{"id":11155,"date":"2015-04-28T14:52:02","date_gmt":"2015-04-28T05:52:02","guid":{"rendered":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/?page_id=11155"},"modified":"2015-05-27T16:44:21","modified_gmt":"2015-05-27T07:44:21","slug":"%e5%9c%9f%e5%b1%8b-%e9%99%bd-%e4%b8%80","status":"publish","type":"page","link":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/staff-2\/%e5%9c%9f%e5%b1%8b-%e9%99%bd-%e4%b8%80\/","title":{"rendered":"\u571f`\u5c4b\u3000\u967d \u4e00"},"content":{"rendered":"
\"\"<\/div>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
\u7565\u6b74<\/th>\n<\/tr>\n
2001<\/td>\n\u8fd1\u757f\u5927\u5b66\u5927\u5b66\u9662\u7dcf\u5408\u7406\u5de5\u5b66\u7814\u7a76\u79d1
\u7269\u8cea\u7cfb\u5de5\u5b66\u5c02\u653b\u3000\u535a\u58eb\u524d\u671f\u8ab2\u7a0b\u3000\u4fee\u4e86<\/td>\n<\/tr>\n
2004<\/td>\n\u5948\u826f\u5148\u7aef\u79d1\u5b66\u6280\u8853\u5927\u5b66\u9662\u5927\u5b66\u7269\u8cea\u5275\u6210\u79d1\u5b66\u7814\u7a76\u79d1
\u7269\u8cea\u5275\u6210\u79d1\u5b66\u5c02\u653b\u3000\u535a\u58eb\u5f8c\u671f\u8ab2\u7a0b\u3000\u4fee\u4e86<\/td>\n<\/tr>\n
2004-2007<\/td>\n\uff08\u72ec\uff09\u7523\u696d\u6280\u8853\u7dcf\u5408\u7814\u7a76\u6240\u3000\u535a\u58eb\u7814\u7a76\u54e1<\/td>\n<\/tr>\n
2007-2010<\/td>\n\uff08\u72ec\uff09\u7406\u5316\u5b66\u7814\u7a76\u6240\u57fa\u5e79\u7814\u7a76\u6240
\u5206\u5b50\u60c5\u5831\u751f\u547d\u79d1\u5b66\u7814\u7a76\u63a8\u9032\u30b0\u30eb\u30fc\u30d7\u3000\u5354\u529b\u7814\u7a76\u54e1<\/p>\n

\n\u4e5d\u5dde\u5927\u5b66\u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u9662
\u5206\u5b50\u60c5\u5831\u9023\u643a\u7814\u7a76\u30bb\u30f3\u30bf\u30fc\u3000\u535a\u58eb\u7814\u7a76\u54e1\uff08\u517c\u4efb\uff09<\/td>\n<\/tr>\n

2010-2015<\/td>\n(\u8ca1)\u4e5d\u5dde\u5148\u7aef\u79d1\u5b66\u6280\u8853\u7814\u7a76\u6240 \u30ca\u30ce\u30c6\u30af\u7814\u7a76\u5ba4 \u7814\u7a76\u54e1
\u4e5d\u5dde\u5927\u5b66 \u672a\u6765\u79d1\u5b66\u5275\u9020\u30bb\u30f3\u30bf\u30fc \u5ba2\u54e1\u52a9\u6559<\/td>\n<\/tr>\n
2015-<\/td>\n\u4e5d\u5dde\u5927\u5b66\u3000\u6700\u5148\u7aef\u6709\u6a5f\u5149\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u7814\u7a76
\u30bb\u30f3\u30bf\u30fc\u3000\u5b66\u8853\u7814\u7a76\u54e1<\/td>\n<\/tr>\n
\u5b66\u4f4d<\/th>\n<\/tr>\n
\u535a\u58eb\uff08\u5de5\u5b66\uff09\uff08\u5948\u826f\u5148\u7aef\u5927\u30012004\u5e74\uff09<\/td>\n<\/tr>\n
\u6240\u5c5e\u5b66\u4f1a<\/th>\n<\/tr>\n
\u65e5\u672c\u5316\u5b66\u4f1a\u3001\u9ad8\u5206\u5b50\u5316\u5b66\u4f1a\u3001\u30b7\u30af\u30ed\u30c7\u30ad\u30b9\u30c8\u30ea\u30f3\u5b66\u4f1a<\/td>\n<\/tr>\n
\u7814\u7a76\u5206\u91ce<\/th>\n<\/tr>\n
\u8d85\u5206\u5b50\u5316\u5b66\uff08\u754c\u9762\u5316\u5b66\u3001\u751f\u4f53\u95a2\u9023\u5316\u5b66\u3001\u8907\u5408\u6750\u6599\u5316\u5b66\u3001\u9ad8\u5206\u5b50\u5316\u5b66\u3001\u69cb\u9020\u5316\u5b66\u306a\u3069\uff09<\/td>\n<\/tr>\n
\u8da3\u5473<\/th>\n<\/tr>\n
\u30c9\u30e9\u30a4\u30d6\u3001\u30ab\u30e1\u30e9\u3001\u9152\u3001\u80b4<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

\u7814\u7a76\u6210\u679c<\/h3>\n

\u8ad6\u6587\u767a\u8868<\/h4>\n
\n
\n
[35]<\/dt>\n
Tailoring of the desired selectivity and the turn-on detection range in a self-assembly-based fluorescence sensory system
\nChem. Sci.<\/strong>, (in press)
\nT. Noguchi, B. Roy, D. Yoshihara, Y. Tsuchiya<\/span><\/strong>, T. Yamamoto, S. Shinkai*\n<\/dd>\n

<\/p>\n

[34]<\/dt>\n
One-pot Optical Sensing of Keto Acids through a Combination of Oxime-click Reaction and Aggregation-induced Emission (AIE)
\nChem. Lett<\/strong>, (in press)
\nD. Yoshihara, T. Noguchi, Y. Tsuchiya<\/span><\/strong>, B. Roy, T. Yamamoto, S. Shinkai*\n<\/dd>\n

<\/p>\n

[33]<\/dt>\n
Molecular recognition directed supramolecular control over perylene-bisimide aggregation resulting in aggregation induced enhanced emission (AIEE) and induced chiral amplification
\nJ. Mater. Chem. C<\/strong>, 3, 2310-2318 (2015)
\nB. Roy, Y. Tsuchiya<\/span><\/strong>, T. Noguchi, D. Yoshihara, T. Yamamoto, S. Shinkai*
\nDOI:10.1039\/C4TC02538E<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[32]<\/dt>\n
Translation of Dicarboxylate Structural Information to Fluorometric Optical Signals through Self-Assembly of Guanidinium-Tethered Oligophenylenevinylene
\nChem. Eur. J.<\/strong>, 20, 13938-13944 (2014)
\nT. Noguchi, B. Roy, Y. Tsuchiya<\/span><\/strong>, D. Yoshihara, T. Yamamoto, S. Shinkai*
\nDOI: 10.1002\/chem.2014404028<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[31]<\/dt>\n
Cyclization-Induced Turn-On Fluorescence System Applicable to Dicarboxylate Sensing
\n Chem. Eur. J.<\/strong>, 20, 381-384 (2014)
\nT. Noguchi, B. Roy, D. Yoshihara, Y. Tsuchiya<\/span><\/strong>, T. Yamamoto, S. Shinkai*
\n[Chemistry Views highlight (Wiley-VHC).]<\/span><\/strong>
\nDOI: 10.1002\/chem.201304031<\/a> <\/strong>\n<\/dd>\n

<\/p>\n

[30]<\/dt>\n
Nucleotide Sensing with a Perirene-based Molecular Receptor via Amplified Fluorescence Quenching
\n Org. Biomol. Chem.<\/strong>, 12, 561-565 (2014)
\nB. Roy, T. Noguchi, D.Yoshihara, Y. Tsuchiya<\/span><\/strong>, T. Yamamoto, S. Shinkai*
\nDOI: 10.1039\/C3OB41586D<\/a> <\/strong>\n<\/dd>\n

<\/p>\n

[29]<\/dt>\n
Creation of Circularly Polarized Luminescence from an Achiral Polyfluorene Deriivative through Complexation with Helix-forming Polysaccharides: Important of the meta-Linkage Chain for Heliix formation
\nChem. Asian J.<\/strong>, 9, 218-222 (2014)
\nT. Shiraki, Y. Tsuchiya<\/span><\/strong>, T. Noguchi, S. Tamaru, N. Suzuki, M. Taguchi, M. Fujiki, S. Shinkai*
\nDOI: 10.1002\/asia.201301216<\/a> <\/strong>\n<\/dd>\n

<\/p>\n

[28]<\/dt>\n
Cyclodextrin-Assisted Synthesis of a Metallosupramolecular Tb(III) Polymer and Its Fluorescence Properties and Chiral Recognition
\nChem. Eur. J.<\/strong> 19, 15485-15488 (2013)
\nD. Yoshihara, Y. Tsuchiya<\/span><\/strong>, T. Noguchi, T. Yamamoto, S. Shinkai*
\nDOI: 10.1002\/chem.201302138<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[27]<\/dt>\n
Dye-sensitized Preparation of Chiral Plasmonic Ag Nanoparticles on Helical Polysaccharides
\nSupramol. Chem.<\/strong>, 25, 748-755 (2013)
\nY. Tsuchiya*<\/span><\/strong>, T. Noguchi, D. Yoshihara, T. Yamamoto, T. Shiraki, S. Tamaru, S. Shinkai*
\nDOI: 10.1080\/10610278.2013.835049<\/a> <\/strong>\n<\/dd>\n

<\/p>\n

[26]<\/dt>\n
Selective Detection of NADPH among Four Pyridine-Nucleotide Cofactors by a Fluorescent Probe Based on Aggregation-Induced Emission
\nMacromol. Rapid Commun<\/strong>, 34, 779-784 (2013)
\nT. Noguchi, A. Dawn, D. Yoshihara, Y. Tsuchiya<\/span><\/strong>, T. Yamamoto, S. Shinkai*
\n[Materials Views (Wiley-VHC).]<\/span><\/strong>
\nDOI: 10.1002\/marc.201300015<\/a> <\/strong>\n<\/dd>\n

<\/p>\n

[25]<\/dt>\n
Nonlinear Fluorescence Response Driven by ATP-induced Selfassembly of Guanidium-tethered Tetraphenylethene
\nChem. Commun<\/strong>, 48, 8090-8092 (2012)
\nT. Noguchi, T. Shiraki, A. Dawn, Y. Tsuchiya<\/span><\/strong>, T. N. L. Le, T. Yamamoto, S. Shinkai*
\n[Selected as Newsworthy Chemistry (ACS).]<\/span><\/strong>
\nDOI: 10.1039\/c2cc33262k<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[24]<\/dt>\n
Unexpected Chiral induction from achiral cationic polythiophene aggregates and its application to the sugar pattern recognition
\nChem. Commun<\/strong>, 48, 7091-7093 (2012)
\nT. Shiraki, A. Dawn, Y. Tsuchiya<\/span><\/strong>, T. Yamamoto, S. Shinkai*
\nDOI: 10.1039\/c2cc33162d<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[23]<\/dt>\n
Creation of Chiral Thixotropic Gels through a Crown-Ammonium Interaction and Their Application to a Memory-Erasing Recycle System
\nChem. Eur. J.<\/strong>, 18, 2832-2838 (2012)
\nA. A. Sobczuk, Y. Tsuchiya<\/span><\/strong>, T. Shiraki, S. Tamaru, S. Shinkai*
\nDOI: 10.1002\/chem.201103249<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[22]<\/dt>\n
Stereochemistry Dependent, Mechanoresponsive Supramolecular Host Assemblies for Fullerenes: A Guest Induced Enhancement of Thixotropy
\nJ. Am. Chem. Soc.<\/strong>, 134, 2161-2171 (2012)
\nA. Dawn, T. Shiraki, H. Ichikawa, A. Takada, Y. Takahashi, Y. Tsuchiya<\/span><\/strong>, T. N. L. Le, S. Shinkai*
\nDOI: 10.1021\/ja211032m<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[21]<\/dt>\n
Fine Wettability Control Created by a Photochemical Combination Method for Inkjet Printing on Self-Assembled Monolayers
\nAdv. Mater.<\/strong>, 24, 968-972 (2012)
\nY. Tsuchiya<\/span><\/strong>, S. Haraguchi, M. Ogawa, T. Shiraki, H. Kakimoto, O. Gotou, T. Yamada, K. Okumoto, S. Nakatani, K. Sakanoue, S. Shinkai*
\nDOI: 10.1002\/adma.201104277<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[20]<\/dt>\n
Supramolecular Dye Inclusion Single Crystals Created from 2,3,6-Trimethyl-\u03b2-cyclodextrin and Porphyrins
\nChem. Eur. J.<\/strong>, 18, 456-465 (2012)
\nY. Tsuchiya*<\/span><\/strong>, T. Shiraki, T. Matsumoto, K. Sugikawa, K. Sada, A. Yamano, S. Shinkai*
\n[Selected as Frontispiece.]<\/span><\/strong>
\nDOI: 10.1002\/chem.201102075<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[19]<\/dt>\n
Heat and light dual switching of a single walled carbon nanotube\/thermo-responsive helical polysaccharide complex: a new responsive system applicable to photodynamic therapy
\nChem. Commun<\/strong>, 47, 7065-7067 (2011)
\nT. Shiraki, A. Dawn, T. N. L. Le, Y. Tsuchiya<\/span><\/strong>, S. Tamaru, N. Enomoto, J. Hojo, S. Shinkai*
\nDOI: 10.1039\/C1CC11288K<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[18]<\/dt>\n
A pH-responsive carboxylic \u03b2-1,3-glucan polysaccharide for complexation with polymeric guests
\nOrg. Biomol. Chem.<\/strong> 9, 4266-4275 (2011)
\nT. N. L. Le, T. Shiraki, A. Dawn, Y. Tsuchiya<\/span><\/strong>, D. Tokunaga, S. Tamaru, N. Enomoto, J. Hojo, S. Shinkai*
\nDOI: 10.1039\/C1OB05114H<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[17]<\/dt>\n
Facile Fabrication of CD-Active One Dimensional Polypyrrole by the Templating Effect of Helix-Forming Anionic Polysaccharide
\nSupramol. Chem.<\/strong>, 23, 239-243 (2011)
\nK. Sugikawa, T. Shiraki, Y. Tsuchiya<\/span><\/strong>, S. Haraguchi, K. Sada, S. Shinkai*
\nDOI: 10.1080\/10610278.2010.521837<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[16]<\/dt>\n
Single-crystal Structure of Porphyrin Bicapped with Trimethyl-\u03b2-cyclodextrins: A Novel Dye-oriented Material
\nChem. Lett.<\/strong>, 40, 99-101 (2011)
\nY. Tsuchiya*<\/span><\/strong>, A. Yamano, T. Shiraki, K. Sada, S. Shinkai*
\n[Selected as Editor\u2019s Choice.]<\/span><\/strong>
\nDOI: 10.1246\/cl.2011.99<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[15]<\/dt>\n
Thermo- and Solvent-Responsive Polymer Complex Created from Supramolecular Complexation between a Helix-Forming Polysaccharide and Cationic Polythiophene
\nJ. Am. Chem. Soc<\/strong>, 132, 13928-13935 (2010)
\nT. Shiraki, A. Dawn, Y. Tsuchiya<\/span><\/strong>, S. Shinkai*
\nDOI: 10.1021\/ja1067349<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[14]<\/dt>\n
Ratiometric Fluorescent Sensor for 2,4,6-Trinitrotoluene Designed Based on Energy Transfer between Size-different Quantum Dots
\nChem. Lett<\/strong>, 39, 156-158 (2010)
\nT. Shiraki, Y. Tsuchiya<\/span><\/strong>, S. Shinkai*
\nDOI: 10.1246\/cl.2010.156<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[13]<\/dt>\n
A Polysaccharide-Based Container Transportation System Powered by Molecular Motors
\nAngew. Chem. Int. Ed.<\/strong>, 49, 724-727 (2010)
\nY. Tsuchiya<\/span><\/strong>, T. Komori, M. Hirano, T. Shiraki, A. Kakugo, T. Ide, J.-P. Gong, S. Yamada, T. Yanagida*, S. Shinkai*
\n[Selected as Newsworthy Paper.]<\/span><\/strong>
\nDOI: 10.1002\/anie.200904909<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[12]<\/dt>\n
Alignment of Polysaccharide-SWNT Composites by Metal-Ligand Interactions
\nChem. Lett.<\/strong>, 38, 812-813 (2009)
\nY. Tsuchiya<\/span><\/strong>, S. Haraguchi, K. Sugikawa, T. Shiraki, K. Kaneko, S. Shinkai*
\nDOI: 10.1246\/cl.2009.812<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[11]<\/dt>\n
On the Helical Motif of the Complexes Created by Association of Helix-Forming Schizophyllan (SPG) and Helix-Forming Polythiophene Derivatives
\nChem. Eur. J.<\/strong>, 15, 11221-11228 (2009)
\nS. Haraguchi, Y. Tsuchiya<\/span><\/strong>, T. Shiraki, K. Sugikawa, K. Sada, S. Shinkai*
\nDOI: 10.1002\/chem.200901003<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[10]<\/dt>\n
Control of polythiophene redox potentials based on supramolecular complexation with helical schizophyllan
\nChem. Commun<\/strong>, 45, 6086-6088 (2009)
\nS. Haraguchi, Y. Tsuchiya<\/span><\/strong>, T. Shiraki, K. Sada, S. Shinkai*
\nDOI: 10.1039\/b910085g<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[9]<\/dt>\n
Quantum Dots Arrangement and Energy Transfer Control via Charge-Transfer Complex Achieved on Poly(Phenylene Ethynylene)\/Schizophyllan Nanowires
\nChem. Asian J.<\/strong>, 4, 1434-1441 (2009)
\nT. Shiraki, S. Haraguchi, Y. Tsuchiya<\/span><\/strong>, S. Shinkai*
\nDOI: 10.1002\/asia.200900175<\/a><\/strong>\n<\/dd>\n

<\/p>\n

[8]<\/dt>\n
Photocurrent generators derived from non-covalently assembled soft-matter molecular system
\nJ. Oleo Sci.<\/strong>, 56, 603-610 (2007)
\nY. Tsuchiya<\/span><\/strong>, T. Arimura*, N. Minami, M. Tashiro, M. Tachiya\n<\/dd>\n

<\/p>\n

[7]<\/dt>\n
13C NMR longitudinal relaxation time studies of a molecular tweezers derived from a calixarene-porphyrin conjugate
\nJ. Oleo Sci.<\/strong>, 56, 155-158 (2007)
\nT. Arimura*, T. Nishioka, Y. Suga, S. Kumamoto, Y. Tsuchiya<\/span><\/strong>, T. Yamaguchi, M. Tachiya\n<\/dd>\n

<\/p>\n

[6]<\/dt>\n
Carbon-13 NMR longitudinal relaxation time study of an ionophoric 1,3-alternate-shaped calix[4]arene ester
\nJ. Oleo Sci.<\/strong>, 55, 75-78 (2006)
\nT. Arimura*, T. Nishioka, S. Kumamoto, Y. Tsuchiya<\/span><\/strong>, T. Yamaguchi, M. Tachiya\n<\/dd>\n

<\/p>\n

[5]<\/dt>\n
Sodium-23 NMR studies of sodium ion ensembles with a 1,3-alternate-shaped calix[4]arene
\nJ. Oleo Sci.<\/strong>, 55, 71-74 (2006)
\nT. Arimura*, T. Nishioka, S. Kumamoto, Y. Tsuchiya<\/span><\/strong>, T. Yamaguchi, M. Tachiya\n<\/dd>\n

<\/p>\n

[4]<\/dt>\n
Photocurrent-Boosting by Intramembrane Electron Mediation between Titania Nanoparticles Dispersed into Nafion-Porphyrin Composites
\nChem. Mater.<\/strong>, 17, 4018-4022 (2005)
\nA. Ikeda*, Y. Tsuchiya<\/span><\/strong>, T. Konishi, S. Ogasawara, J. Kikuchi\n<\/dd>\n

<\/p>\n

[3]<\/dt>\n
A photocurrent-generator utilizing a polyelectrolyte as a matrix of dyes
\nJ. Mater. Chem.<\/strong>, 14, 1128-1131 (2004)
\nY. Tsuchiya<\/span><\/strong>, A. Ikeda*, T. Konishi, J. Kikuchi\n<\/dd>\n

<\/p>\n

[2]<\/dt>\n
Improvement of Quantum Yields for Photoinduced Energy\/Electron Transfer by Isolation of Self-Aggregative Zinc Tetraphenyl Porphyrin-Pendant Polymer Using Cyclodextrin Inclusion in Aqueous Solution
\nJ. Phys. Chem. B<\/strong>, 107, 11261-11266 (2003)
\nT. Konishi, A. Ikeda*, M. Asai, T. Hatano, O. Ito*, Y. Tsuchiya<\/span><\/strong>, J. Kikuchi\n<\/dd>\n

<\/p>\n

[1]<\/dt>\n
Electrochemical Polymerization of Pyrrole-substituted Tetrathiafulvalenyl-thiol, sulfone, and disulfide
\nElectrochemistry<\/strong>, 70, 584-586 (2002)
\nY. Tsuchiya<\/span><\/strong>, H. Fujihara*\n<\/dd>\n<\/div>\n<\/dl>\n

Proceeding<\/h4>\n
\n
[2]<\/dt>\n
Photocurrent generators derived from non-covalently assembled cyclodextrin nano-system.
\nJ. Photopolym. Sci. Technol.(Proc. 24th International Conference of Photopolymer Science and Technology), 20<\/strong>, 533-538 (2007) (Chiba, Japan).
\nT. Arimura, Y. Tsuchiya<\/span><\/strong>, M. Tashiro, M. Tachiya\n<\/dd>\n
[1]<\/dt>\n
Photocurrent generations derived from non-covalently assembled porphyrin conjugate nano-system.
\nJ. Photopolym. Sci. Technol.(Proc. 24th International Conference of Photopolymer Science and Technology), 19<\/strong>, 409-411 (2006) (Chiba, Japan).
\nY. Tsuchiya<\/span><\/strong>, T. Arimura, M. Tachiya\n<\/dd>\n<\/dl>\n

\u7dcf\u8aac\u3001\u89e3\u8aac\u3001\u8457\u66f8<\/h4>\n
\n
[5]<\/dt>\n
\u201cDye Inclusion Single Crystals; Preparations, Structures and Functions\u201d
\nChapter 11 in \u201cCyclodextrins: Synthesis, Chemical Applications and Role in Drug Delivery\u201d, F. G. Ramirez (Ed)
\nNova Science Publishers: New York, USA, 2015 (in press)
\nISBN: 978-1-63482-788-1
\n<\/a><\/strong>
\nY. Tsuchiya<\/span>\n<\/dd>\n
[4]<\/dt>\n
\u300c\u591a\u7cd6\u3092\u5229\u7528\u3057\u305f\u30ca\u30ce\u4eba\u5de5\u30b3\u30f3\u30c6\u30ca\u8f38\u9001\u30b7\u30b9\u30c6\u30e0\u306e\u958b\u767a\u300d
\n\u30bb\u30e9\u30df\u30c3\u30af\u30b9\uff08Ceramics Japan\uff09\uff0c2014\u5e74\uff0c49\u5dfb\uff0cNo.5\uff0cpp 406-410\uff0e
\n\u571f\u5c4b \u967d\u4e00<\/span>\n<\/dd>\n
[3]<\/dt>\n
\u300c\u3089\u305b\u3093\u5f62\u6210\u591a\u7cd6\u3092\u30c6\u30f3\u30d7\u30ec\u30fc\u30c8\u3068\u3057\u305f\u5149\u6d3b\u6027\u30d7\u30e9\u30ba\u30e2\u30cb\u30c3\u30af\u91d1\u5c5e\u30ca\u30ce\u7c92\u5b50\u300d
\n\u30b3\u30ed\u30a4\u30c9\u304a\u3088\u3073\u754c\u9762\u5316\u5b66\u90e8\u4f1a\u30cb\u30e5\u30fc\u30b9\u30ec\u30bf\u30fc\uff08Colloid & Interface Commun.\uff09\uff0c2013\u5e74\uff0c38\u5dfb\uff0cNo.4\uff0cpp 12-15\uff0e
\n\u571f\u5c4b \u967d\u4e00<\/span>\n<\/dd>\n
[2]<\/dt>\n
“New nanomaterial created through complexation with helix-forming polysaccharides”
\n\u300c\u3089\u305b\u3093\u591a\u7cd6\u3068\u6a5f\u80fd\u6027\u6750\u6599\u306e\u8907\u5408\u5316\u306b\u3088\u308b\u30ca\u30ce\u30de\u30c6\u30ea\u30a2\u30eb\u306e\u958b\u767a\u300d
\n\u6708\u520a\u30d5\u30a1\u30a4\u30f3\u30b1\u30df\u30ab\u30eb\uff0c2011\u5e74\uff0c40\u5dfb\uff0cpp7-14\uff0e
\n\u767d\u6728 \u667a\u4e08\uff0c\u571f\u5c4b \u967d\u4e00<\/span>\uff0c\u65b0\u6d77 \u5f81\u6cbb\n<\/dd>\n
[1]<\/dt>\n
“Advanced Functionalities of Macromolecular Assemblies Designed by Molecular Recognition”
\n\u300c\u5206\u5b50\u8a8d\u8b58\u3092\u6d3b\u7528\u3059\u308b\u9ad8\u5206\u5b50\u7d44\u7e54\u4f53\u306e\u30c7\u30b6\u30a4\u30f3\u3068\u9ad8\u6b21\u6a5f\u80fd\u306e\u5275\u51fa\u300d
\n\u79d1\u5b66\u3068\u5de5\u696d\uff0c2010\u5e74\uff0c84\u5dfb\uff0cpp367-375\uff0e
\n\u571f\u5c4b \u967d\u4e00<\/span>\uff0c\u767d\u6728 \u667a\u4e08\uff0c\u65b0\u6d77 \u5f81\u6cbb\n<\/dd>\n<\/dl>\n

\u53d7\u8cde<\/h4>\n
\n
<\/dt>\n
\u7b2c30\u56de\u3000\u30b7\u30af\u30ed\u30c7\u30ad\u30b9\u30c8\u30ea\u30f3\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u30dd\u30b9\u30bf\u30fc\u8cde<\/b>\uff082013\u5e749\u6708\uff09\n<\/dd>\n
\u7b2c9\u56de\u3000\u7a4d\u6c34\u5316\u5b66\u3000\u81ea\u7136\u306b\u5b66\u3076\u3082\u306e\u3065\u304f\u308a\u3000\u7814\u7a76\u52a9\u6210\u30d7\u30ed\u30b0\u30e9\u30e0\u3000\u5968\u52b1\u8cde<\/b>\uff082010\u5e7410\u6708\uff09\n<\/dd>\n<\/dl>\n

\u4f9d\u983c\u30fb\u62db\u5f85\u8b1b\u6f14<\/h4>\n
\n
[8]<\/dt>\n
\u300c\u30b7\u30af\u30ed\u30c7\u30ad\u30b9\u30c8\u30ea\u30f3\uff0d\u91d1\u5c5e\u30dd\u30eb\u30d5\u30a3\u30ea\u30f3\u5305\u63a5\u932f\u4f53\u7d50\u6676\u306e\u5358\u7d50\u6676\uff38\u7dda\u69cb\u9020\u89e3\u6790\u300d
\n\u5206\u5b50\u30fb\u7269\u8cea\u5408\u6210\u30d7\u30e9\u30c3\u30c8\u30d5\u30a9\u30fc\u30e0\u5e73\u621025\u5e74\u5ea6\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\uff0c2014\u5e743\u670811\u65e5\n<\/dd>\n
[7]<\/dt>\n\n\u7b2c11\u56de \u7a4d\u6c34\u5316\u5b66 \u81ea\u7136\u306b\u5b66\u3076\u3082\u306e\u3065\u304f\u308a\u30d5\u30a9\u30fc\u30e9\u30e0\uff0c2013\u5e7410\u670817\u65e5\n<\/dd>\n
[6]<\/dt>\n
\u300c\u5206\u5b50\u8a8d\u8b58\u3092\u5229\u7528\u3057\u305f\u30ca\u30ce\u30c6\u30af\u30ce\u30ed\u30b8\u30fc\u3000\uff5e\u751f\u7269\u3092\u304a\u624b\u672c\u306b\u3057\u305f\u3082\u306e\u3065\u304f\u308a\uff5e\u300d
\n\u5d07\u57ce\u5927\u5b66\u5de5\u5b66\u90e8\u30ca\u30ce\u30b5\u30a4\u30a8\u30f3\u30b9\u5b66\u79d1\u7279\u5225\u8b1b\u6f14\u4f1a\uff0c2013\u5e746\u670827\u65e5\n<\/dd>\n
[5]<\/dt>\n
\u300c\u9ad8\u6b21\u6a5f\u80fd\u7d44\u7e54\u4f53\u306b\u3088\u308b\u30ca\u30ce\u6750\u6599\u30fb\u30ca\u30ce\u30b7\u30b9\u30c6\u30e0\u306e\u69cb\u7bc9\u300d
\n\u798f\u5ca1\u65b0\u30c6\u30af\u30ce\u30ed\u30b8\u30fc\u5275\u6210\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\uff0c2012\u5e7411\u670827\u65e5\n<\/dd>\n
[4]<\/dt>\n
\u300c\u9ad8\u6b21\u5206\u5b50\u8a8d\u8b58\u3092\u99c6\u4f7f\u3057\u305f\u30ca\u30ce\u30b7\u30b9\u30c6\u30e0\u3068\u30ca\u30ce\u6750\u6599\u300d
\n\u7b2c4\u56de\u30cd\u30a4\u30c1\u30e3\u30fc\u30c6\u30af\u30ce\u30ed\u30b8\u30fc\u7814\u7a76\u4f1a\u5e79\u4e8b\u4f1a\uff0c2012\u5e747\u670811\u65e5\n<\/dd>\n
[3]<\/dt>\n
\u300c\u30d0\u30a4\u30aa\u30df\u30e1\u30c6\u30a3\u30c3\u30af\u5305\u63a5\u8907\u5408\u4f53\u306e\u5358\u7d50\u6676\u300d
\n\u65e5\u672c\u5316\u5b66\u4f1a\u7b2c92\u6625\u5b63\u5e74\u4f1a\u3000Advanced Technology Program\uff0c2012\u5e743\u670825\u65e5\n<\/dd>\n
[2]<\/dt>\n
\u300c\u751f\u4f53\u5206\u5b50\u30e2\u30fc\u30bf\u30fc\u3092\u7528\u3044\u305f\u4eba\u5de5\u30b3\u30f3\u30c6\u30ca\u8f38\u9001\u30b7\u30b9\u30c6\u30e0\u306e\u52d5\u4f5c\u5236\u5fa1\u306b\u95a2\u3059\u308b\u7814\u7a76\u300d
\n\u7b2c9\u56de \u7a4d\u6c34\u5316\u5b66 \u81ea\u7136\u306b\u5b66\u3076\u3082\u306e\u3065\u304f\u308a\u30d5\u30a9\u30fc\u30e9\u30e0\uff0c2011\u5e7410\u670817\u65e5\n<\/dd>\n
[1]<\/dt>\n
\u300c\u7523\u5b98\u5b66\u5354\u50cd\u306b\u3088\u308b\u5171\u540c\u7814\u7a76\u4e8b\u4f8b\u306b\u3064\u3044\u3066: \u64a5\u6cb9\u754c\u9762\u306e\u5149\u30d1\u30bf\u30fc\u30cb\u30f3\u30b0\u6280\u8853\u306e\u958b\u767a\u300d
\n\u4e5d\u5dde\u5927\u5b66G-COE \u7b2c\uff14\u56de\u7523\u5b66\u9023\u643a\u30bb\u30df\u30ca\u30fc\uff0c2011\u5e748\u67083\u65e5\n<\/dd>\n<\/dl>\n

\u7279\u8a31<\/h4>\n
\n
[3]<\/dt>\n
\u7279\u8a315561780\u300c\u5305\u63a5\u932f\u4f53\u7d50\u6676\u6750\u6599\u300d<\/dd>\n
[2]<\/dt>\n
\u7279\u8a315561780\u300c\u30ab\u30ea\u30c3\u30af\u30b9\u30a2\u30ec\u30fc\u30f3\u8a98\u5c0e\u4f53\u3092\u7528\u3044\u308b\u5e0c\u571f\u985e\u91d1\u5c5e\u306e\u691c\u51fa\u6cd5\u300d<\/dd>\n
[1]<\/dt>\n
\u7279\u958b2005-251426\u300c\u5149\u96fb\u5909\u63db\u7d20\u5b50\u3092\u7528\u3044\u305f\u8272\u7d20\u91cf\u306e\u6e2c\u5b9a\u65b9\u6cd5\u300d<\/dd>\n<\/dl>\n

\u5b66\u4f1a\u767a\u8868<\/h4>\n
\n
\u56fd\u969b\u5b66\u4f1a<\/dd>\n
[6]<\/dt>\n
Supramolecular Dye Inclusion Single Crystals Created from Cyclodextrins and Porphyrin
\nthe 2012 International Symposium on Macrocyclic and Supramolecular Chemistry, ISMSC-7, Otago, Dunedin, New Zealand, February, 2012.
\nY. Tsuchiya<\/span><\/strong>, T. Shiraki, T. Matsumoto, K. Sugikawa, K. Sada, A. Yamano, S. Shinkai\n<\/dd>\n
[5]<\/dt>\n
Artificial Container Transportation System (Oral)
\nThe 2010 International Chemical Congress of Pacific Basin Societie, Honolulu, Hawaii, USA, December, 2010.
\nY. Tsuchiya<\/span><\/strong>, T. Komori, T. Shiraki, A. Kakugo, J.-P. Gong, T. Yanagida, S. Shinkai\n<\/dd>\n
[4]<\/dt>\n
Novel Polysaccharide-Based Container Transportation System Powered by Molecular Motors
\nThe 5th International Symposium on Macrocyclic & Supramolecular Chemistry, Nara, Japan, June, 2010.
\nY. Tsuchiya<\/span><\/strong>, T. Komori, T. Shiraki, T. Yanagida, S. Shinkai\n<\/dd>\n
[3]<\/dt>\n
Container Transportation Model System by Using Polysaccharide
\nThe 1st FAPS Polymer Congress, Nagoya, Japan, September, 2009.
\nY. Tsuchiya<\/span><\/strong>, T. Komori, M. Hirano, T. Shiraki, A. Kakugo, T. Ide, J.-P. Gong, S. Yamada, T. Yanagida, S. Shinkai\n<\/dd>\n
[2]<\/dt>\n
Accumulation of Histidine Tagged Proteins to Sugar-SWNT Composites
\nThe 4th LSW Symposium on Soft & Wet Matter, Sapporo, Japan, January, 2009.
\nY. Tsuchiya<\/span><\/strong>, S. Yamada, S. Shinkai\n<\/dd>\n
[1]<\/dt>\n
Accumulation of Histidine Tagged Proteins to Sugar-SWNT Composites Bearing Metal Ligands
\nInternational Symposium on Molecular and System Life Sciences, Kobe, Japan, December, 2008.
\nY. Tsuchiya<\/span><\/strong>, Sunao Yamada, Seiji Shinkai\n<\/dd>\n<\/dl>\n","protected":false},"excerpt":{"rendered":"

\u7565\u6b74 2001 \u8fd1\u757f\u5927\u5b66\u5927\u5b66\u9662\u7dcf\u5408\u7406\u5de5\u5b66\u7814\u7a76\u79d1\u7269\u8cea\u7cfb\u5de5\u5b66\u5c02\u653b\u3000\u535a\u58eb\u524d\u671f\u8ab2\u7a0b\u3000\u4fee\u4e86 2004 \u5948\u826f\u5148\u7aef\u79d1\u5b66\u6280\u8853\u5927\u5b66\u9662\u5927\u5b66\u7269\u8cea\u5275\u6210\u79d1\u5b66\u7814\u7a76\u79d1\u7269\u8cea\u5275\u6210\u79d1\u5b66\u5c02\u653b\u3000\u535a\u58eb\u5f8c\u671f\u8ab2\u7a0b\u3000\u4fee\u4e86 2004-2007 \uff08\u72ec\uff09\u7523\u696d\u6280\u8853\u7dcf\u5408\u7814\u7a76\u6240\u3000 […]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":11,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-11155","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/pages\/11155","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\/2"}],"replies":[{"embeddable":true,"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/comments?post=11155"}],"version-history":[{"count":0,"href":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/wp-json\/wp\/v2\/pages\/11155\/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=11155"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}