Gas-Chromatographic Identification of Unusual Unstable Products of the Partial Hydrolysis of Tetraethoxysilane

Cover Page

Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Gas chromatographic analysis of a long-stored sample of tetraethoxysilane (tetraethyl orthosilicate) showed that it lacked the main component due to the hydrolysis of this compound by traces of water. Instead, ethanol and three other components with retention indices (RIs) of 537 ± 2 (no. 1), 608 ± 1 (no. 2, the most abundant component), and 727 ± 3 (no. 3) on a column with a HP-5 stationary phase were detected. These components are unstable, and they cannot be isolated preparatively; as a result, they have not been characterized previously. To identify them, the chemical properties of this sample were characterized, and the recurrent approximations of the RIs of the detected components and their correlation with the retention indices of structural analogs were considered. It was established that they were congeners of the initial tetraethoxysilane, namely, exotic products of its partial hydrolysis—triethoxysilanol (C2H5O)3SiOH, diethoxysilanediol (C2H5O)2Si(OH)2, and ethoxysilanetriol (C2H5O)Si(OH)3. In accordance with published data, some silanediols R2Si(OH)2 and silanetriols RSi(OH)3 are stable, especially, compounds containing substituents capable of conjugation with vacant d orbitals of silicon atoms. Among them are phenyl- (π–d conjugation systems) and alkoxy-substituted (p–d systems) silanediols and silanetriols. The identified products of partial hydrolysis of tetraethoxysilane belong to the latter type.

About the authors

I. G. Zenkevich

Institute of Chemistry, St. Petersburg State University

Email: izenkevich@yandex.ru
198504, St. Petersburg, Russia

D. A. Baranov

Institute of Chemistry, St. Petersburg State University

Author for correspondence.
Email: izenkevich@yandex.ru
198504, St. Petersburg, Russia

References

  1. Middleditch B.S. Analytical Artifacts: GC, MS, HPLC, TLC, and PC. Amsterdam: J. Chromatogr. Library. V. 44. 1989. 1033 p.
  2. Zenkevich I.G. Features and new examples of gas chromatographic separation of thermally unstable analytes / Chapter XX in “Recent advances in gas chromatography”. London: IntechOpen Ltd. 2020. P. 1. https://doi.org/10.5772/intechopen.94229
  3. The NIST Mass Spectral Library (NIST/EPA/NIH EI MS Library, 2020 Release). Software/Data Version; NIST Standard Reference Database, Number 69, May 2020. National Institute of Standards and Technology, Gaithersburg, MD 20899: http://webbook.nist.gov (дата обращения: апрель 2022 г.).
  4. Rama S., Zhang Y., Tchuenbou-magala F., Ding Y., Li Y. Encapsulation of 2-amino-2-methyl-1-propanol with tetraethyl orthosilicate for CO2 capture // Frontiers Chem. Sci. Eng. 2019. V. 13. № 4. P. 672. https://doi.org/1007/s11705-019-1856-6
  5. Ramamurthy A.S., Eglal M.M. Degradation of TCE by TEOS coated nZVI in the presence of Cu(II) for groundwater remediation // J. Nanomaterials. 2014. Article 606534. https://doi.org/10.1155/2014/606534
  6. Arkles B., Steinmetz J.R., Zazyczny J., Mehta P. Factors contributing to the stability of alkoxysilanes in aqueous solutions / Silanes and Other Coupling Agents / Ed. Mittal K.L. Utrecht: VSP, 1992. P. 91.
  7. Braddock D.C., Lickiss P.D., Rowley B.C., Pugh B.C.R., Purnomo T., Santhakumar G., Fussell S.J. Tetramethyl orthosilicate (TMOS) as a reagent for direct amidation of carboxylic acids // Org. Lett. 2018. V. 20. P. 950.
  8. The Merck Index – An Encyclopedia of Chemicals, Drugs, and Biological / Ed. O’Neil M.J. Whitehouse Station: Merck and Co. Inc., 2006. 657 p.
  9. Lide R.C. CRC Handbook of Chemistry and Physics. 88th Ed. Boca Raton: CRC Press (Taylor & Francis Group), 2007. P. 3.
  10. Taylor J.H. Gas chromatographic separation and infrared analysis of ethyl propyl silicates // J. Chromatogr. Sci. 1968. V. 6. № 11. P. 557. https://doi.org/10.1093/chromsci/6.11.557
  11. Ellren O., Peetre I.-B., Smith B.E.B. Gas chromatographic investigation of organometallic compounds and their carbon analogues. I. Determination, calculation, and correlation of Kovats retention indices for tetraalkoxysilanes // J. Chromatogr. 1974. V. 88. P. 295. https://doi.org/10.1016/S0021-9673(00)83154-4
  12. Peetre I.-B. Gas chromatographic investigation of organometallic compounds and their carbon analogues. II. Improved method for calculating retention indices of tetraalkoxysilanes // J. Chromatogr. 1974. V. 88. P. 311. https://doi.org/10.1016/S0021-9673(00)83155-6
  13. Крешков А.П., Кириченко Е.А., Марков Б.А. Индексы удерживания алкоксихлорсилано в // Журн. аналит. химии. 1975. Т. 30. № 2. С. 345.
  14. Иванова Н.Т., Франгулян Л.А. Газохроматографический анализ нестабильных и реакционноспособных соединений. М.: Химия, 1979. 232 с.
  15. Kovats’ retention index system / Encyclopedia of Chromatography. 3rd Ed. / Ed. Cazes J. Boca Raton: CRC Press (Taylor & Francis Group), 2010. V. 2. P. 1304.
  16. Stein S.E., Babushok V.I., Brown R.L., Linstrom P.J. Estimation of Kovats retention indices using group contributions // J. Chem. Inf. Model. 2007. V. 47. P. 975. https://doi.org/10.1021/ci600548y
  17. Lim J., Ha S.-W., Lee J.-K. Precise size-control of silica nanoparticles via alkoxy exchange equilibrium of tetraethyl orthosilicate (TEOS) in the mixed alcohol solution // Bull. Korean Chem. Soc. 2021. V. 33. № 3. P. 1067. https://doi.org/10.5012/bkcs.2012.33.3.1067
  18. Derivatization of analytes in chromatography: General aspects / Encyclopedia of Chromatography. 3rd Ed. / Ed. Cazes J. Boca Raton: CRC Press (Taylor & Francis Group), 2010. V. 1. P. 562.
  19. Compounds: Derivatization for GC analysis / Encyclopedia of Chromatography. 3rd Ed. / Ed. Cazes J. Boca Raton, CRC Press (Taylor & Francis Group), 2010. V. 2. P. 1165.
  20. Зенкевич И.Г., Лукина В.М. Хромато-масс-спектрометрическая характеристика диэтилкеталей алифатических карбонильных соединений // Аналитика и контроль. 2019. Т. 23. № 3. С. 410. https://doi.org/10.15826/analitika.2019.23.3.009
  21. Zenkevich I.G. Application of recurrent relationships in chromatography // J. Chemometrics. 2009. V. 23. P. 179. https://doi.org/10.1002/cem.1214
  22. Zenkevich I.G. Recurrent relationships in separation science / Chemometrics in Chromatography / Eds. Komsta L, Heyden Y.V, Sherma J. New York: Taylor & Francis, 2017. Ch. 24. P. 449.
  23. Toyoda T., Matsumoto T., Arakawa T. Jet printing ink composition. Patent USA. 1982. № 4,338,133.
  24. Kazakova V.V., Gorbatsevich O.B., Skvortsova S.A., Demchenko N.V., Muzafarov A.M. Synthesis of triethoxyxilanol // Russ. Chem. Bull. Int. Ed. 2005. V. 54. № 5. P. 1350.
  25. Nobutami K., Masao K. The crystal structure of diallylsilanediol // Bull. Chem. Soc. Jap. 1954. V. 27. № 9. P. 605. https://doi.org/10.1246/bcsj.27.605
  26. Tyler L. Phenylsilanetriol // J. Am. Chem. Soc. 1955. V. 77. № 3. P. 770. https://doi.org/10.1021/ja1608a078
  27. Korkin S.D., Buzin M.I., Matukhina E.V., Zherlitsyna L.N., Auner N., Shchegolikhina O.I. Phenylsilanetriol – Synthesis, stability, and reactivity // J. Organomet. Chem. 2003. V. 686. № 1–2. P. 313. https://doi.org/10.1016/S0022-328X(03)00721-6
  28. Jha S.K., Marina N., Liu C., Hayashi K. Human body odor discrimination by their GC-MS spectra data mining // Anal. Methods. 2015. № 7. P. 9549. https://doi.org/10.1039/C4AY02457A
  29. Pratana R.I., Yuniar I., Hamdani H., Rostini I. Volatile flavor compounds composition of fresh and steamed tiger shrimp (Penaeus monodon) // Int. J. Fish. Aquat. Res. 2019. V. 4. № 1. P. 25.
  30. Stefanikova J., Arvay J., Miskeje M., Kacaniova M. Determination of volatile organic compounds in Slovak bryndza cheese by the electronic nose and the headspace solid-phase microextraction gas chromatography – mass spectrometry // Slovak J. Food Sci. 2020. V. 14. P. 767. https://doi.org/10.5219/1300

Supplementary files

Supplementary Files
Action
1. JATS XML
2.

Download (73KB)
3.

Download (77KB)
4.

Download (15KB)
5.

Download (55KB)
6.

Download (42KB)
7.

Download (40KB)
8.

Download (47KB)

Copyright (c) 2023 И.Г. Зенкевич, Д.А. Баранов

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies