Effective modulation of the donor properties of N-heterocyclic carbene Ligands by Through-Space communication within a planar chiral scaffold

A high yielding approach to planar chiral carbene ligands is described, in which an imidazo[1,5-a]pyridine-3-ylidene unit is embedded into a cyclophane scaffold. As evident from the IR data of the corresponding rhodium complex 18 as the parent member of this family, these new ligands turned out to be exceptionally strong electron donors, rivaling or even outperforming the other diaminostabilized five-membered N-heterocyclic carbenes (NHC) known to date. If the remote ring of the cyclophane is substituted by four fluorine atoms, however, the donor capacity is significantly reduced by the through-space interaction of the tetrafluorobenzene moiety with the underneath carbene entity. Since X-ray data suggest that the steric demand of the fluorinated and the nonfluorinated cyclophane-2-ylidenes are virtually identical, these results illustrate that the electronic properties of an NHC ligand can be tuned over a wide range without the need to change its constitution or steric attributes. The synthesis route leading to the planar chiral imidazopyridinium salts serving as the immediate carbene precursors involves a previously unrecognized 6 pi-Telectrocyclic ring opening reaction upon exposure of the pyridine-N -oxide 12 to N N -dimethyl-carbamoyl chloride and TMSCN, as evident from the crystal structure analysis of the resulting azatriene adduct 13.