Journal
JOURNAL OF MOLECULAR STRUCTURE
Volume 888, Issue 1-3, Pages 204-213Publisher
ELSEVIER
DOI: 10.1016/j.molstruc.2007.11.049
Keywords
s-Triazine; Tri-s-triazine (heptazine); Cyameluric acid; Cyanuric acid; Guanidinium salt
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Funding
- German Research Foundation, Bonn, Germany [KR 1739/9-1]
- Alexander von Humboldt Foundation, Bonn, Germany
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Reactions of cyameluric acid and cyanuric acid with guanidine in water yield colorless crystals of two novel salts: triguanidinium cyamelurate hydrate [C(NH2)(3)](3)center dot[C6N7O3]center dot 3H(2)O (1) and guanidinium dihydrogencyanurate hydrate [C(NH2)(3)](2)center dot[C(3)N(3)o(3)H(2)](2)center dot H2O (2), respectively. The single crystal X-ray structures show that in the case of 2 there are two protons left at the triazine ring and two crystallographically independent cations and anions are present. In the case of triguanidinium cyamelurate 1, the heptazine ring is completely deprotortated with three crystallographically independent cations. Extensive networks of hydrogen bonds, involving all the molecular species, rule the crystal packing of both salts. Raman and FTIR spectra show the typical features expected for the heterocyclic anions and the guanidinium cation. Simultaneous thermal analysis (TG/DTA) indicates several decomposition steps resulting in 100% mass loss at similar to 750 degrees C for 1 and similar to 600 degrees C for 2. (C) 2007 Elsevier B.V. All rights reserved.
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