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Tatewaki Laboratory, Department of Organic and Polymer Materials Chemistry, Faculty of Engineering, Department of Applied Chemistry, The Graduate School of Engineering, Tokyo University of Agriculture and Technology

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Achievements

原著論文

[1] Y. Tatewaki, K.Mizuguchi, C. Kato, S. Nishihara, S. Okada, “NanoaggregatesComposed of Tetrathiafulvalene Derivatives with Ferrocene-Terminated Side Chains”, ChemLet, 43, 1131-1133 (2014.4).
doi:10.1246/cl.140264

[2] M. Imai, Y. Tatewaki, and S. Okada, “Preparation and Physical Properties of Nanoaggregates Composed of Charge-Transfer Complexes Containing Butadiyne Derivatives with Tetrathiafulvalene Moieties”, Jpn. J. Appl. Phys., 53, 05FA02-1-7 (2014.3).
doi:10.7567/JJAP.53.05FA02

[3] T. Matsuura, T. Wada, Y. Tatewaki, S. Okada, “Effective polar orientation of organic polar nanocrystals and their fixation in polymer matrices”, Jpn. J. Appl. Phys., 53, 061601-7 (2014.6).doi:10.7567/JJAP.53.061601

[4] C. Kato, S. Nishihara,R. Tsunashima, Y. Tatewaki,S. Okada, X.-M. Ren, K. Inoue, D.-L. Long, and L. Cronin, “Quick and Selective Synthesis of Li6[α-P2W18O62] ?28H2O Soluble in Various Organic Solvents”, Dalton Trans., 42, 11363-11366 (2013.6).
doi:10.1039/C3DT51120K

[5] Y. Tatewaki, T. Watanabe, K. Watanabe, K.Kikuchi and S. Okada, “Synthesis and Nanostructures of Several Tetrathiafulvalene Derivatives Having the Side Chains Composed of Chiral and Hydrogen-Bonding Groups and Their Charge-TransferComplexes”, Dalton Trans., 42, 16121-16127 (2013.12).
doi:10.1039/c3dt51464a

[6] K. Higuchi, K.Sasamura, K. Mizuguchi, Y. Tatewaki, and S. Okada, “Synthesis and Solid-State Polymerization of Monomers with Conjugated Diyne-Triene-DiyneStructure”, Polymer, 54, 2901-2906 (2013.5).
doi:10.1016/j.polymer.2013.04.018

[7] J. Tsuchida, Y. Saito, S.Sato, U. Yuki, S. Inayama, Y. Tatewaki, S. Okada, A. Shindo, C. Mikura, K. Fushihara, M. Yamada, “Thermal solid-state polymerization of a divalent metal salt of an unsaturated carboxylic acid and the effects of additives”, Polymer Journal, 45, 1007-1012 (2013.10).
doi: 10.1038/pj.2013.22

[8] Y. Tatewaki, A. Sato, S. Ito, S. Inayama and S. Okada, “Synthesis and Solid-State Polymerization of L-Alanine Derivatives with a (1-Pyrenyl)butadiynyl Group”, Mol. Cryst.Liq. Cryst., 580, 58-63 (2013.11).
doi: 10.1080/15421406.2013.804382

[9] S. Ishii, S.Kaneko, Y. Tatewaki, and S. Okada, “Synthesis and Solid-State Polymerization of 4-(Dimethylamino)phenylbutadiyne Derivatives and Their Charge-Transfer Complexes”, Mol. Cryst. Liq. Cryst.,580, 64-68 (2013.11).
doi: 10.1080/15421406.2013.804753

[10] R. Takahashi, T. Nunokawa,T. Shibuya, R. Tomita, Y. Tatewaki, S. Okada, T.Kimura, S. Shimada, H. Matsuda, “Synthesis and solid-state polymerization of butadiyne derivatives with trialkoxyphenylurethane groups”, Bull. Chem. Soc. Jpn., 85(2), 236-244 (2012.2).
doi:10.1246/bcsj.20110219

[11] T. Shibuya, Y. Tatewaki, S. Okada, “Synthesis of Polydiacetyleneswith Pyridyl Groups Directly Bound to the MainChain”, Mol. Cryst. Liq. Cry., 568, 93-97 (2012.9).
doi:10.1080/15421406.2012.710191

[12] Y. Tatewaki, S. Inayama, K.Watanabe, H. Shibata and S. Okada, “Synthesis and Solid-State Polymerization of Diacetylene with Tetrathiafulvalene and the Electronic Properties”, Mol. Cryst. Liq. Cry.,568, 87-92 (2012.9).
doi:10.1080/15421406.2012.710190

[13] Y. Tatewaki, “Preparation of conductive nanowire having charge migration complex and electrical properties”, Mol. Electron. and Bioelectron.,22(1), 29-32 (2011.3). 

[14] Y. Tatewaki, H.Shibata, T. Shibuya, K. Watanabe, S. Ishii, and S. Okada, “Solid-State Polymerization of a Pyrenylbutadiyne Derivative”,Polymer Photonics and Novel Optical Technologies, 152-155 (2011.9).

[15] T. Kinemuchi, T.Matsuura, Y. Tatewaki, and S. Okada, “Preparation of Ionic Polar Nanocrystals in Various Conditions”, Polymer Photonics and Novel Optical Technologies, 146-151 (2011.9).

[16] T. Kinemuchi,Y. Moritani, Y. Tatewaki,and S. Okada, “Fixation of Surface-Modified Polydiacetylene Nano/Microcrystals on Substrates”, Jpn. J. Appl. Phys., 50, 095202-1-095202-5(2011.9).
doi:10.1143/JJAP.50.095202</