RESUMO
A series of naphthalene-diimide (NDI) and perylene-diimide (PDI) connected bis-N-heterocyclic carbene complexes of iridium (III) have been prepared and fully characterized. The analysis of their NMR spectroscopic features, together their molecular structures show that these species display lone pair-p interactions between the chloride ligands of the Ir(III) complex and the heterocycles of the NDI/PDI moieties. The detection of this type of interaction in solution is due to the formation of two atropisomers, which are formed as a result of the restricted rotation about the Ir-Ccarbene bond imposed by the (Cl)lp p interaction. Variable temperature 1H NMR analysis allowed to determine the strength of this non-covalent interaction, which lies between DH = 6.6-10 kcal/mol. The computational studies performed fully support the experimental findings. Our study demonstrates that this type of lp p interaction is comparable to strong hydrogen bonding.