Syntheses of highly lipophilic and stable organic anions of poly-fluoroalkyl-substituted tetraphenylboron ate-complex tipe.
| Project/Area Number |
02650613
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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 |
有機工業化学
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| Research Institution | Kyushu University |
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Principal Investigator |
KOBAYASHI Hiroshi Kyushu University, Institute of Advanced Material Study ; Professor, 機能物質科学研究所, 教授 (10037731)
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| Co-Investigator(Kenkyū-buntansha) |
SONODA Takaaki Kyushu University, Institute of Advanced Material Study ; Associate professor, 機能物質科学研究所, 助教授 (90108770)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1991: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1990: ¥1,200,000 (Direct Cost: ¥1,200,000)
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| Keywords | Tetraarylboron ate-complex / High lipophilicity / Permanent organic anion / Polyfluoroalkyl-substituted benzene / Lithium-ion-catalyzed Diels-Alder reaction / テトラフェニルホウ素錯体 / 多フッ素化芳香族化合物 / 多フッ化芳香族化合物 |
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| Research Abstract |
The present research project is to investigate the formation of bulky and lipophilic stable tetraarylborate ions substituted by many polyfluoroalkyl groups, their solubilities in a range of hydrophobic solvents, and chemical stabilities under acid conditions. Research results are as follows : 1) Convenient methods were developed for the preparation of perfluoro- and polyfluoro-alkyl-substituted iodobenzenes which were useful as precursors for the corresponding tetraarylborates. 2) Efficient Grigrlard reaction methods were developed for the formation of tetraarylborate-s substituted by 3-perfluoroalkyl, 3, 5-bis (polyfluoroalkyl), and 3-trifluoromethyl-5-polyfluoroalkyl on each phenyl group. 3) Introduction of branched polyfluoroalkyl substituents with an increased number of terminal trifluoromethyl groups enhanced the solubilities of tetramethylammonium tetraarylborates in polyhalomethane solvents, especially effective in polyfluorocarbon solvents. Straight-chained perfluoroalkyl substituents seemed to depress the solubility. 4) Chemical stabilities measured in dichloromethane/sulfuric acid two-phases and in methanolic sulfuric acid solutions were in accordance with the electron-withdrawing effect of substituents, among which. trifluoromethyl groups was most effective as presumed. 5) Counter lithium ion, which was dried at higher temperature under high vacuum, was most electrophilic in dichloromethane to accelerate the Diels-Alder reaction and to affect the exo/endo selectivity of the adducts.
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Report
(3 results)
Research Products
(6 results)
