Journal
ORGANOMETALLICS
Volume 29, Issue 3, Pages 549-553Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om900758y
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Funding
- National Natural Science Foundation of China [20672134, 20872164, 20821002]
- Chinese Academy of Sciences
- Shanghai Municipal Commitee of Science and Technology [07JC14063]
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Reactions of 1,3-bis(trimethylsilyl)indene with Ln(CH2SiMe3)(3)(THF)(2) gave half-sandwich rare earth metal complexes (1,3-(SiMe3)(2)C9H5)Ln(CH2SiMe3)(2)(THF) (Ln = Y, Lu, Dy). These complexes were characterized by single-crystal X-ray diffraction, which showed the eta(5) hapticity of indenyl ligands in all of the complexes. The catalytic behaviors of the complexes for intramolecular hydroamination of aminoalkenes were investigated. The catalytic activity increased with increasing the metal ion size. and the Y and Dy complexes showed excellent activities to a variety aminoalkenes.
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