Force‐Induced Control of Circularly Polarized Luminescence With Rotaxane Architecture

K Keigo Nonaka (Department of Materials Science and Engineering, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8552, Japan) T Takumi Kuroda (Department of Materials Science and Engineering Institute of Science Tokyo, Meguro‐ku Tokyo Japan) K Kota Masuda (Department of Materials Science and Engineering Institute of Science Tokyo, Meguro‐ku Tokyo Japan) T Toshiki Nishitani (Department of Materials Science and Engineering Institute of Science Tokyo, Meguro‐ku Tokyo Japan) M Masaki Enokido (Graduate School of Chemical Sciences and Engineering Hokkaido University Sapporo Hokkaido Japan) M Makoto Tsurui (Graduate School of Chemical Sciences and Engineering Hokkaido University Sapporo Hokkaido Japan) Y Yuichi Kitagawa Y Yasuchika Hasegawa K Keiichi Noguchi (Instrumentation Analysis Center, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei-shi, Tokyo 184-8588, Japan) K Koji Nakano Y Yoshimitsu Sagara (Department of Materials Science and Engineering, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8552, Japan)

Abstract

ABSTRACT The reversible molecular motions of mechanically interlocked molecules (MIMs) have played a crucial role in realizing stimuli‐responsive functions. While the reversible switching of circularly polarized luminescence (CPL) properties has been achieved using MIMs through pH change and/or addition of chemicals, the mechanically controlled CPL utilizing the interlocked architecture has not yet been demonstrated. Here, we introduce a rotaxane‐based mechanophore designed for force‐induced CPL on/off switching. The mechanophore consists of a ring featuring a CPL‐active helicene luminophore and an axle with a matching quencher. The rotaxane mechanophores covalently introduced at the cross‐linking points of a double‐network (DN) gel are reversibly activated and deactivated in response to changes in applied force transduced through the polymer chains during the macroscopic swelling and shrinking of the DN gel. The isotropic swelling of the DN gel effectively suppresses artifacts arising from macroscopic sample orientation, enabling accurate detection of reciprocal CPL derived from a single chiral emitter. This work establishes the first example of mechanical control of CPL at the single‐molecule level and provides a robust measurement methodology for force‐induced CPL switching in soft materials.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 24, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

K

Keigo Nonaka

Department of Materials Science and Engineering, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8552, Japan

T

Takumi Kuroda

Department of Materials Science and Engineering Institute of Science Tokyo, Meguro‐ku Tokyo Japan

K

Kota Masuda

Department of Materials Science and Engineering Institute of Science Tokyo, Meguro‐ku Tokyo Japan

T

Toshiki Nishitani

Department of Materials Science and Engineering Institute of Science Tokyo, Meguro‐ku Tokyo Japan

M

Masaki Enokido

Graduate School of Chemical Sciences and Engineering Hokkaido University Sapporo Hokkaido Japan

M

Makoto Tsurui

Graduate School of Chemical Sciences and Engineering Hokkaido University Sapporo Hokkaido Japan

Y

Yuichi Kitagawa

Y

Yasuchika Hasegawa

K

Keiichi Noguchi

Instrumentation Analysis Center, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei-shi, Tokyo 184-8588, Japan

K

Koji Nakano

Y

Yoshimitsu Sagara

Department of Materials Science and Engineering, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8552, Japan