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Publication
出版物

2019

404
W. Zhang, S. Suzuki, SeongYong Cho, Go Watanabe, Hiroyuki Yoshida, T. Sakurai, Mika Aotani, Y. Tsutsui, Masanori Ozaki, S. Seki
Highly Miscible Hybrid Liquid-Crystal Systems Containing Fluorescent Excited-State Intramolecular Proton Transfer Molecules
Langmuir, 35(43), 14031-14041(2019). DOI: 10.1021/acs.langmuir.9b02272

403
F. Zhang, Vincent Lemaur, Wookjin Choi, Prapti Kafle, S. Seki, Jérôme Cornil, David Beljonne, Ying Diao
Repurposing DNA-binding agents as H-bonded organic semiconductors
Nat. Commun., 10(1), 1-11(2019). DOI: 10.1038/s41467-019-12248-9

402
Yuki Tsujimoto, T. Sakurai, Yuichiro Ono, Shusaku Nagano, S. Seki
Cold Crystallization of Ferrocene-Hinged π-Conjugated Molecule Induced by the Limited Conformational Freedom of Ferrocene
J. Phys. Chem. B, 123(39), 8325-8332(2019). DOI: 10.1021/acs.jpcb.9b06880

401
Shohei Kato, Shuhei Akahori, Yuma Serizawa, Xu Lin, Mitsuaki Yamauchi, Shiki Yagai, T. Sakurai, W. Matsuda, S. Seki, Hiroshi Shinokubo, Yoshihiro Miyake
Systematic synthesis of tetrathia [8] circulenes: The influence of peripheral substituents on the structures and properties in solution and solid states
J. Org. Chem., 85(1), 62–69(2019). DOI: 10.1021/acs.joc.9b01655

400
Zichao Lian, Masanori Sakamoto, Yoichi Kobayashi, Naoto Tamai, Jun Ma, T. Sakurai, S. Seki, Tatsuo Nakagawa, Ming-Wei Lai, Mitsutaka Haruta, Hiroki Kurata, Toshiharu Teranishi
Anomalous Photoinduced Hole Transport in Type I Core/Mesoporous-Shell Nanocrystals for Efficient Photocatalytic H2 Evolution
ACS Nano, 13(7), 8356-8363(2019). DOI: 10.1021/acsnano.9b03826

399
Yoshihiro Motomura, Y. Hattori, T. Sakurai, S. Ghosh, S. Seki
Impact of Unsymmetrical Alkyl–Fluoroalkyl Side Chains over Coil-to-Rod Transition of Soluble Polyacetylenes: Modulation of Electronic Conjugation of Isolated Chains and Their Self-Assembly
Macromolecules, 52(13), 4916-4925(2019). DOI: 10.1021/acs.macromol.9b00629

398
Shinya Sugiura, W. Matsuda, W. Zhang, S. Seki, Nobuhiro Yasuda, Hiromitsu Maeda
Ion-Pairing Assemblies Comprising Anion Complexes of π-Extended Anion-Responsive Molecules
J. Org. Chem., 84(14), 8886-8898(2019). DOI: 10.1021/acs.joc.9b00754

397
Ayumi Kawasaki, Takashi Takeda, Norihisa Hoshino, W. Matsuda, S. Seki, Tomoyuki Akutagawa
High Thermally Stable n-Type Semiconductor up to 850 K Based on Dianionic Naphthalenediimide Derivative
J. Phys. Chem. C, 123(25), 15451-15457(2019). DOI: 10.1021/acs.jpcc.9b03023

396
Tomohiro Higashino, Keiichi Ishida, T. Sakurai, S. Seki, Tatsuki Konishi, Kenji Kamada, Kenji Kamada, Hiroshi Imahori
Pluripotent Features of Doubly Thiophene‐Fused Benzodiphospholes as Organic Functional Materials
Chem. Eur. J., 25(25), 6425-6438(2019). DOI: 10.1002/chem.201900661

395
I. Badía-Domínguez, A. Pérez-Guardiola, J. C. Sancho-García, J. T. Lopez Navarrete, V. H. Jolin, Hongxiang Li, D. Sakamaki, S. Seki, M. C. Ruiz Delgado
Formation of Cyclophane Macrocycles in Carbazole-Based Biradicaloids: Impact of the Dicyanomethylene Substitution Position
ACS Omega, 4(3), 4761-4769(2019). DOI: 10.1021/acsomega.8b03418

394
K. Okino, D. Sakamaki, S. Seki
Dicyanomethyl radical-based near-infrared thermochromic dyes with high transparency in the visible region
ACS Materials Lett., 1(1), 25-29(2019). DOI: 10.1021/acsmaterialslett.9b00049

393
I. Badía-Domínguez, D. Sakamaki, S. Seki, F. Hartl, J. T. López-Navarrete, V. Hernández-Jolín, M. Ruíz-Delgado, L. Hongxiang
Impact of the dicyanomethylene substitution position on the cyclophane macrocycle formation in carbazole-based biradicals

392
J. Ma, A. Kumar, Y. Muroya, S. Yamashita, T. Sakurai, S. A. Denisov, M. D. Sevilla, A. Adhikary, S. Seki, M. Mostafavi
Observation of dissociative quasi-free electron attachment to nucleoside via excited anion radical in solution
Nat. Commun., 10(1), 1-7(2019). DOI: 10.1038/s41467-018-08005-z

391
Y. Hattori, N. Nishimura, Y. Tsutsui, S. Ghosh, T. Sakurai, K. Sugiyasu, M. Takeuchi, and S. Seki
Rod-like transition first or chain aggregation first? ordered aggregation of rod-like poly(p-phenyleneethynylene) chains in solution
Chem. Commun., 55(89), 13342–13345(2019). DOI: 10.1039/c9cc06892a

390
D. Sakamaki, S. Ghosh, and S. Seki
Dynamic covalent bonds: approaches from stable radical species
Mater. Chem. Front., 3(11), 2270–2282(2019). DOI: 10.1039/C9QM00488B

389
H. Saeki, D. Sakamaki, H. Fujiwara, and S. Seki
Extreme multi-point van der Waals interactions: isolable dimers of phthalocyanines substituted with pillar-like azaacenes
Chem. Sci., 10(39), 8939–8945(2019). DOI: 10.1039/C9SC01739A

388
A. Kawasaki, T. Takeda, N. Hoshino, W. Matsuda, S. Seki, and T. Akutagawa
High Thermally Stable n-Type Semiconductor up to 850 K Based on Dianionic Naphthalenediimide Derivative
J. Phys. Chem. C, 123(25), 15451-15457(2019). DOI: 10.1021/acs.jpcc.9b03023

387
A. Lopez-Andarias, C. Atienza, J. Lopez-Andarias, W. Matsuda, T. Sakurai, S. Seki, N. Martin
Assembly effect on the charge carrier mobility in quarterthiophene-based n/p-materials
J. Mater. Chem. C, 7(22), 6649-6655(2019). DOI: 10.1039/C9TC00165D

386
S. Ghosh, R. Raveendran, A. Saeki, S. Seki, M. Namboothiry, and A. Ajayaghosh
Charge Carrier Polarity Modulation in Diketopyrrolopyrrole-Based Low Band Gap Semiconductors by Terminal Functionalization
ACS Appl. Mater. Interfaces, 11(1), 1088-1095(2019). DOI: 10.1021/acsami.8b16714

385
S. Ghosh, Y. Tsutsui, K. Suzuki, H. Kaji, K. Honjo, T. Uemura, and S. Seki
Impact of the position of the imine linker on the optoelectronic performance of π-conjugated organic frameworks
Mol. Syst. Des. Eng., 4(2), 325-331(2019). DOI: 10.1039/C8ME00079D

384
J. Ma, A. Kumar, Y. Muroya, S. Yamashita, T. Sakurai, S. A. Denisov, M. D. Sevilla, A. Adhikary, S. Seki, and M. Mostafavi
Observation of Dissociative Quasi-Free Electron Attachment to Nucleoside via Excited Anion Radical in Solution
Nature Commun., 10(102), (2019). DOI: 10.1038/s41467-018-08005-z

383
W. Zhang, T. Sakurai, M. Aotani, G. Watanabe, H. Yoshida, V. S. Padalkar, Y. Tsutsui, D. Sakamaki, M. Ozaki, and S. Seki
Highly Fluorescent Liquid Crystals from Excited-State Intramolecular Proton Transfer Molecules
Adv. Opt. Mater., 7(2), 1801349(2019). DOI: 10.1002/adom.201801349