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http://ir.ncue.edu.tw/ir/handle/987654321/14783
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題名: | Insertion, Reduction, and Carbon-carbon Coupling Induced by Monomeric Aluminum Hydride Compounds Bearing Substituted Pyrrolyl Ligands |
作者: | Lin, Che-Yu;Tsai, Chia-Fu;Chen, Hsing-Jen;Hung, Chen-Hsiung;Yu, Ru-Ching;Kuo, Pei-Cheng;Lee, Hon-Man;Huang, Jui-Hsien |
貢獻者: | 化學系 |
關鍵詞: | Aluminum hydride;C-C coupling;Insertion;Pyrrole |
日期: | 2006-04
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上傳時間: | 2012-12-10T01:39:44Z
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出版者: | WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
摘要: | A monomeric aluminum hydride complex bearing substituted pyrrolyl ligands, AlH[C4H3N(CH2NMe2)-2]2 (1), was synthesized and structurally characterized. To further confirm the presence of AlH bonds, the compound AlD[C4H3N(CH2NMe2)-2]2 ([D]1) was synthesized by reacting LiAlD4 with [C4H4N(CH2NMe2)-2]. Compound 1 and [D]1 react with phenyl isothiocyanate yielding Al[C4H3N(CH2NMe2)-2]2[η3-SCHNPh] (2) and Al[C4H3N(CH2NMe2)-2]2[η3-SCDNPh] ([D]2) by insertion. The reactions of 1 with 9-fluorenone and benzophenone generated the unusual aluminum alkoxide complexes 3 and 4, respectively, through intramolecular proton abstraction and C–C coupling. A mechanistic study shows that 9-fluorenone coordinates to [D]1 and releases one equivalent of HD followed by C–C coupling and hydride transfer to yield the final product. Reduction of benzil with 1 affords aluminum enediolate complex 5 in moderate yield. Mechanistic studies also showed that the benzil was inserted into the aluminum hydride bond of [D]1 through hydroalumination followed by proton transfer to generate the final product [D]5. All new complexes have been characterized by 1H and 13C NMR spectroscopy and X-ray crystallography. |
關聯: | Chemistry-A European Journal, 12(11): 3067-3073 |
顯示於類別: | [化學系] 期刊論文
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