2000
DOI: 10.1021/ed077p724
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Melting Point and Molecular Symmetry

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Cited by 160 publications
(131 citation statements)
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References 17 publications
(27 reference statements)
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“…From those, conglomerates have always higher melting point from their enantiomeric analogues (Carnelley's law), especially with higher molecular symmetry, while the freezing point varies according to the racemic solution and its crystallization type. Thus, special research interest is focused primarily at the in vitro study of the crystallization type of the solutions of racemic mixtures from natural cancer proteins from various malignant neoplasms with their synthetic enantiomers, regarding the increase of their freezing point and their crystallization at higher temperature from that required for the crystallization of natural cancer protein solutions [2][3][4][5][6][7][8].…”
Section: Methodmentioning
confidence: 99%
“…From those, conglomerates have always higher melting point from their enantiomeric analogues (Carnelley's law), especially with higher molecular symmetry, while the freezing point varies according to the racemic solution and its crystallization type. Thus, special research interest is focused primarily at the in vitro study of the crystallization type of the solutions of racemic mixtures from natural cancer proteins from various malignant neoplasms with their synthetic enantiomers, regarding the increase of their freezing point and their crystallization at higher temperature from that required for the crystallization of natural cancer protein solutions [2][3][4][5][6][7][8].…”
Section: Methodmentioning
confidence: 99%
“…In the case of 5, melting processes are preceded by decomposition. As a general rule, melting points do generally increase with the increasing molecular mass and symmetrical molecules in the crystalline form have higher melting points compared with those of similar structure but with a lower symmetry [8][9][10][11]. The structures of the studied compounds are composed of 3-(2-furanyl)-8-aryl-7,8-dihydroimidazo[2,1-c][1,2,4]triazin-4 (6H)-one unit and differently substituted benzene fragments.…”
Section: Comparison Of the Thermal Behaviour Of 1-6 In Airmentioning
confidence: 95%
“…This derogation from the general rule can be associated with the structure of these compounds. In the case of compound 5, it is more likely that the electronegative Cl atoms can be engaged in polar interactions like p-p or H-bonding which can increase the melting point [8][9][10].…”
Section: Comparison Of the Thermal Behaviour Of 1-6 In Airmentioning
confidence: 99%
“…À49.3 8C for 2b and À54.2 8C for 2c). It has been reported that the T m of an organic compound is determined by the strength of its crystal lattice, which is in turn controlled by three main factors: intermolecular forces, molecular symmetry and degree of conformational freedom of the molecule [20,21].…”
Section: Melting Pointmentioning
confidence: 99%