In this report, we investigate the interactions of MexMCl3-x (x = 0-3, M = Al, Go) with various aromatic and alkyl-substituted 1,4-diaza-1,3-butadiene (R)DAB ligands (or a-diimine ligands) to give a variety of structures in solution and in the solid state. In combination with other previously reported structures, certain general trends of reactivity of these species can be deduced, although there are still some unexplained modes of reactivity. The methylated Al species react with aromatic-substituted RDAB ligands to provide final products that result from C=N insertion into the Al-CH3 group followed by rearrangement reactions. The addition of methyl groups onto the backbone of the (R)DAB ligand is insufficient to stop the insertion and rearrangement processes from occurring. In the case of MeAlCl2 with the bulky (DiPP)DAB ligand, the reaction could be followed spectroscopically from the monoadduct through the inserted/rearranged final product. Methylated Ga species, however, are much less predictable in their behavior with aromatic-substituted (R)DAB ligands. Depending on the exact species and ratios used, coordinated adduct; can be formed and identified, or inserted/rearranged products similar to the aluminum Tractions can be obtained. Quite interestingly, cation/anion pairs can also be formed in which GaCl3 or MeGaCl2 act as a chloride acceptors. This behavior was unique and substantially different from the analogous Al reactions which formed either a dicoordinated adduct or an inserted/rearranged complex. When the stronger-donating alkyl-substituted (R)DAB ligands were used with Me2GaCl, only cation/anion pairs were obtained. Surprisingly, when the same reactions were performed using Me2AlC). as a reagent, irreproducible results were obtained.