Structural rationalisation of co-crystals formed between trithiocyanuric acid and molecules containing hydrogen bonding functionality

Ahn, Shinbyoung ; PrakashaReddy, J. ; Kariuki, Benson M. ; Chatterjee, Swati ; Ranganathan, Anupama ; Pedireddi, V. R. ; Rao, C. N. R. ; Harris, Kenneth D. M. (2005) Structural rationalisation of co-crystals formed between trithiocyanuric acid and molecules containing hydrogen bonding functionality Chemistry - A European Journal, 11 (8). pp. 2433-2439. ISSN 0947-6539

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/chem.20...

Related URL: http://dx.doi.org/10.1002/chem.200400340

Abstract

Crystallisation of trithiocyanuric acid (TTCA) from various organic solvents that have hydrogen bonding capability (acetone, 2-butanone, dimethylformamide, dimethyl sulfoxide, methanol and acetonitrile) leads to the formation of co-crystals in which the solvent molecules are incorporated together with TTCA in the crystal structure. Structure determination by single-crystal X-ray diffraction reveals that these co-crystals can be classified into different groups depending upon the topological arrangement of the TTCA molecules in the crystal structure. Thus, three different types of single-tape arrangements of TTCA molecules and one type of double-tape arrangement of TTCA molecules are identified. In all co-crystals, hydrogen-bonding interactions are formed through the involvement of N-H bonds of TTCA molecules in these tapes and the other molecule in the co-crystal. Detailed rationalisation of the structural properties of these co-crystals is presented.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Crystal Engineering; Hydrogen Bonds; Nitrogen Heterocycles; Structure Elucidation
ID Code:39974
Deposited On:20 May 2011 12:06
Last Modified:20 May 2011 12:06

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