Spectroscopic examinations of hydrogen bonding in hydroxy-functionalized ADMET chemistry

Thompson DL, Wagener KB, Schulze U, Voit B, Jehnichen D, Malanin M (2015)


Publication Type: Journal article

Publication year: 2015

Journal

Book Volume: 36

Pages Range: 60-64

Journal Issue: 1

DOI: 10.1002/marc.201400545

Abstract

Wide-angle X-ray scattering (WAXS) and temperature-dependent Fourier transform infrared spectroscopy (FTIR) spectroscopy are used to study hydrogen bonding interactions of a hydroxyl-functionalized polyethylene (PE) prepared by acyclic diene metathesis (ADMET) chemistry. The hydroxyl polymer exhibits an orthorhombic unit cell structure with characteristic reflection planes at (110) and (200), comparable to pure crystalline PE. These data unequivocally demonstrate that the OH branch is excluded from the PE lamellae. Furthermore, the polymer melts 100°C higher than all previous analogous polymers possessing precision placed long aliphatic branches that also are excluded from PE lamellae. Temperature-dependent FTIR spectroscopy from ambient to 150°C, followed by cooling to 125°C supports exclusion of the hydroxyl group from the crystalline lattice. It is concluded that these hydroxyl groups form stable physical networks in the amorphous region via hydrogen bonding and are important for the overall morphology of such polymers. (Graph Presented).

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How to cite

APA:

Thompson, D.L., Wagener, K.B., Schulze, U., Voit, B., Jehnichen, D., & Malanin, M. (2015). Spectroscopic examinations of hydrogen bonding in hydroxy-functionalized ADMET chemistry. Macromolecular Rapid Communications, 36(1), 60-64. https://dx.doi.org/10.1002/marc.201400545

MLA:

Thompson, Donovan L., et al. "Spectroscopic examinations of hydrogen bonding in hydroxy-functionalized ADMET chemistry." Macromolecular Rapid Communications 36.1 (2015): 60-64.

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