The heteroleptic complex LZnEt [(1); L = MeNacac = MeNC(Me)CHC(Me)O] containing the sterically less demanding N,O-chelating ketoiminate (MeNacac) ligand was synthesized by reaction of ZnEt 2 with an equimolar amount of MeNacacH, whereas the reaction with two equivalents MeNacacH gave the homoleptic complex L 2 Zn 5. 1 reacts with ArOH (Ar = 2,6-Me 2 -Ph) with ethane elimination and formation of LZnOAr (2). Addition of the Lewis base dmap (dmap = 4-dimethylamino pyridine) to 1 and 2 yielded the corresponding Lewis acid-base adducts dmap-Zn(L)Et 3 and dmap-Zn(L)OAr 4. Compounds 1-5 were characterized by heteronuclear NMR ( 1 H, 13 C) and IR spectroscopy, elemental analysis, and single-crystal X-ray dif-[a] Synthesis and Characterization The reaction of ketoimine LH [L = MeNacac = MeNC(Me)-CHC(Me)O] with an equimolar amount of diethylzinc in THF at -60°C occurred with elimination of ethane and formation of Scheme 1. Synthesis of 1-5.