Effect of structural fluctuation on excited-state reaction processes revealed by temperature-variable single-molecule fluorescence spectrosocopy
Project/Area Number |
24550018
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Physical chemistry
|
Research Institution | Rikkyo University (2014) Shizuoka University (2012-2013) |
Principal Investigator |
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Project Status |
Completed (Fiscal Year 2014)
|
Budget Amount *help |
¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2013: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2012: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
|
Keywords | 単一分子分光 / 蛍光ブリンキング / 電子移動 / 項間交差 / 光安定性 / 単一分子蛍光分光 / 電荷移動 / 励起状態 / ブリンキング / 超分子 / カプセル / 不均一性 / 高分子薄膜 / 蛍光 / 水素原子移動 |
Outline of Final Research Achievements |
The effect of static/dynamic heterogeneities upon photophysico-chemical processes of fluorescent dyes in various environments were investigated using single-molecule spectroscopy. Consequently, 1) a 10-fold increase in the photostability of the anthracene-based guest due to supramolecular encapsulation was demonstrated. Furthermore, this complex is >30-fold more photostable than rhodamine 6G, 2) an entire picture of heterogeneous photo-induced charge transfer dynamics of single perylenediimide (PDI) molecules in a polymer matrix was revealed, and 3) the photo-induced reaction dynamics occurring in the system of PDI molecules embedded in γ-cyclodextrin (γCD) films were examined. The analyses of fluorescence blinking statistics and theoretical calculations suggest that the hydrogen atom transfer reaction probably occurs between PDI and γCD via higher-lying triplet n,π* states of PDI.
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Report
(4 results)
Research Products
(24 results)