29Si-NMR study of hydrolysis and initial polycondensation processes of organoalkoxysilanes. I. Dimethyldiethoxysilane

Yoshiyuki Sugahara, Seigo Okada, Kazuyuki Kuroda, Chuzo Kato

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The hydrolysis and initial polycondensation processes of dimethyldiethoxysilane (DMDES) have been investigated by high-resolution 29Si nuclear magnetic resonance spectroscopy (NMR) in a variety of acidic system (DMDES:ethyl alcohol:water:HCl = 1:4:x:y; x = 2 or 4, 1 × 10-5 ≤ y ≤ 1 × 10-2). On the basis of the behavior of signal intensities, those due to the following monomers and oligomers have been identified: Me2Si(OEt)(OH), Me2Si(OH)2, Me2(HO)SiOSi(OH)Me2, Me2(EtO)SiOSi(OH)Me2, Me2(EtO)SiOSiMe2OSi(OH)Me2, Me2(HO)SiOSiMe2OSi(OH)Me2, (Me2SiO)3, Me2(HO)SiO(SiMe2O)2Si(OH)Me2, and (Me2SiO)4 (where Me = CH3, Et = C2H5). It was shown that the substitution of the hydroxyl group for the ethoxy group resulted in an upfield shift of a signal, which was not consistent with the previous observations in tetra-functional alkoxysilane systems. In the course of the polycondensation process, cyclization reactions became predominant to form a considerable amount of the cyclic tetramer directly from the completely hydrolyzed dimer (Me2(HO)SiOSi(OH)Me2).

Original languageEnglish
Pages (from-to)25-34
Number of pages10
JournalJournal of Non-Crystalline Solids
Issue numberC
Publication statusPublished - 1992


ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Condensed Matter Physics
  • Materials Chemistry

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