Control and functionalizations of dynamics of radicals and ionic intermediates generated by photocatalysts
| Project/Area Number |
14050069
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| Research Category |
Grant-in-Aid for Scientific Research on Priority Areas
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| Allocation Type | Single-year Grants |
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| Review Section |
Science and Engineering
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| Research Institution | Yamaguchi University |
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Principal Investigator |
ISHIGURO Katsuya Yamaguchi University, Graduate Shcool of Science and Technology, Professor (40202981)
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| Project Period (FY) |
2001 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥27,700,000 (Direct Cost: ¥27,700,000)
Fiscal Year 2006: ¥4,100,000 (Direct Cost: ¥4,100,000)
Fiscal Year 2005: ¥4,100,000 (Direct Cost: ¥4,100,000)
Fiscal Year 2004: ¥6,300,000 (Direct Cost: ¥6,300,000)
Fiscal Year 2003: ¥6,500,000 (Direct Cost: ¥6,500,000)
Fiscal Year 2002: ¥6,700,000 (Direct Cost: ¥6,700,000)
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| Keywords | Photoinduced Electron Transfer / Radical Ions / Photochromism / Norbornadiene / Quadricyclane / Photocatalyst / Conductive Film / Photochemical Doping / 異性化反応 / フリップ・フロップ / 犠牲ドナー / テトラシアノキノジメタン / ラングミュア・ブロジェット膜 / 導雷性有機薄膜 / 光増感反応 / ラジカルイオン中間体 / 一電子酸化 / 電子交換触媒 / 犠牲試薬 / 固相光化学反応 / 大気イオン / 結合開裂 |
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| Research Abstract |
Design and development of photochemical and electron-transfer reactions for novel functionalities have been studied, focusing on unique characteristics of radical and ionic intermediates in organic photochemistry, with three directions as follows: (1) Doping and storage of hole and electron utilizing electron-transfer induced bond formation/cleavage reactions. Generation of electric conductivity of organic thin films was observed upon the irradiation of alternatively layered LB films of a designed sacrificial donor-photo-sensitizer molecule and tetracyanoquinodimethane with long alkyl chain. In addition, electronic acceptors incorporated with a stable radical to form covalent bond by one-electron reduction were prepared which may enable a reversible photochemical doping reaction. (2) Construction of novel reversible systems employing photochemical cyclization of substituted norbornadienes and the electron-transfer valence isomerization of quadricyclanes. (a) Photochromic system designed for recording of repeat counts with quadricyclanes carrying sacrificial electron donors, which undergo bond-cleavage upon reverse reaction by the one-electron oxidation. (b) Flip-flop type photochromic system, which repeats on and off cycles by every pulsed light irradiation, utilizing the acidity change of a norbornadiene-quadricyclae system substituted with carboxylic acid. (3) The development of novel functional interfacial reactions: In addition, formation of electrochromic and conductive thin films by oxidative polymerization of triphenylamine olygomers, electrostatic control of photocatalytic reactions, generation of the high spin states by photodissociation reactions have been studied.
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Report
(6 results)
Research Products
(16 results)
