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Ken-ichi Shinohara Associate Professor
School of Materials Science¡¢Materials Chemistry Area
B.S. from Niigata University (1992), M.S. from Niigata University (1994), Ph.D. from Niigata University (1997)
Research Fellow of Japan Society for the Promotion of Science (JSPS) at Niigata University (1996-1997). Research Associate at Tohoku University (1997-2002). Associate Professor at Japan Advanced Institute of Science and Technology (2002-- ). Visiting Associate Professor at Tohoku University (2003-2004). Lecturer (part-time) at Niigata University (2008-2009).
Polymer Chemistry, Molecular Machine, Artificial Life-Function
Nanomachine, Functional Polymer Synthesis, Single-Molecule Imaging, AFM Video Imaging
Spectral Fluctuation of Single-Molecules of a Conjugated Polymer in a Solution
Polymer considered in this study is an extremely complicated example due to its generally varied and dynamic structure, so we have had difficulty in clearly defining the correlation between structure and function at the molecular level. In other words, questions such as "What kind of polymer structures indicate the molecular functions?" have been very difficult to clearly answer at the molecular level. This introduces uncertainty as to whether a proposed molecular design is beneficial or not when we are trying to synthesize novel conjugated polymers with improved functions at the molecular level. Therefore, we thought that if we could directly observe an individual molecular structure and its functionality for a single conjugated polymer, it might then become possible to keep this speculation to a minimum, thus enabling a very clear discussion of the relationship between the molecular structure and function at the molecular level. Their observation of a single molecular spectrum for a conjugated substituted poly(phenylenevinylene) in a polystyrene matrix have been reported, but this was not a in solvo system. If the direct measurement of single molecules of a conjugated polymer in solution can be achieved, the observation of unique phenomena can be expected, e.g., the host-guest interaction of single molecules, leading towards the development of novel systems consisting of molecular devices in solution. We have already reported the results of fluorescence imaging experiments conducted on single molecules of the conjugated poly(9,10-anthracenediyl-ethynylene-1,4-phenylene-ethynylene) [poly(AEPE)], which has a rigid-rod main chain, in a tetrahydrofuran (THF) solution at room temperature using a total internal reflection microscope (TIRFM). In the present study, we conducted single molecule fluorescence imaging and single molecule spectroscopy for conjugated poly(AEPE) having a rigid-rod main chain in methanol at room temperature, and we could successfully detect a unique light-emitting phenomenon which fluctuated dynamically with in the time-scale of several seconds.
The creation of the flexible molecular machine
What function does a synthetic polymer have in the single-molecular-level? Does it have such a dynamic multi-functions as protein which a kind of biopolymer? Mankind does not understand the fundamental properties of synthetic polymers yet and still cannot bring the maximum of capabilities out of them. Polymer is highly capable, useful and indispensable material. Especially, conjugated polymers investigated as advanced materials for photonic and electronic applications have made progress, and has caused an ever-increasing interest from both academic research and industrial development. The conjugated polymers are used as laser dyes, organic light-emitting diodes, and so on. In addition recently, there are some applications as an optical resolution membrane materials. Although conjugated polymers are very interesting and important materials, the mechanism in single-molecular-level of these photonic and electronic function are still not clear owing to the various and complicated structure of the conjugated system in the polymer molecules. Thus, the polymers are the complex system of molecules. Therefore, we thought that if direct observation of single molecule of conjugated polymer were achieved, the polymer function would be clear in molecular level toward the polymer functioning at single molecule unit, that is the single-molecule device. In the other, recently, imaging of single protein molecules using fluorescence microscopy has made remarkable progress after development of single fluorophore imaging methods which were used for specimen on an air-dried surface. Single fluorophores in aqueous solution have been imaged using a total internal reflection fluorescence microscope (TIRFM), in which the background fluorescence is greatly reduced, when a laser beam is totally reflected in the interface between the glass surface and solution, illumination is limited to only the vicinity near the glass surface. In our previous study, this single molecules imaging method was expanded to the organic polymer solution system for the direct observation of single molecules of photofunctional rigid-rod conjugated polymer that is a poly(aryleneethynylene) having anthracene units in the main chain. In this study, we report that single molecule imaging of a stereo-regular ¦Ð-conjugated polymer and detection of single molecule slow-twinkling of the photoluminescence in tetrahydrofuran solution at room temperature for the first time.
Single-Molecule Imaging of Synthetic Polymer
¦Ð-Conjugated polymers have been developed as advanced materials for photonic or electronic applications. If the ¦Ð-conjugated polymer chain can be controlled in the higher order structure, novel functions at the molecular level will become available due to the unique ¦Ð-electron system. Many studies confirming the fact that a ¦Ð-conjugated polymer has a helical structure have already been completed. Most of these studies have provided us with data on molecular aggregates or data on the average of many molecules. Although we now understand that the main chain of the polymer takes the form of a helix, does one chain have both right- and left-handed helices? What is the ratio of the right-handed helices to the left-handed ones? What about the regions where the helix is reversed and how does it dynamically change? The answers already provided to all these fundamental questions have been based only on conjecture. Therefore, it is necessary to establish a technique that can determine the structure at the single-molecule level in order to achieve the above-mentioned objective. Here we show that a scanning tunneling microscope (STM) allows us to see the ¦Ð-electron orbital of a chiral quaternary structure, where it was directly observed and its size was even measured with high resolution.
- Applied Scanning Probe Methods X - Biomimetics and Industrial Applications -, Chapter 31: Scanning Probe Microscope Application for Single Molecules in a ¦Ð-Conjugated Polymer toward the Molecular Devices based on Polymer Chemistry,¡¤Ken-ichi Shinohara¡¤Springer (Berlin), ISBN: 978-3-540-74084-1¡¤2008¡¤pp 153-182
- Direct Observation of the Chiral Quaternary Structure in a ¦Ð-Conjugated Polymer at Room Temperature¡¤Ken-ichi Shinohara, Satoshi Yasuda, Gen Kato, Machiko Fujita, and Hidemi Shigekawa¡¤J. Am. Chem. Soc. 123, 3619-3620 (2001); Editors' Choice, Science 292, 15 (2001)
- Impact of a minority enantiomer on the polymerization of alanine-based isocyanides with an oligothiophene pendant¡¤Tomoyuki Ikai, Yuya Wada, Yugaku Takagi, Ken-ichi Shinohara¡¤Polym. Chem.¡¤7¡¤7057-7067¡¤2016 =Front Cover=
- Synthesis of two well-defined quadruple-stranded copolymers having two kinds of backbones by post polymerization of a helical template polymer¡¤Yu Zang, Toshiki Aoki, Hiroyoki Tanagi, Kana Matsui, Masahiro Teraguchi, Takashi Kaneko, Liqun Ma, Hongge Jia, Ken-ichi Shinohara¡¤Macromol. Rapid Commun.¡¤39¡¤2018¡¤1700556¡¤2018
¡þLectures and Presentations
- Single-Molecule Imaging of a Polymer and a Molecular Machine Driven by a Thermal Fluctuation¡¤Ken-ichi Shinohara¡¤International Symposium on Pure & Applied Chemistry (ISPAC) 2017, No. ANC 04. ¡ÚINVITED¡Û¡¤Ho Chi Minh City, Vietnam¡¤Jun. 8-10, 2017
- Single-Molecule Imaging of a Polymer and a Macromolecular Machine ¡ÚInvited Lecture¡Û¡¤Ken-ichi Shinohara¡¤International Symposium on Pure & Applied Chemistry (ISPAC) 2016¡¤Borneo Convention Centre, Kuching, Malaysia¡¤Aug. 15-18, 2016
- A Short Polymer Chain Walks Processively with the 3-nm Step along a Long Chain of a Synthetic Helical Polymer Driven by a Thermal Fluctuation in a Non-Aqueous Media¡¤¡ûKen-ichi Shinohara¡¤XXVI International Conference on Organometallic Chemistry (ICOMC 2014), 3P166¡¤Sapporo, Japan¡¤2014/07/13-18
¡þAcademic Society Affiliations
- Biophysics Society of Japan¡¤Member¡¤1998-
- American Chemical Society¡¤Member¡¤1994-
- The Society of Polymer Science, Japan¡¤Member¡¤1994-
- The 9th Japanese-French Frontier of Science Symposium (JFFoS), Japan Society for the Promotion of Science (JSPS) and the French Ministry of National Education (Kyoto, Japan)¡¤Researcher (Invited) (Polymer Chemistry)¡¤2015/01/22 - 2015/01/25
- Invited: The 2nd SANKEN International Symposium on Chemical and Physical Perspective for Molecular Devices, Osaka University (1999)
- Committee: Colloquium of Tohoku Branch of the Society of Polymer Science, Japan (2001)
¢£Academic Awards Received
- ¥Ý¥ê¥Þ¡¼1Ê¬»Ò¤ÎÄ¾»ë¡§¦Ð¶¦Ìò¹âÊ¬»Òº¿1ËÜ¤Î¹½Â¤¤Èµ¡Ç½¤Î¥¤¥á¡¼¥¸¥ó¥°¡¤Society of Polymer Science, Japan¡¤2005
- Marquis Who's Who in Science and Engineering, 2008-2009, 10th Edition¡¤Marquis Who¡Çs Who LLC (New Providence, NJ, USA)¡¤2009
- Marquis Who¡Çs Who in the World, 2010 Edition¡¤Marquis Who¡Çs Who LLC (New Providence, NJ, USA)¡¤2009