Catalytic Generation of Borenium Ions by Cooperative B–H Bond Activation: The Elusive Direct Electrophilic Borylation of Nitrogen Heterocycles with Pinacolborane

The
B–H bond of typical boranes is heterolytically split
by the polar Ru–S bond of a tethered ruthenium­(II) thiolate
complex, affording a ruthenium­(II) hydride and borenium ions with
a dative interaction with the sulfur atom. These stable adducts were
spectroscopically characterized, and in one case, the B–H bond
activation step was crystallographically verified, a snapshot of the
σ-bond metathesis. The borenium ions derived from 9-borabicyclo[3.3.1]­nonane
dimer [(9-BBN)2], pinacolborane (pinBH), and catecholborane
(catBH) allowed for electrophilic aromatic substitution of indoles.
The unprecedented electrophilic borylation with the pinB cation was
further elaborated for various nitrogen heterocycles.