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@ARTICLE{Staropoli:838854,
author = {Staropoli, Mariapaola and Raba, Andreas and Hövelmann,
Claas H. and Appavou, Marie-Sousai and Allgaier, Jürgen and
Krutyeva, Margarita and Pyckhout-Hintzen, Wim and
Wischnewski, Andreas and Richter, Dieter},
title = {{M}elt dynamics of supramolecular comb polymers:
{V}iscoelastic and dielectric response},
journal = {Journal of rheology},
volume = {61},
number = {6},
issn = {1520-8516},
address = {Melville, NY [u.a.]},
publisher = {Inst.},
reportid = {FZJ-2017-07364},
pages = {1185 - 1196},
year = {2017},
abstract = {The structure and the dynamics of supramolecular comblike
polymers in the melt state is studied by a combination of
linear rheology, dielectric spectroscopy, and small angle
neutron scattering. The system consists of blends of
1,2-polybutyleneoxide (PBO) entangled backbones, randomly
functionalized with thymine (thy) and barely entangled PBO
graft chains—modified with 2,4-diamino-1,3,5-triazine
(DAT) end groups. These bioinspired groups associate into a
transiently branched comb architecture through
heterocomplementary interaction involving the two different
hydrogen bonding groups thy and DAT. In the present
manuscript, we focus on the comparison of the macroscopic
dynamics of the associating blends and permanent comb
analogs. The viscoelastic and dielectric response of
covalent and reversible combs are found to be comparable.
The viscoelastic response of mixtures of thy-functionalized
entangled backbones and DAT-end-modified barely entangled
chains show a relaxation mechanism, which is mostly
attributed to the association/breakage dynamics of the
transient bonds with characteristic time ∼1 s at
T=−25 °C. In the parallel dielectric investigation, the
reversible branched structure is still evident from the
comparison with the corresponding permanent combs and allows
the distinction between fixed arms relaxation and the
lifetime. A α∗ process of the thy-thy association is
likewise detected. The time scale of the supramolecular
association makes the thy-DAT pair an ideal candidate for
the development of responsive materials that combine
permanent and transient linkages for novel applications and
self-healing properties},
cin = {JCNS (München) ; Jülich Centre for Neutron Science JCNS
(München) ; JCNS-FRM-II / Neutronenstreuung ; JCNS-1 /
JCNS-2 / ICS-1},
ddc = {530},
cid = {I:(DE-Juel1)JCNS-FRM-II-20110218 /
I:(DE-Juel1)JCNS-1-20110106 / I:(DE-Juel1)JCNS-2-20110106 /
I:(DE-Juel1)ICS-1-20110106},
pnm = {531 - Condensed Matter and Molecular Building Blocks
(POF3-531) / 551 - Functional Macromolecules and Complexes
(POF3-551)},
pid = {G:(DE-HGF)POF3-531 / G:(DE-HGF)POF3-551},
experiment = {EXP:(DE-MLZ)KWS2-20140101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000414273200012},
doi = {10.1122/1.5001059},
url = {https://juser.fz-juelich.de/record/838854},
}