Статья
2021
Structure and Polymorphism of Imidazole Derivatives
I. N. Karaseva, M. O. Karasev, S. V. Kurbatova
Российский журнал физической химии А
https://doi.org/10.1134/S0036024421010118
Abstract / Full Text
A crystal chemical analysis is performed of the structures of some imidazole derivatives capable of polymorphic transformations. Characteristics of molecular Voronoi–Dirichlet polyhedra are used to analyze nonvalent intra- and intermolecular interactions in the crystal structures of imidazole conformational polymorphs.
Author information
- Samara National Research University, Samara, RussiaI. N. Karaseva, M. O. Karasev & S. V. Kurbatova
References
- A. Katritzky, V. Lobanov, and M. Karelson, Chem. Soc. Rev. 24, 279 (1995).
- R. Kaliszan, Chem. Rev. 107, 3212 (2007).
- V. I. Minkin, B. Ya. Simkin, and R. M. Minyaev, The Theory of Molecule Structure (Feniks, Rostov-on-Don, 1997) [in Russian].
- A. K. Buryak, Russ. Chem. Rev. 71, 695 (2002).
- A. V. Kiselev, Intermolecular Interactions in Adsorption and Chromatography (Vysshaya Shkola, Moscow, 1986) [in Russian].
- A. R. Katritzsky, U. Maran, V. S. Labanov, and M. Karelson, J. Chem. Inform. Comput. Sci. 40, 1 (2000).
- P. M. Zorkii, Ros. Khim. Zh. 45 (2), 3 (2001).
- V. P. Belousov and M. Yu. Panov, Thermodynamics of Aqueous Solutions of Nonelectrolytes (Khimiya, Leningrad, 1983) [in Russian].
- N. A. Smirnova, Molecular Theories of Solutions (Khimiya, Leningrad, 1987) [in Russian].
- E. V. Radchenko, V. A. Palyulin, and N. S. Zefirov, Ros. Khim. Zh. 50 (2), 76 (2006).
- A. M. Banaru, P. M. Zorkii, and A. E. Obodovskaya, Crystallogr. Rep. 52, 623 (2007).
- C. H. Gu, V. Young, and D. J. W. Grant, J. Pharm. Sci. 90, 1878 (2001).
- S. L. Price, Chem. Soc. Rev. 43, 2098 (2014).
- M. Rogalski, U. Domańska, D. Czyrny, and D. Dyczko, Chem. Phys. 285, 355 (2002).
- G. Aromi, L. A. Darrios, O. Roubeaou, and P. Gamez, Coord. Chem. Rev. 255, 485 (2011).
- Y. Polyakova, L. M. Jin, and K. H. Row, J. Liq. Chromatogr. Rel. Technol. 29, 533 (2006).
- U. Domańska, A. Pobudkowska, et al., J. Chem. Eng. Data 49, 1082 (2004).
- X. Li, C. Du, and H. Zhao, J. Chem. Thermodyn. 104, 189 (2017).
- S. N. Lanin, S. A. Rychkova, A. E. Vinogradov, K. S. Lanina, and I. A. Shatalov, Russ. Chem. Bull. 65, 110 (2016).
- A. S. Savchenkova, A. K. Buryak, and S. V. Kurbatova, Russ. J. Phys. Chem. A 89, 1662 (2015).
- V. N. Serezhkin, L. B. Serezhkina, A. P. Shevchenko, and D. V. Pushkin, Russ. J. Phys. Chem. A 79, 918 (2005).
- V. N. Serezhkin, D. V. Pushkin, and L. B. Serezhkina, Crystallogr. Rep. 55, 554 (2010).
- Cambridge Structural Database System, Version 5.32 (Crystallogr. Data Centre, Cambridge).
- A. P. Shevchenko and V. N. Serezhkin, Russ. J. Phys. Chem. A 78, 1598 (2004).
- T. Steiner, Angew. Chem. 41, 48 (2002).
- C. H. Gu, V. Young, and D. J. W. Grant, J. Pharm. Sci. 90, 1878 (2001).
- N. Yu. Bogdanov, K. A. Gorchakov, V. S. Puchnin, V. A. Stepanov, and V. S. Khmelevskaya, Crystallogr. Rep. 56, 608 (2011).