The behavior of a variety of Lewis bases toward diphenylberyllium has been investigated, demonstrating the high Lewis acidity and electron deficiency of diphenylberyllium. A range of monodentate donors with vastly different steric and electronic properties were used, namely, pyridine, NEt 3 , THF, THT, and PMe 3 . The Be-donor bond strength was investigated through application of vacuum, and transformations between the mono-and disubstituted beryllium centers were investigated through stoichiometric addition of additional BePh 2 . Strong electron donors (Nheterocyclic carbenes) with vastly different steric profiles were then investigated, highlighting that steric interactions are more dominant than electronics. Adducts of bidentate ligands with O-, N-, and Pdonating sites were also produced.