4.5 Article

Triptycene Boronates, Boranes, and Boron Ate-Complexes: Toward Sterically Hindered Triarylboranes and Trifluoroborates

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2021, Issue 9, Pages 1440-1445

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.202001672

Keywords

Lewis acids; Organoboron chemistry; Sterically hindered compounds; Triptycenes

Funding

  1. University of Namur
  2. Namur Institute of Structured Matter (NISM)
  3. FNRS [F.4513.18, 1.B.087.21F, 1.E.097.20F]

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Two synthetic strategies were developed to synthesize triptycene-derived bulky boranes, boronates, and boron ate-complexes with various boron substituents. The study showed the quantitative information on the effect of the triptycene scaffold on the photophysical and electronic properties of the obtained compounds through single-crystal X-ray diffraction analysis and UV-Vis/photoluminescence measurements.
We developed two synthetic strategies towards triptycene-derived bulky boranes, boronates, and boron ate-complexes. Starting from borylated or brominated anthracenes and using a Br/Li exchange and [4+2] cycloaddition reaction with in-situ generated benzyne, we produced a series of triptycene boronates and borates with various boron substituents in positions 1 and 9, such as BPin, Bneo, BF3K and B(Mes)(2). Single-crystal X-ray diffraction analysis and UV-Vis/photoluminescence measurements provided quantitative information on the effect of the triptycene scaffold on the photophysical and electronic properties of the obtained compounds.

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