ABSTRACT
p-Diarylboryl halothiophenols are developed and unequivocally characterized. Their photophysical properties and catalytic performance are unveiled by experimental and theoretical investigations. This novel class of triarylboranes behaves as a Brønsted acid to generate the corresponding borylthiophenolate that can absorb visible light to undergo intramolecular charge transfer to form a radical pair consisting of a boron radical anion and thiyl radical, which acts as a single-electron reductant while engaging in hydrogen atom transfer to regenerate the parent borylthiophenol. The synthetic relevance of this mode of action is demonstrated by the establishment of unique catalysis that integrates three different yet tunable functions in a single catalytic cycle, thereby allowing borylthiophenols to solely promote the assembly of sterically congested 1,2-diols and 1,2-aminoalcohol derivatives via radical-radical cross-coupling.
