Isolation of a three-coordinate boron cation with a boron-sulfur double bond.

The reaction of the bulky bis(imidazolin-2-iminato) ligand precursor (1,2-(L(Mes)NH)2-C2H4)[OTs]2 (1(2+)  2[OTs](-); L(Mes) = 1,3-dimesityl imidazolin-2-ylidene, OTs = p-toluenesulfonate) with lithium borohydride yields the boronium dihydride cation (1,2-(L(Mes)N)2-C2H4)BH2[OTs] (2(+)  [OTs](-)). The boronium cation 2(+)  [OTs](-) reacts with elemental sulfur to give the thioxoborane salt (1,2-(L(Mes)N)2-C2H4)BS[OTs] (3(+)  [OTs](-)). The hitherto unknown compounds 1(2+)  2[OTs](-), 2(+)  [OTs](-), and 3(+)  [OTs](-) were fully characterized by spectroscopic methods and single-crystal X-ray diffraction. Moreover, DFT calculations were carried out to elucidate the bonding situation in 2(+) and 3(+). The theoretical, as well as crystallographic studies reveal that 3(+) is the first example for a stable cationic complex of three-coordinate boron that bears a B=S double bond.