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Polymerization of N-methyl B-methyl amino borazine

  • Hicham Moutaabbid EMAIL logo and Mohammed Moutaabbid
Published/Copyright: August 17, 2011
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Journal of Polymer Engineering
From the journal Volume 31 Issue 5

Abstract

A large quantity of high-quality poly[N-methyl B-methyl amino borazine] was synthesized via a solventless method from the monomer 1,3,5-trimethyl-2,4,6-tri(methyl amino)borazine. The thermal polymerization profile was investigated with differential scanning calorimetry (DSC), Fourier transform infrared (FTIR), size exclusion chromatography (SEC), gas chromatography, and mass spectrometry. A polymerization mechanism involving the condensation reaction of two –N(H)CH3 groups releasing methylamine was proposed and compared with the literature. As a result of cross-linking via the amino­methyl moiety, the cured polymer exhibited a molecular weight Mn of 790 g mol-1, glass transition temperature of 64°C, high cross-link density, and thermal stability with a decomposition temperature of 165°C. Functionalized poly[N-methyl B-methyl amino borazine] with chemical stability was fully characterized by 1H, 13C, 11B nuclear magnetic resonance, FTIR, DSC, and SEC analyses. Ultraviolet absorption spectra evidenced changes in the structure of the aforementioned oligomers.

Published Online: 2011-08-17
Published in Print: 2011-09-01

©2011 by Walter de Gruyter Berlin Boston

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