Crystallization, spectral, crystallographical, and thermoanalytical studies of succinobucol polymorphism
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
22323097
DOI
10.1002/jps.23068
PII: S0022-3549(15)31608-7
Knihovny.cz E-zdroje
- MeSH
- diferenciální skenovací kalorimetrie MeSH
- krystalizace MeSH
- krystalografie rentgenová MeSH
- magnetická rezonanční spektroskopie MeSH
- molekulární modely MeSH
- prášková difrakce MeSH
- probukol analogy a deriváty analýza chemie MeSH
- spektrofotometrie infračervená MeSH
- termogravimetrie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- probukol MeSH
- succinobucol MeSH Prohlížeč
Four different polymorphs, A, C, D, and E, of succinobucol were isolated and characterized by means of solid-state nuclear magnetic resonance spectroscopy, single crystal and powder X-ray diffraction, differential scanning calorimetry, thermogravimetry, and attenuated total reflection-infrared spectroscopy. From a number of experiments, the same polymorphs (C, D, and E) and an equilibrium phase mixture B consisting of polymorphs C and D were repeatedly gained using different solvents or their mixtures. Although polymorph A was obtained directly from recrystallization only on few occasions, polymorphs C, D, and E proved to be metastable kinetic polymorphs, which slowly transform to a thermodynamically more stable form A during long-term storage. The single-crystal structures of polymorph C and D were determined by X-ray single-crystal diffraction.
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