Step-growth titanium-catalysed dehydropolymerisation of amine–boranes

Abstract

Precatalysts active for the dehydropolymerisation of primary amine–boranes are generally based on mid or late transition metal. We have found that the activity of the precatalyst system formed from Cp^R₂TiCl₂ and 2nBuLi towards the dehydrogenation of the secondary amine–borane Me₂NH·BH₃, to yield the cyclic diborazane [Me₂N–BH₂]₂, increases dramatically with increasing electron-donating character of the cyclopentadienyl rings (Cp^R). Application of the most active precatalyst system (Cp^R = η-C₅Me₅) to the primary amine–borane MeNH₂·BH₃ enabled the first synthesis of high molar mass poly(N-methylaminoborane), [MeNH–BH₂]_n, the BN analogue of polypropylene, by an early transition metal such as catalyst. Significantly, unlike other dehydropolymerization precatalysts for MeNH₂·BH₃ such as [Ir(POCOP)H₂], skeletal nickel, and [Rh(COD)Cl]₂, the Ti precatalyst system was also active towards a range of substrates including BzNH₂·BH₃ (Bz = benzyl) yielding high molar mass polymer. Moreover, in contrast to the late transition metal catalysed dehydropolymerisation of MeNH₂·BH₃ and also the Ziegler–Natta polymerisation of olefins, studies indicate that the Ti-catalyzed dehydropolymerization reactions proceed by a step-growth rather than a chain-growth mechanism.