| Project/Area Number |
06403014
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
物質変換
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| Research Institution | Chiba University |
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Principal Investigator |
IMAMOTO Tsuneo Chiba University, Faculty of Science Professor, 理学部, 教授 (10134347)
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| Project Period (FY) |
1994 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥33,000,000 (Direct Cost: ¥33,000,000)
Fiscal Year 1996: ¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 1995: ¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 1994: ¥26,800,000 (Direct Cost: ¥26,800,000)
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| Keywords | Boron Anion / Organoboron Compound / Phosphine-Borane / Borane / Amino-Borane / Nucleophilic Substitution / Organophosphorus Compound / Electrophilic Substitution / アミン・ボラン / ホウ素ジアニオン / ホスフィンボラン / 求核反応 / カルボアニオン / 電子環状反応 / 親電子試剤 |
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| Research Abstract |
The generation and reactions of tricoordinate boron anions have been investigated using phosphine-boranes. Tricyclohexylphosphine-monoiodoboranes were reduced by two equivalents of lithium 4,4'-di-tert-butylbiphenylide (LDBB) in tetrahydrofuran at -78ﾟC.The generated chemical species reacted with a variety of electrophiles such as chlorotrimethylsilane, diphenyl disulfide, methyl trifluoromethanesulfonate, ethylene oxide, benzaldehyde, diethyl carbonate, and carbon dioxide to affordphosphine-boranes possessing a sub stituent at the boron atom. Reaction of tri-tert-butylphosphine-monoiodoborane with LDBB,followed by treatment with water or benzyl bromide, provided di-tert-butylphosphine-borane or benzyl (di-tert-butyl) phosphine-borane, respectively. These reactions clearly indicate that tricoordinate boron anions were generated as the reactive intermediates.
Phosphine-boranes possessing trifluoromethanesulfonyloxy group at the boron atom were synthesized by treatment of phosphine-borans with trifluoromethanesulfonic acids. The structures of the obtained compounds were unequivocally determined by single crystal X-ray analyzes. These compounds underwent nucleophilic substitution reaction with various nucleophiles such as organocopper reagents to give B-substituted phosphineboranes in good yields.
Novel heterocyclic compounds containing P-B-S linkages were also synthesized, and their structures and chemical properties were characterized.
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