Abstract
Two trinitromethanide (TNM) salts containing weakly coordinating cations (tetrabutylammonium and cesium) were synthesized via incomplete nitration of acetic anhydride followed by cation exchange with tetrabutylammonium bromide and cesium fluoride. Their structural characteristics were determined by single crystal X-ray crystallography [J.C. Bryan, M.N. Burnett, A.A. Gakh, Acta Crystallogr., Sect. C (Cr. Str. Comm.) 54 (1998) 1229] followed by comparative analysis with the literature data. In all cases, the TNM anion was found to be a non-planar system. The sum of dihedral angles between the central (C-N3) plane of the anion and the planes of the individual nitro groups varies from 60 to 100°. C-N and N-O interatomic distances in TNM anion can be correlated with the dihedral angles of the corresponding nitro groups: The 13C and 14N NMR spectra of the TNM anion are very simple (broad singlets), an indication of the equivalence (on the NMR time scale) of the nitro groups in solution. The distribution ratio between organic phase (tributyl phosphate) and water is 5000 times higher for Cs+-C(NO2)3 compared to Cs+NO3/-, presumably due to size and/or charge delocalization differences between nitrate and TNM anions. (C) 2000 Elsevier Science B.V.
Original language | English |
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Pages (from-to) | 221-228 |
Number of pages | 8 |
Journal | Journal of Molecular Structure |
Volume | 520 |
Issue number | 1-3 |
DOIs | |
State | Published - Mar 14 2000 |
Funding
The research was sponsored by the Initiatives for Proliferation Prevention (IPP) program and by the Division of Chemical Sciences, Office of Science, US Department of Energy under contract DE-AC05-96OR22464 with Oak Ridge National Laboratory, managed by Lockheed Martin Energy Research Corporation.
Funders | Funder number |
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Division of Chemical Sciences | |
Lockheed Martin Energy Research Corporation | |
U.S. Department of Energy | DE-AC05-96OR22464 |
Office of Science | |
Oak Ridge National Laboratory |
Keywords
- Dendritic anions
- NMR
- Nitration
- Trinitromethane
- X-ray crystallography
- Y-conjugation