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题名: Synthesis and Protonolysis of Neutral Aluminum Dihydride Compounds Stabilized by Tridentate-substituted Pyrrolyl Ligands: Synthesis, structural Characterization and Ring-opening Polymerization of ɛ-caprolactone
作者: Chang, Jr-Chiuan;Chen, Ya-Chi;Datta, Amitabha;Lin, Chia-Her;Hsiao, Ching-Sheng;Huang, Jui-Hsien
贡献者: 化學系
关键词: Pyrrole;Aluminum;Ring-opening polymerization
日期: 2011-11
上传时间: 2012-12-10T01:40:12Z
出版者: Elsevier
摘要: A series of aluminum compounds containing tridentate pyrrolyl ligands were obtained from related aluminum dihydride compounds via protonolysis. Treatment of tetranuclear aluminum compound [C4H2N{2,5-(CH2NMe2)2}Al2H5]2 (1) with two equivalents of [C4H3N{2,5-(CH2NMe2)2}] in methylene chloride at 0 °C led to the formation of [C4H2N{2,5-(CH2NMe2)2}]AlH2 (2). Similarly, when the deuterated aluminum compound 1D was used, the corresponding aluminum compound [C4H2N{2,5-(CH2NMe2)2}]AlD2 (2D) could be isolated. The reaction of 2 with one or two equivalents of phenylethyne, triphenylmethanethiol, 2,6-diisopropylaniline, or triphenylsilanol generated mononuclear aluminum compounds [[C4H2N{2,5-(CH2NMe2)2}]AlRR′ (3, R = –CCPh, R′ = H; 4, R = R′ = –CCPh; 5, R = –SCPh3, R′ = H; 6, R = R′ = –SCPh3; 7, R = –NH(2,6-iPr2Ph), R′ = H; 8, R = R′ = –NH(2,6-iPr2Ph); 9, R = –OSiPh3, R′ = H; 10, R = R′ = –OSiPh3). Related Al–D compounds of 3, 5, 7 and 9 were also synthesized and corresponding IR spectroscopic data well matched in comparison of the stretching frequencies of Al–H and Al–D. The molecular structures of 2D, 4, 5, 5D, 7, and 10 have been determined by X-ray crystallography. Compounds 2, 5, and 7 initiated the ring-opening polymerization of ɛ-caprolactone and produced high-molecular weight of poly-ɛ-caprolactone.
關聯: Journal of Organometallic Chemistry, 696(23): 3673-3680
显示于类别:[化學系] 期刊論文


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