An NHC-Stabilized H2 GeBH2 Precursor for the Preparation of Cationic Group 13/14/15 Hydride Chains.

The synthesis, characterization and reactivity studies of the NHC-stabilized complex IDipp ⋅ GeH2 BH2 OTf (1) (IDipp=1,3-bis(2,6-diisopropylphenyl)imidazolin-2-ylidene) are reported. Nucleophilic substitution of the triflate (OTf) group in 1 by phosphine or arsine donors provides access to the cationic group 13/14/15 chains [IDipp ⋅ GeH2 BH2 ERR1 R2 ]+ (2 E=P; R, R1 =H; R2 =t Bu; 3 E=P; R=H; R1 , R2 =Ph; 4 a E=P; R, R1 , R2 =Ph; 4 b E=As; R, R1 , R2 =Ph). These novel cationic chains were characterized by X-ray crystallography, NMR spectroscopy and mass spectrometry. Moreover, the formation of the parent complexes [IDipp ⋅ GeH2 BH2 PH3 ][OTf] (5) and [IDipp ⋅ GeH3 ][OTf] (6) were achieved by reaction of 1 with PH3 . Accompanying DFT computations give insight into the stability of the formed chains with respect to their decomposition.