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Packing Polymorphism on the Example of 5-Hydroxy-1-(4-Methylbenzyl)-3-Chloro-4-[(4-Chlorophenyl)Sulfanyl]-1,5-Dihydro-2H-Pyrrol-2-One: A Crystallographic, Thermochemical, and Spectroscopic Study
Gerasimova D.P., Saifina A.F., Zakharychev D.V., Vandyukova I.I., Fayzullin R.R., Kurbangalieva A.R., Lodochnikova O.A.
© 2020, Pleiades Publishing, Ltd. Two packing polymorphs of 5-hydroxy-1-(4-methylbenzyl)-3-chloro-4
Betti base in the synthesis of chiral bisphosphorylated thioureas
Metlushka K., Sadkova D., Nikitina K., Lodochnikova O., Kataeva O., Alfonsov V.
packing polymorphism
Computational, Structural and Spectroscopic Investigations of Two Polymorphs of 5,7-Dinitro-8-(N-phenylamino)Quinoline
Strashnov P.V., Tkachev V.V., Utenyshev A.N., Kazachenko V.P., Kovalchukova O.V.
Two polymorph modifications of 5,7-dinitro-8-(N-phenylamino) quinoline (DNPAQ) are isolated
Crystal structure and Hirshfeld surface analysis of a new polymorph of (E)-2-(4-bromophenyl)-1-[2,2-dibromo-1-(3-nitrophenyl)ethenyl]diazene
Atioǧlu Z., Akkurt M., Shikhaliyev N.Q., Mammadova N.A., Babayeva G.V., Khrustalev V.N., Bhattarai A.
A new polymorph of the title compound, C14H8Br3N3O2, (form-2) was obtained in the same manner
Betti base in the synthesis of chiral bisphosphorylated thioureas
Metlushka K., Sadkova D., Nikitina K., Lodochnikova O., Kataeva O., Alfonsov V.
packing polymorphism
Smart Polymorphism of Thiacalix[4]arene with Long-Chain Amide Containing Substituents
Gataullina K., Ziganshin M., Stoikov I., Klimovitskii A., Gubaidullin A., Suwińska K., Gorbatchuk V.
for polymorphism than the other two conformations. Thus, 10 polymorphs with essentially different crystal packing
Smart control of calixarene polymorphic states
Gabdulkhaev M.N., Ziganshin M.A., Buzyurov A.V., Schick C., Solovieva S.E., Popova E.V., Gubaidullin A.T., Gorbatchuk V.V.
collapse to a stable packing. In total, seven polymorphs of 1 were identified and characterized. Single
Extraordinary behavior of β-hydroxy sulfoxides and sulfone of pinane series
Nikitina L., Lodochnikova O., Startseva V., Bodrov A., Artemova N., Klimovitskii A., Klochkov V.
-called “packing polymorphs”—monoclinic and triclinic ones. By transition from the room temperature to 150 К
Binuclearopper(I) borohydrideomplexontaining bridging bis(diphenylphosphino) methane ligands: Polymorphic structuresf [(μ2-dppm)2Cu2(η2-BH4)2] dichloromethane solvate
Belkova N.V., Golub I.E., Gutsul E.I., Lyssenko K.A., Peregudov A.S., Makhaev V.D., Filippov O.A., Epstein L.M., Rossin A., Peruzzini M., Shubina E.S.
polymorphic forms (orthorhombic, 1, and monoclinic, 2) The details of molecular geometry and the crystal-packing
Competitive Hydrogen Bonding and Unprecedented Polymorphism in Selected Chiral Phosphorylated Thioureas
Ivshin K., Metlushka K., Zinnatullin R., Nikitina K., Pashagin A., Zakharychev D.V., Efimova A., Kiiamov A., Latypov S., Kataeva O.
lability of compounds and competitive intermolecular H-bonding, multiple polymorphic modifications

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