

FOLLOWUS
School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China
azhang@shu.edu.cn (A.Z.)
wli@shu.edu.cn (W.L.)
Received:01 March 2026,
Accepted:14 April 2026,
Online First:22 June 2026,
Published:05 September 2026
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Wang, L.; Li, Q. S.; Yun, L.; Zhang, A.; Li, W. Multiple-responsive chiral hydrogels from helical dendronized poly(phenylacetylene)s. Chinese J. Polym. Sci. 2026, 44, 2880–2890
Lei Wang, Quan-Sheng Li, Lin Yun, et al. Multiple-Responsive Chiral Hydrogels from Helical Dendronized Poly(phenylacetylene)s[J]. Chinese Journal of Polymer Science, 2026, 44(9): 2880-2890.
Wang, L.; Li, Q. S.; Yun, L.; Zhang, A.; Li, W. Multiple-responsive chiral hydrogels from helical dendronized poly(phenylacetylene)s. Chinese J. Polym. Sci. 2026, 44, 2880–2890 DOI: 10.1007/s10118-026-3715-5.
Lei Wang, Quan-Sheng Li, Lin Yun, et al. Multiple-Responsive Chiral Hydrogels from Helical Dendronized Poly(phenylacetylene)s[J]. Chinese Journal of Polymer Science, 2026, 44(9): 2880-2890. DOI: 10.1007/s10118-026-3715-5.
Chiral hydrogels were fabricated from helical dendronized poly(phenylacetylene)s through acylhydrazone linkage with a disulfide crosslinker. They exhibited responsiveness to temperature
pH
and redox
and possessed characteristic stabilized helicity
reversible compression
and low cytotoxicity.
Chiral hydrogels derived from helical polymers are attractive as intelligent chiral materials due to the combination of polymer helicity and hydrogel characteristics. Here
we report the synthesis and characterization of chiral hydrogels from helical thermoresponsive dendronized poly(phenylacetylene)s
via
dynamic covalent acylhydrazone crosslinking
which are responsive to temperature
pH and redox. Two types of helical copolymers
featuring dendritic oligoethylene glycol (OEG) units terminated with either methoxyl or ethoxyl groups
were employed as precursors to afford distinct overall hydrophilicity. These precursors exhibited unprecedented thermoresponsive behavior attributed to the densely grafted dendritic OEGs
with cloud points (
T
cp
s) primarily governed by the terminal groups (methoxyl versus ethoxyl). To impart multi-responsiveness
a disulfide-containing crosslinker was selected for hydrogel formation. Gelation was conducted at three different tempe
ratures—freezing temperature
room temperature (below
T
cp
)
and elevated temperature (above
T
cp
)—yielding hydrogels with tunable responsiveness to temperature
pH
and redox conditions. The resulting hydrogels displayed stabilized helicity
along with good self-healing properties
excellent compressibility and robust mechanical performance. Preliminary biocompatibility assays indicated low cytotoxicity
underscoring their potential for biomedical applications.
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