density compounds, offering a promising avenue for the development of novel, high-performance explosives with tailored detonation characteristics.
Methods
Density functional theory (DFT) using Gaussian 16 software was used for all quantum chemical calculations. The optimization of the geometry of the designed compounds is performed at two different levels, e.g., B3LYP/6–311 + + G(d,p) and B3PW91/6-31G(d,p). Molecular surface and other properties are visualized using GaussView 6.0 software. The heat of formation (HOF) of the molecules is estimated using isodesmic reactions. The multiwfn program was used for the calculation of molecular surface properties.
期刊介绍:
The Journal of Molecular Modeling focuses on "hardcore" modeling, publishing high-quality research and reports. Founded in 1995 as a purely electronic journal, it has adapted its format to include a full-color print edition, and adjusted its aims and scope fit the fast-changing field of molecular modeling, with a particular focus on three-dimensional modeling.
Today, the journal covers all aspects of molecular modeling including life science modeling; materials modeling; new methods; and computational chemistry.
Topics include computer-aided molecular design; rational drug design, de novo ligand design, receptor modeling and docking; cheminformatics, data analysis, visualization and mining; computational medicinal chemistry; homology modeling; simulation of peptides, DNA and other biopolymers; quantitative structure-activity relationships (QSAR) and ADME-modeling; modeling of biological reaction mechanisms; and combined experimental and computational studies in which calculations play a major role.