ABSTRACT
Amine-borane dimers and oligomers with varied steric and electronic profiles were prepared via capping agent-controlled AA/BB polycondensations. They were used for transfer hydrogenations to aldehydes, ketones, imines as well as electron-poor alkene/alkyne moieties. The amine-borane Lewis-paired oligomers and the congested bis(amine-borane)s provided the highest yields. This was likely helped by facilitated dissociation (oligomers) or H-bond assistance. In the case of the oligomers, the second equivalent of H2 present was also engaged in the reaction. Solid-state NMR characterization provides evidence that the boron-containing materials obtained after transfer dehydrogenation are highly similar to those obtained from thermal dehydrogenation. The oligomers bridge the gap between simple amine-borane molecular reductants and the poly-amine-boranes and provide a full picture of the reactivity changes at the different scales.
