Click functionalization in the synthesis of sorption materials. Communication I. Preparation and some sorption characteristics of silical gel with immobilized formazan with regard to Pd(II) and Cu(II)
Abstract
One of trends in the chemistry of formazans is the search of approaches to the preparation of tailor-made materials on their basis. Among such approaches is covalent immobilization of formazans onto different matrices, such as celluloses, organic resins, and silica gels. The click reactions is the interesting application creation of the molecules and materials suitable for use in the chemical analysis – ionofor, phases for a chromatography, electrochemical sensors. The examples of use of click chemistry in the field of receiving new substances and materials for analytical chemistry have caused the interest of our research group in receiving clickable hydrazone and formazan. The aims of the present were to obtain a silica gel functionalized with formazan groups through the click reaction between the alkyne group forming a part of the formazan molecule and the azido group at the silica gel surface, as well as to study some its sorption characteristics. The maximum sorption capacity of the obtained sorption material with regard to Pd(II) and Cu(II) was established, and optimum conditions for their concentration in a steady-state mode were determined. It was shown that the sorption kinetics of Cu(II) and Pd(II) on silica gel with covalently immobilized formazan can be described by the pseudo-second-order equation. The modified silica gel was illustrated to retain selectivity upon recovery of Cu(II) from systems containing a pair of competing components Cu(II)-Ni(II), Cu(II)-Co(II), and Cu(II)-Cd(II) when n(sorbate):n(functional groups capable of complexation) = 1:1.
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2. Binder W.H., Sachsenhofer R., Macromolecular Rapid Communications, 2007, Vol. 28, pp. 15-54. DOI: 10.1002/marc.200600625 available at https://onlinelibrary.wiley.com (accessed 06.05.2018)
3. Liang L., Astruc D., Coordination Chemistry Reviews, 2011, Vol. 255, pp. 2933-2945. DOI: 10.1016/j.ccr.2011.06.028 available at https://www.sciencedirect.com (accessed 06.05.2018)
4. Sokolova N.V., Nenajdenko V., RSC Advances, 2013, Vol. 3, pp. 16212-16242. DOI: 10.1039/C3RA42482K available at http://pubs.rsc.org (accessed 06.05.2018)
5. Haldon E., Nicasio M.C., Perez P.J., Organic & Biomolecular Chemistry, 2015, Vol. 13, pp. 9528-9550. DOI: 10.1039/C5OB01457C available at http://pubs.rsc.org (accessed 06.05.2018)
6. Lau Y.H., Rutledge P.J., Watkinson M., Todd M.H., Chemical Society Reviews, 2011, Vol. 40, pp. 2848-2866. DOI: 10.1039/C0CS00143K available at http://pubs.rsc.org (accessed 06.05.2018)
7. Cernat A., Tertis M., Cristea C., Sandulescu R., International Journal of Electrochemical Science, 2015, Issue 10, pp. 6324-6337.
8. Nie J., Li J.-P., Deng H., Pan H.-C., Chinese Journal of Analytical Chemistry, 2015, Vol. 43, No 4, pp. 609-617 DOI: 10.11895/j.issn.0253-3820.140925 available at http://online.analchem.cn (accessed 06.05.2018)
9. Sigeikin G.I., Lipunova G.N., Pervova I.G., Russian Chemical Reviews, 2006, Vol. 75(10), pp. 885-900. DOI: https://doi.org/10.1070/RC2006v075n10ABEH003612 available at http://www.uspkhim.ru (accessed 06.05.2018)
10. Ibrahim Y.A., Abbas A.A., Elwahy A.H.M., Journal of Heterocyclic Chemistry, 2004, Vol. 41, pp. 135-149. DOI: 10.1002/jhet.5570410202 available at https://onlinelibrary.wiley.com (accessed 06.05.2018)
11. Shawali A.S., Samy N.A., Journal of Advanced Research, 2015, Vol. 6, pp. 241-254. DOI: 10.1016/j.jare.2014.07.001 available at https://www.sciencedirect.com (accessed 06.05.2018)
12. Buzykin B.I., Lipunova G.N., Pervova I.G., Ostrovskaia V.M. et al., Progress v himii formazanov: sintez – svojstva – primenenie. Moscow, Nauchnyj mir Publ., 2009, 296 p.
13. Podchainova V.N., Bedniagina N.P., Malkina T.G., Ogloblina R.I. et al., Journal of Analytical Chemistry, 1977, Vol. 32, pp. 822-836.
14. Ostrovskaia V.M., Zaporozhets O.A., Budnikov G.K., CHernavskaia N.M., Voda. Indikatornye sistemy. M., EHKONIKS Publ., 2002, 265 p.
15. Lipunova G.N., Rusinova L.I., Maslakova T.I., Russian Journal of General Chemistry, 1996, Vol. 40, pp. 148-154.
16. Pervova I.G., Lipunova G.N., Rezinskikh Z.G., Lipunov I.N., Russian Journal of General Chemistry, 2009, Vol. 53, No 1, pp. 94-99.
17. Lipunov I.N., Pervova I.G., Lipunova G.N., Molochnikov L.S., Kovaleva E.G., Russian Journal of Coordination Chemistry, 1997, Vol. 23, No 12, pp. 934-937.
18. Pervova I.G., Lipunova G.N., Melnik T.A., Lipunov I.N., Sigeikin G.I., Russian Journal of Applied Chemistry, 2003, Vol. 76, No 7, pp. 1088-1091.
19. Grote M., Schwalk A., Kettrup A., Fresenius' Zeitschrift für analytische Chemie, 1982, Vol. 313, pp. 297-303. DOI: 10.1007/BF00486728 available at https://link.springer.com (accessed 06.05.2018)
20. Pervova I.G., Maslakova T.I., Skorykh T.V., Melnik T.A. et al., Sorbtsionnye i khromatograficheskie protsessy, 2009, Vol. 9, No 3, pp. 383-390.
21. Skorykh T.V., Maslakova T.I., Pervova I.G., Lipunov I.N., Sorbtsionnye i khromatograficheskie protsessy, 2012, Vol. 12, No 2, pp. 205-213.
22 Cestari A.R., Vieira E.F.S., Lopes E.C.N., da Silva R.G., Journal of Colloid and Interface Science, 2004, Vol. 272, pp. 271-276. DOI: 10.1016/j.jcis.2003.09.019 available at https://www.sciencedirect.com (accessed 06.05.2018)
23. Mahmoud M.E., Osman M.M., Amer M.E., Analytica Chimica Acta, 2000, Vol. 415, pp. 33-40. DOI: 10.1016/S0003-2670(00)00839-4 available at https://www.sciencedirect.com (accessed 06.05.2018)
24. Yu H.-M., Song H., Chen M.-L., Talanta, 2011, Vol. 85, pp. 625-630. DOI: 10.1016/j.talanta.2011.04.039 available at https://www.sciencedirect.com (accessed 06.05.2018)
25. Konshin V.V., Konshina Dzh.N., Temerdashev Z.A., Furina A.V. et al., . Patent RF, No 2520099, 2014.
26 Konshina D.N., Furina A.V., Temerdashev Z.A., Gurinov A.A., Konshin V.V., Analytical Letters, 2014, Vol. 47, pp. 2665-2681 DOI: 10.1080/00032719.2014.917421 available at https://www.researchgate.net (accessed 06.05.2018)
27. Schlossbauer A., Schaffert D., Kecht J., Wagner E., Bein T., Journal of the American Chemical Society, 2008, Vol. 130, pp. 12558–12559. DOI: 10.1021/ja803018w available at https://pubs.acs.org (accessed 06.05.2018)
28. Dulog L., Breitenbücher J., Liebigs Annalen der Chemie, 1993, Vol. 1993, pp. 201-202. DOI: 10.1002/jlac.199319930135 available at https://onlinelibrary.wiley.com (accessed 06.05.2018)
27 Ivanov A.V., Figurovskaia V.N., Ivanov V.M., Moscow University Chemistry Bulletin, 1992, Vol. 33, No 6, pp. 570-574.
28 SHlenskaia V.I., KHvostova V.P., Peshkova V.M., Journal of Analytical Chemistry, 1962, Vol. 17, No 5, pp. 598-603.
29. Ho Y.S., McKay G., Water research, 2000, Vol. 34, No 3, pp. 735-742. DOI: https://doi.org/10.1016/S0043-1354(99)00232-8 available at https://www.sciencedirect.com (accessed 06.05.2018)