3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials
The targeted energetic material 3-amino-1,2,4(4H)-oxadiazol-5-one (AOD) was synthesized from sodium dicyanamide using hydroxylamine hydrochloride in a one-step procedure. AOD was prepared by a novel procedure in good yield and characterized using spectroscopic (IR, Raman, NMR) techniques. The high n...
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sg-ntu-dr.10356-872632020-06-01T10:01:30Z 3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials Kumar, Sudheer Ambarkar Sasidharan, Nimesh Ganguly, Rakesh Leow, Dasheng Hng, Huey Hoon School of Materials Science & Engineering School of Physical and Mathematical Sciences Central Instrumentation Facility Energetics Research Institute The targeted energetic material 3-amino-1,2,4(4H)-oxadiazol-5-one (AOD) was synthesized from sodium dicyanamide using hydroxylamine hydrochloride in a one-step procedure. AOD was prepared by a novel procedure in good yield and characterized using spectroscopic (IR, Raman, NMR) techniques. The high nitrogen-containing hydroxylamine and hydrazine salts of AOD (3) were prepared from their respective nitrogen bases in good yields. The solid state structures of the synthesized molecules were confirmed by single X-ray crystallography. 3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD, 3), 3-amino-1,2,4(4H)-oxadiazol-5-one-hydroxylamine (AOD-HyAm, 5) and 3-amino-1,2,4(4H)-oxadiazol-5-one-hydrazine (AOD-Hy, 6) showed densities of 1.76, 1.73 and 1.64 g cc−1 respectively. The thermal stabilities of the molecules were assessed by thermogravimetric analysis. Non-isothermal kinetics was performed on the molecules to derive the activation energy. Constant volume combustion energy was determined using oxygen bomb calorimetry and the heat of formation was calculated from the experimental values. Sensitivities of the molecules were measured by using impact and friction tests. Accepted version 2018-02-01T06:53:36Z 2019-12-06T16:38:26Z 2018-02-01T06:53:36Z 2019-12-06T16:38:26Z 2018 2018 Journal Article Kumar, S. A., Sasidharan, N., Ganguly, R., Leow, D., & Hng, H. H. (2018). 3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials. New Journal of Chemistry, 42(3), 1840-1844. 1144-0546 https://hdl.handle.net/10356/87263 http://hdl.handle.net/10220/44369 10.1039/C7NJ03950F 203263 en New Journal of Chemistry © 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. This is the author created version of a work that has been peer reviewed and accepted for publication by New Journal of Chemistry, The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1039/C7NJ03950F]. |
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The targeted energetic material 3-amino-1,2,4(4H)-oxadiazol-5-one (AOD) was synthesized from sodium dicyanamide using hydroxylamine hydrochloride in a one-step procedure. AOD was prepared by a novel procedure in good yield and characterized using spectroscopic (IR, Raman, NMR) techniques. The high nitrogen-containing hydroxylamine and hydrazine salts of AOD (3) were prepared from their respective nitrogen bases in good yields. The solid state structures of the synthesized molecules were confirmed by single X-ray crystallography. 3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD, 3), 3-amino-1,2,4(4H)-oxadiazol-5-one-hydroxylamine (AOD-HyAm, 5) and 3-amino-1,2,4(4H)-oxadiazol-5-one-hydrazine (AOD-Hy, 6) showed densities of 1.76, 1.73 and 1.64 g cc−1 respectively. The thermal stabilities of the molecules were assessed by thermogravimetric analysis. Non-isothermal kinetics was performed on the molecules to derive the activation energy. Constant volume combustion energy was determined using oxygen bomb calorimetry and the heat of formation was calculated from the experimental values. Sensitivities of the molecules were measured by using impact and friction tests. |
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School of Materials Science & Engineering |
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School of Materials Science & Engineering Kumar, Sudheer Ambarkar Sasidharan, Nimesh Ganguly, Rakesh Leow, Dasheng Hng, Huey Hoon |
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Article |
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Kumar, Sudheer Ambarkar Sasidharan, Nimesh Ganguly, Rakesh Leow, Dasheng Hng, Huey Hoon |
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Kumar, Sudheer Ambarkar Sasidharan, Nimesh Ganguly, Rakesh Leow, Dasheng Hng, Huey Hoon 3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials |
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Kumar, Sudheer Ambarkar |
title |
3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials |
title_short |
3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials |
title_full |
3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials |
title_fullStr |
3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials |
title_full_unstemmed |
3-Amino-1,2,4(4H)-oxadiazol-5-one (AOD) and its nitrogen-rich salts: a class of insensitive energetic materials |
title_sort |
3-amino-1,2,4(4h)-oxadiazol-5-one (aod) and its nitrogen-rich salts: a class of insensitive energetic materials |
publishDate |
2018 |
url |
https://hdl.handle.net/10356/87263 http://hdl.handle.net/10220/44369 |
_version_ |
1681058818684878848 |