Investigating the Interplay of Folding and Aggregation in Supramolecular Polymer Systems

Scientists have developed photoresponsive supramolecular polymers that can undergo both intrachain folding and interchain aggregation

The material properties of polymers are determined by the competition between polymer chain folding and aggregation. For the first time, researchers from Japan developed folded supramolecular polymers that can spontaneously undergo interchain aggregation. Using atomic force microscopy, they revealed that this interchain aggregation proceeded through the unfolding of the main chains. They also demonstrated that the photoisomerization of an azobenzene unit led to the unfolding of the polymer, thus accelerating the process of interchain aggregation.

Image title: Exploring Interchain Aggregation in Folded Supramolecular Polymers
Image caption: (a) Chemical structure of monomer 1 (1_trans and 1_cis), which incorporates a twistable biphenyl and an azobenzene photoswitch. (b) Energy landscape of self-assembled 1 with representative atomic force microscopy images.
Image credit: Kenta Tamaki from Chiba University, Japan
License type: Original Content
Usage restrictions: Cannot be reused without permission.

In polymers, the competition between the folding and aggregation of chains, both at an individual level and between chains, can determine the mechanical, thermal, and conductive properties of such materials. Understanding the interplay of folding and aggregation presents a significant opportunity for the development and discovery of polymeric materials with tailored properties and functionalities.

This also holds true for non-covalent counterparts of conventional covalent polymers, i.e., supramolecular polymers (SPs). SPs are expected to have practical applications as novel stimuli-responsive polymer materials. Most SPs have a monotonous one-dimensional linear structure that tends to cause interchain aggregation, but there are very few reports of SPs that can form various higher-order structures through main chain folding. The development of an SP that exhibits both intrachain folding and interchain aggregation would provide a new guideline for creating novel SP materials whose properties can be controlled by higher-order structures.

A recent study published in the Journal of the American Chemical Society on July 25, 2024, reported a new folded SP that spontaneously undergoes interchain aggregation and converts into crystalline aggregates. With the help of atomic force microscopy (AFM), the research team has demonstrated the relationship between unfolding and aggregation. The study was led by Professor Shiki Yagai from Chiba University, with Kenta Tamaki, a doctoral course student at the Graduate School of Science and Engineering at Chiba University, as the first author.

“Originally, we found a monomer structure that polymerized in a spiral shape. This time, we partially changed the structure of the unit that drives the polymerization of the monomer to investigate the monomer-polymer relationship. To our surprise, we observed a phenomenon where the spiral spontaneously unfolds, and the different chains bundle together. We then incorporated a photo-switchable molecule so that this ‘spontaneous’ phenomenon could occur at ‘arbitrary timing’ through light, which provides the background for our research,” says Prof. Yagai, speaking of the inspiration behind this study.

To design the new system, the team opted for twistable biphenyl and photoresponsive azobenzene units as a core, which self-assembled into the desired SPs. The SPs initially formed in a folded state slowly underwent rearrangement in internal molecular order over half a day and aggregated to a crystalline state. The inclusion of azobenzene units in the SPs led to photoinduced unfolding, which significantly accelerated the process by loosening the intrachain stabilization between folded loops.

The researchers observed that when the folded SP solution was left to stand at 20^oC for several days, the polymers spontaneously underwent structural transition and precipitated. When the precipitate was visualized using AFM, they observed a unique intermediate state that appeared to be a coalescence of curved chains en route to the unified straight fibril structures. This intriguing image reminded the researchers of the interchain aggregation often observed in biological systems when proteins misfold, leading to amyloid fibril formation.

Furthermore, the team revealed the reason behind this structural transformation. This included intrachain molecular ordering due to conformational changes in the biphenyl unit and interchain ordering from the alignment of the aliphatic tails covering the exterior of the main chains. This mechanism is similar to the crystallization of conventional covalent polymers. The team corroborated this mechanism using the photoisomerization of the azobenzene unit. When they irradiated UV light to the folded SP solution to induce conformational changes in the azobenzene units, the unfolding of the main chain immediately occurred, and interchain aggregation was significantly accelerated.

Overall, this study opens unforeseen perspectives on the folding and aggregation phenomenon. The mesoscale SPs formed via self-assembly of a large number of molecules can serve as a useful model system to examine the dynamics between individual main chains at a molecular level. This, in turn, opens up new avenues for innovation in trans-scale materials science.

“These phenomena have traditionally been investigated using spectroscopic or macroscopic observations, reflecting the averaged behavior of the whole system. Therefore, the construction of more observable mesoscale models is expected to contribute significantly to the advancement of materials science. We are hopeful that these insights can encourage the development of meso-scale molecular assemblies with meaningful higher-order structures,” concluded Prof. Yagai.

About Professor Shiki Yagai from Chiba University
Shiki Yagai is a Professor at the Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, Chiba, Japan. In 2002, he received his Ph.D. from Ritsumeikan University, Japan. He joined Chiba University as an Assistant Professor and was promoted to Full Professor in 2017. He has over 160 publications in the fields of organic chemistry, supramolecular chemistry, and nanotechnology, with more than 7,500 citations. He has been bestowed with several awards, the most recent being the Swiss Chemical Society Lectureships (2017). Currently, Prof. Yagai and his team are working on the development of supramolecular functional materials.

Funding:
This study was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI grant nos. JP22KJ0486, JP22H00331, JP23H04873, and JP23H04874 in a Grant-in-Aid for Transformative Research Areas “Materials Science of Meso-Hierarchy.”

Reference:
Title of original paper: Photoresponsive Supramolecular Polymers Capable of Intrachain
Folding and Interchain Aggregation
Authors: Kenta Tamaki¹, Sougata Datta², Hiroki Hanayama³, Christian Ganser⁴, Takayuki Uchihashi^4,5, and Shiki Yagai^2,3
Affiliations:
¹Graduate School of Science and Engineering, Chiba University, Japan
²Institute for Advanced Academic Research (IAAR), Chiba University, Japan
³Graduate School of Engineering, Chiba University, Japan
⁴Exploratory Research Center on Life and Living Systems, National Institutes of Natural Sciences, Japan
⁵Department of Physics, Nagoya University, Japan
Journal: Journal of the American Chemical Society
DOI: 10.1021/jacs.4c07878

Contact: Shiki Yagai
Professor, Graduate School of Engineering, IAAR, Chiba University
Email: yagai@faculty.chiba-u.jp

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