Acta Crystallographica Section E: Crystallographic Communications (Feb 2024)

Synthesis and crystal structures of boryl ortho-silylaryl trifluoromethanesulfonates

  • Fredrik Barnå,
  • Matic Hribersek,
  • Andreas Orthaber,
  • Lukasz T. Pilarski

DOI
https://doi.org/10.1107/S2056989024000264
Journal volume & issue
Vol. 80, no. 2
pp. 143 – 147

Abstract

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We report the synthesis and structural characterization of three crystalline borylated ortho-silylaryl trifluoromethanesulfonates: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trimethylsilyl)phenyl trifluoromethanesulfonate, C16H24BF3O5SSi (1a), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trimethylsilyl)phenyl trifluoromethanesulfonate, C16H24BF3O5SSi (1b), and 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trimethylsilyl)phenyl trifluoromethanesulfonate, C17H26BF3O5SSi (2), which are versatile aryne precursors. For all three compounds, the heteroatom substituents are almost coplanar with the central aromatic moiety. C—heteroatom bonding metrics are unexceptional and fall withing the typical range of C—B, C—Si, and C—O single bonds. Despite numerous electronegative sites, only weak intermolecular interactions are observed in the solid state.

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