Isobornanyl sulfoxides and isobornanyl sulfone: Physicochemical characteristics and the features of crystal structure
Autor: | Patrick Rollin, Alina F. Saifina, I. Z. Rakhmatullin, Olga V. Ostolopovskaya, S. V. Pestova, Roman S. Pavelyev, Vladimir V. Klochkov, D. P. Gerasimova, Svetlana A. Rubtsova, Daut R. Islamov, Dmitry V. Zakharychev, Olga A. Lodochnikova, E. S. Izmest’ev, Liliya E. Nikitina |
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Rok vydání: | 2021 |
Předmět: |
010405 organic chemistry
Chemistry Organic Chemistry Synthon Supramolecular chemistry Diastereomer Infrared spectroscopy Crystal structure 010402 general chemistry 01 natural sciences 0104 chemical sciences Analytical Chemistry Sulfone Inorganic Chemistry Crystal Crystallography chemistry.chemical_compound Molecule Spectroscopy |
Zdroj: | Journal of Molecular Structure. 1239:130491 |
ISSN: | 0022-2860 |
DOI: | 10.1016/j.molstruc.2021.130491 |
Popis: | The physico-chemical characteristics and crystal structure of newly synthesized isobornanyl sulfoxides and sulfone are presented. After purification, diastereomeric sulfoxides were obtained in a 2:1 eutectic ratio, which did not allow either separation or enrichment of the mixture. Based on thermochemical data, the form of the phase diagram of the system was reconstructed, showing that diastereomers have significantly different melting points. According to the X-ray data, the same supramolecular open–chain S=O⋅⋅⋅H–O synthon is built up in the crystals of diastereomeric sulfoxides. The isobornanyl sulfone crystal is formed in a complex way – two crystallographically independent molecules playing different roles in the formation of H-bonds. The IR spectra of a diastereomeric sulfoxides mixture demonstrate the averaging of the synthon-forming functional groups bands. In a counterbalance, the IR spectrum of isobornanyl sulfone shows a doubling of the key bands of synthon-forming functional groups belonging to homochirally homogeneous but crystallographically nonequivalent molecules. |
Databáze: | OpenAIRE |
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