Structural similarity and similarity in thermal properties of the polymorphs: melting and crystallization from the melt of tolbutamide and chlorpropamide

The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into hi...

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Published in:Journal of thermal analysis and calorimetry Vol. 142; no. 2; pp. 841 - 848
Main Authors: Drebushchak, T. N., Drebushchak, V. A.
Format: Journal Article
Language:English
Published: Cham Springer International Publishing 01-10-2020
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Abstract The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into high-temperature I H /ε polymorph, which melts at 128 °C. The crystal structures of the high-temperature polymorphs, I H and ε, are very similar to each other in the unit cell parameters and in the arrangement of z-shaped infinite hydrogen-bonded ribbons. Under cooling, other polymorph crystallizes from the melt, V for tolbutamide and β for chlorpropamide, thus making easy the obtaining of these metastable polymorphs. The polymorphs of tolbutamide and chlorpropamide crystallized from their melts turned out to be also very similar to each other in their structures (space group, unit cell parameters, arrangement of π-shaped infinite hydrogen-bonded ribbons). Solid–solid transformation V ⇒ II in tolbutamide was detected both in samples stored under room conditions and those melted in capillaries, thus providing new easy way for II tolbutamide crystallization. In generalizing our results, one can expect that if evident similarity is found among the polymorphs of similar molecules in their crystal structure, the similarity in their thermal properties can be also found, and vice versa.
AbstractList The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into high-temperature I H /ε polymorph, which melts at 128 °C. The crystal structures of the high-temperature polymorphs, I H and ε, are very similar to each other in the unit cell parameters and in the arrangement of z-shaped infinite hydrogen-bonded ribbons. Under cooling, other polymorph crystallizes from the melt, V for tolbutamide and β for chlorpropamide, thus making easy the obtaining of these metastable polymorphs. The polymorphs of tolbutamide and chlorpropamide crystallized from their melts turned out to be also very similar to each other in their structures (space group, unit cell parameters, arrangement of π-shaped infinite hydrogen-bonded ribbons). Solid–solid transformation V ⇒ II in tolbutamide was detected both in samples stored under room conditions and those melted in capillaries, thus providing new easy way for II tolbutamide crystallization. In generalizing our results, one can expect that if evident similarity is found among the polymorphs of similar molecules in their crystal structure, the similarity in their thermal properties can be also found, and vice versa.
The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into high-temperature I.sup.H/[epsilon] polymorph, which melts at 128 °C. The crystal structures of the high-temperature polymorphs, I.sup.H and [epsilon], are very similar to each other in the unit cell parameters and in the arrangement of z-shaped infinite hydrogen-bonded ribbons. Under cooling, other polymorph crystallizes from the melt, V for tolbutamide and [beta] for chlorpropamide, thus making easy the obtaining of these metastable polymorphs. The polymorphs of tolbutamide and chlorpropamide crystallized from their melts turned out to be also very similar to each other in their structures (space group, unit cell parameters, arrangement of [pi]-shaped infinite hydrogen-bonded ribbons). Solid-solid transformation V â II in tolbutamide was detected both in samples stored under room conditions and those melted in capillaries, thus providing new easy way for II tolbutamide crystallization. In generalizing our results, one can expect that if evident similarity is found among the polymorphs of similar molecules in their crystal structure, the similarity in their thermal properties can be also found, and vice versa.
The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The asymmetry in thermal transformations was revealed for both substances. Under heating, all tolbutamide/chlorpropamide polymorphs transform into high-temperature IH/ε polymorph, which melts at 128 °C. The crystal structures of the high-temperature polymorphs, IH and ε, are very similar to each other in the unit cell parameters and in the arrangement of z-shaped infinite hydrogen-bonded ribbons. Under cooling, other polymorph crystallizes from the melt, V for tolbutamide and β for chlorpropamide, thus making easy the obtaining of these metastable polymorphs. The polymorphs of tolbutamide and chlorpropamide crystallized from their melts turned out to be also very similar to each other in their structures (space group, unit cell parameters, arrangement of π-shaped infinite hydrogen-bonded ribbons). Solid–solid transformation V ⇒ II in tolbutamide was detected both in samples stored under room conditions and those melted in capillaries, thus providing new easy way for II tolbutamide crystallization. In generalizing our results, one can expect that if evident similarity is found among the polymorphs of similar molecules in their crystal structure, the similarity in their thermal properties can be also found, and vice versa.
Audience Academic
Author Drebushchak, T. N.
Drebushchak, V. A.
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Issue 2
Keywords Chlorpropamide
X-ray diffraction
DSC
Tolbutamide
Polymorphism
Language English
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Snippet The polymorphism of tolbutamide and chlorpropamide under melting/crystallization was investigated with using DSC and in situ X-ray powder diffraction. The...
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SubjectTerms Analysis
Analytical Chemistry
Capillaries
Chemistry
Chemistry and Materials Science
Chlorpropamide
Crystal structure
Crystallization
Crystals
Diffraction
High temperature
Hydrogen
Hydrogen bonding
Inorganic Chemistry
Measurement Science and Instrumentation
Melts (crystal growth)
Molecular structure
Parameters
Physical Chemistry
Polymer Sciences
Polymorphism
Similarity
Structure
Thermal properties
Thermal transformations
Thermodynamic properties
Tolbutamide
Unit cell
X ray powder diffraction
X-rays
Title Structural similarity and similarity in thermal properties of the polymorphs: melting and crystallization from the melt of tolbutamide and chlorpropamide
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