nims mana images Frontier Molecules Group(FMG)

Japanese

Publications

2021

Original

  1. “Rheology of Conjugated Polymers with Bulky and Flexible Side Chains”
    Z.-C. Yan,* Y. Li, Z. Guo, A. Shinohara, T. Nakanishi, G. Chen,* C. Pan,* F. J. Stadler*
    Macromolecules, 2021, 54, 4061-4069.
    DOI: 10.1021/acs.macromol.1c00044
  2. “Discrimination of methanol from ethanol in gasoline using membrane-type surface stress sensor coated with copper(I) complex”
    M. Nishikawa,* T. Murata, S. Ishihara, K. Shiba, L. K. Shrestha, G. Yoshikawa,* K. Minami,* K. Ariga*
    Bull. Chem. Soc. Jpn., 2021, 94, 648-654.
    DOI: 10.1246/bcsj.20200347
  3. “Liquid marble patchwork on super-repellent surface”
    M. Tenjimbayashi,* S. Samitsu, Y. Watanabe, Y. Nakamura, M. Naito*
    Adv. Funct. Mater., 2021, 31, 2010957. (Inside Front Cover; Highlighted in “Advanced Science News”; Highlighted in MANA; etc.)
    DOI:10.1002/adfm.202010957
  4. “Disposable NO Generator Based on A Structurally Deformed Nitrite-type Layered Double Hydroxide”
    S. Ishihara,* T. Machino, K. Deguchi, S. Ohki, Y. Mogami, M. Tansho, T. Shimizu, J. P. Hill, Y. Yamauchi, N. Iyi*
    Inorg. Chem., 2021, in press. (Press Release)
    DOI: 10.1021/acs.inorgchem.1c00456
  5. “Dual Surface Architectonics for Directed Self-Assembly of Ultrahigh-Resolution Electronics”
    L.Li, W. Li,* Q. Sun, X. Liu, J. Jiu, M. Tenjimbayashi, M. Kanehara, T. Nakayama,* T. Minari*
    Small, 2021, 17, 2101754.
    DOI: 10.1002/smll.202101754
  6. Estimation of Enantiomeric Excess Based on Rapid Host–Guest Exchange”
    J. Labuta,* S. Ishihara,* D.T. Payne, K. Takimoto, H. Sato, L. Hanyková, K. Ariga, J. P. Hill*
    Chemosensors, 2021, 9, 259.
    DOI: 10.3390/chemosensors9090259
  7. “Post-Programmable Network Topology with Broad Gradients of Mechanical Properties for Reliable Polymer Material Engineering”
    H. H. Wei, M. Tenjimbayashi, S. Wang, Y. Nakamura, I. Watanabe, M. Naito*
    Chem. Mater., 2021, 33, 6876-6884.
    DOI: 10.1021/acs.chemmater.1c01715
  8. “How Liquid Marbles Break Down: Direct Evidence for Two Breakage Scenarios”
    M. Tenjimbayashi,* S. Fujii
    Small, 2021, 17, 2102438.
    DOI: 10.1002/smll.202102438
  9. “Experimental design for the highly accurate prediction of material properties using measurements”
    R. Tamura,* Y. Takei, S. Imai, M. Nakahara, S. Shibata, T. Nakanishi,* M. Demura*
    Sci. Technol. Adv. Mater., Methods, 2021, 1, 152-161.
    DOI: 10.1080/27660400.2021.1963641

Review & Commentary

  1. “Solvent-Free Conjugated Polymer Fluids with Optical Functions”
    A. Shinohara, Z. Guo, C. Pan, T. Nakanishi*
    Org. Mater., 2021, 3, 309-320.
    DOI: 10.1055/a-1491-4818
  2. “Alkyl-π functional molecular liquids towards soft electronics”
    T. Machida, T. Nakanishi*
    J. Mater. Chem. C, 2021, 9, 10661-10667. (Selected as a Hot Paper)
    DOI: 10.1039/d1tc00998b
  3. “Alkyl-Fullerene Materials of Tunable Morphology and Function”
    E. A. Neal, T. Nakanishi*
    Bull. Chem. Soc. Jpn, 2021, 94, 1769-1788. (Inside Front Cover)
    DOI: 10.1246/bcsj.20210129
  4. “Functional Molecular Liquids”
    E. A. Neal, T. Nakanishi*
    System-Material Nanoarchitectonics, Y. Wakayama, K. Ariga (Eds), Springer-Nature, 2021, in press.
    DOI: 10.1007/978-4-431-56912-1_6

2020

Original

  1. “Consistent red luminescence in π-conjugated polymers with tunable elastic moduli over five orders of magnitude”
    Z. Guo, A. Shinohara, C. Pan*, F. J. Stadler*, Z. Liu, Z.-C. Yan, J. Zhao, L. Wang, T. Nakanishi*
    Mater. Horiz., 2020, 7, 1421-1426.
    DOI: 10.1039/D0MH00029A
  2. “A near-infrared fluorescent phthalocyanine liquid developed through controlling intermolecular interactions”
    Y. Chino, T. Nakanishi, M. Kimura*
    New J. Chem., 2020, 44, 1689-1693.
    DOI: 10.1039/C9NJ05195C
  3. “Cascade reaction-based chemiresistive array for ethylene sensing”
    S. Ishihara,* A. Bahuguna, S. Kumar, V. Krishnan, J. Labuta, T. Nakanishi, T. Tanaka, H. Kataura, Y. Kon, D. Hong*
    ACS Sens., 2020, 5, 1405-1410.
    DOI: 10.1021/acssensors.0c00194
  4. “Controlled release of H2S and NO through CO2-stimulated anion exchange”
    S. Ishihara,* N. Iyi*
    Nature Commun., 2020, 11, 453.
    DOI: 10.1038/s41467-019-14270-3
  5. “Pushing property limits in materials discovery via boundless objective-free exploration”
    K. Terayama,* M. Sumita, R. Tamura, D. T. Payne, M. K. Chahal, S. Ishihara, K. Tsuda*
    Chem. Sci., 2020, 11, 5959-5968.
    DOI: 10.1039/d0sc00982b
  6. “meso-tetraphenylporphine as a prochiral solvating agent (pro-CSA): A physicochemical study”
    J. Labuta,* S. Ishihara, J. P. Hill*
    J. Porphyrins Phthalocyanines, 2020, 24, 320-329.
    DOI: 10.1142/S1088424619501141
  7. “Data integration for accelerated materials design via preference learning”
    X. Sun, Z. Hou, M. Sumita, S. Ishihara, R. Tamura, K. Tsuda*
    New J. Phys., 2020, 22, 055001.
    DOI: 10.1088/1367-2630/ab82b9
  8. “Amyloid-like Nano-fibrillation of Metal–Organic Complex Arrays Ruled by Their Precisely Designed Metal Sequences”
    R. Rajmohan, G. Vrla, H. Ueki, K. Sajna, T. Takei, H. Ohtsu, M. Kawano, P. Vairaprakash, K. Tashiro*
    Chem. Asian J., 2020, 15, 766–769.
    DOI: 10.1002/asia.201901674
  9. “Liquid Marbles: Exceptional Robustness and Self-Reconfigurability of Liquid Marbles on Superhydrophobic Substrate”
    M. Tenjimbayashi,* Y. Watanabe, Y. Nakamura, M. Naito*
    Adv. Mater. Interfaces, 2020, 7, 2000160.
    DOI: 10.1002/admi.202070058
  10. “Enantiomeric excess dependent splitting of NMR signal through dynamic chiral inversion and co-ligand exchange in a coordination complex”
    K. Takimoto, S. Ishihara,* J. Labuta,* V. Březina, D. T. Payne, J. P. Hill, K. Ariga, M. Sumita, S. Mori, H. Sato
    J. Phys. Chem. Lett., 2020, 11, 8164−8169.
    DOI: 10.1021/acs.jpclett.0c02284
  11. “Continuous Directional Water Transport on Hydrophobic Slippery Ventral Skin of Lampropeltis pyromelana”
    M. Tenjimbayashi,* K. Kawamura, S. Shiratori
    Adv. Mater. Interfaces, 2020, 7, 2000984.
    DOI:10.1021/admi.202000984
  12. “Alternating Copolymers of Vinyl Catechol or Vinyl Phenol with Alkyl Maleimide for Adhesive and Water-Repellent Coating Materials”
    K. Nishimori, M. Tenjimbayashi, M. Naito,* M. Ouchi*
    ACS Appl. Polym. Mater., 2020, 2, 4604-4612.
    DOI:10.1021/acsapm.0c00682

2019

Original

  1. “Soft chromophore featured liquid porphyrins and their utilization toward liquid electret applications”
    A. Ghosh, M. Yoshida, K. Suemori, H. Isago, N. Kobayashi, Y. Mizutani, Y. Kurashige, I. Kawamura, M. Nirei, O. Yamamuro, T. Takaya, K. Iwata, A. Saeki, K. Nagura, S. Ishihara, T. Nakanishi*
    Nature Commun., 2019, 10, 4210.
    DOI: 10.1038/s41467-019-12249-8
  2. “Viscoelastic Conjugated Polymer Fluids”
    A. Shinohara, C. Pan,* Z. Guo, L. Zhou, Z. Liu, L. Du, Z. Yan, F. J. Stadler, L. Wang,* T. Nakanishi*
    Angew. Chem. Int. Ed., 2019, 58, 9581-9585.
    DOI: 10.1002/anie.201903148 (German Edition: DOI: 10.1002/ange.201903148)
  3. “Luminescence tuning with excellent colour homogeneity and steadiness using fluorescent molecular liquids”
    F. Lu, K. Hagiwara, M. Yoshizawa, K. Nagura, S. Ishihara, T. Nakanishi*
    J. Mater. Chem. C, 2019, 7, 2577-2582.
    DOI: 10.1039/C8TC06254D
    (Open Access)
  4. “Paintable Room Temperature Phosphorescent Liquid Formulations of Alkylated Bromonaphthalimide”
    Goudappagouda, A. Manthanath, V. C. Wakchaure, K. C. Ranjeesh, T. Das, K. Vanka, T. Nakanishi, S. S. Babu*
    Angew. Chem. Int. Ed., 2019, 58, 2284-2288.
    DOI: 10.1002/anie.201811834
  5. “Viscoelastic Change of Block Copolymer Ion Gels in a Photoswitchable Azobenzene Ionic Liquid Triggered by Light”
    C. Wang, K. Hashimoto, R. Tamate, H. Kokubo, K. Morishima, X. Li, M. Shibayama, F. Lu, T. Nakanishi, M. Watanabe*
    Chem. Commun., 2019, 55, 1710-1713.
    DOI: 10.1039/C8CC08203K
  6. “Highly fluorescent polyethyleneimine protected Au8 nanoclusters: One-pot synthesis and application in hemoglobin detection”
    F. Lu, H. Yang, Z. Yuan,* T. Nakanishi, C. Lu, Y. He
    Sens. Actuators B, Chem., 2019, 291, 170-176.
    DOI: 10.1016/j.snb.2019.04.067
  7. “Excellent Oxygen Reduction Reaction Performance in Self-Assembled Amyloid-β/Platinum Nanoparticle Hybrids with Effective Platinum–Nitrogen Bond Formation”
    A. Jindal, K. Tashiro, H. Kotani, T. Takei, S. Reichenberger, G. Marzun, S. Barcikowski, T. Kojima, Y. Yamamoto*
    ACS Appl. Energy Mater., 2019, 2, 6536–6541.
    DOI: 10.1021/acsaem.9b01103
  8. “Increasing the complexity of oxoporphyrinogen colorimetric sensing chromophores: N-alkylation and β-substitution”
    M. K. Chahal, N. Velychkivska, W. A. Webre, J. Labuta, S. Ishihara, K. Ariga, F. D’Souza, J. P. Hill*
    J. Porphyrins Phthalocyanines, 2019, 23, 1184-1194.
    DOI: 10.1142/S1088424619501463
  9. “Why do carbonate anions have extremely high stability in the interlayer space of layered double hydroxides?: case study of layered double hydroxide consisting of Mg and Al (Mg/Al = 2)”
    R. Sasai*, H. Sato, M. Sugata, T. Fujimura, S. Ishihara, K. Deguchi, S. Ohki, M. Tansho, T. Shimizu, N. Oita, M. Numoto, Y. Fujii*, S. Kawaguchi, Y. Matsuoka, K. Hagura, T. Abe, C. Moriyoshi*
    Inorg. Chem., 2019, 58, 10928-10935.
    DOI: 10.1021/acs.inorgchem.9b01365

Review & Commentary

  1. “Self-Assembled and Nonassembled Alkylated-Fullerene Materials”
    F. Lu, E. A. Neal, T. Nakanishi*
    Acc. Chem. Res., 2019, 52, 1834-1843.
    DOI: 10.1021/acs.accounts.9b00217
  2. “Solvent-Free Luminous Molecular Liquids”
    F. Lu, T. Nakanishi*
    Adv. Optical Mater., 2019, 7, 1900176.
    DOI: 10.1002/adom.201900176
  3. “Design of solvent-free functional fluids via molecular nanoarchitectonics approaches”
    A. Shinohara, C. Pan, L. Wang, T. Nakanishi*
    Mol. Syst. Des. Eng., 2019, 4, 78-90.
    DOI: 10.1039/c8me00092a
  4. “Room-Temperature Liquid Dyes”
    B. Narayan, T. Nakanishi*
    Book chapter in Functional Organic Liquids, T. Nakanishi (Ed), John Wiley & Sons, Inc., Chapter 1, 2019, pp.1-20.
  5. “Liquids Based on Nanocarbons and Inorganic Nanoparticles”
    A. Ghosh, T. Nakanishi*
    Book chapter in Functional Organic Liquids, T. Nakanishi (Ed), John Wiley & Sons, Inc., Chapter 9, 2019, pp.151-168.
  6. “Ultra-Flexible, Fluidic, Optoelectronically-Active Molecular/Polymeric Materials”
    A. Shinohara, C. Pan, T. Nakanishi*
    Book chapter in Light-Active Functional Organic Materials, Pan Stanford Publishing, Chapter 1, 2019, pp.1-26.
  7. “Development of Functional Molecular Liquids”
    T. Nakanishi*
    Chemistry & Chemical Industry, 2019, 72, 10-12. (in Japanese)
  8. “Liquid Nanocarbons”
    T. Nakanishi*
    POLYMERS, 2019, 68, 297-299. (in Japanese)

2018

Original

  1. “Supercooling of functional alkyl-π molecular liquids”
    F. Lu, K. Jang, I. Osica, K. Hagiwara, M. Yoshizawa, M. Ishii, Y. Chino, K. Ohta, K. Ludwichowska, K. J. Kurzydlowski, S. Ishihara, T. Nakanishi*
    Chem. Sci., 2018, 9, 6774-6778.
    DOI: 10.1039/C8SC02723D
    (Hot Article, Backside Back Cover, Highlighted in ChemSci Pick of the Week)
  2. “A Spin-Active, Electrochromic, Solvent-Free Molecular Liquid Based on Double-Decker Lutetium Phthalocyanine Bearing Long Branched Alkyl Chains”
    A. Zielinska, A. Takai, H. Sakurai, A. Saeki, M. Leonowicz, T. Nakanishi*
    Chem. Asian J., 2018, 13, 770-774.
    DOI: 10.1002/asia.201800175
  3. “Effect of regioisomerism on the photophysical properties of alkylated-naphthalene liquids”
    B. Narayan, K. Nagura, T. Takaya, K. Iwata, A. Shinohara, H. Shinmori, H. Wang, Q. Li, X. Sun, H. Li, S. Ishihara, T. Nakanishi*
    Phys. Chem. Chem. Phys., 2018, 20, 2970−2975.
    DOI: 10.1039/c7cp05584f
    (Hot Paper & Inside Front Cover)
  4. “Experimental and theoretical investigation of fluorescence solvatochromism of dialkoxyphenyl-pyrene molecules”
    F. Lu, N. Kitamura, T. Takaya, K. Iwata, T. Nakanishi,* Y. Kurashige*
    Phys. Chem. Chem. Phys., 2018, 20, 3258−3264.
    DOI: 10.1039/ c7cp06811e
  5. “The aggregation of an alkyl–C60 derivative as a function of concentration, temperature and solvent type”
    J. Hollamby,* C. F. Smith, M. M. Britton, A. E. Danks, Z. Schnepp, Isabelle Grillo, B. R. Pauw, A. Kishimura, T. Nakanishi
    Phys. Chem. Chem. Phys., 2018, 20, 3373−3380.
    DOI: 10.1039/ c7cp06348b
    (Open Access)
  6. “Posttreatment Technique for SN2 Alkylation of Aromatics with Alkyl Halides: Aiming Toward Large-Scale Synthesis of Building Blocks for Soft π-Molecular Materials”
    K. Okamoto, F. Lu, T. Nakanishi*
    Bull. Chem. Soc. Jpn., 2018, 91, 1258-1263.
    DOI: 10.1246/bcsj.20180075
  7. “Aerogel Photo-Catalyst Composed of Transparent Mesoporous Polymethylsilsesquioxane Softly Post-Modified with a Visible-Light Absorbing Metal Complex”
    S. Sanda, K. Kanamori, T. Takei, K. Tashiro*
    ChemNanoMat, 2018, 2, 52-55.
    DOI: 10.1002/cnma.201700276
    (VIP paper)
  8. “A Glutathione-Responsive Short Sequence of Metal–Organic Complex Array”
    P. Bose, T. Takei, X. Li, T. Minowa, R. Rajmohan, P. Vairaprakash, K. Tashiro*
    ChemBioChem, 2018, 19, 1706−1710.
    DOI: 10.1002/cbic.201800252
    (Cover Feature)
  9. “Platinum(II) Terpyridine Complex That Switches Its Photochemical Reactivity in Response to Its Chromic Behavior in the Crystalline State”
    K. Tashiro,* H. Ohtsu, M. Kawano, T. Kojima, T. Kato
    Inorg. Chem., 2018, 57, 13079−13082.
    DOI: 10.1021/acs.inorgchem.8b02400
  10. “NMR Spectroscopic Determination of Enantiomeric Excess Using Small Prochiral Molecules”
    S. Ishihara,* J. Labuta,* Z. Futera, S. Mori, H. Sato, K. Ariga, J. P. Hill*
    J. Phys. Chem. B, 2018, 122, 5114−5120.
    DOI: 10.1021/acs.jpcb.8b03684
  11. “Hunting for Organic Molecules with Artificial Intelligence: Molecules Optimized for Desired Excitation Energies”
    M. Sumita,* X. Yang, S. Ishihara, R. Tamura, K. Tsuda
    ACS Cent. Sci., 2018, 4, 1126−1133.
    DOI: 10.1021/acscentsci.8b00213
    (Highlighted in ACS Cent. Sci., プレスリリース)
  12. “Structural modulation of chromic response: Effects of binding site blocking in a conjugated calix[4]pyrrole chromophore”
    V. Březina, S. Ishihara, J. Lang, L. Hanyková, K. Ariga, J. P. Hill,* J. Labuta*
    ChemistryOpen, 2018, 7, 323-335.
    DOI: 10.1002/open201800005
    (Open Access)
  13. “A star polymer with a metallo-phthalocyanines core as a tunable charge storage material for nonvolatile transistor memory devices”
    J. Aimi,* P.-H. Wang, C.-C. Shih, C.-F. Huang,* T. Nakanishi, M. Takeuchi, H.-Y. Hsueh, W.-C. Chen*
    J. Mater. Chem. C, 2018, 6, 2724-2732.
    DOI: 10.1039/c7tc05790c
    (Back Cover)

Review & Commentary

  1. “Novel Liquid Materials ~Molecular Liquids Possessing Optoelectronical-functions~”
    T. Nakanishi*
    CROSS T&T, 2018, 59, 19-22. (in Japanese)
  2. “10 Years from the Scientific Incentive Award:From Self-assembly to Non-assembly Strategy”
    T. Nakanishi*
    C & I Commun., 2018, 43, 5-6. (in Japanese)
  3. “π-Figuration for Controlling Stacking of π-Conjugated Molecules and Polymers”
    K. Nagura, R. Inoue, A. Takai,* K. Sugiyasu,* M. Takeuchi*
    J. Synth. Org. Chem., 2018, 76, 200–208. (in Japanese)
    DOI: 10.5059/yukigoseikyokaishi.76.200

2017

Original

  1. “A Guide to Design Functional Molecular Liquids with Tailorable Properties using Pyrene-Fluorescence as a Probe”
    F. Lu, T. Takaya,* K. Iwata, I. Kawamura, A. Saeki, M. Ishii, K. Nagura, T. Nakanishi*
    Sci. Rep., 2017, 7, 3416 (12pp).
    DOI:10.1038/s41598-017-03584-1
  2. “Stimuli-Responsive Viscoelastic Properties for Liquid Phthalocyanines”
    Y. Chino, A. Ghosh, T. Nakanishi,* N. Kobayashi, K. Ohta, M. Kimura*
    Chem. Lett., 2017, 46, 1539−1541.
    DOI:10.1246/cl.170672
  3. “Amperometric Detection of Sub-ppm Formaldehyde using SWCNTs and Hydroxylamines: A Referenced Chemiresistive System”
    S. Ishihara,* J. Labuta, T. Nakanishi, T. Tanaka, H. Kataura
    ACS Sensors, 2017, 2, 1405−1409.
    DOI: 10.1021/acssensors.7b00591
  4. “Metallic vs. Semiconducting SWCNT Chemiresistors: A Case for Separated SWCNTs Wrapped by Metallo-Supramolecular Polymer”
    S. Ishihara,* C. J. O’Kelly, T. Tanaka, H. Kataura, J. Labuta, Y. Shingaya, T. Nakayama, T. Ohsawa, T. Nakanishi, T. M. Swager
    ACS Appl. Mater. Interface, 2017, 9, 38062−38067.
    DOI: 10.1021/acsami.7b12992
  5. “Controlled Self-assembly of Oligopeptides Bearing Electron Donor and Acceptor Units on the Side Chains to Form beta-Sheets with Selective π-Stacking Configuration”
    T. Nakayama, K. Tashiro, T. Takei, Y. Yamamoto*
    Chem. Lett.,2017, 46,423–425.
    DOI: 10.1246/cl.161112
  6. “Manipulation Fullerene Superstructures by Complexing with Polycyclic Aromatic Compounds”
    Q. Tang, S. Zhang, X. Liu, M. Sumita, S. Ishihara, H. Fuchs, Q. Ji*, L. K. Shrestha,* K. Ariga
    Phys. Chem. Chem. Phys., 2017, 19, 29099−29105.
    DOI: 10.1039/C7CP04553K

Review & Commentary

  1. “Frontiers of solvent-free functional molecular liquids”,
    A. Ghosh, T. Nakanishi*
    Chem. Commun., 2017, 53, 10344–10357.
    DOI: 10.1039/c7cc05883g
    (Feature Article)

2016

Original

  1. “Ultratrace Detection of Toxic Chemicals: Triggered Disassembly of Supramolecular Nanotube Wrappers”
    S. Ishihara,* J. M. Azzarelli, M. Krikorian, T. M. Swager
    J. Am. Chem. Soc., 2016, 138, 8221–8227.
    DOI: 10.1021/jacs.6b03869
  2. “A Water-soluble Metal–organic Complex Array as a Multinuclear Heterometallic Peptide Amphiphile That Shows Unconventional Anion Dependency in Its Self-assembly”
    P. K. Sukul, P. Bose, T. Takei, O. M. Yaghi, Y. He, M. Lee, K. Tashiro*
    Chem. Commun., 2016, 52, 1579–1581.
    DOI: 10.1039/C5CC08973E
  3. “Fluorescent liquid pyrene derivative-in-water microemulsions”
    M. J. Hollamby,* A. E. Danks, Z. Schnepp, S. E. Rogers, S. R. Hart, T. Nakanishi
    Chem. Commun., 2016, 52, 7344–7347.
    DOI: 10.1039/c6cc01517d
  4. “Phthalocyanine-Cored Star-Shaped Polystyrene for Nano Floating Gate in Nonvolatile Organic Transistor Memory Device”
    J. Aimi,* C.-T, Lo, H.-C. Wu, C.-F. Huang, T. Nakanishi, M. Takeuchi, W.-C. Chen
    Adv. Electron. Mater., 2016, 2, 1500300.
    DOI: 10.1002/aelm.201500300
  5. “Fluorescent Mesomorphic Pyrazinacenes”
    G. J. Richards,* S. Ishihara, J. Labuta, D. Miklik, T. Mori, S. Yamada, K. Ariga, J. P. Hill*
    J. Mater. Chem. C, 2016, 4, 11514–11523.
    DOI: 10.1039/C6TC04628B

Review & Commentary

  1. “Synthesis of a Water-Soluble Metal–Organic Complex Array”
    P. Bose, P. K. Sukul, O. M. Yaghi, K. Tashiro*
    J. Vis. Exp., 2016, 116, JoVE 54513.
    DOI: 10.3791/54513
  2. “Atomic-architectonics, Nanoarchitectonics and Microarchitectonics for Strategies to Make Junk Materials Work As Precious Catalysts”
    K. Ariga,* S. Ishihara, H. Abe
    CrystEngComm, 2016, 18, 6770–6778.
    DOI: 10.1039/C6CE00986G
    (Front Cover Picture)
  3. “Nanoarchitectonics towards smart chemical sensing“
    S. Ishihara, J. Labuta
    Book chapter in Supra-Materials Nanoarchitectonics, 2016, 265–277.
    DOI: 10.1016/B978-0-323-37829-1.00012-2
  4. “Room Temperature Functional “Liquid” Materials”
    T. Nakanishi*
    EKISHO, 2016, 20 (3), 175–181.
    (Front Cover Picture)
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