福島 研究論文

2017 2016 2015 2014 2013 2012 2011 2010 2009年以前

2017

  • Mesoscopic Structural Aspects of Ca2+-Triggered Polymer Chain Folding of a Tetraphenylethene-Appended Poly(Acrylic Acid) in Relation to Its Aggregation-Induced Emission Behavior
  • K. Morishima, F. Ishiwari, S. Matsumura, T. Fukushima, M. Shibayama
    Macromolecules 2017, In press.
  • Temperature Dependence of Magnetophotoconductance in One-Dimensional Molecular Assembly of Hexabenzocoronene
  • Y. Wakikawa, T. Ikoma, Y. Yamamoto, T. Fukushima, K. Akiyama
    ACS Omega  20172, 3260–3266 (DOI: 10.1021/acsomega.7b00474).
    *共同研究拠点成果
  • Rigid-to-Flexible Conformational Transformatdion: An Efficient Route to Ring-Opening of a Trogers Base-Containing Ladder Polymer
  • F. Ishiwari, N. Takeuchi, T. Sato, H. Yamazaki, R. Osuga, J. N. Kondo, T. Fukushima
    ACS Macro Lett. 2017, 6, 775–780 (DOI: 10.1021/acsmacrolett.7b00385).
  • 2,3,5,6,8,9-Hexabromosumanene: Synthesis and Its Application to Suzuki-Miyaura Cross-Coupling
  • H. Toda, Y. Yakiyama, Y. Shoji, F. Ishiwari, T. Fukushima, H. Sakurai
    Chem. Lett.  2017In press (DOI: 10.1246/cl.170566).
  • Stereoselective Encapsulation for a Triarylmethylium o,o-Dimer by Natural γ-Cyclodextrin: Origin of Chiral Recognition for the Axially Chiral Dicationic Guest.
  • T. Suzuki, J. P. Cerón-Carrasco, H. Tamaoki, Y. Ishigaki, R. Katoono, T. Fukushima, and H. Pérez-Sánchez
    Heterocycles 201794, 1123-1132 (DOI: 10.3987/COM-17-13674).
    *共同研究拠点成果
  • Synthesis and Catalytic Applications of a Triptycene-Based Monophosphine Ligand for Palladium-Mediated Organic Transformations
  • F. K.-C. Leung, F. Ishiwari, Y. Shoji, T. Nishikawa, R. Takeda, Y. Nagata, M. Suginome, Y. Uozumi, Y. M. A. Yamada, T. Fukushima
    ACS Omega 20172, 1930–1937 (DOI: 10.1021/acsomega.7b00200).
  • Formation of an Isolable Divinylborinium Ion through Twofold 1,2-Carboboration between a Diarylborinium Ion and Diphenylacetylene
    N. Tanaka, Y. Shoji, D. Hashizume, M. Sugimoto, T. Fukushima
    Angew. Chem. Int. Ed. 2017, 56, 5312–5316 (DOI: 10.1002/anie.201701730).
    Selected as "Back Cover"
  • Supramolecular Polymerization of Supermacrocycles: Effect of Molecular Conformations on Kinetics and Morphology
  • M. Yamauchi, B. Adhikari, D. D. Prabhu, X. Lin, T. Karatsu, T. Ohba, N. Shimizu, H. Takagi, R. Haruki, S. Adachi, T. Kajitani, T. Fukushima, S. Yagai
    Chem. Eur. J. 201723, 5270–5280 (DOI: 10.1002/chem.201605873). 
  • High-fidelity self-assembly pathways for hydrogen-bonding molecular semiconductors
    X. Lin, M. Suzuki, M. Gushiken, M. Yamauchi, T. Karatsu, T. Kizaki, Y. Tani, K. Nakayama, M. Suzuki, H. Yamada, T. Kajitani, T. Fukushima, Y. Kikkawa, S. Yagai
    Sci. Rep. 20177, 43098 (DOI: 10.1038/srep43098).
  • Unveiling a new aspect of simple arylboronic esters: long-lived room-temperature phosphorescence from heavy-atom-free molecules
    Y. Shoji, Y. Ikabata, Q. Wang, D. Nemoto, A. Sakamoto, N. Tanaka, J. Seino, H. Nakai, T. Fukushima
    J. Am. Chem. Soc. 2017139,  2728–2733 (DOI: 10.1021/jacs.6b11984).
  • Highly air- and moisture-stable hole-doped carbon nanotube films achieved by a boron-based oxidant
    K. Funahashi, N. Tanaka, Y. Shoji, N. Imazu, K. Nakayama, K. Kanahashi, H. Shirae, S. Noda, H. Ohta,T. Fukushima, and T. Takenobu
    Appl. Phys. Express 201710, 035101 (DOI: 10.7567/APEX.10.035101).

2016

  • A design principle of polymers processable into 2D homeotropic order
    Z. Chen, Y.-T. Chan, D. Miyajima, T. Kajitani, A. Kosaka, T. Fukushima, J. M. Lobez, T. Aida
    Nature Commun. 20167, 13640 (doi:10.1038/ncomms13640).
  • A ternary blend of a polymer, fullerene, and insulating self-assembling triptycene molecules for organic photovolatics
    M. Kumano, M. Ide, N. Seiki, Y. Shoji, T. Fukushima, A. Saeki
    J. Mater. Chem. A 20164, 18490–18498. (doi: 10.1039/C6TA07705F).
  • An anion-conductive microporous membrane composed of a rigid ladder polymer with a spirobiindane backbone
    F. Ishiwari, T. Sato, H. Yamazaki, J. N. Kondo, S. Miyanishi, T. Yamaguchi, T. Fukushima
    J. Mater. Chem. A 20164, 17655–17659 (doi: 10.1039/C6TA07576B).
  • Synthesis and Self-Assembly of Cyclic 2,7-Anthrylene Ethynylene 1,3-Phenylene Ethynylene Trimer with a Planar Conformation
    Y. Takaki, R. Ozawa, T. Kajitani, T. Fukushima, M. Mitsui, K. Kobayashi
    Yuta Takaki,
    Ryota Ozawa,
    Dr. Takashi Kajitani,
    Prof. Takanori Fukushima,
    Prof. Masaaki Mitsui,
    Prof. Kenji Kobayashi

    Chem. Eur. J. 201622, 16760–16764 (doi: 10.1002/chem.201603627).
  • Supramolecular Assemblies of Ferrocene-Hinged Naphthalenediimides: Multiple Conformational Changes in Film States
    A. Takai, T. Kajitani, T. Fukushima, K. Kishikawa, T. Yasuda, M. Takeuchi
    J. Am. Chem. Soc. 2016138, 11245–11253 (DOI: 10.1021/jacs.6b05824).
    *新学術領域「π造形科学」共同研究成果
  • Supramolecular Scaffold for Tailoring the Two-Dimensional Assembly of Functional Molecular Units into Organic Thin Films
    F. K.-C. Leung, F. Ishiwari, T. Kajitani, Y. Shoji, T. Hikima, M. Takata, A. Saeki, S. Seki, Y. M. A. Yamada, T. Fukushima
    J. Am. Chem. Soc. 2016138, 11727–11733 (DOI: 10.1021/jacs.6b05513).
  • Discrete Self-Assembly and Functionality of Guest Molecules in an Organic Framework
    S. Ando, T. Fukushima, T. Yamaguchi
    Chem. Mater. 201628, 5847–5854 (DOI: 10.1039/C6RA07173B).
  • Scanning tunnelling microscopy analysis of octameric o-phenylenes on Au(111)
    S. Marqués-González, S. Fujii, T. Nishino, Y. Shoji, F. Ishiwari, T. Fukushima, M. Kiguchi
    RSC Advances 20166, 55970–55975 (DOI: 10.1039/C6RA07173B).
    *新学術領域「π造形科学」共同研究成果
  • Hydrogen-bonded oligothiophene rosettes with a benzodithiophene terminal unit: self-assembly and application to bulk heterojunction solar cells
    H. Ouchi, X. Lin, T. Kizaki, D. D. Prabhu, F. Silly, T. Kajitani, T. Fukushima, K. Nakayama, S. Yagai
    Chem. Commun. 201652, 7874–7877 (DOI: 10.1039/C6CC03430F).
    *新学術領域「π造形科学」共同研究成果
  • Chlorine-based inductively coupled plasma etching of GaAs wafer using tripodal paraffinic triptycene as an etching resist mask
    A. Matsutani, F. Ishiwari, Y. Shoji, T. Kajitani, T. Uehara, M. Nakagawa, T. Fukushima
    Jpn. J. Appl. Phys. 201655, 06GL01-1 to 06GL01-3 (DOI:10.7567/JJAP.55.06GL01).
  • Ultraflexible organic amplifier with biocompatible gel electrodes
    T. Sekitani,  T. Yokota,  K. Kuribara, M. Kaltenbrunner,  T. Fukushima, Y. Inoue,  M. Sekino, T. Isoyama,  Y. Abe, H. Onodera, T. Someya
    Nature Commun. 20167, 11425 (DOI: 10.1038/ncomms11425).
  • Bioinspired design of a polymer gel sensor for the realization of extracellular Ca2+ imaging
    F. Ishiwari, H. Hasebe, S. Matsumura, F. Hajjaj, N. Horii-Hayashi, M. Nishi, T. Someya, T. Fukushima
    Sci. Rep. 20166, 24275 (DOI:10.1038/srep24275).

2015

  • 11B Solid-State NMR Interaction Tensors of Linear Two-Coordinate Boron: The Dimesitylborinium Cation
    A. E. Alain, Y. Shoji, T. Fukushima, D. L. Bryce
    Inorg. Chem. 2015, 54, 11889–11896 (DOI: 10.1021/acs.inorgchem.5b02161).
  • Raising the metal–insulator transition temperature of VO2 thin films by surface adsorption of organic polar molecules
    H. Shioya, Y. Shoji, N. Seiki, M. Nakano, T. Fukushima, Y. Iwasa
    Appl. Phys. Exp. 20158, 1211011–1211014 (DOI:10.7567/APEX.8.121101).
    Selected as "Spotlights Article"
  • Helix sense-selective supramolecular polymerization seeded by a one-handed helical polymeric assembly
    W. Zhang, W. Jin, T. Fukushima, T. Mori, T. Aida
    J. Am. Chem. Soc. 2015in press (DOI:10.1021/jacs.5b09878).
  • Ultrahigh-throughput exfoliation of graphite into pristine ‘single-layer’ graphene using microwaves and molecularly engineered ionic liquids
    M. Matsumoto, Y. Saito, C. Park, T. Fukushima, T. Aida
    Nat. Chem. 20157, 730–736. (doi:10.1038/nchem.2315).
  • The molecular and electronic structures of a thioaroyl cation formed by borinium ion-mediated C=S double bond cleavage of CS2
    Y. Shoji, N. Tanaka, D. Hashizume, T. Fukushima
    Chem. Commun. 201551, 13342–13345 (DOI: 10.1039/C5CC05645D).
    Selected as "Outside Front Cover"
  • Selective Synthesis of Single and Multi-Walled Supramolecular Nanotubes Using Solvophobic/Solvophilic Controls:  Stepwise Radial Growth via “Coil-on-Tube” Intermediates
    S. Prasanthkumar, W. Zhang, W. Jin, T. Fukushima, T. Aida
    Angew. Chem. Int. Ed. 201554, 11168–11172 (DOI: 10.1002/anie.201505806). (Selected as a VIP paper)
  • Rational synthesis of organic thin films with exceptional long-range structural integrity
    N. Seiki, Y. Shoji, T. Kajitani, F. Ishiwari, A. Kosaka, T. Hikima, M. Takata, T. Someya, T. Fukushima
    Science 2015348, 1122-1126. (DOI: 10.1126/science.aab1391).
  • Photoalignment of an azobenzene-based chromonic liquid crystal dispersed in triacetyl cellulose: single-layer alignment films with an exceptionally high order parameter
    M. Matsumori, A. Takahashi, Y. Tomioka, T. Hikima, M. Takata, T. Kajitani, T. Fukushima
    ACS Appl. Mater. Interfaces 2015, 7, 11074–11078. (DOI: 10.1021/acsami.5b02577).
  • An electron-accepting molecular unit exhibiting an orientational preference favorable for organic photovoltaic applications
    K. Akaike, S. Ando, H. Enozawa, A. Kosaka, T. Kajitani, T. Fukushima
    Thin Solid Films 2015583, 34-39. (doi:10.1016/j.tsf.2015.03.002).
  • Synthesis and properties of semi-crystalline anion exchange membrane with well-defined ion channel structure
    S. Miyanishi, T. Fukushima, T. Yamaguchi
    Macromolecules 2015, 48, 2576-2584. (DOI: 10.1021/ma502448g).
  • Translation of assembling trajectory by preorganization: A study of the magnetic properties of 1D polymeric unpaired electrons immobilised  on a discrete nanoscopic scaffold
    V. K. Praveen, Y. Yamamoto, T. Fukushima, Y. Tsunobuchi, K. Nakabayashi, S. Ohkoshi, K. Kato, M. Takata, T. Aida
    Chem. Commun. 201551, 1206-1209. (doi:10.39/C4CC08942A).
  • Three-Way Output Molecular Response System based on Tetrakis(3,4-dialkoxyphenyl)-3,4-dihydro [5]helicenes: Perturbation of Properties by Long Alkyl Chains
    Y. Ishigaki, S. Yoshida, H. Kawai, R. Katoono, K. Fujiwara, T. Fukushima, T. Suzuki
    Heterocycles. 201590, 126-135. (doi:10.3987/COM-14-S(K)31).

2014

  • Electrochromic and unique chiroptical properties of helically deformed tetraarylquinodimethanes generated from less hindered dicationic precursors upon reduction
    T. Suzuki, Y. Sakano, T. Iwai, S. Iwashita, Y. Miura, R. Katoono, H. Kawai, K. Fujiwara, Y. Tsuji, T. Fukushima
    Pure Appl. Chem. 2014, 86, 507–516. *共同研究拠点成果
  • A two-coordinate boron cation featuring C–B+–C bonding
    Y. Shoji,  N. Tanaka,  K. Mikami,  M. Uchiyama, T. Fukushima
    Nature Chem. 20146, 498–503. (10.1038/nchem.1948) =>プレスリリース(東工大ニュース)
    Highlighted in News & Views: C. Reus, M. Wagner "Boron served straight up"
  •             and in Chemical & Engineering News (Volume 92, Issue 20, p. 30, Concentrates) 
  • Electrochiroptical Response in Aqueous Media: 9,10-Dihydrophenanthrene-9,10-diyl Dications with Michlar's Hydrol Blue Chromophores Attached with Oligoethylene Glycol Units
    T. Suzuki, K. Hanada, R. Katoono, Y. Ishigaki, S. Higasa, H. Higuchi, H. Kikuchi, K. Fujiwara, H. Yamada, T. Fukushima
    Chem. Lett. 201443, 982-984. (10.1246/cl.140163) *共同研究拠点成果
  • Oxidative Protonolysis of the Expanded Central C-C Bond in a Di(spiroacridan)-type Hexaphenylethane Derivative Accompanied by UV-vis, FL, and CD Spectral Changes
    T. Suzuki, Y. Kuroda, K. Wada, Y. Sakano, R. Katoono, K. Fujiwara, F. Kakiuchi, T. Fukushima
    Chem. Lett. 201443, 887–889. (10.1246/cl.140192) *共同研究拠点成果
  • Expandability of Ultralong C–C Bonds: Largely Different C1–C2 Bond Lengths Determined by Low-temperature X-ray Structural Analyses on Pseudopolymorphs of 1,1-Bis(4-fluorophenyl)-2,2-bis(4-methoxyphenyl)pyracene
    T. Suzuki, Y. Uchimura, F. Nagasawa, T. Takeda, H. Kawai, R. Katoono, K. Fujiwara, K. Murakoshi, T. Fukushima, A. Nagaki, J. Yoshida
    Chem. Lett. 201443, 86–88. (10.1246/cl.130872) *共同研究拠点成果

 

2013

  • o-Phenylene Octamers as Surface Modifiers for Homeotropic Columnar Ordering of Discotic Liquid Crystals
    T. Kajitani, Y. Suna, A. Kosaka, T. Osawa, S. Fujikawa, M. Takata, T. Fukushima, T. Aida
  • J. Am. Chem. Soc.  2013135, 14564–14567. (10.1021/ja4087853
  • Tetrathiafulvalene Hybridized with Indacenetetraone as a Visible-Light-Harvesting Electron Acceptor Applicable to Bulk-Heterojunction Organic Photovoltaics
    K. Akaike, H. Enozawa, T. Kajitani, M. Koizumi, A. Kosaka, D. Hashizume, Y. Koizumi, A. Saeki, S. Seki, and T. Fukushima
  • Chem. Lett.  201342, 1417–1419. (doi:10.1246/cl.130702
  • Effect of Acceptor Lamination on Photocarrier Dynamics in Hole Transporting Hexabenzocoronene Nanotubular Self-Assembly
    Y. Wakikata, T. Ikoma, Y. Yamamoto, T. Fukushima, T. Aida, K. Akiyama
  • J. Phys. Chem. C, 2013117, 15295–15305. (DOI: 10.1021/jp402640k
  • Preparation, Properties, and X-ray Structures of Bis(10-methyl-9-methyleneacridan)-type Electron Donors with a Thiophene/bithiophene/terthiophene Skeleton: Redox Switching of Thiophene-thienoquinoid Structure Accompanied by UV-Vis-NIR Electrochromic Response
    T. Suzuki, Y. Hoshiyama, K. Wada, Y. Ishigaki, Y. Miura, H. Kawai, R. Katoono, K. Fujiwara,T. Fukushima
  • Chem. Lett.  201352, 1004–1006. (doi:10.1246/cl.130401 )*共同研究拠点成果 
  • Oxidative conversion of tetraaryldihydrodibenzothiepins into elemental sulfur and stable cationic dyes accompanied by dual UV-Vis and CD spectral changes
    T. Suzuki, T. Kuroda, H. Tamaoki, S. Higasa, R. Katoono, K. Fujiwara, T. Fukushima, H. Yamada
    Chem. Lett. 201342, 706–708. (doi:10.1246/cl.130275)*共同研究拠点成果
  • Redox switching of conjugation length using 9,9,10,10-tetraaryl-9,10-dihydrophenanthrene as an ON/OFF unit: Preparation, X-ray structure, and redox properties of perfluorobiphenyl derivative and its SNAr reactions to pi-extended analogues
    T. Suzuki, H. Tamaoki, R. Katoono, K. Fujiwara, J. Ichikawa, T. Fukushima
  • Chem. Lett. 201342, 703–705. (doi:10.1246/cl.130190 ) *共同研究拠点成果 
  • Dynamic or Nondynamic? Helical Trajectory in Hexabenzocoronene Nanotubes Biased by a Detachable Chiral Auxiliary
    W. Zhang, W. Jin, T. Fukushima, N. Ishii, T. Aida
    J. Am. Chem. Soc. 2013135, 114–117. (DOI: 10.1021/ja311738m )
  • Amphiphilic Design of a Discotic Liquid-Crystalline Molecule for Dipole Manipulation: Hierarchical Columnar Assemblies with a 2D Superlattice Structure
    M.-C. Yeh, Y.-L. Su, M.-C. Tzeng, C. W. Ong, T. Kajitani, H. Enozawa, M. Takata, Y. Koizumi, A. Saeki, S. Seki, T. Fukushima
  • Angew. Chem. Int. Ed. 201352, 1031–1034. (DOI: 10.1002/anie.201207708 

2012

  • Discotic Ionic Liquid Crystals of Triphenylene as Excellent Dispersants for Orienting Single-Walled Carbon Nanotubes: Toward Anisotropic Soft Electrical Conductors
    J. J. Lee, A. Yamaguchi, M. A. Alam, Y. Yamamoto, T. Fukushima, K. Kato, M. Takata, N. Fujita, T. Aida
  • Angew. Chem. Int. Ed. 201251, 8490–8494. (DOI:10.1002/anie.201203284) (Accepted as "VIP" paper in Angew. Chem. Int. Ed.)
  • Wide-Range 2D Lattice Correlation Unveiled for Columnarly Assembled Triphenylene Hexacarboxylic Esters
    T. Osawa, T. Kajitani, D. Hashizume, H. Ohsumi, S. Sasaki, M. Takata, Y. Koizumi, A. Saeki, S. Seki, T. Fukushima, T. Aida
  • Angew. Chem. Int. Ed. 201251, 7990–7993. (DOI: 10.1002/anie.201203077)
  • Remarkable Effect of Terminal Groups and Solvents on Helical Folding of o-Phenylene Oligomers
    S. Ando, E. Ohta, A. Kosaka, D. Hashizume, H. Koshino, T. Fukushima, T. Aida
  • J. Am. Chem. Soc. 2012134, 11084-11087. (DOI: 10.1021/ja303117z)
  • Interface Dependence of Charge Formation Dynamics in Hexabezocoronene-C60
    Y. Moritomo, Y. Yonezawa, M. Ito, H. Kamioka, Y. Yamamoto, T. Fukushima, T. Aida
  • Appl. Phys. Express 20125, 062401. (DOI: 10.1143/APEX.5.062401)

2011

  • A 4 V Operation, Flexible Braille Display Using Organic Transistors, Carbon Nanotube Actuators, and Organic Static Random-Access Memory
    K. Fukuda, T. Sekitani, U. Zschieschang, H. Klauk, K. Kuribara, T. Yokota, T. Sugino, K. Asaka, M. Ikeda, H. Kuwabara, T. Yamamoto, K. Takimiya, T. Fukushima, T. Aida, M. Takamiya, T. Sakurai, T. Someya
  • Adv. Funct. Mater. 2011, 21, 4019-4027. (DOI: 10.1002/adfm.201101050)
  • Supramolecular Linear Heterojunction Composed of Graphite-Like Semiconducting Nanotubular Segments
    W. Zhang, W. Jin, T. Fukushima, A. Saeki, S. Seki, T. Aida
  • Science 2011, 334, 340-343. (DOI: 10.1126/science.1210369)
  • Photoconductivity of Self-Assembled Hexabenzocoronene Nanotube: Insight into the Charge Carrier Mobilities on Local and Long-Range Scales
    A. Saeki, Y. Yamamoto, Y. Koizumi, T. Fukushima, T. Aida, S. Seki
  • J. Phys. Chem. Lett. 2011, 20, 2549-2554. (DOI: 10.1021/jz201223e)
  • Redox-Responsive Molecular Helices with Highly Condensed π-Clouds
    E. Ohta, H. Sato, S. Ando, A. Kosaka, T. Fukushima, D. Hashizume, M. Yamasaki, K. Hasegawa, A. Muraoka, H. Ushiyama, K. Yamashita, T. Aida
    Nature Chem. 2011, 3, 68-73. (DOI:10.1038/nchem.900)

2010

  • Large-Area Three-Dimensional Molecular Ordering of a Polymer Brush by One-Step Processing
    N. Hosono, T. Kajitani, T. Fukushima, K. Ito, S. Sasaki, M. Takata, T. Aida
    Science 2010, 330, 808-811. (DOI: 10.1126/science.1195302)
  • Use of Side-Chain Incompatibility for Tailoring Long-Range p/n Heterojunctions: Photoconductive Nanofibers Formed by Self-Assembly of an Amphiphilic Donor-Acceptor Dyad Consisting of Oligothiophene and Perylenediimide
    W.-S. Li, A. Saeki, Y. Yamamoto, T. Fukushima, S. Seki, N. Ishii, K. Kato, M. Takata, T. Aida
    Chem. Asian J. 2010, 5, 1566-1572. (DOI: 10.1002/asia.201000111)
  • Form Factor of an N-Layered Helical Tape and Its Application to Nanotube Formation of Hexa-peri-hexabenzocoronene-Based Molecules
    C. V. Teixeira, H. Amenitsch, T. Fukushima, J. P. Hill, W. Jin, T. Aida, M. Hotokka, M. Linden
    J. Appl. Cryst. 2010, 43, 850-857. (DOI:10.1107/S0021889810015736)
  • Hexabenzocoronene Graphitic Nanotube Appended with Dithienylethene Pendants: Photochromism for Modulation of Photoconductivity
    Y. He, Y. Yamamoto, W. Jin, T. Fukushima, A. Saeki, S. Seki, N. Ishii, T. Aida
    Adv. Mater. 2010, 22, 829-832. (DOI: 10.1002/adma.200902601)
  • Magnetic Field Effect on the Photocarriers in Self-Assembled Hexabenzocoronene Nanotubes
    Y. Wakikawa, T. Ikoma, Y. Yamamoto, T. Fukushima, T. Aida
    Synth. Met. 2010, 160, 275-279. (DOI:10.1016/j.synthmet.2009.08.052)

 

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東京工業大学
科学技術創成研究院
化学生命科学研究所

当研究室は物質理工学院 応用化学系に所属しています。

教授 福島 孝典

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