{"id":241,"date":"2012-08-31T15:59:58","date_gmt":"2012-08-31T06:59:58","guid":{"rendered":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/?page_id=241"},"modified":"2014-07-05T14:29:27","modified_gmt":"2014-07-05T05:29:27","slug":"yasuda","status":"publish","type":"page","link":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/staff-2\/yasuda\/","title":{"rendered":"\u5b89\u7530 \u7422\u9ebf (Dr. Takuma YASUDA)"},"content":{"rendered":"
\"\"<\/div>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
\u7565\u6b74<\/th>\n<\/tr>\n
2005\u5e74<\/td>\n\u6771\u4eac\u5de5\u696d\u5927\u5b66 \u5927\u5b66\u9662\u7dcf\u5408\u7406\u5de5\u5b66\u7814\u7a76\u79d1 \u535a\u58eb\u8ab2\u7a0b\u4fee\u4e86<\/td>\n<\/tr>\n
2005\u5e74~<\/td>\n\u6771\u4eac\u5927\u5b66 \u5927\u5b66\u9662\u7406\u5b66\u7cfb\u7814\u7a76\u79d1 COE\u7279\u4efb\u7814\u7a76\u54e1<\/td>\n<\/tr>\n
2006\u5e74~<\/td>\n\u65e5\u672c\u5b66\u8853\u632f\u8208\u4f1a\u7279\u5225\u7814\u7a76\u54e1(PD) (\u6771\u4eac\u5927\u5b66 \u5de5\u5b66\u7cfb\u7814\u7a76\u79d1)<\/td>\n<\/tr>\n
2008\u5e74~<\/td>\n\u6771\u4eac\u5927\u5b66 \u5927\u5b66\u9662\u5de5\u5b66\u7cfb\u7814\u7a76\u79d1 \u5316\u5b66\u751f\u547d\u5de5\u5b66\u5c02\u653b \u52a9\u6559<\/td>\n<\/tr>\n
2010\u5e74~<\/td>\n\u4e5d\u5dde\u5927\u5b66 \u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u9662 \u5fdc\u7528\u5316\u5b66\u90e8\u9580 \u51c6\u6559\u6388
\n(2011\u5e74~\u3000JST\u3055\u304d\u304c\u3051\u7814\u7a76\u54e1 \u517c\u4efb)<\/td>\n<\/tr>\n
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\u535a\u58eb(\u5de5\u5b66) \uff08\u6771\u4eac\u5de5\u696d\u5927\u5b66\u30012005\u5e74\uff09<\/td>\n<\/tr>\n
\u6240\u5c5e\u5b66\u4f1a<\/th>\n<\/tr>\n
\u65e5\u672c\u5316\u5b66\u4f1a<\/a>\u3001\u9ad8\u5206\u5b50\u5b66\u4f1a<\/a>\u3001\u65e5\u672c\u6db2\u6676\u5b66\u4f1a<\/a>\u3001\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a<\/a>\u3001\u7c73\u56fd\u5316\u5b66\u4f1a<\/a>\u3001\u7c73\u56fdMRS<\/a><\/td>\n<\/tr>\n
\u7814\u7a76\u5206\u91ce<\/th>\n<\/tr>\n
\u6a5f\u80fd\u6027\u6709\u6a5f\u6750\u6599\u5316\u5b66<\/td>\n<\/tr>\n
\u8da3\u5473<\/th>\n<\/tr>\n
\u30b9\u30dd\u30fc\u30c4 (\u91ce\u7403\u3001\u30d0\u30ec\u30fc\u3001\u30b9\u30ad\u30fc\u3001\u30b8\u30e0\u901a\u3044)\u3001\u98df\u3079\u6b69\u304d \ud83d\ude06<\/td>\n<\/tr>\n
Profile<\/th>\n<\/tr>\n
Takuma YASUDA was born in 1977 in Aichi, Japan. He received his PhD in 2005 from Tokyo Institute of Technology under the supervision of Prof. Takakazu Yamamoto. He then began postdoctoral research focusing on functional liquid-crystalline materials with Prof. Takashi Kato at the University of Tokyo. In 2008, he was appointed to an Assistant Professor at the University of Tokyo. Currently, he is an Associate Professor, working in the group of Prof. Chihaya Adachi at Kyushu University. He is also a concurrent researcher of PRESTO, Japan Science and Technology Agency (JST). His research is directed towards the design, synthesis, and functionalization of \u03c0-conjugated molecular materials.\u00a0Current topics of research include their applications\u00a0to organic electronics devices. He received the Chemical Society of Japan Award for Young Chemists (2014), the Hitachi Chemical Award from the Society of Polymer Science, Japan (2013), and the Award for Young Researchers from the Japanese Liquid Crystal Society (2010).<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

\u7814\u7a76\u696d\u7e3e (Achievements)<\/h3>\n

\u539f\u8457\u8ad6\u6587 (Original Papers with Peer Review)<\/h4>\n
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[58]<\/dt>\n
W. Shin, T. Yasuda,* Y. Hidaka, G. Watanabe, R. Arai, K. Nasu, T. Yamaguchi, W. Murakami, K. Makita, and C. Adachi,*
\n\u201c\u03c0-Extended Narrow-Bandgap Diketopyrrolopyrrole-Based Oligomers for Solution-Processed Inverted Organic Solar Cells\u201d
\n Adv. Energy Mater.<\/em> 2014<\/strong>, 4<\/em>, in press<\/a>.\u00a0<\/dd>\n
[57]<\/dt>\n
C. Mayr, S. Y. Lee, T. D. Schmidt, T. Yasuda, C. Adachi, and W. Br\u00fctting,*
\n\u201cEfficiency Enhancement of Organic Light-Emitting Diodes Incorporating a Highly Oriented Thermally Activated Delayed Fluorescence Emitter\u201d
\n Adv. Funct. Mater.<\/em> 2014<\/strong>, 24<\/em>, in press<\/a>.\u00a0<\/dd>\n
[56]<\/dt>\n
H. Nakanotani, T. Higuchi, T. Furukawa, K. Masui, K. Morimoto, M. Numata, H. Tanaka, Y. Sagara, T. Yasuda, and C. Adachi,*
\n\u201cHigh Efficiency Light-Emitting Diodes with Fluorescent Emitters\u201d
\n Nature Commun.<\/em> 2014<\/strong>, 5<\/em>, 4016<\/a>.\u00a0<\/dd>\n
[55]<\/dt>\n
S. Y. Lee, T. Yasuda,* Y. S. Yang, Q. Zhang, and C. Adachi,*
\n\u201cLuminous Butterflies: Efficient Exciton Harvesting by Benzophenone Derivatives for Full-Color Delayed Fluorescence OLEDs\u201d
\n Angew. Chem. Int. Ed.<\/em> 2014<\/strong>, 53<\/em>, 6520-6524<\/a>.\u00a0<\/dd>\n
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[54]<\/dt>\n
H. Ohkuma, T. Nakagawa, K. Shizu, T. Yasuda,* and C. Adachi,*
\n\u201cThermally Activated Delayed Fluorescence from a Spiro-Diazafluorene Derivative\u201d
\n Chem. Lett.<\/em> 2014<\/strong>, 43<\/em>, 1017-1019<\/a>. (Selected as an Editor’s Choice<\/a>)\u00a0<\/dd>\n
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[53]<\/dt>\n
T. Takahashi, K. Shizu, T. Yasuda,* K. Togashi, and C. Adachi,*
\n\u201cDonor\u2013Acceptor Structured 1,4-Diazatriphenylene Derivatives Exhibiting Thermally Activated Delayed Fluorescence: Design and Synthesis, Photophysical Properties and OLED Characteristics\u201d
\n Sci. Technol. Adv. Mater.<\/em> 2014<\/strong>, 15<\/em>, 034202<\/a>.\u00a0<\/dd>\n
[52]<\/dt>\n
T. Komori, H. Nakanotani, T. Yasuda,* and C. Adachi,*
\n\u201cLight-Emitting Organic Field-Effect Transistors Based on Highly Luminescent Single Crystals of Thiophene\/Phenylene Co-Oligomers\u201d
\n J. Mater. Chem. C<\/em> 2014<\/strong>, 2<\/em>, 4918-4921<\/a>.\u00a0<\/dd>\n
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[51]<\/dt>\n
J. Y. Kim, T. Yasuda,* Y. S. Yang, N. Matsumto, and C. Adachi,*
\n\u201cPolymorphism in 9,9-Diarylfluorene-Based Organic Semiconductors: Influence on Optoelectronic Functions\u201d
\nChem. Commun.<\/em> 2014<\/strong>,\u00a050<\/em>, 1523-1526<\/a>. (Highlighted as an Inside Front Cover<\/a>)\u00a0<\/dd>\n
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[50]<\/dt>\n
H. Mieno, T. Yasuda,* Y. S. Yang,\u00a0and C. Adachi,*
\n\u201cSelf-Assembly, Physicochemical, and Field-Effect Transistor Properties of Solution-Crystallized Organic Semiconductors Based on \u03c0-Extended Dithieno[3,2-b<\/em>:2′,3′-d<\/em>]thiophenes\u201d
\nChem. Lett.<\/em> 2014<\/strong>, 43<\/em>, 293-295<\/a>.<\/dd>\n
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[49]<\/dt>\n
T. Nishimoto, T. Yasuda,* Y. S. Yang, R. Kondo, and C. Adachi,*
\n\u201cA Six-Carbazole-Decorated Cyclophosphazene as a Host with High Triplet Energy Host to Realize Efficient Delayed-Fluorescence OLEDs\u201d
\nMater. Horiz.<\/em> 2014<\/strong>, 1<\/em>, 264-269<\/a>.\u00a0<\/dd>\n
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[48]<\/dt>\n
K. Nasu, T. Nakagawa, H. Nomura, C.-J. Lin, C.-H. Cheng, M.-R. Tseng, T. Yasuda, and C. Adachi,*
\n\u201cA Highly Luminescent Spiro-Anthracenone-Based Organic Light-Emitting Diode through Thermally Activated Delayed Fluorescence\u201d
\nChem. Commun.<\/em> 2013<\/strong>, 49<\/em>, 10385\u201310387<\/a>.\u00a0<\/dd>\n
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[47]<\/dt>\n
Y. S. Yang, T. Yasuda,* H. Kakizoe, H. Mieno, H. Kino, Y. Tateyama, and C. Adachi,*
\n\u201cHigh Performance Organic Field-Effect Transistors Based on Single-Crystal Microribbons and Microsheets of Solution-Processed Dithieno[3,2-b<\/em>:2′,3′-d<\/em>]thiophene Derivatives\u201d
\nChem. Commun.<\/em> 2013<\/strong>, 49<\/em>, 6483\u20136485<\/a>. (Highlighted as an Inside\u00a0Back Cover<\/a>)\u00a0<\/dd>\n
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[46]<\/dt>\n
W. Shin, T. Yasuda,* G. Watanabe, Y. S. Yang, and C. Adachi,*
\n\u201cSelf-Organizing Mesomorphic Diketopyrrolopyrrole Derivatives for Efficient Solution-Processed Organic Solar Cells\u201d
\nChem. Mater.<\/em> 2013<\/strong>, 25<\/em>, 2549\u20132556<\/a>.\u00a0<\/dd>\n
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[45]<\/dt>\n
J. Lee, K. Shizu, H. Tanaka, H. Nomura, T. Yasuda, and C. Adachi,*
\n\u201cOxadiazole- and Triazole-Based Highly-Efficient Thermally-Activated Delayed Fluorescence Emitters for Organic Light-Emitting Diodes\u201d
\nJ. Mater. Chem. C<\/em> 2013<\/strong>, 1<\/em>, 4599-4604<\/a>.\u00a0<\/dd>\n
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[44]<\/dt>\n
K. Togashi, Y. Sagara, T. Yasuda, and C. Adachi,*
\n\u201cMolecular Design of High-Molecular-Orientation Electron-Transport Materials and Application to Organic Light-Emitting Diodes\u201d
\nChem.\u00a0Lett.<\/em> 2013<\/strong>, 42<\/em>, 651\u2013653<\/a>.\u00a0<\/dd>\n
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[43]<\/dt>\n
A. Wada, T. Yasuda,* Q. Zhang, Y. S. Yang, I. Takasu, S. Enomoto, and C. Adachi,*
\n\u201cA Host Material Consisting of a Phosphinic Amide Directly Linked Donor\u2013Acceptor Structure for Efficient Blue Phosphorescent Organic Light-Emitting Diodes\u201d
\nJ. Mater. Chem. C<\/em> 2013<\/strong>, 1<\/em>, 2404-2407<\/a>. (Selected as Top 10 most-read Journal of<\/em>
\nMaterials Chemistry C articles<\/em> in February and March 2013)\u00a0<\/dd>\n
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[42]<\/dt>\n
M. Hirade, T. Yasuda, and C. Adachi,*
\n\u201cEffects of Intramolecular Donor\u2013Acceptor Interactions on Bimolecular Recombination in Small-Molecule Organic Photovoltaic Cells\u201d
\nJ. Phys. Chem. C<\/em> 2013<\/strong>, 117<\/em>, 4986\u20134991<\/a>.\u00a0<\/dd>\n
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[41]<\/dt>\n
K. Togashi, T. Yasuda, and C. Adachi,*
\n\u201cTriphenylene-Based Host Materials for Low-Voltage and Highly Efficient Red Phosphorescent Organic Light-Emitting Diodes\u201d
\nChem. Lett.<\/em> 2013<\/strong>, 42<\/em>, 383\u2013385<\/a>.\u00a0<\/dd>\n
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[40]<\/dt>\n
J. Y. Kim, T. Yasuda,* Y. S. Yang, and C. Adachi,*
\n\u201cBifunctional Star-Burst Amorphous Molecular Materials for OLEDs: Achieving Highly Efficient Solid-State Luminescence and Carrier Transport Induced by Spontaneous Molecular Orientation\u201d
\nAdv. Mater.<\/em> 2013<\/strong>, 25<\/em>, 2666\u20132671<\/a>. (Highlighted as an\u00a0Inside Front\u00a0Cover<\/a>)\u00a0<\/dd>\n
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[39]<\/dt>\n
Y. S. Yang, T. Yasuda,* and C. Adachi,*
\n\u201cOrganic Single-Crystal Transistors Based on \u03c0-Extended Heteroheptacene Microribbons\u201d
\nBull. Chem. Soc. Jpn.<\/em> 2012<\/strong>, 85<\/em>, 1186-1191<\/a>. (Selected as a BCSJ Award Article and highlighted as a Cover<\/a>)\u00a0<\/dd>\n
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[38]<\/dt>\n
K. Togashi, S. Nomura, N. Yokoyama, T. Yasuda, and C. Adachi,*
\n\u201cLow Driving Voltage Characteristics of Triphenylene Derivatives as Electron Transport Materials in Organic Light-Emitting Diodes\u201d
\nJ. Mater. Chem.<\/em> 2012<\/strong>, 22<\/em>, 20689-20695.<\/a>\u00a0<\/dd>\n
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[37]<\/dt>\n
S. Y. Lee, T. Yasuda, H. Nomura, and C. Adachi,*
\n\u201cHigh-Performance Organic Light-Emitting Diodes Utilizing Efficient Thermally Activated Delayed Fluorescence from Triazine-Based Donor-Acceptor Hybrid Molecules\u201d
\nAppl. Phys. Lett.<\/em> 2012<\/strong>, 101<\/em>, 093306.<\/a> (Ranked in Top 20 Most Read Articles<\/a>)\u00a0<\/dd>\n
[36]<\/dt>\n
R. Kondo, T. Yasuda,* Y. S. Yang, J. Y. Kim, and C. Adachi,*
\n\u201cHighly Luminescent \u03c0-Conjugated Dithienometalloles: Photophysical Properties and Their Application in Organic Light-Emitting Diodes\u201d
\nJ. Mater. Chem.<\/em> 2012<\/strong>, 22<\/em>, 16810-16816.<\/a> (Selected as Top 10 most-read\u00a0JMC articles<\/a>, and highlighted in Noteworthy Chemistry<\/a> by the American Chemical Society)\u00a0<\/dd>\n
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[35]<\/dt>\n
A. Wada, Q. Zhang, T. Yasuda, I. Takasu, S. Enomoto, and C. Adachi,*
\n\u201cEfficient Luminescence from a Copper(I) Complex Doped in Organic Light-Emitting Diodes by Suppressing C-H Vibrational Quenching\u201d
\nChem. Commun.<\/em> 2012<\/strong>, 48<\/em>, 5340-5342.<\/a>\u00a0<\/dd>\n
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[34]<\/dt>\n
T. Yasuda,* T. Shimizu, F. Liu, G. Ungar, and T. Kato,*
\n\u201cElectro-Functional Octupolar \u03c0-Conjugated Liquid Crystals\u201d
\nJ. Am. Chem. Soc.<\/em> 2011<\/strong>, 133<\/em>, 13437-13444.<\/a>\u00a0<\/dd>\n
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[33]<\/dt>\n
M. Taneda, T. Yasuda, and C. Adachi,*
\n\u201cHorizontal Orientation of a Linear-Shaped Platinum(II) Complex in Organic Light-Emitting Diodes with a High Light Out-Coupling Efficiency\u201d
\nAppl. Phys. Exp.<\/em> 2011<\/strong>, 4<\/em>, 071602.<\/a>\u00a0<\/dd>\n
[32]<\/dt>\n
T. Yasuda, K. Tanabe, T. Tsuji, K. K. Coti, I. Aprahamian, J. F. Stoddart,* and T. Kato,*
\n\u201cA Redox-Switchable [2]Rotaxane in a Liquid-Crystalline State\u201d
\nChem. Commun.<\/em> 2010<\/strong>, 46<\/em>, 1224-1226.<\/a> (Selected as a Hot Article, and\u00a0highlighted in NPG Asia Materials<\/a>)\u00a0<\/dd>\n
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[31]<\/dt>\n
Y. Shoji, M. Yoshio, T. Yasuda, M. Funahashi, and T. Kato,
\n\u201cAlignment of Photoconductive Self-Assembled Fibers Composed of \u03c0-Conjugated Molecules under Electric Fields\u201d
\nJ. Mater. Chem.<\/em> 2010<\/strong>, 20<\/em>, 173-179.\u00a0<\/dd>\n
[30]<\/dt>\n
Y. Hirai, S. S. Babu, V. K. Praveen, T. Yasuda, A. Ajayaghosh, and T. Kato,
\n\u201cAnisotropic Self-Assembly of Photoluminescent Oligo(p-phenylenevinylene) Derivatives in Liquid Crystals: An Effective Strategy for the Macroscopic Alignment of \u03c0-Gels\u201d
\nAdv. Mater.<\/em> 2009<\/strong>, 21<\/em>, 4029-4033.<\/a> (Highlighted as an Inside Front Cover<\/a>)\u00a0<\/dd>\n
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[29]<\/dt>\n
K. Isoda, T. Yasuda, and T. Kato,
\n\u201cTruxene-Based Columnar Liquid Crystals: Self-Assembled Structures and Electro-Active Properties\u201d
\nChem. Asian J.<\/em> 2009<\/strong>, 4<\/em>, 1619-1625.<\/a> (Selected as a VIP paper and highlighted as a Cover Picture<\/a>)\u00a0<\/dd>\n
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[28]<\/dt>\n
E. D. Baranoff, J. Voignier, T. Yasuda, V. Heitz, J.-P. Sauvage, and T. Kato,
\n\u201cMacrocycle-Based Liquid Crystals: A Study of Topological Effects on Mesomorphism\u201d
\nMol. Cryst. Liq. Cryst.<\/em> 2009<\/strong>, 509<\/em>, 165-172.\u00a0<\/dd>\n
[27]<\/dt>\n
M. Kimura, T. Hatano, T. Yasuda, J. Morita, Y. Akama, K. Minoura, T. Shimomura, and T. Kato,
\n\u201cPhotoluminescent Liquid Crystals Based on Trithienylphosphine Oxides\u201d
\nChem. Lett.<\/em> 2009<\/strong>, 38<\/em>, 800-801.\u00a0<\/dd>\n
[26]<\/dt>\n
K. Minoura, Y. Akama, J. Morita, T. Yasuda, T. Kato, and T. Shimomura,
\n\u201cSupramolecular Structure of Columnar Liquid Crystalline \u03c0-Conjugated Oligothiophenes with Highly Polarized Photoluminescent Properties\u201d
\nJ. Appl. Phys.<\/em> 2009<\/strong>, 105<\/em>, 113513-6.\u00a0<\/dd>\n
[25]<\/dt>\n
Y.-L. Zhao, N. Erina, T. Yasuda, T. Kato, and J. F. Stoddart,
\n\u201cA Layered Liquid Crystalline Droplet\u201d
\nJ. Mater. Chem.<\/em> 2009<\/strong>, 19<\/em>, 3469-3474.\u00a0<\/dd>\n
[24]<\/dt>\n
T. Yasuda, H. Ooi, J. Morita, Y. Akama, K. Minoura, M. Funahashi, T. Shimomura, and T. Kato,
\n\u201c\u03c0-Conjugated Oligothiophene-Based Polycatenar Liquid Crystals: Self-Organization and Photoconductive, Luminescent, and Redox Properties\u201d
\nAdv. Funct. Mater.<\/em> 2009<\/strong>, 19<\/em>, 411-419.<\/a> (Highlighted as an Inside Front Cover<\/a>, and selected as a Fast Breaking Paper in Materials Science<\/a> by Thomson Reuters)<\/dd>\n
\"\" \"\"<\/dd>\n
[23]<\/dt>\n
K. Tanabe, T. Yasuda, and T. Kato,
\n\u201cLuminescent Ionic Liquid Crystals Based on Tripodal Pyridinium Salts\u201d
\nChem. Lett.<\/em> 2008<\/strong>, 37<\/em>, 1208-1209.\u00a0<\/dd>\n
[22]<\/dt>\n
K. Isoda, T. Yasuda, and T. Kato,
\n\u201cDipole-Driven Self-Assembly of Redox-Active Mesogenic Tetracyanoanthraquinodimethanes\u201d
\nJ. Mater. Chem.<\/em> 2008<\/strong>, 18<\/em>, 4522-4528.\u00a0<\/dd>\n
[21]<\/dt>\n
T. Morikita, T. Yasuda, and T. Yamamoto,
\n\u201cLuminescent \u03c0-Conjugated Poly(aryleneethynylene)s Consisting of Plural Aromatic Units: Preparation and Systematic Studies on Their Optical Properties\u201d
\nReact. Funct. Polym.<\/em> 2008<\/strong>, 68<\/em>, 1483-1491.\u00a0<\/dd>\n
[20]<\/dt>\n
K. Tanabe, T. Yasuda, M. Yoshio, and T. Kato,
\n\u201cViologen-Based Redox-Active Ionic Liquid Crystals Forming Columnar Phases\u201d
\nOrg. Lett.<\/em> 2007<\/strong>, 9<\/em>, 4271-4274.\u00a0<\/dd>\n
[19]<\/dt>\n
T. Yasuda, K. Namekawa, T. Iijima, and T. Yamamoto,
\n\u201cNew Luminescent 1,2,4-Triazole\/Thiophene Alternating Copolymers: Synthesis, Characterization, and Optical Properties\u201d
\nPolymer<\/em> 2007<\/strong>, 48<\/em>, 4375-4384.\u00a0<\/dd>\n
[18]<\/dt>\n
E. D. Baranoff, J. Voignier, T. Yasuda, V. Heitz, J.-P. Sauvage, and T. Kato,
\n\u201cA Liquid-Crystalline [2]Catenane and Its Copper(I) Complex\u201d
\nAngew. Chem. Int. Ed.<\/em> 2007<\/strong>, 46<\/em>, 4680-4683.\u00a0<\/dd>\n
[17]<\/dt>\n
I. Aprahamian, T. Yasuda, T. Ikeda, S. Saha, W. R. Dichtel, K. Isoda, T. Kato, and J. F. Stoddart,
\n\u201cA Liquid-Crystalline Bistable [2]Rotaxane\u201d
\nAngew. Chem. Int. Ed.<\/em> 2007<\/strong>, 46<\/em>, 4675-4679<\/a>.\u00a0<\/dd>\n
\"\"<\/dd>\n
[16]<\/dt>\n
M. Kimura, T. Yasuda, K. Kishimoto, G. Gotz, P. Bauerle, and T. Kato,
\n\u201cOligothiophene-Based Liquid Crystals Exhibiting Smectic A Phases in Wider Temperature Ranges\u201d
\nChem. Lett.<\/em> 2006<\/strong>, 35<\/em>, 1150-1151.\u00a0<\/dd>\n
[15]<\/dt>\n
T. Yasuda, K. Kishimoto, and T. Kato,
\n\u201cColumnar Liquid Crystalline \u03c0-Conjugated Oligothiophenes\u201d
\nChem. Commun.<\/em> 2006<\/strong>, 3399-3401.\u00a0<\/dd>\n
[14]<\/dt>\n
T. Yamamoto, T. Yasuda, K. Kobayashi, I. Yamaguchi, T. Koizumi, D. Ishii, M. Nakagawa, Y. Mashiko, and N. Shimizu,
\n\u201cUtilization of Industrially Available 2,3-Dichloro-1,3-butadiene for Direct Synthesis of 2,3-Diaryl-1,3-butadienes\u201d
\nBull. Chem. Soc. Jpn.<\/em> 2006<\/strong>, 79<\/em>, 498-500.\u00a0<\/dd>\n
[13]<\/dt>\n
T. Yasuda, Y. Sakai, S. Aramaki, and T. Yamamoto,
\n\u201cNew Coplanar (ABA)n-Type Donor-Acceptor \u03c0-Conjugated Copolymers Constituted of Alkylthiophene and Pyridazine: Synthesis Using Hexamethylditin, Self-Organized Solid Structure, and Optical and Electrochemical Properties of the Copolymers\u201d
\nChem. Mater.<\/em> 2005<\/strong>, 17<\/em>, 6060-6068<\/a>.\u00a0<\/dd>\n
\"\"<\/dd>\n
[12]<\/dt>\n
T. Yasuda, T. Imase, and T. Yamamoto,
\n\u201cSynthesis, Characterization, and Optical and Electrochemical Properties of New 2,1,3-Benzoselenadiazole-Based CT-Type Copolymers\u201d
\nMacromolecules<\/em> 2005<\/strong>, 38<\/em>, 7378-7385.\u00a0<\/dd>\n
[11]<\/dt>\n
T. Yamamoto, T. Yasuda, Y. Sakai, and S. Aramaki,
\n\u201cAmbipolar Field-Effect Transistor (FET) and Redox Characteristics of a \u03c0-Conjugated Thiophene\/1,3,4-Thiadiazole CT-Type Copolymer\u201d
\nMacromol. Rapid Commun.<\/em> 2005<\/strong>, 26<\/em>, 1214-1217. (Highlighted as a Back Cover)\u00a0<\/dd>\n
[10]<\/dt>\n
T. Yamamoto, B.-L. Lee, I. Nurulla, T. Yasuda, I. Yamaguchi, A. Wada, C. Hirose, M. Tasumi, A. Sakamoto, and E. Kobayashi,
\n\u201cTransfer of Photoenergy in \u03c0-Conjugated Polymers. Two Types of Photoluminescence that Involve Energy Transfer along a Polymer Chain\u201d
\nJ. Phys. Chem. B<\/em> 2005<\/strong>, 109<\/em>, 10605-10610.\u00a0<\/dd>\n
[9]<\/dt>\n
T. Yasuda, T. Imase, Y. Nakamura, and T. Yamamoto,
\n\u201cNew Alternative Donor-Acceptor Arranged Poly(Aryleneethynylene)s and Their Related Compounds Composed of Five-Membered Electron-Accepting 1,3,4-Thiadiazole, 1,2,4-Triazole, or ,4-Dinitrothiophene Units: Synthesis, Packing Structure, and Optical Properties\u201d
\nMacromolecules<\/em> 2005<\/strong>, 38<\/em>, 4687-4697.\u00a0<\/dd>\n
[8]<\/dt>\n
T. Yasuda, T. Imase, S. Sasaki, and T. Yamamoto, \u201cSynthesis,
\nSolid Structure, and Optical Properties of New Thiophene-Based Alternating \u03c0-Conjugated Copolymers Containing 4-Alkyl-1,2,4-triazole or 1,3,4-Thiadiazole Unit as the Partner Unit\u201d
\nMacromolecules<\/em> 2005<\/strong>, 38<\/em>, 1500-1503.\u00a0<\/dd>\n
[7]<\/dt>\n
T. Yamamoto, K. Kobayashi, T. Yasuda, Z.-H. Zhou, I. Yamaguchi, T. Ishikawa, and S. Koshihara,
\n\u201cPreparation of Polyacetylenes via Organometallic C-C Coupling Reactions\u201d
\nPolym. Bull.<\/em> 2004<\/strong>, 52<\/em>, 315-319.\u00a0<\/dd>\n
[6]<\/dt>\n
T. Yasuda, I. Yamaguchi, and T. Yamamoto,
\n\u201cPreparation of N-Grafted Polyanilines with Oligoether Side Chains by Using Ring-Opening Graft Copolymerization of Epoxide, and Their Optical, Electrochemical and Thermal Properties and Ionic Conductivity\u201d
\nJ. Mater. Chem.<\/em> 2003<\/strong>, 13<\/em>, 2138-2144.\u00a0<\/dd>\n
[5]<\/dt>\n
T. Yasuda and T. Yamamoto,
\n\u201cSynthesis and Characterization of New Luminescent 1,10-Phenanthroline- and Pyridine-Containing \u03c0-Conjugated Polymers. Their Optical Response to Protic Acid, Mn+<\/sup>, and Solvents\u201d
\nMacromolecules<\/em> 2003<\/strong>, 36<\/em>, 7513-7519.\u00a0<\/dd>\n
[4]<\/dt>\n
T. Yamamoto, Y. Saitoh, K. Anzai, H. Fukumoto, T. Yasuda, Y. Fujiwara, B.-K. Choi, K. Kuboto, and T. Miyamae,
\n\u201cPoly(1,10-phenanthroline-3,8-diyl) and Its Derivatives. Preparation, Optical and Electrochemical Properties, Solid Structure, and Their Metal Complexes\u201d
\nMacromolecules<\/em> 2003<\/strong>, 36<\/em>, 6722-6729.\u00a0<\/dd>\n
[3]<\/dt>\n
T. Yasuda, I. Yamaguchi, and T. Yamamoto,
\n\u201cPreparation of N-Grafted Polyanilines Utilizing Ring-Opening Copolymerization of Epoxide. Tuning of Solubility and Optical and Electrochemical Properties of Polyaniline\u201d
\nSynth. Met.<\/em> 2003<\/strong>, 139<\/em>, 35-38.\u00a0<\/dd>\n
[2]<\/dt>\n
T. Yasuda, I. Yamaguchi, and T. Yamamoto,
\n\u201cA New Soluble 1,10-Phenanthroline-Containing \u03c0-Conjugated Polymer: Synthesis and Effect of Metal Complexation on Optical Properties\u201d
\nAdv. Mater.<\/em> 2003<\/strong>, 15<\/em>, 293-296.\u00a0<\/dd>\n
[1]<\/dt>\n
I. Yamaguchi, T. Yasuda, and T. Yamamoto,
\n\u201cRing-Opening Graft Copolymerization of Epoxide with Polyaniline: Chemical Properties and Lithium Ionic Conductivity of the Copolymer\u201d
\nJ. Polym. Sci., Part A: Polym. Chem. <\/em>2001<\/strong>, 39<\/em>, 3137-3142.\u00a0<\/dd>\n
<\/dt>\n
<\/dd>\n<\/dl>\n

\u7dcf\u8aac\u30fb\u89e3\u8aac (Review Papers)<\/h4>\n
\n
[6]<\/dt>\n
J. Sakuda, T. Yasuda, and T. Kato,
\n\u201cLiquid-Crystalline Catenanes and Rotaxanes\u201d
\nIsr. J. Chem.<\/em> 2012<\/strong>, 52<\/em>, 854-862.\u00a0<\/dd>\n
[5]<\/dt>\n
\u5b89\u7530 \u7422\u9ebf\u30fb\u52a0\u85e4 \u9686\u53f2,
\n\u201c\u96fb\u5b50\u6d3b\u6027\u03c0\u5171\u5f79\u6db2\u6676\u306e\u65b0\u6750\u6599\u8a2d\u8a08\u3068\u6a5f\u80fd\u5316\u201d
\n\u6db2\u6676<\/em> 2011<\/strong>, 15<\/em>, 132-137.\u00a0<\/dd>\n
[4]<\/dt>\n
T. Kato, Y. Shoji, M. Yoshio, S. Yamane, and T. Yasuda,
\n\u201cFunctional Soft Materials: Nanostructured Liquid crystals and Self-Assembled Fibrous Aggregates\u201d
\nJ. Synth. Org. Chem. Jpn.<\/em> 2010<\/strong>, 68<\/em>, 1169-1174.\u00a0<\/dd>\n
[3]<\/dt>\n
T. Kato, T. Yasuda, Y. Kamikawa, and M. Yoshio,
\n\u201cSelf-Assembly of Functional Columnar Liquid Crystals\u201d
\nChem. Commun.<\/em> 2009<\/strong>, 729-739.<\/a> (Ranked as a ChemComm Most Cited Feature Article 2009)\u00a0<\/dd>\n
\"\"<\/dd>\n
[2]<\/dt>\n
I. Aprahamian, O. S. Miljanic, W. R. Dichtel, K. Isoda, T. Yasuda, T. Kato, and J. F. Stoddart,
\n\u201cClicked Interlocked Molecules\u201d
\nBull. Chem. Soc. Jpn.<\/em> 2007<\/strong>, 80<\/em>, 1856-1869.\u00a0<\/dd>\n
[1]<\/dt>\n
T. Yamamoto, I. Yamaguchi, and T. Yasuda,
\n\u201cPAEs with Heteroaromatic Rings\u201d
\nAdv. Polym. Sci.<\/em> 2005<\/strong>, 177<\/em>, 181-208.\u00a0<\/dd>\n
<\/dt>\n
<\/dd>\n<\/dl>\n

\u8457\u66f8 (Book Chapters)<\/h4>\n
\n
<\/dt>\n
<\/dt>\n
[7]<\/dt>\n
K. Isoda, T. Yasuda, M. Funahashi, and T. Kato,
\n\u201cRedox-Active (Electrochromic) Liquid Crystals\u201d
\nHandbook of Liquid Crystals<\/em>, 2nd edition (Ed. J. W. Goodby et al.), Chapter 24, in press, Wiley-VCH, Germany (2014)\u00a0<\/dd>\n
[6]<\/dt>\n
M. Funahashi, T. Yasuda, and T. Kato,
\n\u201cLiquid Crystal Semiconductors: Oligothiophene and Related Materials\u201d
\nHandbook of Liquid Crystals<\/em>, 2nd edition (Ed. J. W. Goodby et al.), Chapter 23, in press, Wiley-VCH, Germany (2014)\u00a0<\/dd>\n
[5]<\/dt>\n
\u5b89\u7530 \u7422\u9ebf,
\n\u6700\u5148\u7aef\u6750\u6599\u30b7\u30b9\u30c6\u30e0One Point<\/a>\uff08\u7b2c3\u5dfb\uff09\uff1a\u81ea\u5df1\u7d44\u7e54\u5316\u3068\u6a5f\u80fd\u6750\u6599\uff08\u9ad8\u5206\u5b50\u5b66\u4f1a \u7de8, \u5206\u62c5\u57f7\u7b46\uff09
\npp. 78-88, \u5171\u7acb\u51fa\u7248 (2012)\u00a0<\/dd>\n
[4]<\/dt>\n
T. Yasuda and T. Kato,
\n\u201cAdvanced Systems of Supramolecular Liquid Crystals\u201d
\nSupramolecular Soft Matter: Applications in Materials and Organic Electronics<\/em><\/a>
\n(Ed: T. Nakanishi), Chapter 14, pp. 283-299, Wiley, Germany (2011)\u00a0<\/dd>\n
[3]<\/dt>\n
\u5b89\u7530 \u7422\u9ebf\u30fb\u52a0\u85e4 \u9686\u53f2,
\n\u201c\u6a5f\u80fd\u6027\u30ca\u30ce\u69cb\u9020\u6db2\u6676\u306e\u65b0\u5c55\u958b\u201d
\n\u6708\u520a\u30d5\u30a1\u30a4\u30f3\u30b1\u30df\u30ab\u30eb\u30002011\u5e743\u6708\u53f7<\/a> (Vol. 40, No. 3)
\npp. 36-41, \u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248 (2011)\u00a0<\/dd>\n
[2]<\/dt>\n
\u821f\u6a4b \u6b63\u6d69\u30fb\u5b89\u7530 \u7422\u9ebf\u30fb\u52a0\u85e4 \u9686\u53f2,
\n\u201c\u6db2\u6676\u6027\u6709\u6a5f\u534a\u5c0e\u4f53\u306e\u30ca\u30ce\u69cb\u9020\u5316\u201d
\n\u6db2\u6676\u2015\u69cb\u9020\u5236\u5fa1\u3068\u6a5f\u80fd\u5316\u306e\u6700\u524d\u7dda<\/a>\uff08\u52a0\u85e4\u9686\u53f2 \u76e3\u4fee, \u5206\u62c5\u57f7\u7b46\uff09
\npp. 151-158, \u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248 (2010)\u00a0<\/dd>\n
[1]<\/dt>\n
\u5b89\u7530 \u7422\u9ebf\u30fb\u52a0\u85e4 \u9686\u53f2,
\n\u201c\u96fb\u5b50\u5171\u5f79\u7cfb\u306e\u81ea\u5df1\u7d44\u7e54\u5316\u3068\u6a5f\u80fd\u201d
\n\u96fb\u5b50\u5171\u5f79\u7cfb\u6709\u6a5f\u6750\u6599\u306e\u5275\u88fd\u30fb\u6a5f\u80fd\u958b\u767a\u30fb\u5fdc\u7528<\/a> \uff08\u6a9c\u5c71\u7232\u6b21\u90ce \u76e3\u4fee, \u5206\u62c5\u57f7\u7b46\uff09
\npp. 254-264, \u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248 (2008)\u00a0<\/dd>\n
<\/dt>\n
<\/dd>\n<\/dl>\n

\u53d7\u8cde (Awards)<\/h4>\n
\n
<\/dt>\n
<\/dt>\n
2014\u5e743\u6708<\/dt>\n
\u65e5\u672c\u5316\u5b66\u4f1a \u9032\u6b69\u8cde<\/a>
\n(The Chemical Society of Japan Award for Young Chemists)\u00a0<\/dd>\n
2013\u5e749\u6708<\/dt>\n
\u9ad8\u5206\u5b50\u5b66\u4f1a\u00a0\u65e5\u7acb\u5316\u6210\u8cde<\/a>
\n(SPSJ Hitachi Chemical Award)\u00a0<\/dd>\n
2013\u5e746\u6708<\/dt>\n
\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u4e5d\u5dde\u5c71\u53e3\u652f\u90e8 \u5968\u52b1\u8cde<\/a>
\n(Award for a Creative Young Chemist, Kyushu-Yamaguchi Branch,\u00a0The Society of Synthetic Organic Chemistry, Japan)\u00a0<\/dd>\n
2012\u5e7411\u6708<\/dt>\n
\u65e5\u672c\u5316\u5b66\u4f1a BCSJ\u8ad6\u6587\u8cde<\/a>
\n(BCSJ Award from the Chemical Society of Japan)\u00a0<\/dd>\n
2012\u5e744\u6708<\/dt>\n
\u65e5\u672c\u5316\u5b66\u4f1a \u512a\u79c0\u8b1b\u6f14\u8cde(\u5b66\u8853)<\/a>
\n(CSJ Presentation Award 2012 from the Chemical Society of Japan)\u00a0<\/dd>\n
2011\u5e742\u6708<\/dt>\n
\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a \u5bcc\u58eb\u30d5\u30a3\u30eb\u30e0\u7814\u7a76\u4f01\u753b\u8cde<\/a>
\n(Fujifilm Award in Synthetic Organic Chemistry, Japan)\u00a0<\/dd>\n
2010\u5e749\u6708<\/dt>\n
\u65e5\u672c\u6db2\u6676\u5b66\u4f1a\u8cde \u5968\u52b1\u8cde<\/a>
\n(Award for Young Researchers from the Japanese Liquid Crystal Society)\u00a0<\/dd>\n
2009\u5e744\u6708<\/dt>\n
\u65e5\u672c\u5316\u5b66\u4f1a \u512a\u79c0\u8b1b\u6f14\u8cde(\u5b66\u8853)<\/a>
\n(CSJ Presentation Award 2009 from the Chemical Society of Japan)\u00a0<\/dd>\n
2007\u5e741\u6708<\/dt>\n
\u65e5\u672cMRS\u5b66\u8853\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0 \u5968\u52b1\u8cde
\n(Award for Encouragement of Research in Materials Science from the Materials Research Society of Japan)\u00a0<\/dd>\n
2006\u5e749\u6708<\/dt>\n
\u65e5\u672c\u6db2\u6676\u5b66\u4f1a \u8679\u5f69\u8cde
\n(Kosai Award from Japanese Liquid CrystalSociety)\u00a0<\/dd>\n
2006\u5e742\u6708<\/dt>\n
\u624b\u5cf6\u8a18\u5ff5\u7814\u7a76\u8cde \u535a\u58eb\u8ad6\u6587\u8cde
\n(Tejima Doctoral Dissertation Award)\u00a0<\/dd>\n
<\/dt>\n
<\/dd>\n<\/dl>\n

 <\/p>\n

 <\/p>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

\u7565\u6b74 2005\u5e74 \u6771\u4eac\u5de5\u696d\u5927\u5b66 \u5927\u5b66\u9662\u7dcf\u5408\u7406\u5de5\u5b66\u7814\u7a76\u79d1 \u535a\u58eb\u8ab2\u7a0b\u4fee\u4e86 2005\u5e74~ \u6771\u4eac\u5927\u5b66 \u5927\u5b66\u9662\u7406\u5b66\u7cfb\u7814\u7a76\u79d1 COE\u7279\u4efb\u7814\u7a76\u54e1 2006\u5e74~ \u65e5\u672c\u5b66\u8853\u632f\u8208\u4f1a\u7279\u5225\u7814\u7a76\u54e1(PD) (\u6771\u4eac\u5927\u5b66 \u5de5\u5b66\u7cfb\u7814\u7a76\u79d1) 2008\u5e74~ […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":11,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-241","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/pages\/241","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/comments?post=241"}],"version-history":[{"count":0,"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/pages\/241\/revisions"}],"up":[{"embeddable":true,"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/pages\/11"}],"wp:attachment":[{"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/media?parent=241"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}