Depending on the nature of the amino group bound to the boron atom, the reactions of various aminodichloroboranes R 2 NBCl 2 with Na[(η Since 1990, when the first transition-metal complex with a two-center, two-electron bond between the metal and a threefold coordinated boron atom was structurally characterized
[1] , such boryl complexes have become of increasing interest, as they are known to be important intermediates in transition-metal-catalyzed hydroboration [2] [3]
[4] , and, very recently, the selective functionalization of alkanes in terminal position was achieved by photolysis of a boryltungsten complex [5] . During the last seven years a large number of structurally authentic boryl complexes have been described and the 1,2-dioxobenzo or "catechol" group, as ligand to boron, has had a pivotal role in obtaining these compounds, since most of them were either obtained by the reaction of an anionic transition-metal complex with CatBCl (Cat ϭ 1,2-O 2 C 6 H 4 )
[ In contrast to the well-developed chemistry of boryl transition metal complexes, knowledge about the corresponding borylene complexes is restricted to only one example (and derivatives of this).