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Tetrazenes listing

The literature listed in Table 2 gives numerous examples of calculated bond lengths and angles with optimized geometry for the tetrazole tautomers. The electronic structures of the substituted 4,5-dihydrotetrazoles (14) have been investigated by MNDO and AM 1 calculations to explain their photoelectron spectra <88CB1213>. Their electronic structure resembles that of the c -2-tetrazene group and is characterized by three occupied n molecular orbitals and two n molecular... [Pg.625]

Guanylnitiosaminoguany I tetrazene or Tetracene Salts. It forms numerous salts, most of which are explosive. Several of them are listed in Beil and other refs... [Pg.814]

Cis-silylated, germylated, or stannylated acyclic tetrazenes have not yet been identified (33). These are, probably in all cases, substantially higher in energy than the corresponding trans compounds. The cyclic tetrazenes (sila- and germatetrazolines) listed in Table III, however, are in the cis configuration. [Pg.213]


See other pages where Tetrazenes listing is mentioned: [Pg.216]    [Pg.216]    [Pg.216]    [Pg.216]    [Pg.207]    [Pg.207]    [Pg.317]    [Pg.160]    [Pg.160]    [Pg.1199]    [Pg.170]   
See also in sourсe #XX -- [ Pg.9 , Pg.9 , Pg.103 ]




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Tetrazen tetrazene

Tetrazene

Tetrazenes

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