The reaction of SrBr2 with 2 equiv of sodium N,N-dimethylaminodiboranate (DMADB; Na(H3BNMe2BH3)) in Et2O at 0 degrees C followed by crystallization and drying under vacuum gives the unsolvated strontium compound Sr(H3BNMe2BH3)(2) (1). Before the vacuumdrying step, the colorless crystals obtained by crystallization consist of the diethyl ether adduct Sr(H3BNMe2BH3)(2) (Et2O)(2) (2). If the reaction of SrBr2 with 2 equiv of Na(H3BNMe2BH3) is carried out in the more strongly coordinating solvent thf, the solvate Sr(H3BNMe2BH3)(2)(thf)(3) (3) is obtained. Treating the thf adduct 3 with 1,2-dimethoxyethane (dme), bis(2-methoxyethyl) ether (diglyme), or N,N,N',N'-tetramethylethylenediamine (tmeda) in thf affords the new compounds Sr(H3BNMe2BH3)(2) (dme)(2) (4), Sr(H3BNMe2BH3)(2) (diglyme) (5), and Sr(H3BNMe2BH3)(2) (tmeda) (6), respectively, in greater than 60% yields. Treatment of 3 with 2 equiv of the crown ether 12-crown-4 affords the charge-separated salt [Sr(H3BNMe2BH3)(12-crown-4)(2)][H3BNMe2BH3] (7). Crystal structures of all the Lewis base adducts are described. Compounds 2-6 all possess chelating kappa(2)-BH3NMe2BH3-kappa(-2) groups, in which two hydrogen atoms on each boron center are bound to strontium. Compound 6 is dinuclear because each metal atom is also coordinated to one hydrogen atom on a BH3NMe2BH3- ligand that chelates to the neighboring metal center. Compound 7 possesses an unusual kappa(1)-BH3NMe2BH3- group owing to the near-complete encapsulation of the Sr atom by two 12-crown-4 molecules; the other BH3NMe2BH3- anion is a charge-separated counterion. When they are heated, the diglyme and tmeda compounds 5 and 6 melt without decomposition and can be sublimed readily under reduced pressure (1 Ton) at 120 degrees C. The diglyme and tmeda adducts are some of the most volatile strontium compounds known and are promising candidates as CVD precursors for the growth of strontium-containing thin films.