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{ | |
"id": "132", | |
"path": "/content/acs/en/molecule-of-the-week/archive/a/11-azobis1h-tetrazole", | |
"title": "1,1'-Azobis(1H-tetrazole)", | |
"date": "09/03/12", | |
"archive": "A", | |
"description": "<p>1,1'-Azobis(1<i>H</i>-tetrazole)<b> </b>was <a href=\"http://pubs.acs.org/doi/abs/10.1021/ic200071q\"><u>synthesized from 1-amino-1<i>H</i>-tetrazole</u></a> by T. M. Klapötke and D. G. Piercey at the Ludwig Maximilian University of Munich in 2011. It contains an unprecedented 10–nitrogen atom chain. As might be expected from its structure, 1,1'-azobis(1<i>H</i>-tetrazole) is a powerful explosive, with a detonation velocity of almost 9200 m/s. Its extreme sensitivity to motion makes it impossible to handle as a dry solid; and in solution, it decomposes slowly with the release of nitrogen gas.</p>\n", | |
"info": "", | |
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"teaserImage1": "/content/dam/acsorg/molecule/archive-new/11-azobis-teaser.png", | |
"answerImage1": "/content/dam/acsorg/molecule/archive-new/11-azobis-3d.png", | |
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] | |
} |
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