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Explosophore

Functional group which gives an organic molecule explosive properties

Explosophores are functional groups in organic chemistry that give organic compounds explosive properties.

01History

The term was first coined by Russian chemist V. Pletz in 1935 and originally mistranslated in some articles as plosophore. Also of note is an auxoexplose concept (similar to chromophore and auxochrome concept), which is a group that modifies the explosive capability of the molecule. The term explosophore has been used more frequently after its use in books such as Organic Chemistry of Explosives by J. Agrawal and R. Hodgson (2007)'.

02Properties

Nitrogen-containing explosophores (groups I, II and III below) are particularly strong because in addition to providing oxygen they react to form molecular nitrogen, which is a very stable molecule, and thus the overall reaction is strongly exothermic. The gas formed also expands, causing the shock wave which is observed.

03Classification

Pletz grouped the explosophores into eight distinct categories.

I. −NO2, −ON=O, −ONO2
These represent:
  • the nitro group, a nitrogen atom bound to two oxygen atoms as well as an organic molecule (e.g. TNT, RDX)
  • the nitrate ion, a nitrogen atom bound to three oxygen atoms, (e.g. nitroglycerin, ANFO)
  • the nitrite ion, a nitrogen atom bound to two oxygen atoms
Most commercially used explosives include the nitrate ion or the nitro group.
II. −N=N−, −N=N+=N
The azo and azide groups respectively, connected to organic/inorganic compounds (e.g. silver azide AgN3, lead azide Pb(N3)2, ammonium azide NH4N3)
III. −RnNXm
The halogenated nitrogen group X:halogen (e.g. nitrogen triiodide NI3 and nitrogen trichloride NCl3)
IV. −C=N−O−
The fulminate group (e.g. fulminic acid HONC and mercury fulminate Hg(ONC)2)
V. −OClO2, −OClO3
The chlorate and perchlorate groups respectively, connected to organics/inorganics (e.g. potassium chlorate KClO3, fluorine perchlorate FOClO3)
VI. −O−O−, −O3
The peroxide and ozonide groups respectively, connected to organics/inorganics (e.g. acetone peroxide, butanone peroxide)
VII. −C≡C M+
The acetylide group with its metal derivatives (e.g. silver acetylide Ag2C2, copper acetylide Cu2C2)
VIII. A metal atom connected by an unstable bond to the carbon of certain organic radicals
This class contains for instance organic compounds of mercury, thallium, and lead.
Other
Other substances have been characterised as explosophores outside of the eight classes as defined by Pletz.
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Sources and credits

This article is adapted from the Wikipedia article Explosophore, written by its contributors and licensed under CC BY-SA 4.0. Fathomly has changed the layout, removed citation markers, navigation and maintenance notices, and adjusted punctuation. This adapted version is shared under the same license. For references, see the original article.

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