Abstract
The exploitation of C-C activation to facilitate chemical reactions is well-known in organic chemistry. Traditional strategies in homogeneous media rely upon catalyst-activated or metal-mediated C-C bonds leading to the design of new processes for applications in organic chemistry. However, activation of a C-C bond, compared with C-H bond activation, is a more challenging process and an underdeveloped area because thermodynamics does not favor insertion into a C-C bond in solution. Carbon-carbon bond cleavage through loss of an oxime moiety has not been reported. In this paper, a new observation of self-coupling via C-C bond cleavage with concomitant loss of oxime in the absence of metals (either metal-complex mediation or catalysis) results in dihydroxylammonium 5,5-bistetrazole-1,10-diolate (TKX-50) as well as N,N′-([3,3′-bi(1,2,4-oxadiazole)]-5,5′-diyl)dinitramine, a potential candidate for a new generation of energetic materials.
| Original language | English |
|---|---|
| Pages (from-to) | 3560-3563 |
| Number of pages | 4 |
| Journal | Journal of the American Chemical Society |
| Volume | 140 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 14 Mar 2018 |
| Externally published | Yes |
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