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6 citations found for Kaur, R

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Acta Cryst. (2017). A73, C759
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Acta Cryst. (2023). A79, C1415
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Cocrystallization of cyclic imides with benzoic acid and some of its hydroxyl analogues resulted in cocrystals and eutectics in a mutually exclusive manner depending on the presence or absence and position of the hydroxyl group and consequent supramolecular effect for different combinations.

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The title compound, C38H50O5 {systematic name: 10-(3-hy­droxy­benzo­yl)-2,2,7,7-tetra­methyl-3,6,8-tris­(3-methyl­but-2-en­yl)-3,4,4a,5,6,7-hexa­hydro-4a,8-methano-2H-cyclo­octa­[b]pyran-9,11(8H)-dione}, is a polyisoprenylated benzophenone, isolated for the first time from the fruits of Garcinia indica during our investigation of bioactive compounds from this plant and their large-scale extraction. The relative configuration of the title compound was chosen based on comparison of its spectroscopic and optical rotation data with that of the isomorphous and isostructural compound isogarcinol, whose absolute configuration is known. The crystal packing features O—H...O hydrogen bonds. A Cambridge Structural Database analysis revealed that the crystal structure reported here is isomorphous and isostructural with that of isogarcinol.

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High-energy X-ray diffraction data modelling, reverse Monte Carlo simulations, pair distribution function analysis and Rietveld refinement are described for strontium tellurite glass, anti-glass and crystalline samples.

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A comprehensive list of organic crystalline polymorphs has been assembled using the Cambridge Structural Database (CSD) and the structures categorized by crystal type, uncovering significant variations in the polymorphism prevalence of each group. Phenomena such as the high prevalence of temperature-induced phase transitions in organic salts and the diminishing percentage of polymorphic crystal entries in the CSD over the last 20 years, with the exception of cocrystals, highlight areas of prospective study.

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