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dc.contributor.authorSireenart Surinwongen_US
dc.contributor.authorTimothy J. Prioren_US
dc.contributor.authorApinpus Rujiwatraen_US
dc.date.accessioned2018-09-04T09:46:07Z-
dc.date.available2018-09-04T09:46:07Z-
dc.date.issued2014-01-01en_US
dc.identifier.issn01252526en_US
dc.identifier.other2-s2.0-84899621441en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84899621441&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/53269-
dc.description.abstractSingle crystals of cyanuric acid in its keto form have been hydrothermally synthesized via the acid catalyzed hydrolysis of 1, 3,5-triazine-2,4,6-triamine triacetic acid. The crystal structure has been solved and refined in a standard monoclinic C2/c which is better preferable than the commonly employed C2/n with b >> 90. The original cell in C2/c are a = 7.9070(13)Å, b = 6.7347(14)Å, c = 9.0788(15)Å, b = 90.794(14)°, V = 483.41(15)Å3, R = 0.0473, Rw = 0.1288, S = 1.073, and the transformed C2/n cell are a = 7.907Å, b = 6.7347Å, c = 11.9564Å, b =130.602°. Relationships between different crystallographic settings are discussed. The molecular motifs are assembled into two-dimensional layer in (10-1) plane by the 2 4 N-H···O type of hydrogen bonding interactions with graph sets R 22(8) and R 44(16). The molecule shows partial aromatic character, corresponding to the harmonic-oscillator model of aromaticity index of 0.89.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.subjectMathematicsen_US
dc.subjectPhysics and Astronomyen_US
dc.titleCyanuric acid: Hydrothermal crystal growth and alternative crystallographic descriptionen_US
dc.typeJournalen_US
article.title.sourcetitleChiang Mai Journal of Scienceen_US
article.volume41en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Hullen_US
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