Why Does the Intramolecular Trimethylene-Bridged Frustrated Lewis Pair Mes2 PCH2 CH2 CH2 B(C6 F5 )2 Not Activate Dihydrogen?

Abstract

The methyl labelled C3 -bridged frustrated phosphane borane Lewis pair (P/B FLP) 2 b was prepared by treatment of Mes2 PCl with a methallyl Grignard reagent followed by anti-Markovnikov hydroboration with Piers' borane [HB(C6 F5 )2 )]. The FLP 2 b is inactive toward dihydrogen under typical ambient conditions, in contrast to the C2 - and C4 -bridged FLP analogues. Dynamic NMR spectroscopy showed that this was not due to kinetically hindered P⋅⋅⋅B dissociation of 2 b. DFT calculations showed that the hydrogen-splitting reaction of the parent compound 2 a is markedly endergonic. The PH(+) /BH(-) H2 -splitting product of 2 b was indirectly synthesized by a sequence of H(+) /H(-) addition. It lost H2 at ambient conditions and confirmed the result of the DFT analysis.

Keywords: boron; density functional calculations; dihydrogen activation; frustrated Lewis pair; phosphorus.