N-Silylaminotitanium Chlorides - Synthesis, Structures, Multinuclear Magnetic Resonance, and some Applications

N‐Silylaminotitanium trichlorides, Me3S(R)N‐TiCl3 (18) [R = tBu (a), SiMe3 (b), 9‐borabicyclo[3.3.1]nonyl (9‐BBN)(c)], and (CH2SiMe2)2N‐TiCl3 (18d) were obtained in high yield and high purity from the reaction of the respective bis(silylamino)plumbylene with an excess of titanium tetrachloride. The crystal structure of 18a was determined by X‐ray analysis. The reactions of the analogous stannylenes with an excess of TiCl4 did not lead to 18. N‐Lithio‐trimethylsilyl[9‐(9‐borabicyclo[3.3.1]nonyl)]amine (8) was prepared, structurally characterized and used for the synthesis of a new bis(amino)stannylene 10 and a plumbylene 11. The compounds 18a—d served as ideal starting materials for the synthesis of bis(silylamino)titanium dichlorides, where the silylamino groups can be identical (19) or different (20). This was achieved either by the reaction of 18 again with bis(amino)plumbylenes or with lithium N‐silylamides. In contrast to the direct synthesis starting from titanium tetrachloride and two equivalents of the respective lithium amide, which in general affords 19 with identical amino groups only in low yield, the procedure starting from 18 is much more versatile and gave the pure compounds 19 or 20 in almost quantitative yield. Further treatment of the dichlorides 19 or 20 with lithium amides led to tris(amino)titanium chlorides 21. The dichlorides 19 or 20 reacted with two equivalents of alkynyllithium reagents to give the first well characterized examples of di(alkyn‐1‐yl)bis(N‐silylamino)titanium compounds 22—27. These compounds reacted with trialkylboranes (triethyl or tripropylborane) by 1, 1‐organoboration. In some cases, the extremely reactive reaction products could be identified as novel 1, 1‐bis(silylamino)titana‐2, 4‐cyclopentadienes 28—31 bearing a dialkylboryl group in 3‐position. In solution, the proposed structures of all products were deduced from a consistent set of data derived from multinuclear magnetic resonance spectroscopy (1H, 11B, 13C, 14N, 15N, 29Si, 35Cl NMR). N‐Silylaminotitanchlorides — Synthese, Strukturen, Multikern magnetische Resonanz und einige Anwendungen N‐Silylaminotitantrichloride (18), Me3S(R)N‐TiCl3 [R = tBu (a), SiMe3 (b), 9‐borabicyclo[3.3.1]nonyl (9‐BBN)(c)] und (CH2SiMe2)2N‐TiCl3 18d wurden in hoher Ausbeute und Reinheit über die Reaktion des entsprechenden Bis(silylamino)plumbylens mit einem Überschuß an Titantetrachlorid erhalten. Die Kristallstruktur von 18a wurde mittels Röntgenstrukturanalyse bestimmt. Reaktio