113748-68-8Relevant articles and documents
Contributions to the Chemistry of Boron, 191. - Addition and Insertion Reactions of Amino-imino-boranes with the Trihalides of Main-Group V Elements
Brandl, Andreas,Noeth, Heinrich
, p. 1321 - 1328 (2007/10/02)
The tetramethylpiperidino-imino-boranes 1a, b react with the trihalides of phosphorus, arsenic, and antimony (Hal = F, Cl, Br, with PF3 as an exception) to yield novel N-boryl-substituted amino elements dihalides 2 and 3.However, 1:1 adducts having a structure analogous to allene result with the iodides as well as with BiCl3.NMR spectra reveal no intramolecular interaction of the tetramethylpiperidino group with the element E atom in the insertion products in contrast to the X-ray result on 3b and 3e.Both molecules adapt a Ψ-trigonal bipyramidal coordination at E in the solid state.