Synthesis and Structural Diversity of Barium (N,N-Dimethylamino)diboranates
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The reaction of a slurry of BaBr2 in a minimal amount of tetrahydrofuran (THF) with 2 equiv of Na(H3BNMe2BH3) in diethyl ether followed by crystallization from diethyl ether at 鈭?0 掳C yields crystals of Ba(H3BNMe2BH3)2(Et2O)2 (1). Drying 1 at room temperature under vacuum gives the partially desolvated analogue Ba(H3BNMe2BH3)2(Et2O)x (1鈥?/b>) as a free-flowing white solid, where the value of x varies from <0.1 to about 0.4 depending on whether desolvation is carried out with or without heating. The reaction of 1 or 1鈥?/b> with Lewis bases that bind more strongly to barium than diethyl ether results in the formation of new complexes Ba(H3BNMe2BH3)2(L), where L = 1,2-dimethoxyethane (2), N,N,N鈥?N鈥?tetramethylethylenediamine (3), 12-crown-4 (4), 18-crown-6 (5), N,N,N鈥?N鈥?tetraethylethylenediamine (6), and N,N,N鈥?N鈥?N鈥?pentamethylethylenetriamine (7). Recrystallization of 4 and 5 from THF affords the related compounds Ba(H3BNMe2BH3)2(12-crown-4)(THF)路THF (4鈥?/b>) and Ba(H3BNMe2BH3)2(18-crown-6)路2THF (5鈥?/b>). In addition, the reaction of BaBr2 with 2 equiv of Na(H3BNMe2BH3) in the presence of diglyme yields Ba(H3BNMe2BH3)2(diglyme)2 (8), and the reaction of 1 with 15-crown-5 affords the diadduct [Ba(15-crown-5)2][H3BNMe2BH3]2 (9). Finally, the reaction of BaBr2 with Na(H3BNMe2BH3) in THF, followed by the addition of 12-crown-4, affords the unusual salt [Na(12-crown-4)2][Ba(H3BNMe2BH3)3(THF)2] (10). All of these complexes have been characterized by IR and 1H and 11B NMR spectroscopy, and the structures of compounds 1鈥?b>3, 4鈥?/b>, 5鈥?/b>, and 6鈥?b>10 have been determined by single-crystal X-ray diffraction. As the steric demand of the Lewis bases increases, the structure changes from polymers to dimers to monomers and then to charge-separated species. Despite the fact that several of the barium complexes are monomeric in the solid state, none is appreciably volatile up to 200 掳C at 10鈥? Torr.

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