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Synthesis and Structures of Dimesityldiboranes(4)

✍ Scribed by Herbert Hommer; Heinrich Nöth; Jörg Knizek; Werner Ponikwar; Holger Schwenk-Kircher


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
385 KB
Volume
1998
Category
Article
ISSN
1434-1948

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✦ Synopsis


  1. / B,BЈ-Di-tert-butyloxy-B,BЈdimesityldiborane(4) / B,BЈ-Dimesityl-B, BЈ-di(organylthio)diborane(4) / NMR spectroscopy / X-ray structures An efficient route to B, BЈ-dihalo-B,BЈ-dimesityldiboranes(4) observed in mes 2 B 2 I 2 , indicating that the iodide is the strongest Lewis acid in the reported series of mes 2 B 2 Y 2 is reported, as well as the conversion of these and of B,BЈdimesityl-B,BЈ-dimethoxydiborane(4) into other B,BЈ-compounds. This is also reflected in short B-C bonds. Moreover, the two mes(Y)B units also approach orthogonality dimesityldiboranes B 2 mes 2 X 2 (X = OR, SR, NR 2 , NHR). The substituents X influence the shielding of the 11 B nucleus in in these diborane(4) compounds, and thus enforce this as a typical structural feature of diborane( 4) derivatives. For this the expected manner. Hindered rotation about the B-N bond is observed for X = pyrrolyl, while in solution there is free reason, the planar C(N)B-B(N)C unit of B,BЈdi(benzylamino)-B,BЈ-dimesityldiborane( 4) is regarded as rotation about the B-C bond. However, X-ray structural results reveal that the mesityl group is almost orthogonal to exceptional for aminodiboranes(4). the B(B)CY plane in the solid state. The shortest B-B bond is

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