- PII
- 10.31857/S0044457X23600895-1
- DOI
- 10.31857/S0044457X23600895
- Publication type
- Status
- Published
- Authors
- Volume/ Edition
- Volume 68 / Issue number 10
- Pages
- 1373-1378
- Abstract
- The behavior of borylated iminols based on the closo-decaborate and closo-dodecaborate anions in the dichloromethane–water system has been studied as a function of the pH of the aqueous phase. The distribution coefficients of compounds in the n-octanol–water system have been determined: for (Bu4N)[B12H11NHC(OH)CH3], log Kow = –0.46; for (Bu4N)[2-B10H9NHC(OH)CH3], log Kow = –0.51. These compounds show hydrophilic properties similar to those of formic and acetic acids. It has been shown that this method can be used to purify target compounds from hydrolysis products in the preparation of various derivatives as a result of nucleophilic addition of the closo-borate anions to nitrilium derivatives.
- Keywords
- <i>клозо</i>-додекаборатный анион <i>клозо</i>-декаборатный анион нитрилиевые производные иминолы ВЭЖХ
- Date of publication
- 01.10.2023
- Year of publication
- 2023
- Number of purchasers
- 0
- Views
- 40
References
- 1. Zhang Y., Liu J., Duttwyler S. // Eur. J. Inorg. Chem. 2015. V. 2015. № 31. P. 5158. https://doi.org/10.1002/ejic.201501009
- 2. Messina M.S., Axtell J.C., Wang Y. et al. // J. Am. Chem. Soc. 2016. V. 138. № 22. P. 6952. https://doi.org/10.1021/jacs.6b03568
- 3. Bolli C., Derendorf J., Jenne C. et al. // Chem. Eur. J. 2014. V. 20. № 42. P. 13783. https://doi.org/10.1002/chem.201403625
- 4. Grüner B., Bonnetot B., Mongeot H. // Collect. Czech. Chem. Commun. 1997. V. 62. № 8. P. 1185. https://doi.org/10.1135/cccc19971185
- 5. Sivaev I.B., Bregadze V.I., Sjöberg S. // Collect. Czech. Chem. Commun. 2002. V. 67. № 6. P. 679. https://doi.org/10.1135/cccc20020679
- 6. Nelyubin A.V., Klyukin I.N., Novikov A.S. et al. // Inorganics. 2022. V. 10. № 11. P. 196. https://doi.org/10.3390/inorganics10110196
- 7. Bogdanova E.V., Stogniy M.Yu., Suponitsky K.Yu. et al. // Molecules. 2021. V. 26. № 21. P. 6544. https://doi.org/10.3390/molecules26216544
- 8. Laskova J., Ananiev I., Kosenko I. et al. // Dalton Trans. 2022. V. 51. № 8. P. 3051. https://doi.org/10.1039/D1DT04174F
- 9. Nelyubin A.V., Selivanov N.A., Bykov A.Yu. et al. // Int. J. Molecular Sci. 2021. V. 22. № 24. P. 13391. https://doi.org/10.3390/ijms222413391
- 10. Losytskyy M.Yu., Kovalska V.B., Varzatskii O.A. et al. // J. Lumin. 2016. V. 169. P. 51. https://doi.org/10.1016/j.jlumin.2015.08.042
- 11. Kimura S., Masunaga S., Harada T. et al. // Bioorg. Med. Chem. 2011. V. 19. № 5. P. 1721. https://doi.org/10.1016/j.bmc.2011.01.020
- 12. Fedotova M.K., Usachev M.N., Bogdanova E.V. et al. // Bioengineering. 2021. V. 9. № 1. P. 5. https://doi.org/10.3390/bioengineering9010005
- 13. Zhang Y., Sun Y., Wang T. et al. // Molecules. 2018. V. 23. № 12. P. 1. https://doi.org/10.3390/molecules23123137
- 14. Varkhedkar R., Yang F., Dontha R. et al. // ACS Central Sci. 2022. V. 8. № 3. P. 322. https://doi.org/10.1021/acscentsci.1c01132
- 15. Sun Y., Zhang J., Zhang Y. et al. // Chem. Eur. J. 2018. V. 24. № 41. P. 10364. https://doi.org/10.1002/chem.201801602
- 16. Nelyubin A.V., Sokolov M.S., Selivanov N.A. et al. // Russ. J. Inorg. Chem. 2022. V. 67. № 11. P. 1751. https://doi.org/10.1134/S003602362260109X
- 17. Nelyubin A.V., Selivanov N.A., Bykov A.Yu. et al. // Russ. J. Inorg. Chem. 2022. V. 67. № 11. P. 1776. https://doi.org/10.1134/S0036023622601106
- 18. Nelyubin A.V., Klyukin I.N., Novikov A.S. et al. // Mendeleev Commun. 2021. V. 31. № 2. P. 201. https://doi.org/10.1016/j.mencom.2021.03.018
- 19. Zhdanov A.P., Klyukin I.N., Bykov A.Y. et al. // Polyhedron. 2017. V. 123. P. 176. https://doi.org/10.1016/j.poly.2016.11.035
- 20. Nelyubin A.V., Klyukin I.N., Zhdanov A.P. et al. // Russ. J. Inorg. Chem. 2019. V. 64. № 14. P. 1750. https://doi.org/10.1134/S0036023619140043
- 21. Šícha V., Plešek J., Kvíčalová M. et al. // Dalton Trans. 2009. № 5. P. 851. https://doi.org/10.1039/B814941K
- 22. Stogniy M.Y., Erokhina S.A., Sivaev I.B. et al. // Phosphorus, Sulfur Silicon Relat. Elem. 2019. V. 194. P. 1. https://doi.org/10.1080/10426507.2019.1631312
- 23. Guangxian X., Jimei X., Technolgy S. // New Frontiers in Rare Earth Science and Applications. 1985. https://doi.org/10.1016/c2013-0-11730-8
- 24. Нелюбин А.В., Клюкин И.Н., Селиванов Н.А. и др. // Журн. неорган. химии. 2023. Т. 68. № 6. С. 768. https://doi.org/10.31857/S0044457X22602310
- 25. Yang S.T., White S.A., Hsu S.T. // Ind. Eng. Chem. Res. 1991. V. 30. № 6. P. 1335. https://doi.org/10.1021/ie00054a040
- 26. Dupont-Leclercq L., Giroux S., Henry B. et al. // Langmuir. 2007. V. 23. № 21. P. 10463. https://doi.org/10.1021/la7017488
- 27. Fu H., Sun Y., Teng H. et al. // Sep. Purif. Technol. 2015. V. 139. P. 36. https://doi.org/10.1016/j.seppur.2014.11.001
- 28. Zhdanov A.P., Bykov A.Y., Kubasov A.S. et al. // Russ. J. Inorg. Chem. 2017. V. 62. № 4. P. 468. https://doi.org/10.1134/S0036023617040210
- 29. Dearden J.C., Bresnen G.M. // Quantitative Structure-Activity Relationships. 1988. V. 7. № 3. P. 133. https://doi.org/10.1002/qsar.19880070304
- 30. Grüner B., Plzák Z. // J. Chromatogr. A. 1997. V. 789. № 1–2. P. 497. https://doi.org/10.1016/S0021-9673 (97)00497-4
- 31. Horáček O., Papajová-Janetková M., Grüner B. et al. // Talanta. 2021. V. 222. P. 121652. https://doi.org/10.1016/j.talanta.2020.121652
