Research

Tokyo Tech News

No Assembly Required: Self-assembling Silicone-based Polymers

RSS

October 25, 2018

Scientists at Tokyo Tech, RIKEN and Tohoku University have developed a silicone polymer chain that can self-assemble into a 3D periodic structure. They achieved this by using their recently reported self-assembling triptycene molecules to modify the ends of the polymer chains.

Self-assembling 2D+1D polymer structures

Figure 1. Self-assembling 2D+1D polymer structures


1,8,13-Trip is a triptycene molecule that can self-assemble into 2D hexagonal arrays, which then stack on top of each other to form a periodic polymer structure, shown in middle of the figure. Can silicone (PDMS) chains with the ends substituted with triptycene molecules self-assemble in a similar fashion?

The development of novel soft materials for various optical, mechanical, heat/charge transportation and nanotechnological applications would greatly benefit from techniques to create polymer assemblies in periodically ordered structures. Such ordered structures are created using molecular scaffolds or by modifying certain parts of the polymers used so that they self-assemble into the desired shape.

However, researchers nowadays consider that terminal functionalization (modifying both ends of a polymer chain) is not very effective for creating periodically ordered structures. That's why scientists from Tokyo Institute of Technology (Tokyo Tech), led by Fumitaka Ishiwari, were interested in revisiting one of their recently developed triptycene molecules, called 1,8,13-Trip. The team had already demonstrated that this molecule can reliably self-assemble into a periodic 3D structure made of parallel 2D sheets separated from each other by a fixed distance (see Fig. 1). "We were interested in investigating whether the powerful self-assembling ability of this triptycene motif would also operate in polymer systems," explains Ishiwari.

Therefore, the team designed polydimethylsiloxane (PDMS) chains with the ends replaced by a triptycene molecule. They hoped that these modified silicone chains would also exhibit the promising self-assembling behavior observed for 1,8,13-Trip alone, and thus had to run many different experiments to prove it, including Synchrotron-Radiation X-ray diffraction/scattering using the BL45XU beamline at SPring-8outer (Hyogo, Japan), differential scanning calorimetry and spectroscopy measurements. Fortunately, all results seemed to indicate that the modified PDMS chains had self-assembled into the 3D periodic structure shown in Fig. 2. This was also verified by analyzing the differences in the flow characteristics of the modified PDMS chains and regular PDMS chains.

Structure of the modified PDMS molecules

Figure 2. Structure of the modified PDMS molecules


The PDMS molecules modified with triptycene could self-assemble into the desired 2D hexagonal arrays (shown in upper right of the figure) and then stacked to form a 2D+1D structure (shown in the lower right of the figure), which cause dramatic increase of viscosity. As a result, liquid PDMS turned into a highly viscous solid.

The team's findings are very promising because the triptycene motif used is simple and easy to synthesize via short steps, and may provide a powerful tool for organizing polymers and reinforcing their structural and physical properties. "The present finding will update the general notion that terminal functionalization is not effective for achieving the controlled assembly of polymers into a periodically ordered structure," concludes Ishiwari. The team will carry on investigating the self-organization of polymers, and it is hoped that the results will lead to the development of novel materials and synthesis techniques.

Professor Masaki Takata of Tohoku University attributed the success of the study to the collaborative efforts of the Network Joint Research Center for Materials and Devices and the large scale Synchrotron Radiation facility, SPring-8, managed by RIKEN. He added that "this would hopefully also trigger a big demand for further high quality materials, which can be developed at the next-generation 3GeV synchrotron facility, due to begin construction at Tohoku University next year."

Professor Takanori Fukushima at work in the laboratory
Professor Takanori Fukushima at work in the laboratory

Lead author and Assistant Professor Fumitaka Ishiwari(left) and former master's student Gen Okabe in front of the high-performance liquid chromatography
Lead author and Assistant Professor Fumitaka Ishiwari(left)
and former master's student Gen Okabe
in front of the high-performance liquid chromatography

Reference

Authors :
Fumitaka Ishiwari1,2, Gen Okabe1,2, Hibiki Ogiwara1,2, Takashi Kajitani1,2, Masatoshi Tokita3, Masaki Takata2,4, and Takanori Fukushima1
Title of original paper :
Terminal Functionalization with a Triptycene Motif That Dramatically Changes the Structural and Physical Properties of an Amorphous Polymer
Journal :
Journal of the American Chemical Society
DOI :
Affiliations :

1 Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology

2 RIKEN SPring-8 Center

3 Department of Chemical Science and Engineering, Tokyo Institute of Technology

4 Institute of Multidisciplinary Research for Advanced Materials, Tohoku University

Further Information

Assistant Professor Fumitaka Ishiwari

Laboratory for Chemistry and Life Sciences,
Institute of Innovative Research,
Tokyo Institute of Technology

Email ishiwari@res.titech.ac.jp
Tel +81-45-924-5232

Professor Takanori Fukushima

Laboratory for Chemistry and Life Sciences,
Institute of Innovative Research,
Tokyo Institute of Technology

Email fukushima@res.titech.ac.jp
Tel +81-45-924-5220

Contact

Public Relations Section,
Tokyo Institute of Technology

Email media@jim.titech.ac.jp
Tel +81-3-5734-2975

RSS