Surface Organometallic Chemistry of Tin: Thermal Transformation, under Vacuum, of ⪫Si-O-Sn(n-Bu)3 Supported on Silica

C. Nódez, F. A. Choplin, Jean-Marie Maurice Basset, E. Benazzi

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35 Scopus citations

Abstract

The reactivity of the well-defined surface organometallic fragment ⪫Si-O-Sn(n-C4H9)31 grafted on silica200 and on silica500 has been studied by thermal treatment of 1 at increasing temperatures in vacuo. The surface reactions have been followed by quantitative measurements of the evolved gases, infrared and Mössbauer spectroscopies, 13C CP-MAS and 119Sn NMR spectroscopy, XPS measurements, and electron microscopy (CTEM and STEM EDAX). On both types of silicas, the surface reactions are similar in nature, although differences are noticeable. First, there is formation of (⪫Si-O)2(Sn(n-C4H9)2) 2, which undergoes a second solvolysis process by silanols leading to (⪫Si-O)3Sn(n-C4H9) 3 and finally surface Sn(II) and Sn(IV) atoms (as determined by XPS and Mdssbauer experiments). Although the well-defined surface organometallic compound (⪫Si-O)2Sn(n-C4H9)2 can be prepared on silica by another route, no unique surface compound can be obtained during the thermal decomposition which transforms progressively 1 into 2 and 3. A mechanism of decomposition of the various surface organometallic complexes has been deduced from a comparison of the results obtained on both solids. The alkyl groups seem to follow a β-H elimination mechanism leading to tin hydrides and 1-butene rather than a disproportionation mechanism leading to equimolar amounts of 1-butene and butane.

Original languageEnglish (US)
Pages (from-to)3039-3046
Number of pages8
JournalJournal of the American Chemical Society
Volume116
Issue number7
DOIs
StatePublished - Apr 1 1994

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

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