English / Japanese

太田英輔のWebsite



学歴:

博士(理学) 2008年,北海道大学
鈴木孝紀教授
修士 2005年,北海道大学
鈴木孝紀教授
学士 2003年,北海道大学
(辻孝名誉教授,鈴木孝紀教授

職歴:

2011–現在 大阪府立大学 助教
池田浩教授
2009–2011年 理化学研究所 特別研究員
相田卓三教授福島孝典教授
2008–2009年 理化学研究所 訪問研究員
相田卓三教授福島孝典教授
2007–2009年 日本学術振興会(JSPS) 特別研究員

業績リスト:

原著論文
  1. Bis(10-methylacridinium)s as a Versatile Platform for Redox-active Functionalized Dyes and Novel Structures
    T. Suzuki, T. Takeda, E. Ohta, K. Wada, R. Katoono, H. Kawai, and K. Fujiwara
    Chem. Rec. 2015, 15, 280–294.

  2. The "Excited State C–C Bond Cleavage—Luminescence" Phenomenon of a Biphenyl-substituted Methylenecyclopropane Triggered by Intermolecular Energy Transfer from Triplet Benzophenone
    Y. Matsui, T. Kido, E. Ohta, and H. Ikeda
    Chem. Commun. 2014, 50, 13963–13966.

  3. Unexpected Formation of a Phenonium Ion-containing Salt by Single Electron-transfer Oxidation of a Cage Compound Possessing Triphenylamine Moieties
    Y. Kuramoto, Y. Matsui, E. Ohta, H. Sato, and H. Ikeda
    Tetrahedron Lett. 2014, 55, 4366–4369.

  4. One-pot Photochemical Synthesis of Novel Thienobis[1]benzothiophene with an Angularly-fused Structure that Promotes Unique Intermolecular S•••S Contacts in the Crystalline State
    T. Ogaki, E. Ohta, A. Yamamoto, H. Sato, K. Mizuno, and H. Ikeda
    Tetrahedron Lett. 2014, 55, 4269–4273.

  5. Theoretical Study Demonstrating that Silylene Bridging Brings about LUMO Energy Lowering without Increasing the Reorganization Energy for Single Electron Transfer
    E. Ohta, T. Ogaki, T. Aoki, and H. Ikeda
    Chem. Lett. 2014, 43, 755–757.

  6. Remarkable Difference in Fluorescence Lifetimes of the Crystalline States of Dibenzoylmethanatoboron Difluoride and Its Diisopropyl Derivative
    M. Tanaka, E. Ohta, A. Sakai, Y. Yoshimoto, K. Mizuno, and H. Ikeda
    Tetrahedron Lett. 2013, 54, 4380–4384.

  7. Synthesis and Basic Properties of Tetrathieno[2,3-a:3′,2′-c:2″,3″-f:3‴,2‴-h]naphthalene: A New π-Conjugated System Obtained by Photoinduced Electrocyclization–Dehydrogenation Reactions of Tetra(3-thienyl)ethene
    A. Yamamoto, E. Ohta, N. Kishigami, N. Tsukahara, Y. Tomiyori, H. Sato, Y. Matsui, Y. Kano, K. Mizuno, and H. Ikeda
    Tetrahedron Lett. 2013, 54, 4049–4053.

  8. The Lifetime and Efficiency of Triplet–Triplet Fluorescence from the Excited State of a TMM Biradical Determined Using Transient Emission Spectroscopy on Two-color Two-laser Flash Photolysis
    Y. Matsui, D. Kawahara, E. Ohta, and H. Ikeda
    Phys. Chem. Chem. Phys. 2013, 15, 7064–7069.

  9. Remarkable Effects of Terminal Groups and Solvents on Helical Folding of o-Phenylene Oligomers
    S. Ando, E. Ohta, A. Kosaka, D. Hashizume, H. Koshino, T. Fukushima, and T. Aida
    J. Am. Chem. Soc. 2012, 134, 11084–11087.

  10. White Light Emission from a Single Component System: Remarkable Concentration Effects on the Fluorescence of 1,3-Diaroylmethanatoboron Difluoride
    A. Sakai, M. Tanaka, E. Ohta, Y. Yoshimoto, K. Mizuno, and H. Ikeda
    Tetrahedron Lett. 2012, 53, 4138–1441.

  11. DFT Studies of Unique Stereoelectronic Effects of Substituents on Divergent Reaction Pathways of Methylenecyclobutanone Radical Cations
    Y. Kano, F. Tanaka, E. Ohta, K. Mizuno, and H. Ikeda
    Tetrahedron 2012, 68, 5564–5571.

  12. Redox-responsive Molecular Helices with Highly Condensed π-Clouds
    E. Ohta, H. Sato, S. Ando, A. Kosaka, T. Fukushima, D. Hashizume, M. Yamasaki, K. Hasegawa, A. Muraoka, H. Ushiyama, K. Yamashita, and T. Aida
    Nature Chem. 2011, 3, 68–73.

  13. Drastic Change in Racemization Barrier upon Redox Reactions: Novel Chiral-memory Units Based on Dynamic Redox Systems
    T. Suzuki, K. Wada, Y. Ishigaki, Y. Yoshimoto, E. Ohta, H. Kawai, and K. Fujiwara
    Chem. Commun. 2010, 46, 4100–4102.

  14. Four-way-output Molecular Response System based on the Dihydrodibenzo[c,g]phenanthrene Skeleton: Modulation of CD and FDCD Activity by Acid and Electron-transfer
    E. Ohta, T. Nehira, H. Kawai, K. Fujiwara, and T. Suzuki
    Tetrahedron Lett. 2008, 49, 777–781.

  15. Unprecedented Four-way-output Molecular Response System Based on Biphenyl-2,2'-diyldiacridiniums: Induction of Axial Chirality through Intramolecular Hydrogen Bonds between Chiral Amide Groups
    T. Suzuki, K. Ohta, T. Nehira, H. Higuchi, E. Ohta, H. Kawai, and K. Fujiwara
    Tetrahedron Lett. 2008, 49, 772–776.

  16. Chromic and Fluorescence Response System Based on the Dihydrophenanthroline—Bipyridine Skeleton: Dynamic Redox Behavior and Metal Binding Properties
    T. Suzuki, R. Tamaki, E. Ohta, T. Takeda, H. Kawai, K. Fujiwara, and M. Kato
    Tetrahedron Lett. 2007, 48, 3823–3827.

  17. Electrochiroptical Systems Based on Biphenyl-2,2'-diyl-type Dicationic Dyes: Strong Chiroptical Signals through the Transmission of Point Chirality to Axial Chirality
    T. Suzuki, T. Iwai, E. Ohta, H. Kawai, and K. Fujiwara
    Tetrahedron Lett. 2007, 48, 3599–3603.

  18. Butane-1,4-diyl Dications Stabilized by Steric Factors: Electrochiroptical Response Systems Based on Reversible Interconversion between Dihydro[5]helicene-type Electron Acceptors and Electron-donating 1,1'-Binaphthyls
    E. Ohta, H. Higuchi, H. Kawai, K. Fujiwara, and T. Suzuki
    Org. Biomol. Chem. 2005, 3, 3024–3031.

  19. First Stable 7,7,8,8-Tetraaryl-o-quinodimethane: Isolation, X-ray Structure, Electrochromic Response of 9,10-Dihydrophenanthrene
    S.-i, Iwashita, E. Ohta, H. Higuchi, H. Kawai, K. Fujiwara, K. Ono, M. Takenaka, and T. Suzuki
    Chem. Commun. 2004, 2076–2077.

  20. Electrochiroptical Response of 2,2'-(2,2-Diarylethenyl)binaphthyl-type Electron Donors that Undergo Reversible C–C Bond Formation/Breaking upon Two-electron Transfer
    H. Hiroki, E. Ohta, H. Kawai, K. Fujiwara, T. Tsuji, and T. Suzuki
    J. Org. Chem. 2003, 68, 6605–6610.

総説
  1. Dynamic Redox Systems as Electrochromic Materials: Bistability and Advanced Response
    T. Suzuki, E. Ohta, H. Kawai, K. Fujiwara, and T. Fukushima
    Synlett 2007, 6, 851–869.

氏名:

太田英輔(Eisuke OHTA)

生年月日:

1979年7月17日

出身地:

北海道

現所属:

大阪府立大学大学院 工学研究科
物質化学系専攻 応用化学分野
助教(池田浩研究室

研究分野:

有機化学,構造有機化学,有機光化学,
有機電子移動科学,高分子化学

所属学会:

日本化学会
高分子学会
近畿化学協会
有機合成化学協会
基礎有機化学会
光化学協会
ケイ素化学協会



連絡先

博士(理学) 太田英輔
大阪府立大学 大学院工学研究科
物質化学系専攻 応用化学分野
居室:B5棟 6C-65
住所:〒599-8531 大阪府堺市中区学園町1-1
電話:072-254-9389