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Updated: Dec 27, 2025

A Simple and Efficient Protocol for the Catalytic Insertion Polymerization of Functional Norbornenes
Published on: February 27, 2017
Dehydropolymerisation of Methylamine Borane and an N-Substituted Primary Amine Borane Using a PNP Fe Catalyst
Felix Anke1, Susanne Boye2, Anke Spannenberg1
1Leibniz-Institut für Katalyse e.V., Albert-Einstein-Str. 29a, 18059, Rostock, Germany.
Abstract:
Dehydropolymerisation of methylamine borane (H3 B⋅NMeH2 ) using the well-known iron amido complex [(PNP)Fe(H)(CO)] (PNP=N(CH2 CH2 PiPr2 )2 ) (1) gives poly(aminoborane)s by a chain-growth mechanism. In toluene, rapid dehydrogenation of H3 B⋅NMeH2 following first-order behaviour as a limiting case of a more general underlying Michaelis-Menten kinetics is observed, forming aminoborane H2 B=NMeH, which selectively couples to give high-molecular-weight poly(aminoborane)s (H2 BNMeH)n and only traces of borazine (HBNMe)3 by depolymerisation after full conversion. Based on a series of comparative experiments using structurally related Fe catalysts and dimethylamine borane (H3 B⋅NMe2 H) polymer formation is proposed to occur by nucleophilic chain growth as reported earlier computationally and experimentally. A silyl functionalised primary borane H3 B⋅N(CH2 SiMe3 )H2 was studied in homo- and co-dehydropolymerisation reactions to give the first examples for Si containing poly(aminoborane)s.
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