Ecternal Control of Electron Transfer Reaction at an Interface
| Project/Area Number |
03650655
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
工業物理化学・複合材料
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| Research Institution | Hokkaido University |
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Principal Investigator |
NAKAMURA Hiroshi Hokkaido Univ., Fac. of Sci., Professor, 理学部, 教授 (00117194)
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| Co-Investigator(Kenkyū-buntansha) |
YONEMURA Hiroaki Kyushu Univ., Fac. of Eng., Assistant Professor, 工学部, 助手 (40220769)
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| Project Period (FY) |
1991 – 1992
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| Project Status |
Completed (Fiscal Year 1992)
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| Budget Amount *help |
¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 1992: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1991: ¥1,300,000 (Direct Cost: ¥1,300,000)
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| Keywords | Reverse micelle / Radical pair / Electron Transfer / Exchange term / Electron spin echo / Time resolved ESR / CIDEP / 励起三重項 / 時間分解ESRスペクトル / トリプレットメカニズム / ラジカル間相互作用 |
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| Research Abstract |
Photoinduced electron transfer reactions between electron donor and acceptor was investigated in an interface of molecular assemblies such as AOT reversed micelle.
1. Conformation of the D-A linked compound was studied in an aqueous media. Through-ring cyclodextrin (CD) complex of D-A linked compound were investigated by means of high resolution NMR spectra, and thermodynamic parameter such as complex formation constants and formation rate constants with DELTAGs were obtained. These parameter shows that the hydrophobic interaction between the cavity of CD and the alkyl chain of D-A dominantly determined the stabilities of the complexes, statically. However, the repulsion between the hydrophilicity of the head group of D-A molecule and hydrophilic cavity of CD cased the anomalously stable complexation.
2. Electron spin-echo investigation shows the situation of a radical moiety of the donor molecule in the micelles. And, the alkyl chain length and the charge of the radical and the surface of the micelles governs the situation in the molecular assemblies.
3. Time resolved electron spin resonace equipment was manufactured, and time resolved ESR (or CIDEP) spectra were able to be obtained. In aqueous media, the spectra were hardly obtained by low Q-values, but AOT reversed micelle media gave a good result for measurements of CIDEP spectra. The CIDEP spectra shows that the magnetic field effects for the reverse electron transfer are governed by the electron exchange interaction between the radical pairs of the D-A systems.
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Report
(3 results)
Research Products
(22 results)
