YAMADA, Hiroko Achievement
Papers
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Polyazaacene and Cyclazaacene Precursors Synthesized by Dehydration Condensation from a Versatile Bis-α-diketone Unit Having an Anthracene Skeleton
Y. S. Chan, H. Hayashi,* S. Sato, S. Kasahara, K. Matsuo, N. Aratani, H. Yamada*,
Eur. J. Org. Chem. 2022, e202200621. [Selected as Very Important Paper, Front Cover.]
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Synthesis of Planar meso-Aryl Rosarins: A Reversible Antiaromatic/ Aromatic Interconversion
N. Liu, H. Morimoto, F. Wu, X. Lv, B. Xiao, D. Kuzuhara, J. Pan, F. Qiu,* N. Aratani, Z. Shen,* H. Yamada,* S. Xue*,
Org. Lett. 2022, 14, 3609-3613.
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Gram-Scale Diversity-Oriented Synthesis of Dinaphthothiepine Bisimides as Soluble Precursors for Perylene Bisimides
Y. Tanaka, K. Matsuo*, H. Yamada*, N. Fukui*, H. Sinokubo*,
Eur. J. Org. Chem. 2022, e202200770.
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Exploration of alkyl-group effects on the molecular packing of 5,15-disubstituted tetrabenzoporphyrins toward efficient charge-carrier transport
E. Jeong, T. Ito, K. Takahashi, T. Koganezawa, H. Hayashi, N. Aratani, M. Suzuki*, H. Yamada*,
ACS Appl. Mater. Interfaces 2022, 14, 32319-32329.
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A Porphyrin(2.1.2.1) Bis-boron Complex as Deep-red AIE
N. Liu, X. Lv, B. Xiao, D. Kuzuhara, P. Mei, N. Aratani, H. Yamada, F. Qiu*, J. Pan*, S. Xue*,
Dalton Trans. 2022, 51, 9606-9610.
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Synthesis of Porphyrin(2.1.2.1) with Embedded Naphthalene
X. Lv, N. Liu, B. Xiao, H. Morimoto, D. Kuzuhara*, N. Aratani, H. Yamada, F. Qiu*, S. Xue*,
J. Porphyrins Phthalocyanines 2022, 26, 510-516.
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Facile Post-synthesis and Redox Behavior of π-Expanded Ferrocene and ansa-Ferrocene
H. Morimoto, K. Matsuo, H. Hayashi, H. Yamada *, N. Aratani*,
Chem. Lett. 2022, 51, 428-430.
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Effect of aromatic solvents residuals on electron mobility of organic single crystals
G. Xue, B. Peng, T. Ye, K. Takahashi, J. Wu, Y. Liu, H. Yamada, H. Chen, H. Li*,
Adv. Electron. Mater. 2022, 2200158/1-7.
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Cross-conjugated isothianaphthene quinoids: a versatile strategy for controlling electronic structures
K. Yamamoto, S. M. Quintero, S. Jinnai, E. Jeong, K. Matsuo, M. Suzuki, H. Yamada, J. Casado*, Y. Ie*,
J. Mater. Chem. C 2022, 10, 4424-4433.
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Synthesis, Characterization, and Electrochemistry of Copper Dibenzoporphyrin(2.1.2.1) Complexes N. Liu, W. R. Osterloh, H. Huang, X. Tang, P. Mei, D. Kuzuhara, Y. Fang, J. Pan, H. Yamada, F. Qiu*, K. M. Kadish*, S. Xue*, Inorg. Chem. 2022, 61, 3563-3572.
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Reversible Photoluminescence Control of Azobenzene Crystals by Light and Heat Stimulation
M. Yamauchi*, M. Okaji, N. Aratani, H. Yamada, S. Masuo*,
ChemPhotoChem 2022, e202100301.
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On-Surface Synthesis and Characterization of Nitrogen-Substituted Undecacenes
K. Eimre*, José I. Urgel*, H. Hayashi, M. Di Giovannantonio, P. Ruffieux, S. Sato, S. Otomo, Y. S. Chan, N. Aratani, D. Passerone, O. Gröning, H. Yamada*, R. Fasel,* C. A. Pignedoli*,
Nat. Commun. 2022, 13, 511. [Selected as Editor’s Choice]
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Single crystal field-effect transistor of tetrabenzoporphyrin with one-dimensionally extended columnar packing motif exhibiting efficient charge transport property
J. Zhu, H. Hayashi*, M. Chen, C. Xiao, K. Matsuo, N. Aratani, L. Zhang, H. Yamada*,
J. Mater. Chem. C 2022, 10, 2527-2531. [Selected as Hot Paper, Inside Front Cover.]
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Porphyrin(2.1.2.1) as a novel binucleating ligand: synthesis and molecular structures of mono- and di-rhodium(i) complexes
S. Xue*, N. Liu, P. Mei, D. Kuzuhara, M. Zhou, Jianming Pan, H. Yamada, F. Qiu*,
Chem. Commun. 2021, 57, 12808-1811.
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Binuclear Rhodium(I) Complex of a Dimethylvinylene-Bridged Distorted Hexaphyrin(2.1.2.1.2.1)
S. Xue, N. Liu, P. Mei, D. Kuzuhara*, N. Aratani, F. Qiu*, H. Yamada*,
Inorg. Chem. 2021, 60, 16070-16073.
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Mirror-Image Cofacial Coronene Dimers Characterized by CD and CPL Spectroscopy: A Molecular-scale Twisted Bilayer Graphene
K. Uehara, H. Kano, K. Matsuo, H. Hayashi, M. Fujiki, H. Yamada*, N. Aratani*,
ChemPhotoChem 2021, 5, 974-978. [Very Important Paper, Selected as Cover Picture]
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Synthesis of 10,20-substituted tetrabenzo-5,15-diazaporphyrin copper complexes from soluble precursors
Y. Sugano, K. Matsuo*, H. Hayashi, N. Aratani, H. Yamada*,
J. Porphyrins Phthalocyanines 2021, 25, 1186-1192.
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Nature of Local Charge Carrier Motions in Porphyrin-Based Bulk Heterojunction Films Revealed by Time-Resolved Optical Pump-Terahertz Probe Spectroscopy
K. Ohta, Y. Hiramatsu, M. Suzuki, H. Yamada*, K. Tominaga*,
Chem. Lett. 2021, 50, 1859-1862.
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Efficient photogeneration of nonacene on nanostructured graphene
C. Ayani, M. Pisarra, J. Urgel, J. Navarro, C. Díaz, H. Hayashi, H. Yamada, F. Calleja, R. Miranda, R. Fasel, F. Martín*, A. Vázquez de Parga*,
Nanoscale Horiz. 2021, 6, 744-750.
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Deep-red circularly polarised luminescent C70 derivatives
H. Kano, H. Hayashi, K. Matsuo, M. Fujiki, H. Yamada*, N. Aratani*,
Sci. Rep. 2021, 11, 12072.
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Synthesis and Properties of the Doubly Oxonium-Embedded Picenes as Electron-Deficient Polycyclic Aromatic Hydrocarbons
K. Matsuo*, N. Toda, N. Aratani, H. Yamada*,
Org. Lett. 2021, 23, 3986-3990.
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Buckyball as an Electron Donor in a Dyad of C60 and Xanthene Dye
H. Kano, K. Matsuo, H. Hayashi, K. Kato, A. Yamakata, H. Yamada*, N. Aratani*,
Eur. J. Org. Chem. 2021, 23, 3377-3381.
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Acridino[2,1,9,8‐klmna]acridine Bisimides: An Electron‐Deficient π‐System for Robust Radical Anions and n‐Type Organic Semiconductors
K. Tajima, K. Matsuo, H. Yamada*, S. Seki*, N. Fukui*, H. Shinokubo*,
Angew. Chem. Inter. Ed. 2021, 60, 14060-14067. [プレスリリース]
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Synthesis and Evaluation of Charge Transport Property of Ethynylene-Bridged Anthracene Oligomers
J. Zhu, H. Hayashi*, M. Chen, C. Xiao, K. Matsuo, N. Aratani, L. Zhang, H. Yamada*,
Macromol. Chem. Phys. 2021, 222, 2100024.
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One-Pot Synthesis of a Cyclic Pyrene Octamer from Two Bifunctionalized
P. Mei, R. Kurosaki, A. Matsumoto, H. Yamada*, N. Aratani*,
Synthesis 2021, 53, 344-347.
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Molecular organized isoindigo based small molecules with terminal thermally cleavable protecting group
M. Shaker*, H. Hayashi, H. Yamada*,
Dyes and Pigments 2021, 184, 108806.
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Direct borylation of terrylene and quaterrylene
H. Kano, K. Uehara, K. Matsuo, H. Hayashi, H. Yamada*, N. Aratani*,
Beilstein J. Org. Chem. 2020, 16, 621-627.
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Facilitated Interfacial Electronic Processes by the π−π Stacked Edgeon Tetrabenzoporphyrin/Graphene Layer Enables Broadband Ultrasensitive Photodetecting with Prompt Response
M. Shao, M. Yu, M. Suzuki, H. Yamada, Y. Wang, Y. Chen, C. Lu, D. Wang, Z. Yang*,
ACS Appl. Electron. Mater. 2020, 2, 3459-3467.
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Vinylene-Bridged Cyclic Dipyrrin and BODIPY Trimers
S. Xue, D. Kuzuhara*, N. Aratani, H. Yamada*,
Int. J. Mol. Sci. 2020, 21, 8041.
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Dinaphthothiepine Bisimide and Its Sulfoxide: Soluble Precursors for Perylene Bisimide
S. Hayakawa, K. Matsuo, H. Yamada*, N. Fukui*, H. Shinokubo*,
J. Am. Chem. Soc. 2020, 142, 11663-11668. [プレスリリース]
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Dynamic Behavior of Photogenerated Charge Carriers in Diketopyrrolopyrrole-Linked Tetrabenzoporphyrin-Based Bulk Heterojunction Thin Films Probed with Time-Resolved Terahertz Spectroscopy
K. Ohta, Y. Hiramatsu, K. Takahashi, M. Suzuki, H. Yamada,* K. Tominaga*,
J. Photochem. Photobiol. A: Chemistry 2020, 400, 112623.
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A Windmill-Shaped Molecule with Anthryl Blades to Form Smooth Hole-Transport Layers via a Photoprecursor Approach
A. Maeda, A. Nakauchi, Y. Shimizu, K. Terai, S. Sugii, H. Hayashi, N. Aratani, M. Suzuki*, H. Yamada*,
Materials 2020, 13, 2316.
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A Directly-linked Cyclic Pyrene Tetramer as a Back-to-back Receptor for Two Fullerenes
R. Kurosaki, K. Matsuo, H. Hayashi, H. Yamada*, N. Aratani*,
Chem. Lett. 2020, 49, 892-895. [Selected as Editor’s Choice]
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Visible‐light‐induced Heptacene Generation under Ambient Conditions: Utilization of Single‐crystal Interior as an Isolated Reaction Site
H. Hayashi*, N. Hieda, M. Yamauchi, Y. Chan, N. Aratani, S. Masuo*, H. Yamada*,
Chem. Eur. J. 2020, 26, 15079-15083. [Selected as Hot Paper, Inside Cover]
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Small bandgap features achieved in atomically precise 17-atom-wide armchair-edged graphene nanoribbons
J. Yamaguchi*, H. Hayashi, H. Jippo, A. Shiotari, M. Ohtomo, M. Sakakura, N. Hieda, N. Aratani, M. Ohfuchi, Y. Sugimoto, H. Yamada*, S. Sato,
Commun. Mater. 2020, 1, 36. [Selected as Editor’s Choice TOP 15, プレスリリース]
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Robust Unipolar Electron Conduction using an Ambipolar Polymer Semiconductor with Solution-Processable Blends
M. Ford*, M. Suzuki, C. Bridges, K. Bustillo, M. Seifrid, M. Wang, H. Yamada, T. Nguyen, G. Bazan,
Chem. Mater. 2020, 32, 6831-6837.
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Retro-Diels–Alder Reaction on Surface: Generating Energy-Prohibited Structures in Bulk Film Condition through Surface-Adsorbing Neutralization Effect
M. Shao, M. Yu, Z. Yang*, M. Suzuki*, H. Yamada*,
J. Phys. Chem. C 2020, 124, 5723-5733.
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Cyclic butadiyne-linked porphyrin(2.1.2.1) oligomers
D. Kuzuhara*, W. Furukawa, N. Aratani, H. Yamada*,
J. Porphyrins Phthalocyanines 2020, 24, 489-497.
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Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
M. Suzuki*, K. Terai, C. Quinton, H. Hayashi, N. Aratani, H. Yamada*,
Chem Sci. 2020, 11, 1825-1831.
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Orbital-Energy Modulation of Tetrabenzoporphyrin-Derived Non-Fullerene Acceptors for Improved Open-Circuit Voltage in Organic Solar Cells
E. Jeong, K. Takahashi, S. K Rajagopal, T. Koganezawa, H. Hayashi, N. Aratani, M. Suzuki*, T. Nguyen*, H. Yamada*,
J. Org. Chem. 2020, 85, 168-178. [Selected as Back Cover]
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Torsional chirality generation based on cyclic oligomers constructed from an odd number of pyrenes
R. Kurosaki, M. Suzuki, H. Hayashi, M. Fujiki, N. Aratani*, H. Yamada*,
Chem. Commun. 2019, 55, 9618-9621. [Selected as Back Cover]
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Effect of Edge Functionalization on the Bottom-Up Synthesis of Nano-Graphenes
M. Ohtomo*, H. Hayashi*, K. Hayashi, H. Jippo, J. Zhu, R. Hayashi, J. Yamaguchi, M. Ohfuchi, H. Yamada*, S. Sato*,
ChemPhysChem 2019, 20, 3366-3372.
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Synthesis of Anthracene Derivatives with Azaacene‐containing Iptycene Wings and the Utilization as a Dopant for Solution‐processed Organic Light‐emitting Diodes
H. Hayashi*, Y. Kato, A. Matsumoto, S. Shikita, N. Aizawa, M. Suzuki, N. Aratani, T. Yasuda, H. Yamada*,
Chem. Eur. J. 2019, 25, 15565-15571.
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2,7,12,17-Tetra(2,5-thienylene)-substituted porphycenes
D. Kuzuhara*, H. Nakaoka, K. Matsuo, N. Aratani, H. Yamada*,
J. Porphyrins Phthalocyanines 2019, 23, 898-907.
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Short Excited-State Lifetimes Enable Photo-Oxidatively Stable Rubrene Derivatives
J. Ly, K. Martin, S. Thomas, M. Yamashita, B. Yu, C. A. Pointer, H. Yamada, K. R. Carter, S. Parkin, L. Zhang*, J.-L. Bredas*, E. R. Young,* A. L. Briseno*,
J. Phys. Chem. A 2019, 123, 7558-7566.
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Crystallization-Induced Emission of Azobenzene Derivatives
M. Yamauchi*, K. Yokoyama, N. Aratani, H. Yamada, S. Masuo*,
Angew. Chem. Inter. Ed. 2019, 58, 14173-14178.
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Overcoming steric hindrance in aryl‐aryl homocoupling via on‐surface copolymerization
J. I. Urgel*, M. D. Giovannantonio, G. Gandus, Q. Chen, X. Liu, H. Hayashi, P. Ruffieux, S. Decurtins, A. Narita, D. Passerone, H. Yamada, S. Liu, K. Müllen, C. A. Pignedoli, R. Fasel*,
ChemPhysChem 2019, 20, 2360-2366.
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Control of Aromaticity and cis‐/trans‐Isomeric Structure of Non‐Planar Hexaphyrin(2.1.2.1.2.1) and Metal Complexes
S. Xue, D. Kuzuhara*, N. Aratani, H. Yamada*,
Angew. Chem. Int. Ed. 2019, 58, 12524-12528.
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A remarkably strained cyclopyrenylene trimer that undergoes metal-free direct oxygen insertion into the biaryl C–C σ-bond
R. Kurosaki, H. Hayashi, M. Suzuki, J. Jiang, M. Hatanaka, N. Aratani, H. Yamada,
Chem. Sci. 2019, 10, 6785-6790.
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Organic Heterojunctions Formed by Interfacing Two Single Crystals from a Mixed Solution
H. Li, J. Wu, K. Takahashi, J. Ren, R. Wu, H. Cai, J. Wang, H. Xin, Q. Miao, H. Yamada, H. Chen, H. Li*,
J. Am. Chem. Soc. 2019, 141, 10007-10015.
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Solid-State, Near-Infrared to Visible Photon Upconversion via Triplet–Triplet Annihilation of a Binary System Fabricated by Solution Casting
A. Abulikemu*, Y. Sakagami, C. Heck, K. Kamada*, H. Sotome, H. Miyasaka, D. Kuzuhara, H. Yamada*,
ACS Appl. Mater. Interfaces 2019, 11, 20812-20819. [プレスリリース]
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Synthesis of the Soluble Precursors of Tetrabenzoporphyrin: Control of the Solubility and the Conversion Temperature
T. Okujima*, Y. Hashimoto, T. Furuta, R. Yamanaka, G. Jin, S. Ohtsuobo, S. Aramaki, S. Mori, H. Yamada, H. Uno, N. Ono*,
Bull. Chem. Soc. Jpn. 2019, 92, 1370-1378.
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Synthesis of a Porphyrin(2.1.2.1) Nanobelt and Its Ability To Bind Fullerene
S. Xue, D. Kuzuhara*, N. Aratani , H. Yamada*,
Org. Lett. 2019, 21, 2069-2072.
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On-surface light-induced generation of higher acenes and elucidation of their open-shell character
J. I. Urgel, S. Mishra, H. Hayashi, J. Wilhelm, C. A. Pignedoli, M. D. Giovannantonio, R. Widmer, M. Yamashita, N. Hieda, P. Ruffieux, H. Yamada*, R. Fasel*,
Nat. Commun. 2019, 10, 861.
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Photoconversion of 6,13-a-diketopentacene single crystals exhibiting light intensity-dependent morphological change
M. Yamauchi, Y. Miyamoto, M. Suzuki, H. Yamada, S. Masuo*,
Phys. Chem. Chem. Phys. 2019, 21, 6348-6353. [Selected as Back Cover]
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Inter-Polymer Self-Assembly of Bottom-up Graphene Nanoribbons Fabricated from Fluorinated Precursors
M. Ohtomo*, H. Jippo, H. Hayashi, J. Yamaguchi, M. Ohfuchi, H. Yamada, S. Sato*,
ACS Appl. Mater. Interfaces 2018, 10, 31623-31630.
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Improvement in interlayer structure of p–i–n-type organic solar cells with the use of fullerene-linked tetrabenzoporphyrin as additive
Y. Tamura, M. Suzuki, T. Nakagawa, T. Koganezawa, S. Masuo, H. Hayashi, N. Aratani, H. Yamada*,
RSC Advances 2018, 8, 35237-35245.
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An ethynylene-Bridged Pentacene Dimer: Two-Step Synthesis and Charge Transport Property
K. Kawano, H. Hayashi*, S. Yoshimoto, N. Aratani, M. Suzuki, J. Yoshinobu*, H. Yamada*,
Chem. Eur. J. 2018, 24, 14916-14920.
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[30]Hexaphyrin(2.1.2.1.2.1) as Aromatic Planar Ligand and its Trinuclear Rhodium(I) Complex
S. Xue, D. Kuzuhara*, N. Aratani, H. Yamada*,
Inorg. Chem. 2018, 57, 9902-9906.
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Photochemical layer-by-layer solution process for preparing organic semiconducting thin films having right materials at right places
M. Suzuki*, Y. Yamaguchi, K. Uchinaga, K. Takahira, C. Quinton, S. Yamamoto, N. Nagami, M. Furukawa, K. Nakayama*, H. Yamada*,
Chem. Sci. 2018, 9, 6614-6621. [Selected as Back Cover]
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1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C60
P. Mei, A. Matsuomoto, H. Hayashi, M. Suzuki, N. Aratani*, H. Yamada*,
RSC Adv. 2018, 8, 20872-20876.
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An Anomalous Antiaromaticity that Arises from the Cycloheptatrienyl Anion Equivalent
K. Uehara, P. Mei, T. Murayama, F. Tani, H. Hayashi, M. Suzuki, N. Aratani,* H. Yamada*,
Eur. J. Org. Chem. 2018, 33, 4508-4511. [Selected as Front Cover]
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Synthesis of [14]Oxatriphyrins(2.1.1) and Their Transformation into Ethane-Bridged Oxatripyrrins by Boron Complexation
D. Kuzuhara*, S. Kawatsu, W. Furukawa, H. Hayashi, N. Aratani, H. Yamada*,
Eur. J. Org. Chem. 2018, 18, 2122-2129.
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Macrocyclic Polyradicaloids with Unusual Super-ring Structure and Global Aromaticity
C. Liu, M. E. Sandoval-Salinas, Y. Hong, T. Y. Gopalakrishna, H. Phan, N. Aratani, T. S. Herng, J. Ding, H. Yamada, D. Kim*, D. Casanova*, J. Wu*,
Chem 2018, 4, 1586-1595.
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Structure Engineering: Extending the Length of Azaacene Derivatives through Quinone Bridge
Z. Wang, Z. Wang, Y. Zhou, P. Gu, G. Liu, K. Zhao, L. Nie, Q. Zeng, J. Zhang, Y. Li, R. Gangly, N. Aratani, L. Huang, Z. Liu, H. Yamada*, W. Hu*, Q. Zhang*,
J. Mater. Chem. C 2018, 6, 3628-3633.
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Benzonorcorrole NiII Complexes: Enhancement of Paratropic Ring Current and Singlet Diradical Character by Benzo-Fusion
T. Yoshida, K. Takahashi, Y. Ide, R. Kishi, J. Fujiyoshi, S. Lee, Y. Hiraoka, D. Kim, M. Nakano*, T. Ikeue, H. Yamada, H. Shinokubo*,
Angew. Chem. Inter. Ed. 2018, 57, 2209-2213.
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Universality of Giant Seebeck Effect in Organic Small Molecules
H. Kojima*, R. Abe, F. Fujiwara, M. Nakagawa, K. Takahashi, D. Kuzuhara, H. Yamada, Y. Yakiyama, H. Sakurai, T. Yamamoto, H. Yakushiji, M. Ikeda, M. Nakamura*,
Mater. Chem. Frontiers 2018, 2, 1276-1283.
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Transient Photocurrent Elucidating Carrier Dynamics and Potential of Bulk Heterojunction Solar Cells Fabricated by Thermal Precursor Approach
N. Kudo, K. Uchida, T. Ikoma*, K. Takahashi, D. Kuzuhara, M. Suzuki, H. Yamada, D. Kumagai, Y. Yamaguchi, K. Nakayama,
Solar RRL 2018, 2, 1700234.
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Photophysical properties and structural analysis of modified methylene blues as near infrared dyes
A. Tamoto, N. Aratani*, H. Yamada*,
J. Photochem. Photobiol. A: Chemistry 2018, 358, 441-446.
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Probing Charge Carrier Dynamics in Porphyrin-Based Organic Semiconductor Thin Films by Time-Resolved THz Spectroscopy
K. Ohta, S. Tokonami, L. Takahashi, Y. Tamura, H. Yamada*, K. Tominaga*,
J. Phys, Chem. B 2017, 121, 10157-10165.
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Synthesis, Characterization and Protonation Behavior of Quinoxaline-Fused Porphycenes
D. Kuzuhara*, M. Sakaguchi, W. Furukawa, T. Okabe, N. Aratani, H. Yamada*,
Molecules 2017, 22, 908.
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Contraction of π-Conjugated Rings upon Oxidation from Cyclooctatetraene to Benzene via Tropylium Cation
A. Tamoto, N. Aratani*, H. Yamada*,
Chem. Eur. J. 2017, 23, 16388-16392.
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On-Surface Synthesis of Heptacene Organometallic Complexes
J. I. Urgel, H. Hayashi, M. D. Giovannantonio, C. A. Pignedoli, S. Mishra, O. Deniz, M. Yamashita, T. Dienel, P. Ruffieux, H. Yamada*, R. Fasel*,
J. Am. Chem. Soc. 2017, 139, 11658-11661.
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Understanding the structure-determining solid fluorescence of an azaacene derivative
P. Gu, G. Liu, J. Zhao, N. Aratani, X. Ye, Y. Liu, H. Yamada, L. Nie, H. Zhang, J. Zhu, D.-S. Li*, Q. Zhang*,
J. Mater. Chem. C 2017, 5, 8869-8874.
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Highly anisotropic mobility in solution processed TIPS-pentacene film studied by independently driven four GaIn probes.
S. Yoshimoto*, K. Takahashi, M. Suzuki, H. Yamada, R. Miyahara, K. Mukai, J. Yoshinobu,
Appl. Phys. Lett. 2017, 111, 073301.
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Dinaphthotetrathiafulvalene Bisimides: A New Member of the Family of π-Extended TTF Stable p-Type Semiconductors
M. Yamashita, K. Kawano, A. Matsumoto, N. Aratani, H. Hayashi, M. Suzuki, L. Zhang, A. L. Briseno, H. Yamada*,
Chem. Eur. J. 2017, 23, 15002-15007. [Selected as Front Cover]
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Side-chain engineering in a thermal precursor approach for efficient photocurrent generation with insoluble tetrabenzoporphyrin–diketopyrrolopyrrole conjugates
K. Takahashi, D. Kumagai, N. Yamada, D. Kuzuhara, Y. Yamaguchi, N. Aratani, T. Koganezawa, S. Koshika, N. Yoshimoto, S. Masuo, M. Suzuki*, K. Nakayama*, H. Yamada*,
J. Mater. Chem. A 2017, 5, 14003-14011. [Selected as Inside Front Cover]
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Experimental and Theoretical Investigations of Surface-Assisted Graphene Nanoribbon Synthesis Featuring Carbon–Fluorine Bond Cleavage
H. Hayashi*, J. Yamaguchi, H. Jippo, R. Hayashi, N. Aratani, M. Ohfuchi, S. Sato*, H. Yamada*,
ACS Nano 2017, 11, 6204-6210.
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Rearrangement of an aniline linked perylene bisimide under acidic conditions and visible to near-infrared emission from the intramolecular charge-transfer state of its fused derivatives
M. Kojima, A. Tamoto, N. Aratani*, H. Yamada*,
Chem. Commun. 2017, 53, 5698-5701. [Selected as Inside Back Cover]
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Studies on Pyrene and Perylene Derivatives upon Oxidation and Application to a Higher Analogue
A. Matsumoto, M. Suzuki, H. Hayashi, D. Kuzuhara, J. Yuasa, T. Kawai, N. Aratani*, H. Yamada*,
Bull. Chem. Soc. Jpn. 2017, 90, 667-677.
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Semiconducting Self-assembled Nanofibers Prepared from Photostable Octafluorinated Bisanthene Derivative
H. Hayashi*, N. Aratani, H. Yamada*,
Chem. Eur. J. 2017, 23, 7000-7008. [Selected as Hot Paper, Inside Cover]
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Engineering Thin Films of a Tetrabenzoporphyrin toward Efficient Charge-Carrier Transport: Selective Formation of a Brickwork Motif
K. Takahashi, B. Shan, X. Xu, S. Yang, T. Koganezawa, D. Kuzuhara, N. Aratani, M. Suzuki*, Q. Miao*, H. Yamada*,
ACS Appl. Mater. Interfaces 2017, 9, 8211-8218.
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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. 2017, 7, 43098.
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Fullerene-Based n-Type Materials That Can Be Processed by a Photoprecursor Approach for Photovoltaic Applications
K. Kawajiri, T. Kawanoue, M. Yamato, K. Terai, M. Yamashita, M. Furukawa, N. Aratani, M. Suzuki*, K. Nakayama*, H. Yamada*,
ECS J. Solid State Sci. Tech. 2017, 6, 6.
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Rylene Ribbons with Unusual Diradical Character
W. Zeng, H. Phan, T. S. Herng, T. Y. Gopalakrishna, N. Aratani, Z. Zeng, H. Yamada, J. Ding, J. Wu*,
Chem 2017, 2, 81-92.
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An Azulene-Fused Tetracene Diimide with a Small HOMO– LUMO Gap
T. Koide, M. Takesue, T. Murafuji, K. Satomi, Y. Suzuki, J. Kawamata, K. Terai, M. Suzuki, H. Yamada, Y. Shiota, K. Yoshizawa, F. Tani*,
ChemPlusChem 2017, 82, 1010-1014.
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Applicability of Density Functional Tight Binding Method with Dispersion Correction to Investigate the Adsorption of Porphyrin/Porphycene Metal Complexes on Graphene
Y. Kanematsu*, K. Gohara, H. Yamada, Y. Takano*,
Chem. Lett. 2017, 46, 51-52.
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Synthesis and Characterization of an Iridium Triphyrin Complex
S. Xue, D. Kuzuhara*, N. Aratani, H. Yamada*,
Inorg. Chem. 2016, 55, 10106-10109.
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Fullerene-linked tetrabenzoporphyrins for solution-processed organic photovoltaics: flexible vs. rigid linkers
Y. Tamura, D. Kuzuhara, M. Suzuki, H. Hayashi, N. Aratani, H. Yamada*,
J. Mater. Chem. A. 2016, 4, 15333-15342. [Selected as Inside Front Cover]
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Synthesis, Characterization and Electronic Structures of Porphyrins Fused with Polycyclic Aromatic Ring Systems
T. Okujima*, J. Mack*, J. Nakamura, G. Kubheka, T. Nyokong, H. Zhu, N. Komobuchi, N. Ono, H. Yamada, H. Uno, N. Kobayashi*,
Chem. Eur. J. 2016, 22, 14730-14738.
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Benzo[4,5]cyclohepta[1,2-b]fluorene: an isomeric motif for pentacene containing linearly fused five-, six- and seven-membered rings
X. Yang, X. Shi, N. Aratani, T. P. Gonçalves, K. Huang, H. Yamada, C. Chi*, Q. Miao*,
Chem. Sci. 2016, 7, 6176-6181.
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Switching charge-transfer characteristics from p-type to n-type through molecular “doping” (cocrystallization)
J. Zhang, P. Gu, G. Long, R. Ganguly, Y. Li, N. Aratani, H. Yamada, Q. Zhang*,
Chem. Sci. 2016, 7, 3851-3856.
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Bisanthra-thianthrene: synthesis, structure and oxidation propertie
M. Yamashita, H. Hayashi, M. Suzuki, D. Kuzuhara*, J. Yuasa, T. Kawai, N. Aratani*, H. Yamada*,
RSC Adv. 2016, 6, 70700-70703.
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Aromaticity Relocation in Perylene Derivatives upon Two-electron Oxidation to Form Anthracene and Phenanthrene
A. Matsumoto, M. Suzuki, H. Hayashi, D. Kuzuhara, J. Yuasa, T. Kawai, N. Aratani*, H. Yamada*,
Chem. Eur. J. 2016, 22, 14462-14466.
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Porphycene Dimer–Based Non-Fullerene Acceptor for Organic Solar Cell
T. Okabe, D. Kuzuhara, M. Suzuki, N. Aratani, H. Yamada*,
J. Porphyrins Phthalocyanines 2016, 20, 1350-1360.
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Synthesis and Metalation of Doubly o-Phenylene-Bridged Cyclic Bis(dipyrrin)s with Highly Bent Skeleton of Dibenzoporphyrin(2.1.2.1)
D. Kuzuhara*, W. Furukawa, A. Kitashiro, N. Aratani, H. Yamada*,
Chem. Eur. J. 2016, 22, 10671-10678.
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Photoprecursor Approach Enables Preparation of Well-Performing Bulk-Heterojunction Layers Comprising a Highly Aggregating Molecular Semiconductor
M. Suzuki, Y. Yamaguchi, K. Takahashi, K. Takahira, T. Koganezawa, S. Masuo, K. Nakayama*, H. Yamada*,
ACS Appl. Mater. Interface 2016, 8, 8644-8651.
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A laterally π-expanded fluorone dye as an efficient near infrared fluorophore
K. Sezukuri, M. Suzuki, H. Hayashi, D. Kuzuhara, N. Aratani*, H. Yamada*,
Chem. Commun. 2016, 52, 4872-4875.
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A Diradical Approach towards BODIPY-Based Dyes with Intense Near-Infrared Absorption around λ =1100 nm
Y. Ni, S. Lee, M. Son, N. Aratani, M. Ishida, A. Samanta, H. Yamada, Y. Chang, H. Furuta, D. Kim*, J. Wu*, Angew,
Chem. Int. Ed. 2016, 55, 2815-2819.
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Towards Tetraradicaloid: The Effect of Fusion Mode on Radical Character and Chemical Reactivity
P. Hu, S. Lee, T. Herng, N. Aratani, T. Gonçalves, Q. Qi, X. Shi, H. Yamada, K. Huang, J. Ding*, D. Kim*, J. Wu*,
J. Am. Chem. Soc. 2016, 138, 1065-1077.
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Z-Shaped Pentaleno- Acene Dimers with High Stability and Low Band Gap
G. Dai, J. Chang, J. Luo, S. Dong, N. Aratani, B. Zheng, K. Huang, H. Yamada, C. Chi*, Angew,
Chem. Int. Ed. 2016, 55, 2693-2696.
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Fusing N-heteroacene Analogues into One “Kinked” Molecule with Slipped Two-dimensional Ladder-like Packing
J. Zhang, C. Wang, G. Long, N. Aratani, H. Yamada, Q. Zhang*,
Chem. Sci. 2016, 7, 1309-1313.
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Full Characterization and photoelectrochemical behaviors of Pyrene-fused Octaazadecacene and Tetraazaoctacene
Z. Wang, J. Miao, G. Long, P. Gu, J. Li, N. Aratani, H. Yamada, B. Liu, Q. Zhang*,
Chem. Asian J. 2016, 11, 482-485.
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Charge-Carrier Dynamics in Benzoporphyrin Films Investigated by Time-Resolved THz Spectroscopy
K. Ohta, S. Hiraoka, Y. Tamura, H. Yamada, K. Tominaga,
Appl. Phys. Lett. 2015, 107, 183302/1-5.
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Facile synthesis of indolizino[3,4,5-ab]isoindoles by an acid-induced cyclization of 1,2-di(1H-pyrrol-2-yl)benzenes
D. Kuzuhara*, S. Miyake, H. Moriyama, Y. Tamura, N. Aratani, H. Yamada*,
Tetrahedron Lett. 2015, 56, 5564-5567.
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Catalytic two-electron reduction of dioxygen catalysed by metal-free [14]triphyrin(2.1.1)
K. Mase, K. Ohkubo, Z. Xue, H. Yamada, S. Fukuzumi*,
Chem. Sci. 2015, 6, 6496-6504.
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Indolizino[5,6-b]quinoxaline Derivatives: Intramolecular Charge Transfer Characters and NIR Fluorescence
M. Kojima, H. Hayashi, T. Aotake, S. Ikeda, M. Suzuki, N. Aratani, D. Kuzuhara, H. Yamada*,
Chem. Asian J. 2015, 10, 2337-2341. [Selected as Inside Cover]
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A Novel D-π-A Small Molecule with N-heteroacene as Acceptor Moiety for Photovoltaic Application
C. Wang, T. Okabe, G. Long, D. Kuzuhara, Y. Zhao, N. Aratani*, H. Yamada*, Q. Zhang*,
Dyes and Pigments 2015, 122, 231-237.
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Evaluation of semiconducting molecular thin films solution-processed via the photoprecursor approach: the case of hexyl-substituted thinoanthracenes
C. Quinton, M. Suzuki*, Y. Kaneshige, Y. Tatenaka, C. Katagiri, Y. Yamaguchi, D. Kuzuhara, N. Aratani, K. Nakayama, H. Yamada*,
J. Mater. Chem. C 2015, 3, 5995-6005.
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Tetrabenzoperipentacene: Stable Five-Electron Donating Ability and a Discrete Triple-Layered β-Graphite Form in the Solid State
A. Matsumoto, M. Suzuki, D. Kuzuhara, H. Hayashi, N. Aratani*, H. Yamada*, Angew,
Chem. Int. Ed. 2015, 54, 8175-8178. [Selected as Hot Paper]
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An electron-deficient tetrathiafulvalene-conjugated bistetracene
M. Yamashita, H. Hayashi, N. Aratani*, H. Yamada*,
Tetrahedron Lett. 2015, 56, 3804-3808.
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Synthesis, Characterization and Memory Performance of Two Organic Small Molecules through Donor-acceptor Design
C. Wang, M. Yamashita, B. Hu, Y. Zhou, J. Wang, J. Wu, F. Huo, P. S. Lee, N. Aratani, H. Yamada, Q. Zhang*,
Asian J. Org. Chem. 2015, 4, 646-651.
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Synthesis, Structure, and Air-stable N-type Field-Effect Transistor Behaviors of Functionalized Octaazanonacene-8,19-dione
C. Wang, J. Zhang, G. Long, N. Aratani, H. Yamada, Y. Zhao, Q. Zhang*,
Angew. Chem. Int. Ed. 2015, 54, 6292-6296.
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Evaluation of Charge Transfer Efficiency of Organic Thin-Film Photovoltaic Devices Fabricated Using Fluorescence Microspectroscopy
S. Masuo*, W. Sato, Y. Yamaguchi, M. Suzuki, K. Nakayama, H. Yamada,
Photochem. Photobiol. Sci. 2015, 14, 883-890.
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Effect of alkyl substituents: 5,15-bis(trimethylsilylethynyl)- vs 5,15-bis(triisopropylsilylethynyl)-tetrabenzoporphyrins and their metal complexes
K. Takahashi, N. Yamada, D. Kumagai, D. Kuzuhara, M. Suzuki, Y. Yamaguchi, N. Aratani, K. Nakayama*, H. Yamada*,
J. Porphyrins Phthalocyanines 2015, 19, 473-478.
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9,9’-Anthryl-Anthroxyl Radicals: Strategic Stabilization of Highly Reactive Phenoxyl Radicals
T. Aotake, M. Suzuki, N. Aratani, J. Yuasa, D. Kuzuhara, H. Hayashi, H. Nakano, T. Kawai, J. Wu*, H. Yamada*,
Chem. Commun. 2015, 51, 6734-6737. [Selected as Inside Back Cover]
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An Optically- and Thermally-Switchable Electronic Structure Based on Anthracene–BODIPY Conjugate
T. Aotake, M. Suzuki, K. Tahara, D. Kuzuhara, N. Aratani, N. Tamai, H. Yamada*,
Chem. Eur. J. 2015, 21, 4966-4974. [Selected as Inside Cover]
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Synthesis, Properties and Crystal Structures of 2,7,12,17-Tetraarylporphycenes
D. Kuzuhara, H. Nakaoka, T. Okabe, N. Aratani, H. Yamada,
Heterocycles 2015, 90, 1214-1227.
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Rewritable Multilevel Memory Performance of a Tetraazatetracene Donor-Acceptor Derivative with Good Endurance
C. Wang, B. Hu, J. Wang, J. Gao, G. Li, W.-W. Xiong, B.-h. Zou, M. Yamashita, A. Matsumoto, N. Aratani, H. Yamada, F. Huo, P. S. Lee, Q. Zhang*,
Chem. Asian. J. 2015, 10, 116-119.
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Tautomerism in Porphycenes: Analysis of Rate-Affecting Factors
P. Ciąćka, P. Fita, A. Listkowski, M. Kijak, S. Nonell, D. Kuzuhara, H. Yamada, C. Radzewicz, J. Waluk,
J. Phys. Chem. B 2015, 119,2292-2301.
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Synthesis and electronic properties of acetylene- and butadiyne-linked 3,3'-porphycene dimers
T. Okabe, D. Kuzuhara*, N. Aratani, H. Yamada*,
J. Porphyrins Phthalocyanines 2014, 18, 849-855.
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Photoprecursor approach as an effective means for preparing multilayer organic semiconducting thin films by solution processes
Y. Yamaguchi, M. Suzuki, T. Motoyama, S. Sugii, C. Katagiri, K. Takahira, S. Ikeda, H. Yamada*, K. Nakayama*,
Sci. Rep. 2014, 4, 7151
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A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species A. Matsumoto, M. Suzuki, D. Kuzuhara, J. Yuasa, T. Kawai, N. Aratani*, H. Yamada*, Chem. Commun. 2014, 50, 10899-11064. [Selected as Inside Cover]
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Direct comparison of covalently-linked dyad and a 1:1 mixture of tetrabenzoporphyrin and fullerene as organic photovoltaic materials
Y. Tamura, H. Saeki, J. Hashizume, Y. Okazaki, D. Kuzuhara, M. Suzuki, N. Aratani, H. Yamada*,
Chem. Commun. 2014, 50, 10379-10381.
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Synthesis and Electrochemical Properties of Porphycene–Diketopyrrolopyrrole Conjugates
T. Okabe, D. Kuzuhara*, M. Suzuki, N. Aratani, H. Yamada*,
Org. Lett. 2014, 16, 3508-3511.
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Design Amphiphilic Dipolar π-Systems for Complex Stimuli-Responsive Luminescent Materials Designed Using Metastable States
S. Yagai*, S. Okamura, Y. Nakano, M. Yamauchi, K. Kishikawa, T. Karatsu, A. Kitamura, A. Ueno, D. Kuzuhara, H. Yamada,
Nat. Commun. 2014, 5, 4013.
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Photoconversion of 6, 13-α-Diketopentacene in the Crystalline Phase
S. Masuo*, K. Tanaka, M. Oe, Hiroko Yamada,
Phys. Chem. Chem. Phys. 2014, 16, 13483-13488.
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Synthesis of opp-Dibenzohexaphyrins(1.1.1.1.1.1) by Retro-Diels-Alder Reaction
S. Ishida, D. Kuzuhara, H. Yamada, A. Osuka*,
Asian. J. Org. Chem. 2014, 3, 716–722.
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Effect of Crystallinity in Small Molecular Weight Organic Heterojunction Solar Cells
H. Saeki, O. Kurimoto, H. Nakaoka, M. Misaki, D. Kuzuhara, H. Yamada*, K. Ishida*, Y. Ueda,
J. Mater. Chem. C 2014, 2, 5357-5364.
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Time-Resolved Fluorescence Spectroscopy Study of Excited State Dynamics of Alkyl- and Benzo-Substituted Triphyrin(2.1.1)
Y. Iima, D. Kuzuhara, Z.-L. Xue, S. Akimoto, H. Yamada*, K. Tominaga*,
Phys. Chem. Chem. Phys. 2014, 16, 13129-13135.
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Synthesis and Solid State Structures of a Tetrathiafulvalene-conjugated Bistetracene
M. Yamashita, D. Kuzuhara, N. Aratani*, H. Yamada*,
Chem. Eur. J. 2014, 20, 6309-6314.
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Synthesis and optical reactivity of 6,13-a-diketoprecursors of 2,3,9,10-tetraalkylpentacenes in solution, film and crystals
S. Katsuta, H. Saeki, K. Tanaka, Y. Murai, D. Kuzuhara, M. Misaki, N. Aratani, S. Masuo, Y. Ueda, H. Yamada*,
J. Mater. Chem. C 2014, 2, 986-993. [Selected as Inside Back Cover]
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Synthesis and Molecular Structure of Cyclo[8](9,10-Dihydro-9,10-Anthraceno)Pyrrole
T. Okujima*, C. Ando, S. Mori, T. Nakae, H. Yamada, H. Uno,
Heterocycles 2014, 88, 417-424.
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Bulk-Heterojunction Organic Photovoltaic Devices Fabricated Using Asymmetric Soluble Anthracene Core Photoprecursors
T. Motoyama, S. Sugii, S. Ikeda, Y. Yamaguchi, H. Yamada*, K. Nakayama*,
Jpn. J. Appl. Phys. 2014, 53, 01AB02/1-4.
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New 2,6-Distyryl-Substituted BODIPY Isomers: Synthesis, Photophysical Properties, and Theoretical Calculations
L. Gai, J. Mack, H. Lu*, H. Yamada, D. Kuzuhara, G. Lai, Z. Li*, Z. Shen*,
Chem. Eur. J. 2014, 20, 1091-1102.
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Yellow NIR dye: π-Fused bisbenzoBODIPYs with electron-withdrawing groups
M. Nakamura, M. Kitatsuka, K. Takahashi, T. Nagata, S. Mori, D. Kuzuhara, T. Okujima, H. Yamada, T. Nakae, H. Uno*,
Org. Biol. Chem. 2014, 12, 1309-1317.
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Solution-processed anthradithiophene–PCBM p–n junction photovoltaic cells fabricated by using the photoprecursor method
H. Yamada*, Y. Yamaguchi, R. Katoh, T. Motoyama, T. Aotake, D. Kuzuhara M. Suzuki, T. Okujima, H. Uno, N. Aratani, K. Nakayama*,
Chem. Commun. 2013, 49, 11638-11640.
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Fabrication of Phase-Separated Benzoporphycene/[6,6]-Phenyl-C61-Butyric Acid Methyl Ester Films for Use in Organic Photovoltaic Cells
H. Saeki, M. Misaki, D. Kuzuhara, H. Yamada, Y. Ueda*,
Jpn. J. Appl. Phys. 2013, 53, 111601-111606.
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Synthesis and Crystal Structures of 5,15-bis(triisopropylsilylethynyl)-tetrabenzoporphyrins
K. Takahashi, D. Kuzuhara, N. Aratani, H. Yamada*,
J. Photopol. Sci. Tech. 2013, 26, 213-216.
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Photo-conversion and structural properties of the drop-cast films of 6,13-pentacene diketone
C. Ohashi, H. Yamada, K. Nakayama*,
Mol. Cryst. Liq. Cryst. 2013, 580, 103-109.
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Characterization and Field-Effect Transistor Performance of Printed Pentacene Films Prepared by Photoconversion of the Soluble Precursor
K. Nakayama*, C. Ohashi, Y. Oikawa, T. Motoyama, H. Yamada*,
J. Mater. Chem. C 2013, 1, 6244-6251.
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Synthesis and Properties of Boron Complexes of [14]Triphyrins(2.1.1)
D. Kuzuhara*, Z. Xue, S. Mori, T. Okujima, H. Uno, N. Aratani, H. Yamada*,
Chem. Commun. 2013, 49, 8955-8957.
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MCD spectroscopy and TD-DFT calculations of low-symmetry acenaphthoporphyrins with dual fluorescence
J. Mack, J. Nakamura, T. Okujima*, H. Yamada, H. Uno, N. Kobayashi*,
J. Porphyrins Phthalocyanines 2013, 17, 996-1007.
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Acenaphthylene-fused cyclo[8]pyrroles with intense NIR region absorption bands
T. Okujima*, C. Ando, J. Mack, S. Mori, I. Hisaki, T. Nakae, H. Yamada, K. Ohara, N. Kobayashi*, H. Uno,
Chem. Eur. J. 2013, 19, 13970–13978.
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A soluble bispentacenequinone precursor for creation of directly 6,6′-linked bispentacenes and a tetracyanobipentacenequinodimethane
K. Tanaka, N. Aratani, D. Kuzuhara, S. Sakamoto, T. Okujima, N. Ono, H. Uno, H. Yamada*,
RSC Adv. 2013, 3, 15310-15315.
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Effect of the orthoquinone moiety in 9,10-phenanthrenequinone on its ability to induce apoptosis in HCT-116 and HL-60 cells
N. Hatae*, J. Nakamura. T. Okujima, M. Ishikura, T. Abe, S. Hibino, T. Choshi, C. Okada, H. Yamada, H. Uno, E. Toyota*,
Bioorg. Med. Chem. Lett. 2013, 23, 4637-4640.
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η5-Cyclopentadienyl-Iron(II)-[14]Triphyrin(2.1.1) Sandwich Compounds: Synthesis, Characterization, and Stable Redox Interconversion
Z. Xue, D. Kuzuhara, S. Ikeda, Y. Sakakibara, K. Ohkubo, N. Aratani, T. Okujima, H. Uno, S. Fukuzumi, H. Yamada*,
Angew. Chem. Int. Ed. 2013, 52, 7306-7309.
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In Situ Preparation of Highly Fluorescent Pyrene-Dyes from Non-luminous Precursors Upon Photoirradiation
T. Aotake, H. Tanimoto, H. Hotta, D. Kuzuhara T. Okujima, H. Uno, H. Yamada*,
Chem. Commun. 2013, 49, 3661-3663.
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Covalent Modular Approach for Dimension-Controlled Self-Organization of Perylene Bisimide Dyes
X. Lin, H. Misaki, T. Seki, H. Kurata, T. Karatsu, A. Kitamura, D. Kuzuhara, H. Yamada, T. Ohba, A. Saeki, S. Seki, S. Yagai*,
Chem. Eur. J. 2013, 19, 6561-6565
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Hetero-Layered Organic Photovoltaic Devices Fabricated Using Soluble Pentacene Photoprecursors
T. Motoyama, T. Kiyota, H. Yamada*, K. Nakayama*,
Solar Energy Materials Solar Cells 2013, 114, 138-160.
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Thermal Conversion Behavior and Morphology Control of Benzoporphycene from a Novel Soluble Precursor H. Saeki, O. Kurimoto, M. Misaki, D. Kuzuhara, H. Yamada, Y. Ueda, Appl. Phys. Exp. 2013, 6, 035601-3.
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Thiatriphyrin(2.1.1): A Core-Modified Contracted Porphyrin
D. Kuzuhara, Y. Sakakibara, S. Mori, T. Okujima, H. Uno, H. Yamada*,
Angew. Chem. Inter. Ed. 2013, 52, 3360-3363.
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Photochemical synthesis of naphthacene and its derivatives for irreversible photo-responsive fluorescent molecules
T. Aotake, Y. Yamashita, T. Okujima,, N. Shirasawa, Y. Jo, S. Fujimori, H. Uno, N. Ono, H. Yamada*,
Tetrahedron Lett. 2013, 54, 1790-1793.
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Synthesis and Characterization of New Platinum(II) and Platinum(IV) Triphyrin Complexes
Z. Xue, D. Kuzuhara, S. Ikeda, T. Okujima, S. Mori, H. Uno, H. Yamada*,
Inorg. Chem 2013, 52, 1688-1690.
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FET performance and substitution effect on 2,6-dithienylanthracence devices prepared by photoirradiation of their diketone precursors
H. Yamada*, C. Ohashi, T. Aotake, S. Katsuta, Y. Honsho, H. Kawano, T. Okujima, H. Uno, N. Ono, S. Seki*, K. Nakayama*,
Chem. Commun. 2012, 48, 11136-11138.
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π-Fused bis-BODIPY as a candidate for NIR dyes
M. Nakamura, H. Tahara, K. Takahashi, T. Nagata, H. Uoyama, D. Kuzuhara, S. Mori, T. Okujima, H. Yamada, H. Uno*,
Org. Biomol. Chem. 2012, 10, 6840-6849. [Selected as Front Cover]
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Synthesis and properties of azulene-substituted thiophenes, terthiophenes and dithienothiophenes
T. Okujima*, A. Toda, Y. Miyashita, A. Nonoshita, H. Yamada, N. Ono and H. Uno,
Heterocycles, 2012, 86, 637-648,
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Synthesis of bis-naphthoporphyrins
H. Uoyama, H. Yamada, T. Okujima, H. Uno*,
Heterocycles 2012, 86, 515-534.
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Retro-Diels-Alder approach to the synthesis of π-expanded azuliporphyrins and their porphyrinoid aromaticity
T. Okujima*, T. Kikkawa, H. Nakano, H. Kubota, N. Fukugami, N. Ono, H. Yamada, H. Uno,
Chem. Eur. J. 2012, 18, 12854-12863.
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Self-Organization of Hydrogen-Bonding Naphthalene Chromophores into J-type Nanorings and H-type Nanorods: Impact of Regloisomerism
S. Yagai*, Y. Goto, X. Lin, T. Karatsu, A. Kitamura, D. Kuzuhara, H. Yamada, Y. Kikkawa, A. Saeki, S. Seki,
Angew. Chem. Int. Ed. 2012, 51, 6643-6647.
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Synthesis and spectroscopic properties of ring-fused thiophene bridged push–pull dyes and their application in dye-sensitized solar cells
Q. Liu, F-T. Kong, T. Okujima, H. Yamada, S-Y. Dai, H. Uno, N. Ono, X-Z. You, Z. Shen*,
Tetrahedron Lett. 2012, 53, 3264-3267.
-
Solution-processed zinc tetrabenzoporphyrin thin-finls and transistors
P. B. Shea*, H. Yamada, N. Ono, J. Kanicki,
Thin Solid Film 2012, 520, 4031-4035.
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Synthesis, Structure and Photochemistry of 5,14-Diketopentacene
T. Aotake, S. Ikeda, D. Kuzuhara, S. Mori, T. Okujima, H. Uno, H. Yamada*,
Eur. J. Org. Chem. 2012, 9, 1723-1729
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Tuning the spectroscopic, electrochemical and photovoltaic properties of triarylamine-based sensitizers through ring-fused thiophene bridge
Q. Liu, Q.-Y. Feng. H. Yamada*, Z.-S. Wang, N. Ono,.X.-Z. You, Z. Shen*,
Chem. Asian J. 2012, 7, 1312-1319.
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Synthesis of p-expanded O-chelated boronedipyrromethene as an NIR dye
Y. Tomimori, T. Okujima*, T. Yano, S. Mori, N. Ono, H. Yamada, H. Uno,
Tetrahedron, 2011, 67, 3187-3193.
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Synthesis of pentacene-, tetracene- and anthracene bisimides using double-cyclization reaction mediated by bismuth(III) triflate
S. Katsuta, K. Tanaka, Y. Maruya, S. Mori, S. Masuo, T. Okujima, H. Uno, K. Nakayama, H. Yamada*,
Chem. Commun. 2011, 47, 10112-10114.
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Photophysical properties of triphyrin(2.1.1) investigated by time-resolved fluorescence measurements
Y. Iima, D. Kuzuhara, Z. Xue, H. Uno, S. Akimoto, H. Yamada*, K. Tominaga*,
Chem. Phys. Lett. 2011, 513, 67-71.
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Porphyrin Molecular Tweezers for Fullerenes
H. Uno*, M. Furukawa, A. Fujimoto, H. Uoyama, H. Watanabe, T. Okujima, H. Yamada, S. Mori, M. Kuramoto, T. Iwamura, N. Hatae, F. Tani, N. Komatsu,
J. Porphyrins Phrhalocyaniens 2011, 15, 951-963.
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Synthesis, Structures and Properties of Benzoporphycenes and Naphthoporphycenes
D. Kuzuhara, H. Yamada*, S. Mori, T. Okujima, H. Uno,
J. Porphyrins Phrhalocyaniens 2011, 15, 930-942.
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Tetrabenzodiazaporphyrin: The semiconducting hybrid of tetrabenzoporphyrin and phthalocyanine
T. Okujima*, G. Jin, S. Ohtsubo, S. Aramaki, N. Ono, H. Yamada, H. Uno,
J. Porphyrins Phrhalocyaniens 2011, 15, 697-703.
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Cyclo[8]isoindoles: Ring-Expanded and Annelated Porphyrinoids
T. Okujima*, G. Jin, N. Matsumoto, J. Mack, S. Mori, K. Ohara, D. Kuzuhara, C. Ando, N. Ono, H. Yamada, H. Uno, N. Kobayashi*,
Angew. Chem. Int. Ed. 2011, 50, 5699-5703. [Selected as Hot Paper]
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The Synthesis and Properties of Free-Base [14]Triphyrin(2.1.1) Compounds and the Formation of Subporphyrinoid Metal Complexes
Z.-L. Xue, J. Mack, H. Lu,. L. Zhang, X.-Z. You,. D. Kuzuhara, M. Stillman, H. Yamada*, S. Yamauchi, N. Kobayashi*, Z. Shen*,
Chem. Eur. J. 2011, 17, 4396-4407. [Selected as Inside Cover]
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First Synthesis of Dodeca-substituted Porphycenes
D. Kuzuhara, H. Yamada*, K. Yano, T. Okujima, S. Mori, H. Uno,
Chem. Eur. J. 2011, 17, 3376-3383.
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Synthesis, Properties and Ambipolar Organic Field-Effect Transistor Performances of Symmetrically Cyanated Pentacene and Naphthacene as Air-Stable Acene Derivatives
S. Katsuta, D. Miyagi, H. Yamada*, T. Okujima, S. Mori, K. Nakayama*, H. Uno,
Org. Lett. 2011, 13, 1454-1457.
-
New Synthesis of meso-free-[14]triphyrin(2.1.1) by McMurry coupling and its derivatization to Mn(I) and Re(I) complexes
D. Kuzuhara, H. Yamada,* Z. Xue, T. Okujima, S. Mori, Z. Shen, H. Uno,
Chem. Commun. 2011, 47, 722-724. [Selected as Hot Article]
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Vitamin K analogue as a new fluorescence probe for quantitative antioxidant assay
K. Ohara*, R. Mitsuimori, M. Takebe, D. Kuzuhara, H. Yamada, S. Nagaoka,
J. Photochem. Photobiol. A 2010, 215, 52-58.
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Synthesis, crystal structure, and photodynamics of π-expanded porphyrin-fullrene dyads synthesized by Diels-Alder reaction.
H. Yamada*, K. Ohkubo, D. Kuzuhara, T. Takahashi, A. S. D. Sandanayaka, T. Okujima, K. Ohara, O. Ito, H. Uno, N. Ono, S. Fukuzumi*,
J. Phys. Chem. B 2010, 114, 14717-14728.
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Synthesis and photochemical properties of a-diketoporphyrins as precursors for π-expanded porphyrins
H. Yamada*, D. Kuzuhara, K. Ohkubo, T. Takahashi, T. Okujima, H. Uno, N. Ono, S. Fukuzumi*,
J. Mater. Chem., 2010, 20, 3011-3024.
-
Photochemical synthesis of tetraaryl-substituted pentacenes
S. Katsuta, H. Yamada*, T. Okujima, H. Uno,
Tetrahedron Lett., 2010, 51, 1397-1400.
-
Synthesis and properties of BCOD-fused trithiasapphyrin and trithiabenzosapphyrins
T. Okujima*, T. Kikkawa, S. Kawakami, Y. Shimizu, H. Yamada, N. Ono, H. Uno*,
Tetrahedron, 2010, 66, 7213-7218.
-
Synthesis of π-expanded BODIPYs and their fluorescent properties in the visible-near-infrared region
T. Okujima*, Y. Tomimori, J. Nakamura, H. Yamada, H. Uno, N. Ono,
Tetrahedron 2010, 66, 6895-6900.
-
Pentacene precursors for solution-processed OFETs
H. Uoyama, H. Yamada, T. Okujima, H. Uno*,
Tetrahedron 2010, 66, 6889-6894.
-
Synthesis of tetrabenzoporphyrins fused with fluoranthenes
J. Nakamura, T. Okujima*, Y. Tomimori, N. Komobuchi, H. Yamada, H. Uno, N. Ono,
Heterocycles 2010, 80, 1165-1175.
-
Thermal behavior of bicyclo[2.2.2]octadiene-installed precursors for 2H-anthra[2,3-c]pyrroles and anthra[2,3-c]thiophene
H. Uoyama, C. Chenxin, H. Tahara, Y. Shimizu, H. Hagiwara, Y. Hanasaki, H. Yamada, T. Okujima, H. Uno*,
Heterocycles 2010, 80, 1187-1196.
-
Synthesis of 2,3-dihydrobenzo[1,4]dithiin-fused porphyrins
G. Jin, T. Okujima*, Y. Hashimoto, H. Yamada, H. Uno, N. Ono,
Phosphorus, Sulfur Silicon Relat. Elem. 2010, 185, 1108-1116.
-
Highly pure synthesis, spectral assignments, and two-photon properties of cruciform porphyrin pentamers fused with benzene units
H. Uoyama, K. S. Kim, K. Kuroki, J.-Y. Shin, T. Nagata*, T. Okujima, H. Yamada, N. Ono, Kim, D. Kim*, H. Uno*,
Chem. Eur. J. 2010, 16, 4063-4074.
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Preparation of highly conjugated oligoaza-pahs based on the oxidative intramolecular coupling of bicyclo[2.2.2]octadiene-huzed pyrrole
H. Uno*, T. Takiue, H. Uoyama, T. Okujima, H. Yamada, G. Masuda,
Heterocycles 2010, 80, 791-802.
-
Absorption and Emission Properties of Acenaphthoporphyrins
J. Nakamura, N. Ono, H. Yamada, T. Okujima*,
Mol. Cryst. Liq. Cryst. 2009, 505, 349-355.
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Synthesis, structures, and optical and electrochemical properties of benzoporphycenes
D. Kuzuhara, J. Mack, H. Yamada, T. Okujima, N. Ono, N. Kobayashi*,
Chem. Eur. J. 2009, 15, 10060-10069.
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Organic thin-film transistor from a pentacene photo precursor
A. Masumoto, Y. Yamashita, S. Go, T. Kikuchi, H. Yamada*, T. Okujima, N. Ono*, H. Uno,
Jpn J. Appl. Phys. 2009, 48, 051505/1-5.
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Synthesis of mono-, di- and tribenzoporphyrins from their soluble precursors
T. Okujima*, Y. Hashimoto, G. Jin, H. Yamada, N. Ono,
Heterocycles 2009, 77, 1235-1248.
-
First Synthesis of Porphyrin-Fused 1,10-Phenanthroline-Ruthenium(II) Complexes
T. Okujima*, A. Mifuji, J. Nakamura, H. Yamada, H. Uno, N. Ono,
Org. Lett. 2009, 11, 4088-4091.
-
Aminoisoindole as a useful π-system elongation unit
T. Akiyama, H. Uoyama, T. Okujima, H. Yamada, N. Ono, H. Uno*,
Tetahedron 2009, 65, 4345-4350.
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Soluble precursors of 2,3-naphthalocyanine and phthalocyanine for use in thin film transistors
A. Hirao, T. Akiyama, T. Okujima, H. Yamada, H. Uno, Y. Sakai, S. Aramaki*, N. Ono*,
Chem. Commun. 2008, 4714-4716.
-
A facile one pot synthesis of meso-aryl-substituted [14]triphyrin(2.1.1)
Z.-L. Xue, Z. Shen*, J. Mack, D. Kuzuhara, H. Yamada*, T. Okujima, N. Ono, X.-Z. You*, N. Kobayashi*,
J. Am. Chem. Soc. 2008, 130, 16478-16479, [Selected as Front Cover, Highlighted in Angew. Chem. Int. Ed.]
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Synthesis and characterization of tetraanthroporphyrins
H. Yamada*, D. Kuzuhara, T. Takahashi, Y. Shimizu, K. Uota, T. Okujima, H. Uno, N. Ono,
Org. Lett. 2008, 10, 2947-2950.
-
Selective synthesis of 5-alkenyl-15-alkynyl-porphyrin and 5,15-dialkynyl-porphyrin by 2+2 acid-catalyzed condensation of dipyrrylmethane and TMS propynal
H. Yamada*, K. Kushibe, S. Mitsuogi, T. Okujima, H. Uno, N. Ono,
Tetrahedron Lett. 2008, 49, 4731-4733.
-
Synthesis of extremely soluble precursors of tetrabenzoporphyrins
T. Okujima*, Y. Hashimoto, G. Jin, H. Yamada, H. Uno, and N. Ono*,
Tetrahedron 2008, 64, 2405-2411.
-
Synthesis of phthalocyanine fused with bicycle[2.2.2]octadienes and thermal conversion into naphthalocyanine
T. Akiyama, A. Hirao, T. Okujima, H. Yamada, H. Uno, and N. Ono*,
Heterocycles 2007, 74, 835-843.
-
Solution-processed polycrystalline copper tetrabenzoporphyrins thin-film transistors
P. B. Shea, L.R. Pattison, M. Kawano, C. Chen, J. Chen, P. Petroff, D. C. Martin, H. Yamada, N. Ono, J. Kanicki*,
Synth. Metals 2007, 157, 190-197.
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Polycrystalline tetrabenzoporphyrin organic field-effect transistors with nanostructuired channels
P. B. Shea, C. Chen, J. Kanicki*, L.R. Pattison, P. Petroff, H. Yamada, N. Ono,
Appl. Phys. Lett. 2007, 90, 233107/0-3.
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Photocurrent generation of benzoporphyrin films prepared by solution process
H. Yamada*, N. Kamio, A. Ohishi, M. Kawano, T. Okujima, N. Ono
J. Porphyrins Phthalocyanines 2007, 11, 383-389.
-
A new synthesis of tetra(quinoxalino)tetraazaporphyrin by retro Diels-Alder reaction of a soluble precursor
T. Okujima*, M. Kikuchi, H. Yamada, H. Uno, N. Ono*,
J. Porphyrins Phthalocyanines 2006, 10, 1197-1201.
-
Effective photochemical synthesis of an air-stable anthracene-based organic semiconductor from its diketone precursor
H. Yamada*, E. Kawamura, S. Sakamoto, Y. Yamashita, T. Okujima, H. Uno, N. Ono*,
Tetrahedron Lett. 2006, 47, 7501-7504.
-
Solution-processed nickel tetrabenzoporphyrin thin-film transistors
P. B. Shea, J. Kanicki*, L.R. Pattison, P. Petroff, M. Kawano, H. Yamada, N. Ono,
J. Appl. Phys. 2006, 100, 034502/0-7.
-
Novel one-pot synthesis of 5-alkenyl-15-alkynylporphyrins and their derivatisation to a butadiyne-linked benzoporphyrin dimer
H. Yamada*, K. Kushibe, T. Okujima, H. Uno, and N. Ono*,
Chem. Commun. 2006, 383-385.
-
Synthesis of 4,7-dihydro-2H-isoindole derivatives via Diels-Alder reaction of tosylacetylene
T. Okujima*, G. Jin, Y. Hashimoto, H. Yamada, H. Uno, N. Ono*,
Heterocycles 2006, 70, 619-626.
-
Photo precursor for pentacene
H. Uno*, Y. Yamashita, M. Kikuchi, H. Watanabe, H. Yamada, T. Okujima, T. Ogawa, N. Ono*,
Tetrahedron Lett. 2005, 46, 1981-1983. [Selected as Front Cover]
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Photochemical synthesis of pentacene and its derivatives
H. Yamada*, Y. Yamashita, M. Kikuchi, H. Watanabe, T. Okujima, H. Uno, T. Ogawa, K. Ohara, N. Ono*,
Chem. Eur. J. 2005, 11, 6212-6221.
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A molecular tetrad allowing efficient energy storage for 1.6 s at 163 K
D. M. Guldi*, H. Imahori*, K. Tamaki, Y. Kashiwagi, H. Yamada, Y. Sakata, S. Fukuzumi*,
J. Phys. Chem. A 2004, 108, 541-548.
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Effects of metal ions on photoinduced electron transfer in zinc porphyrin-naphthalenediimide linked systems
K. Okamoto, Y. Mori, H. Yamada, H. Imahori*, and S. Fukuzumi*,
Chem. Eur. J. 2004, 10, 474-483.
-
C70 vs. C60 in zinc porphyrin–fullerene dyads: prolonged charge separation and ultrafast energy transfer from the second excited singlet state of porphyrin
T. Kesti*, N. Tkachenko, H. Yamada, H. Imahori*, S. Fukuzumi, and H. Lemmetyinen,
Photochem. Photobiol. Sci. 2003, 2, 251-258.
-
Layer-by-layer assembly of porphyrin-fullerene dyads
I. Zilbermann, G. Anderson, D. M. Guldi*, H. Yamada, H. Imahori*, S. Fukuzumi,
J. Porphyrins Phthalocyanines 2003, 7, 357-364.
-
Structure and photoelectrochemical properties of ITO electrodes modified with self-assembled monolayers of meso,meso-linked porphyrin oligomers
T. Hasobe, H. Imahori*, K. Ohkubo, H. Yamada, T. Sato, Y. Nishimura, I. Yamazaki*, S. Fukuzumi*,
J. Porphyrins Phthalocyanines 2003, 7, 296-312.
-
Photovoltaic properties of self-assembled monolayers of porphyrins and porphyrin-fullerene dyads on ITO and gold surfaces
H. Yamada, H. Imahori*, Y. Nishimura, I. Yamazaki*, T. K. Ahn, S. K. Kim, D. Kim*, S. Fukuzumi*,
J. Am. Chem. Soc. 2003, 125, 9129-9139.
-
Enhancement of light harvesting and photocurrent generation by ITO electrodes modified with meso, meso-linked porphyrin oligomers
T. Hasobe, H. Imahori*, H. Yamada, T. Sato, K. Ohkubo, S. Fukuzumi*,
Nano Lett. 2003, 3, 409-412.
-
Porphyrin-fullerene dyad with a long linker: formation of charge transfer conformer in Langmuir-Blodgett film
N. V. Tkachenko*, V. Vehmanen, J.-P. Nikkanen, H. Yamada, H. Imahori, S. Fukuzumi, H. Lemmetyinen,
Chem. Phys. Lett. 2002, 366, 245-252.
-
Electron transfer properties of singlet oxygen and promoting effects of scandium ion
S. Fukuzumi*, S. Fujita, T. Suenobu, H. Yamada, H. Imahori, Y. Araki, O. Ito*,
J. Phys. Chem. A 2002, 106, 1241-1247.
-
Exciplex intermediates in photoinduced electron transfer of porphyrin-fullerene dyads
T. J. Kesti*, N. V. Tkachenko, V. Vehmanen, H. Yamada, H. Imahori*, S. Fukuzumi*, and H. Lemmetyinen,
J. Am. Chem. Soc.,2002, 124, 8067-8077.
-
Comparison of reorganization energies for intra- and intermolecular electron transfer
H. Imahori*, H. Yamada, D. M. Guldi*, Y. Endo, A. Shimomura, S. Kundu, K. Yamada, T. Okada*, Y. Sakata, S. Fukuzumi*,
Angew. Chem. Inter. Ed. 2002, 114, 2450-2453.
-
Photocurrent generation using gold electrodes modified with self-assembled monolayers of a fullerene-porphyrin dyad
H. Yamada, H. Imahori*, S. Fukuzumi*,
J. Mater. Chem. 2002, 12, 2034-2040.
-
Enhancement of photocurrent generation by ITO electrodes modified chemically with self-assembled monolayers of porphyrin-fullerene dyads
H. Yamada, H. Imahori*, Y. Nishimura, I. Yamazaki*, S. Fukuzumi*,
Adv. Mater. 2002, 14, 892-895.
-
Large photocurrent generation of gold electrodes modified with [60]fullerene-linked oligothiophenes bearing a tripodal rigid anchor
D. Hirayama, K. Takimiya, Y. Aso*, T. Ohtubo*, T. Hasobe, H. Yamada, H. Imahori*, S. Fukuzumi, Y. Sakata,
J. Am. Chem. Soc. 2002, 124, 532-533.
-
Uphill photooxidation of NADH analogues by hexyl viologen catalyzed by zinc porphyrin-linked fullerenes
S. Fukuzumi*, H. Imahori*, K. Okamoto, H. Yamada, M. Fujitsuka, O. Ito, D. M. Guldi*,
J. Phys. Chem. A 2002, 106, 1903-1908.
-
Concentration effects of porphyrin monolayers on the structure and photoelectrochemical properties of mixed self-assembled monolayers of porphyrin and alkanethiol on gold electrodes
H. Imahori*, T. Hasobe, H. Yamada, Y. Nishimura, I. Yamazaki*, S. Fukuzumi*,
Langmuir 2001, 17, 4925-4931.
-
Spectroscopy and photocurrent generation in nanostructured thin films of porphyrin-fullerene dyad clusters
H. Imahori*, T. Hasobe, H. Yamada, P. V. Kamat*, S. Barazzoulk, M. Fujitsuka, O. Ito*, S. Fukuzumi*,
Chem. Lett. 2001, 784-785.
-
Catalytic effects of dioxygen on intramolecular electron transfer in radical ion pairs of zinc porphyrin-linked fullerenes
S. Fukuzumi*, H. Imahori*, H. Yamada, M. E. El-Khouly, M. Fujitsuka, O. Ito*, D. M. Guldi*,
J. Am. Chem. Soc. 2001, 123, 2571-2575.
-
Light-harvesting and photocurrent generation by gold electrodes modified with mixed self-assembled monolayers of boron-dipyrrin and ferrocene-porphyrin-fullerene triad
H. Imahori*, H. Norieda, H. Yamada, Y. Nishimura, I. Yamazaki*, Y. Sakata, S. Fukuzumi*,
J. Am. Chem. Soc. 2001, 123, 100-110.
-
Remarkable enhancement of photocurrent generation by ITO electrodes modified with a self-assembled monolayer of porphyrin
H. Yamada, H. Imahori*, Y. Nishimura, I. Yamazaki*, S. Fukuzumi*,
Chem. Commun. 2000, 1921-1922.
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Photosynthetic electron transfer using fullerenes as novel acceptors
H. Imahori*, K. Tamaki, H. Yamada, K. Yamada, Y. Sakata*, Y. Nishimura, I. Yamazaki*, M. Fujitsuka, O. Ito*,
Carbon 2000, 38, 1599-1605.
-
Vectorial multistep electron transfer at the gold electrodes modified with self-assembled monolayers of ferrocene-porphyrin-fullerene triads
H. Imahori*, H. Yamada, Y. Nishimura, I. Yamazaki*, Y. Sakata*
J. Phys. Chem. B 2000, 104, 2099-2108.
-
Chain length effect on the structure and photoelectrochemical properties of self-assembled monolayers of porphyrins on gold electrodes
H. Imahori*, H. Norieda, Y. Nishimura, I. Yamazaki*, K. Higuchi*, N. Kato, T. Motohiro, H. Yamada, K. Tamaki, M. Arimura, Y. Sakata*,
J. Phys. Chem. B 2000, 104, 1253-1260.
-
An investigation of photocurrent generation by gold electrodes modified with self-assembled monolayers of C60
H. Imahori*, T. Azuma, A. Ajavakom, H. Norieda, H. Yamada, Y. Sakata*,
J. Phys. Chem. B 1999, 103, 7233-7237.
-
Long-lived charge separation with high quantum yield in a ferrocene-porphyrin-fullerene triad
M. Fujitsuka, O. Ito*, H. Imahori*, K. Yamada, H. Yamada, Y. Sakata*
Chem. Lett. 1999, 721-722.
-
Synthesis and photoelectrochemical properties of a self-assembled monolayer of a ferrocene-porphyrin-fullerene triad on a gold electrode
H. Imahori*, H. Yamada, S. Ozawa, K. Ushida, and Y. Sakata*,
Chem. Commun 1999, 1165-1166.
-
Photoinduced electron transfer at a gold electrode modified with a self-assembled monolayer of fullerene
H. Imahori*, T. Azuma, S. Ozawa, H. Yamada, K. Ushida, A. Ajavakom, H. Norieda, Y. Sakata*,
Chem. Commun. 1999, 557-558.
-
Chain length effect on photocurrent from polymethylene-linked porphyrins in self-assembled monolayers
H. Imahori*, H. Norieda, S. Ozawa, K. Ushida, H. Yamada, T. Azuma, K. Tamaki, Y. Sakata*,
Langmuir 1998, 14, 5335-5338.
-
Fucoxanthin-pyropheophorbide and zeaxanthin-pyropheophorbide dyads as new models for study on carotenoid-chlorophyll excited state interactions
A. Osuka*, S. Shinoda, S. Marumo, H. Yamada, T. Katoh, I. Yamazaki*, Y. Nishimura, Y. Tanaka, S. Taniguchi, T. Okada*, K. Nozaki, T. Ohno*,
Bull. Chem. Soc. Jpn. 1995, 68, 3255-3268.
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Electric field effects of photogenerated ion pairs on nearby molecules: a model for the carotenoid band shift in photosynthesis
D. Gosztola, H. Yamada, M. R. Wasielewski*,
J. Am. Chem. Soc. 1995, 117, 2041-2048.
-
Charge separation in zinc diporphyrin-zinc porphyrin-pyromellitimide-quinone tetrads
A. Osuka*, H. Yamada, K. Maruyama, T. Ohno, K. Nozaki, T. Okada*, Y. Tanaka, N. Mataga,
Chem. Lett. 1995, 591-592.
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Intramolecular charge recombination in carotenoid-porphyrin-pyromellitimide triads
A. Osuka, H. Yamada, S. Shinoda, K. Nozaki, T. Ohno,
Chem. Phys. Lett.1995, 238, 37-41.
-
Direct observation of a consecutive two step electron transfer in some zinc porphyrin-pyromellitimide-quinone triads which undergo the same mode of electron transfers as in the bacterial photosynthetic reaction center
M. Ohkohchi, A. Takahashi, N. Mataga*, T. Okada, A. Osuka*, H. Yamada, K. Maruyama,
J. Am. Chem. Soc. 1993, 115, 12137-12143.
-
Synthesis and photoexcited-state dynamics of aromatic group-bridged carotenoid-porphyrin dyads and carotenoid-porphyrin-pyromellitimide triads
A. Osuka*, H. Yamada, K. Maruyama, N. Mataga*, T. Asahi, M. Ohkouchi, T. Okada, I. Yamazaki, Y. Nishimura,
J. Am. Chem. Soc. 1993, 115, 9439-9452.
-
Covalently linked tyrosine-pyropheophorbide a and tryptophan-pyropheophorbide a compounds: synthesis and photo-induced cross coupling with 1,4-benzoquinone
K. Maruyama*, H. Yamada, A. Osuka,
Photochem. Photobiol. 1991, 53, 617-626.
-
Picosecond dynamics of intramolecular singlet excitation energy transfer and photoinduced electron transfer in covalently-linked carotenoid-porphyrin and carotenoid-porphyrin-pyromellitimide molecules
A. Osuka, H. Yamada, K. Maruyama, N. Mataga, T. Asahi, I. Yamazaki, Y. Nishimura,
Chem. Phys. Lett. 1991, 181, 419-426.
-
Synthesis of conformationally restricted carotenoid-linked porphyrins
A. Osuka, H. Yamada, K. Maruyama*,
Chem. Lett. 1990, 1905-1908.
-
The anion radicals of pheophytin a and its derivatives studied by means of CIDNP technique
K. Maruyama*, H. Yamada, A. Osuka,
Bull. Chem. Soc. Jpn.1990, 63, 3462-3466.
-
Photoinduced cross coupling reaction of covalently linked tyrosine-pyropheophorbide a and tyrosine-9-desoxopyropheophorbide a to 1,4-benzoquinone
K. Maruyama*, H. Yamada, A. Osuka,
Chem. Lett. 1989, 833-836.
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Microscopic Structures, Dynamics, and Spin Configuration of the Charge Carriers in Organic Photovoltaic Solar Cells Studied by Advanced Time-Resolved Spectroscopic Methods
K. Ohta, K. Tominaga,* T. Ikoma,* Y. Kobori,* H. Yamada,
Langmuir 2022, 38, 7365-7382.
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Synthesis of oligoacenes using precursors for evaluation of their electronic structures
H. Yamada*, H. Hayashi,
Photochem. Photobiol. Sci. 2022, 21, 1511-1532.
-
Impacts of substituents on the morphology and performance of small-molecule semiconductors in organic photovoltaic devices
M. Suzuki*, K. Suzuki, T. Wona, H. Yamada*,
J. Mater. Chem. C 2022, 10, 1162-1195. [Selected as Back Cover]
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Porphyrinoides with Vinylene_Bridges
D. Kuzuhara*, H. Yamada*,
Synlett 2021, 32, 1072-1084.
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Synthesis and Morphological Control of Organic Semiconducting Materials using the Precursor Approach
H. Yamada*, D. Kuzuhara, M. Suzuki, H. Hayashi, N. Aratani,
Bull. Chem. Soc. Jpn. 2020, 93, 1234-1267.
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Semiconducting p-Extended Tetrathiafulvalene Derivatives
H. Yamada*, M. Yamashita, H. Hayashi, M. Suzuki, and N. Aratani,
Chem. Eur. J. 2018, 24, 18601-18612. [Selected as Frontispiece]
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Synthesis and photoreactivity of p-diketone-type precursors of acenes and their use in organic-device fabrication
M. Suzuki, T. Aotake, Y. Yamaguchi, N. Noguchi, H. Nakano*, K. Nakayama*, H. Yamada*,
J. Photochem. Photobiol. C: Photochem. Reviews 2014, 18, 50-70.
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Synthesis and characterization of [14]triphyrin(2.1.1) and its metal complexes
D. Kuzuhara, H. Yamada*,
Heterocycles 2013, 87, 1209-1240.
-
Organic semiconductors based on small molecules with thermally or photochemically removable groups
H. Yamada*, T. Okujima, N. Ono,
Chem. Commun. 2008, 2957-2974.
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「光変換型前駆体法」を利用した高次アセンおよび高次アセン複合体の作製
林宏暢, 山田容子
光化学協会誌 2019, 50, 114-117.
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拡張 π 共役有機材料の機能開拓 と溶液塗布によるデバイス作製 プロセスへの応用
林宏暢、鈴木充朗、葛原大軌、荒谷直樹、山田容子
有機合成化学協会誌 2015, 73, 1232-1244.
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前駆体法を利用した機能性π共役拡張化合物の合成と物性
山田容子, 葛原大軌, 勝田修平, 奥島鉄雄, 宇野英満
有機合成化学協会誌 2011, 69, 802-813.
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可溶性前駆体の光反応による有機半導体の高効率合成.
山田容子
光化学協会誌, 2008, 39, 209-213.
-
On-surface synthesis of polyacenes and narrow band-gap graphene nanoribbons
Hironobu Hayashi, Hiroko Yamada, in “Atomically Precise Nanochemistry” ed. by Rongchao Jin and De-en Jiang, in press, Wiley.
-
α-Diketone-Type Precursors of Acenes for Solution-Processed Organic Solar Cells
Mitsuharu Suzuki, Hiroko Yamada, in “Light – Active Functional Organic Materials” ed. by Hiroko Yamada and Shiki Yagai, pp173-194, 2019, Pan Stanford Publishing.
-
Nano-structure control of crystalline organic thin films by a solution process
Hiroko Yamada, in “Physics and Chemistry of Carbon-Based Materials, Basic and Applications” ed. by Yoshihiro Kubozono, pp253-292, 2019, Springer.
-
Materials for Organic Electronics and Bioelectronics
Yoshihiro Kubozono, Hidenori Goto, Hiroko Yamada in “3D local structure and functionality design of materials” ed. by Hiroshi Daimon and Yuji C. Sasaki, pp173-195, 2019, World Scientific Publishing, Maruzen Publishing.
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Synthesis of Porphyrins Fused with Aromatic Rings.
Noboru Ono, Hiroko Yamada, Tetsuo Okujima, in “Handbook of Porphyrin Science Vol. 2”, ed. by K. M. Kadish, K. M. Smith, R. Guilard, pp. 1-102, 2010, World Scientific.
-
Supramolecules Based on Porphyrins,
Hiroko Yamada, Tetsuo Okujima, Noboru Ono, in “Topics in Heterocyclic Chemistry” Vol.17. pp.123-159, 2008. Springer.
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有機デバイス
久保園芳博,山田容子『機能構造科学入門―3D活性サイトと物質デザイン』大門寛,佐々木裕次編, 分担執筆,
pp139-155, 2016, 丸善出版.
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付加:光Barton反応.
山田容子, 『光化学の事典』光化学協会・光化学の事典編集委員会編, 分担執筆,
pp208, 2014, 朝倉書店
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光変換型前駆体法による有機デバイスの開発.
山田容子, 中山健一『有機デバイスのための塗布技術』監修竹谷純一, 分担執筆,
pp32-41, シーエムシー出版
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変換型半導体材料の開発とその応用. 小野 昇, 山田容子, 荒牧晋司『低分子有機半導体の高性能化』分担執筆,
pp. 139-156, 2009, サイエンス&テクノロジー株式会社.
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低分子有機半導体材料の開発. 小野 昇, 山田容子, 『有機薄膜太陽電池の高効率化と耐久性向上』分担執筆,
pp. 78-96, 2009, サイエンス&テクノロジー株式会社.
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山田容子, 『はじめての有機スペクトル解析−IR,NMR,MSデータを読む CD-ROM付』宇野英満、築部 浩編, 分担執筆,
pp.34-44, 2004, 丸善株式会社.
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すべてはペンタセン光前駆体から始まった-『前駆体法』が見せてくれた世界
山田容子
化学と工業 2021, 74, 1, 35.
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どこまで伸びる?ベンゼン環の連結競争
林宏暢, 山田容子
化学 2020, 75, 68-69.
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基板上グラフェンナノリボン合成における前駆体分子へのフッ素の導入効果
林宏暢, 山田容子
New Diamond 2020, 36, 1, 15-18. [表紙]
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高次アセンの合成とナノカーボン材料創成への展開
林宏暢, 山田容子
月刊ファインケミカル 2020, 49, 1, 32-38.
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カルボカチオンの最新事情-ついに終結?非古典的カルボカチオンの構造を巡る挑戦
鈴木充朗, 山田容子
化学 2013, 68, 12, 70-71.
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光前駆体法による有機半導体材料の開発
山田容子
同仁ニュース 2012, 143, 1-5.
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前駆体法を利用したπ共役拡張化合物の開発
山田容子, 葛原大軌
未来材料 2012, 2, 20-27.
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革新的塗布型材料による有機薄膜太陽電池の構築
山田容子, 中山健一
化学工業 2012, 63, 13-17.
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機能性有機材料の開発.
山田容子
化学経済 2011, 5, 58-61
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前駆体法を利用した溶液塗布型有機低分子半導体の開発.
山田容子
化学工業 2009, 60, 4, 58-63.
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子供向けの科学絵本の中から.
山田容子
化学と工業, 2007, 60, 12, 1184.
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