Self-Diffusion of Ferulic and Sinapic Acids in the Binary Carbon Tetrachloride–Acetone-d6 System
- Autores: Golubev V.1, Gurina D.1
-
Afiliações:
- G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences
- Edição: Volume 97, Nº 2 (2023)
- Páginas: 247-251
- Seção: ФИЗИЧЕСКАЯ ХИМИЯ РАСТВОРОВ
- URL: https://journals.rcsi.science/0044-4537/article/view/136518
- DOI: https://doi.org/10.31857/S0044453723020061
- EDN: https://elibrary.ru/DRIXVM
- ID: 136518
Citar
Resumo
1H NMR with a pulsed magnetic field gradient method are used to measure the coefficients of self-diffusion of ferulic and sinapic acids in binary carbon tetrachloride–acetone-d6 solvent at temperatures of 278 and 298 K. Data show that the acids’ coefficients of self-diffusion grow along with the concentration of acetone-d6 and temperature. It is shown that the effective hydrodynamic radii of acids do not depend on the composition of the binary solvent within the experimental error. In light of molecular association, this behavior can be explained by the competition between two processes: acid–acetone heteroassociation and acid–acid self-association.
Palavras-chave
Sobre autores
V. Golubev
G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences
Email: vag@isc-ras.ru
153045, Ivanovo, Russia
D. Gurina
G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences
Autor responsável pela correspondência
Email: vag@isc-ras.ru
153045, Ivanovo, Russia
Bibliografia
- Sun Y., Li Sh., Song H. et al. // Natural Product Research. 2006. V. 20 (9). P. 835. https://doi.org/10.1080/14786410500462579
- Ju H.S., Li X.J., Zhao B.L. et al. // Acta Pharmacol. Sin. 1990. V. 11. P. 466.
- Meng S., Lu Z. J., Zhang Z.N. et al. // Chin. Pharmacol. Bull. 1994. V. 10. P. 439.
- Kikuzaki H., Hisamoto M., Hirose K. et al. // J. Agricultural and Food Chemistry. 2002. V. 50. P. 2161. https://doi.org/10.1021/jf011348w
- Kumar N., Pruthi V. // Biotechnol. Rep. 2014. V. 4. P. 86.
- El-Seedi H.R., El-Said A.M.A., Khalifa S.A.M. et al. // J. Agric. Food Chem. 2012. V. 60. P. 10877. https://doi.org/10.1021/jf301807g
- Puupponen-Pimia R., Nohynek L., Alakomi H.-L. et al. // Appl. Microbiol. Biotechnol. 2005. V. 67. P. 8. https://doi.org/10.1007/s00253-004-1817-x
- Lay H.L., Shih I.J., Yeh C.H. et al. // J. Food Drug Anal. 2000. V. 8. P. 304.
- Pereira C.G., Meireles M.A.A. // Food Bioprocess Technol. 2010 V. 3. P. 340. https://doi.org/10.1007/s11947-009-0263-2
- Yamamoto M., Iwai Y., Nakajima T. et al. // J. Phys. Chem. A. 1999. V. 103. P. 3525. https://doi.org/10.1021/jp984604p
- Ke J., Jin Sh., Han B. et al. // J. Supercrit. Fluids. 1997. V. 11. P. 53. https://doi.org/10.1016/S0896-8446(97)00029-6
- Gohres J.L., Shukla C.L., Popov A.V. et al. // J. Phys. Chem. B. 2008. V. 112. P. 14993. https://doi.org/10.1021/jp806135s
- Gurina D.L., Antipova M.L., Odintsova E.G. et al. // J. Supercrit. Fluids. 2018. V. 139. P. 19. https://doi.org/10.1016/j.supflu.2018.05.004
- Gurina D.L., Antipova M.L., Odintsova E.G. et al. // Ibid. 2017. V. 126. P. 47. https://doi.org/10.1016/j.supflu.2017.02.008
- Gurina D.L., Odintsova E.G., Golubev V.A. et al. // Ibid. 2017. V. 124. P. 50.https://doi.org/10.1016/j.supflu.2017.01.012
- Golubev V.A., Gurina D.L. // Russ. J. Phys. Chem. A. 2019. V. 93. P. 447. https://doi.org/10.1134/S0036024419030075
- Price W.S. NMR Studies of Translational Motion: Principles and Applications. Cambridge University Press: Cambridge, 2009. 393 p.
- Hardt A.P., Anderson D.K., Rathbun R. et al. // J. Phys. Chem. 1959. V. 63. P. 2059. https://doi.org/10.1021/j150582a021
- Golubev V.A., Gurina D.L. // J. Mol. Liq. 2019. V. 283. P. 1. https://doi.org/10.1016/j.molliq.2019.03.038
- Vignes A. // Ind. Eng. Chem. Fundam. 1966. V. 5. P. 189. https://doi.org/10.1021/i160018a007
- Golubev V.A. // J. Mol. Liq. 2020. V. 305. P. 112813. https://doi.org/10.1016/j.molliq.2020.112813
- Monakhova Yu.B., Pozharov M.V., Zakharova T.V. et al. // J. Solution. Chem. 2014. V. 43. P. 1963. https://doi.org/10.1007/s10953-014-0249-1
- Macchioni A., Ciancaleoni G., Zuccaccia C., Zuccaccia D. // Chem. Soc. Rev. 2008. V. 37. P. 479. https://doi.org/10.1039/B615067P
- Крестов Г.А., Афанасьев В.Н., Ефремова Л.С. Физико-химические свойства бинарных растворителей. Л.: Химия, 1988. 688 с.
- Holz M., Mao X., Seiferling D. // J. Chem. Phys. 1996. V. 104. P. 669. https://doi.org/10.1063/1.470863
- Golubev V.A., Gurina D.L., Kumeev R.S. // Russ. J. Phys. Chem. A. 2018. V. 92. P. 75. https://doi.org/10.1134/S0036024418010090
- Golubev V.A., Kumeev R.S., Gurina D.L. et al. // J. Mol. Liq. 2017. V. 241. P. 922. https://doi.org/10.1016/j.molliq.2017.06.102
- Golubev V.A. // Ibid. 2018. V. 264. P. 314. https://doi.org/10.1016/j.molliq.2018.05.083
- Golubev V.A., Gurina D.L. // Ibid. 2021. V. 326. P. 115230. https://doi.org/10.1016/j.molliq.2020.115230
- Cabrita E.J., Berger S. // Magn. Reson. Chem. 2001. V. 39. P. 142. https://doi.org/10.1002/mrc.917