The decomposition behavior of energetic materi- als is very important for the safety problems concerning their production, transportation, use and storage, because molecular decomposition is intimately connected to their explosive properties. Nitroaromatic compounds, particularly nitrobenzene derivatives, are often considered as prototypi- cal energetic molecules, and some of them are commonly used as high explosives. Quantitative structure-activity rela- tionship (QSAR) represents a potential tool for predicting the thermal stability properties of energetic materials. But it is reported that constructing general reliable models to predict their stability and their potential explosive proper- ties is a very difficult task. In this work, we make our efforts to investigate the relationship between the molecular structures and corresponding thermal stabilities of 77 nitro- benzene derivatives with various substituent functional groups (in ortho , meta and/or para positions). The pro- posed best MLR model, developed by the new software QSARINS, based on Genetic Algorithm for variable selection and with various validation tools, is robust, stable and pre- dictive with R 2 of 0.86, Q LOO 2 of 0.79 and CCC of 0.90. The results indicated that, though difficult, it is possible to build predictive, externally validated QSAR models to estimate the thermal stability of nitroaromatic compounds

Structure-Activity Relationship Analysis of the Thermal Stabilities of Nitroaromatic Compounds Following Different Decomposition Mechanisms

GRAMATICA, PAOLA
2013-01-01

Abstract

The decomposition behavior of energetic materi- als is very important for the safety problems concerning their production, transportation, use and storage, because molecular decomposition is intimately connected to their explosive properties. Nitroaromatic compounds, particularly nitrobenzene derivatives, are often considered as prototypi- cal energetic molecules, and some of them are commonly used as high explosives. Quantitative structure-activity rela- tionship (QSAR) represents a potential tool for predicting the thermal stability properties of energetic materials. But it is reported that constructing general reliable models to predict their stability and their potential explosive proper- ties is a very difficult task. In this work, we make our efforts to investigate the relationship between the molecular structures and corresponding thermal stabilities of 77 nitro- benzene derivatives with various substituent functional groups (in ortho , meta and/or para positions). The pro- posed best MLR model, developed by the new software QSARINS, based on Genetic Algorithm for variable selection and with various validation tools, is robust, stable and pre- dictive with R 2 of 0.86, Q LOO 2 of 0.79 and CCC of 0.90. The results indicated that, though difficult, it is possible to build predictive, externally validated QSAR models to estimate the thermal stability of nitroaromatic compounds
2013
J., Li; H., Liu; X., Huo; Gramatica, Paola
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/1811120
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