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Construction of dioxetane-type high-efficiency chemiluminescence system assisted by intermolecular hydrogen bonding in solid phase

Research Project

Project/Area Number 16K05707
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Organic chemistry
Research InstitutionKanagawa University

Principal Investigator

Watanabe Nobuko  神奈川大学, 理学部, 助教 (40291744)

Co-Investigator(Kenkyū-buntansha) 松本 正勝  神奈川大学, 付置研究所, 名誉教授 (10260986)
Project Period (FY) 2016-10-21 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2018: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords光有機化学 / ジオキセタン / 固体化学 / 有機光化学 / 固体発光 / 固相発光 / 化学発光
Outline of Final Research Achievements

Deprotonation of a dioxetane bearing a hydroxyaryl group generates an unstable dioxetane having oxidoaryl anion, which undergoes intramolecular charge-transfer-induced decomposition (CTID) to produce a singlet-excited carbonyl fragment while effectively emitting light especially in an aprotic polar solvent.
To realize highly efficient chemiluminescence of dioxetane in the solid state, we attempted CTID-type decomposition of dioxetane by using of intermolecular hydrogen bonding between a phenolic OH of dioxetane and an additive such as organic super base. As a preliminary study, we found that organic super bases can be used for CTID of dioxetane bearing a hydroxyaryl group in an organic solvent. In addition, we investigated base-induced decomposition of dioxetanes bearing a 3-hydroxyphenyl substituted with 4-p-oligophenylene moiety. Thus, we found that base-induced decomposition of these dioxetanes rapidly proceeded to give bright light even in water as well as in acetonitrile or DMSO.

Academic Significance and Societal Importance of the Research Achievements

3-ヒドロキシフェニル置換ジオキセタンに代表されるCTID型ジオキセタンは、蛍光性化合物からの発光と異なり光源を必要とせず、また感度も高く、医療衛生分野での生体内微量物質の検出に使用されているほか、分子イメージングへの応用も行なわれている。さらにポリマーへジオキセタンを導入し、ポリマーの機械的な応答をジオキセタンの分解発光で検出する検討も行なわれている。この様な背景のもと、固体状態でジオキセタンの発光効率の良いCTID型発光系を組み上げることはジオキセタンの応用に大きく貢献すると期待できる。

Report

(5 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (7 results)

All 2020 2018 2017

All Journal Article (4 results) (of which Peer Reviewed: 4 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results) Presentation (3 results) (of which Invited: 1 results)

  • [Journal Article] Highly effective and rapid emission of light from bicyclic dioxetanes bearing a 3-hydroxyphenyl substituted with a 4-p-oligophenylene moiety in an aqueous system: two different ways for the enhancement of chemiluminescence efficiency2020

    • Author(s)
      Nobuko Watanabe,* Hikaru Takatsuka, Hisako K. Ijuin, Masakatsu Matsumoto*
    • Journal Title

      Tetrahedron

      Volume: ‐ Issue: 23 Pages: 131203-131203

    • DOI

      10.1016/j.tet.2020.131203

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Organic superbase-induced chemiluminescent decomposition of a hydroxyaryl-substituted dioxetane: Unique effect of a bifunctional guanidine base on the chemiluminescence profile of a bicyclic dioxetane bearing a 4-(benzoxazol-2-yl)-3,5-dihydroxyphenyl moiety2018

    • Author(s)
      ①N. Watanabe, A. Wakatsuki, H. K. Ijuin, Y. Kabe and M. Matsumoto
    • Journal Title

      Tetrahedron Letters

      Volume: 59 Issue: 11 Pages: 971-977

    • DOI

      10.1016/j.tetlet.2018.01.045

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Journal Article] Notable difference between tetrabutylammonium fluoride and organic superbases as triggers for the chemiluminescent decomposition of bicyclic dioxetanes bearing a 4-(N-phenylbenzoimidazole-2-yl)-3-hydroxyphenyl moiety2018

    • Author(s)
      ②N. Watanabe, K. Kumagai, R. Ohtuka, A. Wakatsuki, H. K. Ijuin, Y. Kabe and M. Matsumoto
    • Journal Title

      Heterocycles

      Volume: 印刷中

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Journal Article] Solvent- and temperature-controlled inversion of π-facial selectivity in the 1,2-cycloaddition of singlet oxygen to hydroxyphenyl-substituted cyclohexadihydrofurans2017

    • Author(s)
      N. Watanabe, K. Hiragaki, K. Tsurumi, H. K. Ijuin, and M. Matsumoto
    • Journal Title

      Tetrahedron

      Volume: 73 Issue: 14 Pages: 1845-1853

    • DOI

      10.1016/j.tet.2017.02.038

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Presentation] 水素結合とジオキセタン型化学発光2018

    • Author(s)
      渡邉信子
    • Organizer
      生物発光化学発光研究会34回学術講演会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] 有機強塩基に誘発されるフェノール置換ジオキセタンの化学発光2017

    • Author(s)
      若月 愛結・渡邉 信子・伊集院 久子・加部 義夫・松本 正勝
    • Organizer
      2017年光化学討論会
    • Related Report
      2017 Research-status Report
  • [Presentation] 有機強塩基に誘発されるフェノール置換ジオキセタンの化学発光2017

    • Author(s)
      若月 愛結・渡邉 信子・伊集院 久子・加部 義夫・松本 正勝
    • Organizer
      生物発光化学発光研究会 第33回学術講演会
    • Related Report
      2017 Research-status Report

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Published: 2016-10-24   Modified: 2021-02-19  

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