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Dinitramidoborates,...
Dinitramidoborates, a Fascinating Case of Competing Oxygen and Nitrogen Donors and Tautomerism
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- Belanger-Chabot, Guillaume (author)
- University of Southern California
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- Rahm, Martin, 1982 (author)
- Chalmers tekniska högskola,Chalmers University of Technology
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- Haiges, Ralf (author)
- University of Southern California
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- Christe, Karl O. (author)
- University of Southern California
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(creator_code:org_t)
- 2017-07-27
- 2017
- English.
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In: Angewandte Chemie. - : Wiley. - 1521-3773 .- 1433-7851. ; 56:36, s. 10881-10885
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Abstract
Subject headings
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- Reactions of the BH4- anion with equimolar amounts of HN(NO2)2 or of BH3*THF with K+[N(NO2)2]- produced a mono-substituted [BH3N(NO2)2]- anion which contains a B-N connected dinitramido ligand. The reaction of BH4- with two equivalents of HN(NO2)2 afforded the di-substituted borate anion consisting of two isomers, one with both nitramido ligands attached to B through N and the other one with one ligand attached through N and the other one through O. The disubstituted dinitramidoborates are marginally stable under ambient conditions, and the isomer with two N-connected ligands was characterized by its crystal structure. A tri-substituted borate was tentatively identified by NMR in the reaction of BH4- with a large excess of HN(NO2)2. All anions are highly energetic. Theoretical calculations show that the energy differences between the B-N and B-O tautomers are small, explaining the observed ease of ligand exchange.
Subject headings
- NATURVETENSKAP -- Kemi -- Oorganisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)
Keyword
- boron chemistry
- tautomerism
- dinitramides
- high energy density materials
- dinitramidoborate
Publication and Content Type
- art (subject category)
- ref (subject category)
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