Binary interpnictogen compounds bearing diaryl bismuth fragments bound to all lighter pnictogens.
Tobias DunajKevin DollbergCarsten von HänischPublished in: Dalton transactions (Cambridge, England : 2003) (2022)
Multiple interpnictogen compounds with covalent single bonds between a diarylbismuth fragment and all lighter pnictogens were prepared from the corresponding diarylhalido bismuthanes. The aminobismuthanes Ph 2 BiNMe 2 (1) and Mes 2 BiNMe 2 (2) (Mes = 2,4,6-trimethylphenyl-) have been obtained via a salt metathesis reaction and compound 2 was successfully reacted with t BuNH 2 in a condensation reaction to yield Mes 2 BiNH t Bu (3). The bismuthanyl phosphanes Ar 2 BiP t Bu 2 (Ar = Ph: 4 and Ar = Mes: 5) and arsanes Ar 2 BiAs t Bu 2 (Ar = Ph: 8 and Ar = Mes: 9) were also obtained via salt metathesis. Through a trimethylsilyl halide abstraction reaction of the diaryl halido bismuthanes and E t Bu(SiMe 3 ) 2 (E = P and As), the bismuthanyl phosphanes Ar 2 BiP t Bu(SiMe 3 ) (Ar = Ph: 6; Ar = Mes: 7) and the arsanes Ar 2 BiAs t Bu(SiMe 3 ) (Ar = Ph: 10; Ar = Mes: 11) have been prepared. Bismuthanyl stibanes were accessed via a condensation reaction of Mes 2 SbH with 1 or 2, respectively. The compound Ph 2 BiSbMes 2 (12), which has different substituents at the bismuth and antimony atoms, was isolated and fully characterised. In contrast, the isolation of Mes 2 BiSbMes 2 (13) was not possible due to a dynamic equilibrium with Mes 4 Bi 2 and Mes 4 Sb 2 which was investigated via low-temperature 1 H-NMR spectroscopy in solution. The isolated compounds with a single bond between bismuth and the heavy pnictogens arsenic and antimony are rare examples of their kind. All isolated compounds (1-12) were characterised by NMR and IR spectroscopy, mass spectrometry, elemental analysis and single crystal X-ray diffraction.