Fixing Pillar[5]Arene‐Based Rotaxanes Into Epoxy Networks to Produce Toughened Epoxy Resins

ABSTRACT Introducing mechanical interlocking into epoxy thermosets can enhance material performance. However, this method typically requires complex monomer design and elaborate synthesis. Here, we demonstrate a simple strategy that exploits the dual functionality of a commercially available hydroxylated pillar[5]arene, which acts simultaneously as a macrocyclic host and a rigid cross‐linking unit. By threading polymer chains through the macrocycles, poly(pseudo)rotaxanes consisting of rigid wheels and flexible axles were formed. Then, in situ curing fixed the pillar[5]arene into the epoxy networks through both mechanical and covalent bonding. The resulting materials exhibited a balanced combination with tensile strength of 29.7 MPa and toughness of 21.6 MJ·m −3 . This approach enabled fine‐tuning of the mechanical properties of the epoxy networks by varying the pillar[5]arene content and epoxy precursor lengths. By combining supramolecular threading with covalent network formation using a single macrocycle, this work provides a convenient and practical route to regulating epoxy network properties.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-07-02
DOI
https://doi.org/10.1002/anie.5980142
Primary Topic
Supramolecular Chemistry and Complexes
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Fixing Pillar[5]Arene‐Based Rotaxanes Into Epoxy Networks to Produce Toughened Epoxy Resins

Tan‐Hao Shi, Shunsuke Ohtani, Motohiro Mizuno, Kenichi Kato et al.
Angewandte Chemie International Edition
Supramolecular Chemistry and Complexes
article

Fixing Pillar[5]Arene‐Based Rotaxanes Into Epoxy Networks to Produce Toughened Epoxy Resins

Tan‐Hao Shi, Shunsuke Ohtani, Motohiro Mizuno, Kenichi Kato, De‐Hui Tuo, Yoshito Tanaka, Toyomitsu Seki, Shingo Okuno, Xin Geng, Tomoki Ogoshi
article en

Abstract

ABSTRACT Introducing mechanical interlocking into epoxy thermosets can enhance material performance. However, this method typically requires complex monomer design and elaborate synthesis. Here, we demonstrate a simple strategy that exploits the dual functionality of a commercially available hydroxylated pillar[5]arene, which acts simultaneously as a macrocyclic host and a rigid cross‐linking unit. By threading polymer chains through the macrocycles, poly(pseudo)rotaxanes consisting of rigid wheels and flexible axles were formed. Then, in situ curing fixed the pillar[5]arene into the epoxy networks through both mechanical and covalent bonding. The resulting materials exhibited a balanced combination with tensile strength of 29.7 MPa and toughness of 21.6 MJ·m −3 . This approach enabled fine‐tuning of the mechanical properties of the epoxy networks by varying the pillar[5]arene content and epoxy precursor lengths. By combining supramolecular threading with covalent network formation using a single macrocycle, this work provides a convenient and practical route to regulating epoxy network properties.

Angewandte Chemie International Edition
Kanazawa University (JP), Kyoto University (JP), Daikin (Japan) (JP), Life Science Institute (JP)
Japan Society for the Promotion of Science, Japan Science and Technology Agency
Openalex Percentile: Top 14%
Supramolecular Chemistry and Complexes
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Fixing Pillar[5]Arene‐Based Rotaxanes Into Epoxy Networks to Produce Toughened Epoxy Resins — Tan‐Hao Shi, Shunsuke Ohtani, et al. · Angewandte Chemie International Edition (2026) | TGRS Research Map | TGRS