Position-Dependent Segmental Relaxation in Bottlebrush Polymers

  • Karin J. Bichler
  • , Bruno Jakobi
  • , Alice Klapproth
  • , Richard A. Mole
  • , Gerald J. Schneider

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Segmental dynamics of specifically labeled poly(propylene oxide), PPO, based bottlebrush polymers, PNB-g-PPO, were studied using quasi-elastic neutron scattering. The focus was set to different parts of the side chains to investigate the hypothetical gradual relaxation behavior within the side chains of a bottlebrush polymer. Different sections of the side chains were highlighted for QENS via sequential polymerization of protonated and deuterated monomers to allow the study of the relaxation behavior of the inner and outer parts of the side chain separately. A comparison of these two parts reveals a slowdown due to the grafting process happening across the different regions. This is seen for the segmental relaxation time as well as on the time-dependent mean-square displacement. Additionally, the non-Gaussian parameter, α, shows a decreasing difference from Gaussian behavior with the distance to the backbone. Altogether, this leads to the conclusion that gradual relaxation behavior exists.

Original languageEnglish
Pages (from-to)4729-4736
Number of pages8
JournalMacromolecules
Volume57
Issue number10
DOIs
StatePublished - May 28 2024
Externally publishedYes

Funding

We acknowledge funding by the U.S. Department of Energy (DoE) under Grant DE-SC0019050. We are also grateful for the access to the neutron scattering instruments, provided by ACNS, Sydney, Australia (Pelican: P15734 and Emu: P15710). Mass spectrometry experiments were performed at the LSU Mass Spectrometry Facility (MSF). The Bruker UltrafleXtreme MALDI instrument was supported by NIH (Grant 1S10RR024520-01A1).

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