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机构地区:[1]Department of Chemtstry, Shanghat Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, China [2]Department of Chemistry, East China University of Science and Technology, Shanghai 200237, China
出 处:《Chinese Journal of Chemistry》2006年第2期231-234,共4页中国化学(英文版)
基 金:Project supported by the National Natutral Science Foundation of China (No. 20372016).
摘 要:[Cp2Ln(μ-SR)]2 was reacted with Ph2C=C=O to yield ketene mono-insertion products [Cp2Ln(μ-η1:η2-OC(SR)=CPh2)]2 [R=Bn, Ln=Yb (1), Er (2), Y (3) and R--Ph, Ln=Yb (4)], indicating that the reactions of organolanthanide thiolates with ketenes are independent of the nature of the thiolate ligand and the ketene as well as the reaction condition. These reactions could provide an efficient method for the synthesis of organolanthanide complexes with the a-thiolate-substituted enolate ligand. All these complexes were characterized by elemental analysis and spectroscopic properties and the structure of complex 1 was determined through X-ray single crystal diffraction analysis.[Cp2Ln(μ-SR)]2 was reacted with Ph2C=C=O to yield ketene mono-insertion products [Cp2Ln(μ-η1:η2-OC(SR)=CPh2)]2 [R=Bn, Ln=Yb (1), Er (2), Y (3) and R--Ph, Ln=Yb (4)], indicating that the reactions of organolanthanide thiolates with ketenes are independent of the nature of the thiolate ligand and the ketene as well as the reaction condition. These reactions could provide an efficient method for the synthesis of organolanthanide complexes with the a-thiolate-substituted enolate ligand. All these complexes were characterized by elemental analysis and spectroscopic properties and the structure of complex 1 was determined through X-ray single crystal diffraction analysis.
关 键 词:organolanthanide INSERTION KETENE structure CYCLOPENTADIENYL
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