| Project/Area Number |
15550043
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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 | Kanagawa University |
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Principal Investigator |
WATANABE Nobuko Kanagawa University, Faculty of Science, Assistant Professor, 理学部, 助手 (40291744)
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| Co-Investigator(Kenkyū-buntansha) |
MATSUMOTO Masakatsu Kanagawa University, Faculty of Science, Professor, 理学部, 教授 (10260986)
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| Project Period (FY) |
2003 – 2004
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| Project Status |
Completed (Fiscal Year 2004)
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| Budget Amount *help |
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 2004: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2003: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Keywords | Chemiluminescence substrate / Triggering / Dioxetane / Aryl sulfide anion / Aryl methanide anion / Aryl amide anion / 化学発光 / CIEEL / アリルチオラートアニオン / アリールメチル型カルバニオン |
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| Research Abstract |
New CIEEL-active dioxetanes having a new triggering system were designed and synthesized. The dioxetanes realized were 5-t-butyl-4,4-dimethyl-2,6,7-trioxabicyclo-[3.2.0]heptanes, which bear an electron-donor, such as aryl sulfide anion, arylmethanide anion, and arylamide anion at the 1-position instead of typical areneoxide anion.
1.Aryl sulfide anion (aryl-S^-) system : Dioxetanes bearing an acylthiophenyl group was synthesized. Since benzenethiol is stronger acid than phenol, dioxetanes bearing a thiophenolic moiety could be triggered by a weak base such as amines. In fact, they decomposed on treatment with a primary amine to emit yellow light with moderate chemiluminescent efficiency in DMSO. Even in an aqueous system, they gave light without significant decrease of chemiluminescent efficiency. A dimeric dioxetane having a disulfide function could be also triggered with Bu_4N hydroxide.
2.Arylmethanide anion (aryl-C^-) system : Dioxetanes bearing a phenyl moiety substituted with a methyl having an electron-withdrawing group were treated with TBAF/DMSO to emit light with maximum wavelength at 758〜530 nm. The order of the base-induced decomposition rates coincided with the order of acidity for parent carbon acids. A dioxetane bearing a 3-(1-cyanoethenyl)phenyl group was also found to undergo the Michael-addition-induced chemiluminescent decomposition. When chlorobis (methoxycarbonyl)methanide was used as a nucleophile, the CT-induced decomposition of an intermediary dioxetane bearing a phenymethanide competed with the intramolecular cyclopropanation. These results show a possibility that the rate of an intramolecular competitive reaction can be estimated by examining the product ratio in the spent reaction mixture,.
3.Arylamide anion (aryl-N^-) system : Dioxetane bearing acylaminophenyl and iridole were synthesized and confirmed to emit light by the treatment with base. These are a first example of dioxetane active toward N-triggering.
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