Abstract
This paper describes “Hydroboration Polymerization” as a novel methodology for the preparation of organoboron polymers. A polyaddition between diene and thexylborane produced a polymer consisting of C-B bonds in the main chain. The resulting organoboron polymers can be regarded as a polymer homologue of trialkylborane and can be expected as a novel type of reactive polymers. On the other hand, hydroboration polymerization of diene with monobromoborane produced poly(organoboron halide)s as a polymeric Lewis acid. Furthermore, hydroboration polymerization of dicyano compounds such as isophthalonitrile with t-butylborane produced an air-stable boroncontaining polymer (polycyclodiborazane) having B-N four-membered rings via dimerization of iminoborane species.
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© 1994 Springer-Verlag Berlin Heidelberg
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Chujo, Y. (1994). Hydroboration Polymerization. In: Ghiggino, K.P. (eds) Progress in Pacific Polymer Science 3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-78759-1_4
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DOI: https://doi.org/10.1007/978-3-642-78759-1_4
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-78761-4
Online ISBN: 978-3-642-78759-1
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