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Posted:May 22, 2026 Research Highlights

Revealing molecular cooperation: macrocyclic host molecules work together on a surface

A collaborative research team from Kanazawa University and Kyoto University reports in the Journal of the American Chemical Society the successful visualization of how densely assembled macrocyclic host molecules cooperatively capture guest molecules on a surface. Using two advanced atomic force microscopy (AFM) techniques, the team directly observed host–guest complex formation as well as reversible association–dissociation dynamics at the single-molecule level.

The study reveals that when one macrocyclic molecule captures a guest molecule, this event influences neighboring host molecules and promotes further guest capture. This cooperative behavior emerges only when the host molecules are densely assembled on a surface. The findings provide new insight into how surface-confined molecular interactions give rise to cooperative behavior and could contribute to the design of next-generation chemical sensors, separation systems, and storage materials.

The results of this study were published in the online edition of Journal of the American Chemical Society on May 20, 2026 (Open access).
This article was made Open Access with support from the Kanazawa University 2026 Open Access Promotion APC Support Program.

Background
Reversible association and dissociation processes are fundamental to the function of many molecular systems and play key roles in applications such as chemical sensors, separation materials, pharmaceuticals, and energy-related materials. Host–guest complexation,*1 in which a host molecule selectively captures a guest molecule, provides a representative model for studying these processes. Host–guest interactions have mainly been studied in solution using techniques such as NMR, calorimetry, and spectroscopy, which provide averaged information rather than direct observation of individual molecules. However, in functional materials and devices, host molecules are often immobilized on solid surfaces, where densely assembled neighboring molecules can strongly influence one another. To understand such surface-specific behavior, techniques that can visualize association and dissociation at the single-molecule level are needed. In this study, the research team employed two atomic force microscopy (AFM)*2 techniques to investigate host–guest complex formation on a substrate: frequency modulation AFM, which provides high spatial resolution, and high-speed AFM, which visualizes dynamic processes.

 Summary of the Research Findings
The research team used pillar[5]arene (P[5]A), a ring-shaped host molecule with a nanoscale cavity, densely assembled on a substrate. Frequency modulation AFM visualized structural changes of 100 picometers or less caused by guest capture and revealed that the complexes were not uniformly distributed. Instead, guest binding at one host molecule promoted further binding at sites about 3 nanometers away, indicating cooperative behavior. Molecular dynamics simulations suggested that this behavior originates from interactions and steric constraints among densely assembled host molecules. High-speed AFM further revealed repeated association and dissociation of individual complexes, with lifetimes ranging from milliseconds to seconds. These results show that reversible host–guest binding can be directly visualized at the single-molecule level.

Fig. 1:Atomic force microscopy observation of cooperative guest capture by densely assembled macrocyclic host molecules on a substrate at the single-molecule level.

Future Perspectives
The findings in this study show that new molecular functions, which emerge only when functional molecules are densely assembled on substrates, can be understood at the single-molecule level using two AFM techniques. The insights gained from this work provide important guidelines for the precise design of functional molecules and their assembled states. They are also expected to contribute to the development of next-generation functional materials and molecular devices.

Glossary

*1 Host–guest chemistry
A molecular assembly process in which a host molecule with a cavity or internal space selectively captures a guest molecule with a compatible shape and properties. Similar to a key fitting into a lock, this molecular fit enables selective recognition and capture.
*2 Atomic force microscopy
A microscopy technique that uses an atomically sharpened tip to observe structural changes on material surfaces.

Article

Title
Cooperative host–guest complexation in densely assembled host structures on surfaces revealed at the single-molecular level
Author
Hitoshi Asakawa, Hiroka Hatano, Shixin Fa, Takashi Sumikama, Mikihiro Shibata, Shu Takashima, Moe Ogasawara, Akio Ohta, Tada-aki Yamagishi, and Tomoki Ogoshi
Journal
Journal of the American Chemical Society
Publication date
May 20, 2026
DOI
10.1021/jacs.6c00891
URL
https://pubs.acs.org/doi/10.1021/jacs.6c00891

Funder

This work was supported by JST, PRESTO (Grant Number JPMJPR1411 and JPMJPR1313), Japan. This work was also supported by JSPS KAKENHI Grant Number JP24K01509 and JP19H00909. This work was also supported by the World Premier International Research Center Initiative, MEXT, Japan and Kanazawa University SAKIGAKE Projects 2022 and 2024. Calculations were partly conducted on a supercomputer at the Research Center for Computational Science in Okazaki, Japan (project: 25-IMS-C097).