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机构地区:[1]Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials,Fudan Uni-versity,Shanghai 200433, China [2]Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials,Fudan Uni-versity,Shanghai 200433, China State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
出 处:《Chinese Journal of Chemistry》2004年第9期935-940,共6页中国化学(英文版)
基 金:the National Natural Science Foundation of China and the Research Funds of Excellent Young Teacher and the New Century Distinguished Scientist of National Education Ministry of China.
摘 要:Six new ethylthioethylcyclopentadienyl-containing organolanthanide complexes CpTh 2LnCl [Ln=Gd (1), Dy (2)] and Cp2LnCpTh [Cp=C5H5, Ln=Yb (3), Sm (4), Dy (5), Y (6)] were synthesized by the reaction of ethylthioethyl-cyclopentadienyl (CpTh) sodium salt with LnCl3 or Cp2LnCl in THF. Complexes 16 were characterized by ele-mental analyses, infrared and mass spectroscopies. The molecular structures of complexes 13 were also deter-mined by the X-ray single crystal diffraction. The results show that the side-chain sulfur atom on the ethylthio-ethylcyclopentadienyl ring can form intramolecular chelating coordination to the central lanthanide ion, improving the stability of organolanthanide complexes and reducing the number of coordinated THF molecules.Six new ethylthioethylcyclopentadienyl-containing organolanthanide complexes CpTh 2LnCl [Ln=Gd (1), Dy (2)] and Cp2LnCpTh [Cp=C5H5, Ln=Yb (3), Sm (4), Dy (5), Y (6)] were synthesized by the reaction of ethylthioethyl-cyclopentadienyl (CpTh) sodium salt with LnCl3 or Cp2LnCl in THF. Complexes 16 were characterized by ele-mental analyses, infrared and mass spectroscopies. The molecular structures of complexes 13 were also deter-mined by the X-ray single crystal diffraction. The results show that the side-chain sulfur atom on the ethylthio-ethylcyclopentadienyl ring can form intramolecular chelating coordination to the central lanthanide ion, improving the stability of organolanthanide complexes and reducing the number of coordinated THF molecules.
关 键 词:organolanthanide substituted cyclopentadienyl crystal structure synthesis
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