Abstract
The crystal structure of the 1∶1 adduct of 2-aminopyrimidine with indole-2-carboxylic acid has been determined by single crystal X-ray diffraction, revealing a novel interactive mode. The utility of 2-aminopyrimidine in formation of stable hydrogen-bonded networks with carboxylic acids is discussed and the modes of interaction are reviewed.
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Part 28.,Aust. J. Chem., 1997, (submitted).
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Lynch, D.E., Latif, T., Smith, G. et al. Molecular co-crystals of carboxylic acids, part 29. The effect of competitive interactions on adduct formation involving 2-aminopyrimidine: the crystal structure of the 1∶1 adduct of 2-aminopyrimidine with indole-2-carboxylic acid. J Chem Crystallogr 27, 567–575 (1997). https://doi.org/10.1007/BF02576455
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DOI: https://doi.org/10.1007/BF02576455