Development of Sensitizers and Chemiluminescent Reagents intending to create new Super-function
| Project/Area Number |
15550037
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Organic chemistry
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| Research Institution | OKAYAMA UNIVERSITY |
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Principal Investigator |
KIMURA Masaru Okayama University, Graduate School, Professor, 大学院自然科学研究科, 教授 (30033442)
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| Project Period (FY) |
2003 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2005: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2004: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2003: ¥2,000,000 (Direct Cost: ¥2,000,000)
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| Keywords | Functional Chemistry / Super Function / Chemiluminescence / Chemosensor / Bioluminescence / Lophine / Lophine peroxide / Imidazole / 光増感剤 / ジアザペリレン / アゼピニウムカチオン / ルミノール / シアニン色素 / 化学発光剤 / 太陽電池 / 増感剤 / ルテノセン |
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| Research Abstract |
We have explored function-accumulating system for generation of a new super-function. Recently many investigations on chemo-sensors as the super-function have employed chelation-enhanced fluorescence. However, metal ion-based functional chemi luminescent systems have not been reported for the lophines. We presented the first potential signaling system incorporating a chelating ability and CL property. We have prepared 4,5-diphenyl-2-(2-pyridyl)-imidazole and developed to 2-(2-hydroxyphenyl)-4,5-diphenylimidazole 1 bearing a chelating function. The CL efficiency of 1 was 0.28 times that of lophine peroxide on initiation with KOH/MeOH. When the trigger base was changed to TBAF/THF, the efficiency was 530-fold in dry DMF. Singlet oxygen was detected from the reaction of lophine hydroperoxides in the presence of a singlet oxygen detector. In order to examine the substituent effect on the formation of singlet oxygen, 2-(p-substituted phenyl) lophine peroxides were tested. An electron-attracting group contributed to the efficient formation of singlet oxygen, while an electron-donating group enhanced the chemiluminescence. As the second example, a 2,11-diaza[3,3]paracyclo(9,10)anthracenophane derivative possessing an ethylenediamine host function has been prepared.
Further we reported a unique-unexpected rearrangement from [benzene anthracene]biplanemers to energy-stored compounds and a azepine chemistry as a side work.
We have achieved outstanding research goals in their functional chemistry and photochemistry of biplanemers as shown above. We are very much grateful for the financial support from the KAKEN fund.
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Report
(4 results)
Research Products
(31 results)
