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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 NH3‐BH3 (borazane) allows for a direct access to organic/inorganic hybrid dihydrogen reservoirs with a maximal H2 loading of 8 wt %. These exhibit a dehydrogenation temperature lower than that of either the borazane or the polystyrene‐g‐boramines taken separately.
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Ledoux et al. (2019) studied this question.
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