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Explosophore

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This is an old revision of this page, as edited by Wostr (talk | contribs) at 18:19, 19 May 2022 (citation needed; Polish sources from around 1950. and 1960. state that plosophore/auxoplose was a similar theory by Lothrop & Handrick (1948)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

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

History

The term was first coined by Russian chemist V. Pletz in 1935[1] and originally mistranslated in some articles as plosophore[citation needed]. 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)'.[citation needed]

Properties

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.

Classification

Pletz grouped the explosophores into eight distinct categories.[2][3]

I. −NO2, −ON=O and −ONO2

These represent

Most commercially used explosives include the nitrate ion or the nitro group.

II. −N=N− and −N=N+=N

The azo and azide groups respectively, connected to organic/inorganic compounds (e.g. AgN3, Pb(N3)2, NH4N3)

III. −RnNXm

The halogenated nitrogen group X:halogen (for example NI3 and NCl3)

IV. −C=N−O−

The fulminate group (example HONC and Hg(ONC)2)

V. −OClO2 and −OClO3

The chlorate and perchlorate groups respectively, connected to organics/inorganics (e.g. KClO3, FOClO3)

VI. −O−O− and −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. Ag2C2, 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.

References

  1. ^ Pletz, V. J. Gen. Chem. (U.S.S.R.) 5, 173 (1935)
  2. ^ Handrick, G.R., Lothrop, W.C. Chem. Rev., 1949, 44 (3) p 419–445
  3. ^ Warey, Philip. B. ed. New Research on Hazardous Materials, Nova Science Publishers, 2007