2009
DOI: 10.1016/j.tca.2008.12.001
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Temperature- and moisture-dependent phase changes in crystal forms of barbituric acid

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Cited by 42 publications
(44 citation statements)
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“…1.87 [10]) also resulting from the presence of two methylene hydrogen atoms. The existence of three polymorphs of anhydrous H2ba and deihydrate [11][12][13], and six polymorphs of anhydrous thiobarbituric acid and hydrate [14] make these molecules interesting from the viewpoint of crystal engineering. They can be used as a building block to construct the supramolecular assemblies with distinctive properties.…”
Section: Fig 1 Schemes Of Pefloxacin (A) and Barbituric Acids (B): Xmentioning
confidence: 99%
“…1.87 [10]) also resulting from the presence of two methylene hydrogen atoms. The existence of three polymorphs of anhydrous H2ba and deihydrate [11][12][13], and six polymorphs of anhydrous thiobarbituric acid and hydrate [14] make these molecules interesting from the viewpoint of crystal engineering. They can be used as a building block to construct the supramolecular assemblies with distinctive properties.…”
Section: Fig 1 Schemes Of Pefloxacin (A) and Barbituric Acids (B): Xmentioning
confidence: 99%
“…Typically hydrate stability is evaluated by characterizing the dehydration conditions and observed phase changes. The most common techniques for studying dehydration are powder X-ray diffraction (PXRD), [3][4][5][6][7] thermal analysis, 3,5,6,[8][9][10][11][12][13][14] spectroscopic methods, 8,12,[15][16][17] and particle morphology and particle size characterization of the original and dehydrated products. [18][19][20] By using these methods, it is possible to determine the dehydration conditions and understand the behavior of hydrate upon dehydration.…”
Section: Introductionmentioning
confidence: 99%
“…3. A broad double-band (3564 and 3543 cm À1 ) and a single-band at 3478 cm À1 corresponding to the different hydroxyl in the enoltautomer structure of barbituric acid [26] given in Fig. 4 can be easily found in Fig.…”
Section: Characterization Of Zinc Barbituratementioning
confidence: 96%
“…3 (Fig. 4, ketotautomer) around 1750 cm À1 [26] (i.e. 1768, 1758, 1745 and 1716 cm À1 ) are replaced by a single sharp peak at 1711 cm À1 , and two intense peaks appeared at 1591 and 1262 cm À1 corresponding to carbonyl and carbon-oxygen (CeO) bonds in ZnL 2 , respectively.…”
Section: Characterization Of Zinc Barbituratementioning
confidence: 99%