Tunable Hydrogen Release from Amine-Boranes via their Insertion into Functional Polystyrenes.

Polystyrene-g-boramine random copolymers are dihydrogen reservoirs with tunable dehydrogenation temperatures, which can be adjusted by selecting the boramine content in the copolymers. They display a unique dihydrogen thermal release profile, which is a direct consequence of the insertion of the amine-boranes in a polymeric scaffold, and not from a direct modification of the electronics or sterics of the amine-borane function. Finally, the mixture of polystyrene-g-boramines with conventional NH -BH (borazane) allows for a direct access to organic/inorganic hybrid dihydrogen reservoirs with a maximal H loading of 8 wt %.

Polyboramines for Hydrogen Release: Polymers Containing Lewis Pairs in their Backbone.

The one-step polycondensation of diamines and diboranes triggered by the in situ deprotonation of the diammonium salts and concomitant reduction of bisboronic acids leads to the assembly of polymer chains through multiple Lewis pairing in their backbone. These new polyboramines are dihydrogen reservoirs that can be used for the hydrogenation of imines and carbonyl compounds. They also display a unique dihydrogen thermal release profile that is a direct consequence of the insertion of the amine-borane linkages in the polymeric backbone.