Abstract

The solventless reaction of diisopropylaminoborane with n-butylamine, at room temperature, leads to a mixture of B(sp2) H-, B(sp3) H2 -, and B(sp3) H3 -containing species. At low temperature, the reaction outcome is completely modified, thus leading selectively to the formation of high-mass polybutylaminoborane. When extended to a variety of primary amines, under solventless conditions and at low temperature, this reaction provides a new, efficient, and direct metal-free access to high-molecular-mass polyaminoboranes in good to high yields under mild reaction conditions.

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