Synthesis of the Smallest Member of the Silylketene Family: H3SiC(H)=C=O

György Tarczay, Marko Förstel, Sándor Góbi, Pavlo Maksyutenko, Ralf I. Kaiser

Research output: Contribution to journalArticle

5 Citations (Scopus)


Exploiting photoionization reflectron time-of-flight mass spectrometry (PI-ReTOF-MS) combined with electronic structure calculations, it is shown that the hitherto elusive silylketene molecule (H3SiC(H)=C=O)—the isovalent counterpart of the well-known methylketene molecule—is forming via interaction of energetic electrons with low-temperature silane–carbon monoxide ices. In combination with the infrared spectroscopically detected triplet dicarbon monoxide reactant, electronic structure calculations suggest that dicarbon monoxide reacts with silane via a de facto insertion of the terminal carbon atom into a silicon–hydrogen single bond. This is followed by non-adiabatic reaction dynamics triggered by the heavy silicon atom intersystem crossing from the triplet to the singlet manifold, eventually leading to the formation of silylketene. The non-equilibrium nature of the elementary reactions within the exposed ices results in an exciting and novel chemistry which cannot be explored via traditional preparative chemistry. Since the replacement of hydrogen in silane can introduce side groups such as silyl or alkyl, the reaction of triplet dicarbon monoxide with silane represents the parent system for a previously disregarded reaction class revealing an elegant path to access the largely reactive group of silylketenes.

Original languageEnglish
Pages (from-to)882-889
Number of pages8
Issue number8
Publication statusPublished - Apr 19 2017


  • VUV laser ionization time-of-light mass spectrometry
  • astrochemical ices
  • formation mechanism
  • reactive molecules
  • silicon compounds

ASJC Scopus subject areas

  • Atomic and Molecular Physics, and Optics
  • Physical and Theoretical Chemistry

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