Tuning N-heterocyclic carbenes in T-shaped Pt ^II complexes for intermolecular C-H bond activation of arenes

Small change matters: T-shaped Pt ^II complexes with less flexible substituents, than, for example, isopropyl or tert-butyl groups, on N-heterocyclic carbene (NHC) ligands allow for C-H bond activation reactions of aromatic compounds (see scheme; BAr ^f ₄ ^-= tetrakis[(3,5-trifluoromethyl)phenyl]borate; F yellow, Pt red). NHC substituents that are not highly branched prevent agostic interactions and reduce the barriers to achieve the C-H bond cleavage.