A funadamental study on the reaction of boronic acid with saccharide-determination of saccharide with metal complexes having boronic acid moiety-
Project/Area Number |
25410150
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Analytical chemistry
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Research Institution | Waseda University |
Principal Investigator |
Ishihara Koji 早稲田大学, 理工学術院, 教授 (20168248)
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Co-Investigator(Kenkyū-buntansha) |
ODANI Akira 金沢大学, 薬学系, 教授 (60143913)
TAKAGI D. Hideo 名古屋大学, 物質科学国際研究センター, 准教授 (70242807)
INAMO Masahiko 愛知教育大学, 教育学部, 教授 (20176407)
IWATSUKI Satoshi 甲南大学, 理工学部, 教授 (80373033)
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Co-Investigator(Renkei-kenkyūsha) |
SUGAYA Tomoaki 早稲田大学, 理工学術院, 助教 (30633367)
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2015: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2014: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2013: ¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
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Keywords | ボロン酸 / 糖の定量 / 金属錯体 / 反応機構 / 発光性金属錯体 / D-フルクトース / ホウ素の定量 / ボロン酸金属錯体 / 糖 / 定量 |
Outline of Final Research Achievements |
A number of luminescent boronic acid-based sensors for sugars, which utilize a reversible reaction between boronic acid and diol, have been exploited so far. However, a fundamental study on how efficiently progresses the sensing reaction is lacking. In this study, we have performed at first equilibrium and kinetic study on the reactions of some boronic acids with diols in aqueous solution in order to get fundamental information for their reactions, which resulted in proposing an universal reaction mechanism of boronic acid with diol. Then, we have performed similar study on the reactions of boronic acid with sugars to identify the reactive species of boronic acid and a sugar in the sensing reaction, and proposed a comprehensive sensing mechanism. Based on the mechanism, we have designed and synthesized highly luminescent metal complexes with boronic acid moiety, and tried to determine a sugar with monitoring the change in luminescence due to its reactions with these complexes.
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Report
(4 results)
Research Products
(56 results)
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[Journal Article] Flipping of Coordinated Triazine Moiety in Cu(I)-L2 and Small Electronic Factor, κ el, for Direct Outer-Sphere Cross Reactions: Syntheses, Crystal Structures and Redox Behavior of Copper(II)/(I)-L2 Complexes (L = 3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine)2015
Author(s)
Atsutoshi Yamada, Takuya Mabe, Ryohei Yamane, Kyoko Noda, Yuko Wasada, Masahiko Inamo, Koji Ishihara, Takayoshi Suzuki, and Hideo D. Takagi
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Journal Title
Dalton Trans.
Volume: 44
Issue: 31
Pages: 13979-13990
DOI
Related Report
Peer Reviewed / Acknowledgement Compliant
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[Journal Article] Syntheses, Crystal Structures and Ligand Field Properties of Iron(II) Complexes with PNP Ligands: Origin of Large Ligand Field by Phosphorous Donor Atom2014
Author(s)
Takuya Mabe, Hiroshi Yamaguchi, Masayuki Fujiki, Kyoko Noda,Koji Ishihara, Masahiko Inamo, Refat Moustafa Hassan, Satoshi Iwatsuki, Takayoshi Suzuki, and Hideo D. Takagi
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Journal Title
J. Sol. Chem.
Volume: 43
Issue: 9-10
Pages: 1574-1587
DOI
Related Report
Peer Reviewed
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[Journal Article] Relative kinetic reactivities of boronic acids and boronate ions toward 1,2-diols.2014
Author(s)
Okamoto T, Tanaka A, Watanabe E, Miyazaki T, Sugaya T, Iwatsuki S, Inamo M, Takagi H D, Odani A, Ishihara K.
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Journal Title
Eur J Inorg Chem
Volume: 2014(14)
Issue: 14
Pages: 2389-2395
DOI
Related Report
Peer Reviewed
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[Journal Article] Universal Reaction Mechanism of Boronic Acid with Diol in Aqueous Solution, Based on Kinetics, and Basic Concept of Conditional Formation Constant2014
Author(s)
Furikado Y, Nagahata T, Okamoto T, Sugaya T, Iwatsuki S, Inamo M, Takagi H D, Odani A, Ishihara K
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Journal Title
Chem. Eur. J.
Volume: 20(41)
Issue: 41
Pages: 13194-13202
DOI
Related Report
Peer Reviewed
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[Presentation] Flipping of Coordinated Triazine Moiety in Cu(I)-L2 and Small Electronic Factor, κel, for Direct Outer-Sphere Cross Reactions (L = 3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine)2015
Author(s)
Takuya Mabe, Atsutoshi Yamada, Yuko Wasada, Masahiko Inamo, Koji Ishihara, Takayoshi Suzuki, Hideo D. Takagi
Organizer
第65回錯体化学討論会
Place of Presentation
奈良女子大学
Year and Date
2015-09-22
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