Symmetry‐Breaking in Carbon Nanohoops Enables Room‐Temperature Ternary Single‐Molecule Switching

K Kaili Chang (Beijing National Laboratory for Molecular Sciences CAS Key Laboratory of Organic Solids Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China) Q Qing‐Song Deng (State Key Laboratory for Physical Chemistry of Solid Surfaces and Department of Chemistry College of Chemistry and Chemical Engineering Xiamen University Xiamen P. R. China) K Kai Song (Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry) J Jia‐Yin Yang (Department of Chemistry College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 China) C Chengjia Jing (Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry) B Bingchen Liu (Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry) X Xuwei Song (Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry) Y Yuan‐Zhi Tan (Department of Chemistry College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 China) D Daoben Zhu (Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry) Y Yaping Zang (Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids)

Abstract

Abstract Single‐molecule electronics offers chemically encoded routes to ultra‐dense information processing, yet room‐temperature operation is often limited to binary conductance states due to thermal broadening and electronic averaging. Here we demonstrate robust ternary switching at room temperature using symmetry‐engineered carbon nanohoops. Embedding a pyrene unit into the [12]cycloparaphenylene backbone via a symmetry‐breaking 1,6‐linkage disrupts the electronic equivalence of π –segments and localizes frontier orbitals. Under controlled mechanical elongation in single–molecule junctions, the molecule exhibits three well‐resolved conductance plateaus, each separated by ∼one order of magnitude, affording unambiguous and reproducible readout. First‐principles transport calculations reveal that symmetry‐breaking–induced orbital localization discretizes coherent tunneling pathways, accounting for the observed plateaus. These findings establish molecular symmetry control as a general design principle for room‐temperature multistate charge transport in conjugated macrocycles, opening a pathway to high‐density single‐molecule logic architectures.

Article Details

Volume / Issue Vol. 65, Issue 1
Published January 02, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

K

Kaili Chang

Beijing National Laboratory for Molecular Sciences CAS Key Laboratory of Organic Solids Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China

Q

Qing‐Song Deng

State Key Laboratory for Physical Chemistry of Solid Surfaces and Department of Chemistry College of Chemistry and Chemical Engineering Xiamen University Xiamen P. R. China

K

Kai Song

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry

J

Jia‐Yin Yang

Department of Chemistry College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 China

C

Chengjia Jing

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry

B

Bingchen Liu

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry

X

Xuwei Song

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry

Y

Yuan‐Zhi Tan

Department of Chemistry College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 China

D

Daoben Zhu

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry

Y

Yaping Zang

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids