posted on 2019-05-24, 00:00authored byKazuaki Kato, Yuta Ikeda, Kohzo Ito
The
universal relationship between the elastic modulus and the
cross-link density of a conventional rubber/gel has been demonstrated
experimentally to be inapplicable to gels with slidable cross-links.
Herein, we describe the synthesis of slide-ring (SR) gel networks
devoid of intramolecular cross-links by the cross-coupling of two
differently functionalized polyrotaxanes. The cross-link density was
determined from the characteristic UV absorption attributed to the
asymmetric cross-linked moiety. The cross-link density was shown to
correlate considerably more weakly with the Young’s modulus
than conventional gels and rubbers that follow a universal proportional
dependence. In addition, even at a similar cross-link density, the
modulus appeared to be lower due to a lower density of cyclic components
along the threading chain, i.e., the “coverage”, though
the data were limited in the narrow cross-link density range. These
results might suggest a considerably lower contribution from the conformational
entropy of chains associated with sliding through the cross-links
and the counteracting entropy attributed to ring arrangement, though
effects of the different persistence length due to the coverage difference
could affect the modulus.