Mono- and dinuclear group 3 metal complexes incorporating polydentate bis(imino)phenoxy {(NO)-O-2}(-) and bis(amido)phenoxy {(NO)-O-2}(3-) ligands were synthesized by alkane elimination reactions from the tris(alkyl) M(CH2SiMe3)(3) (THF)(2) and M(CH2C6H4-o-NMe2)(3) (M = Sc, Y) precursors. Complex laY was used for the selective C-H activation of 2-phenylpyridine at the 2'-phenyl position affording the corresponding bis(aryl) product 3a-Y, which was found to be reacted reluctantly with weak electrophiles (styrene, imines, hydrosilanes). The mechanism of formation of 3a-Y was established by DFT calculations, which also corroborated high stability of the complex toward insertion of styrene, apparently stemming from the inability to form the corresponding adduct. Copolymerization of cyclohexene oxide and CO2 promoted by 1a-Y (0.1-0.5 mol %) was demonstrated to proceed under mild conditions (toluene, 70 P-CO2 = 12 bar) giving polycarbonates with high efficiency (maximal TON of 460) and selectivity (97-99% of carbonate units).