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Acta Chimica Sinica ›› 1992, Vol. 50 ›› Issue (10): 1024-1032. Previous Articles Next Articles
Original Articles
邓道利;郑晓帆;钱长涛;金松春;林永华
发布日期:
DENG DAOLI;ZHENG XIAOFAN;QIAN CHANGTAO;JIN SONGCHUN;LIN YONGHUA
Published:
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Bis(2-methoxyethylcyclopentadienyl)yttrium and -ytterbium tetrahydroborates have been synthesized in good yields by the reaction of bis(2-methoxyethylcyclopentadienyl)lanthanide chlorides with sodium borohydride in THF at room temperature The title complexes were characterized by elemental analyses, MS, 1H NMR and IR spectra. The crystal structures of the title compounds have been determine by x-ray diffraction. The x-ray structures and IR reveal the bidentate yttrium and ytterbium tetrahydroborate complexes with the intramol. coordination bonds between lanthanide metal and ligand oxygen atoms.
Key words: CRYSTAL STRUCTURE DETERMINATION, INFRARED SPECTROPHOTOMETRY, X-RAY DIFFRACTION ANALYSIS, CYCLOPENTADIENE P, PROTON MAGNETIC RESONANCE SPECTROMETRY, YTTRIUM COMPLEX, YTTERBIUM COMPLEX, BORANES
CLC Number:
O611.662
O627
DENG DAOLI;ZHENG XIAOFAN;QIAN CHANGTAO;JIN SONGCHUN;LIN YONGHUA. Studies organolanthanide.XL.synthesis and X-ray structure of bis(2-methoxyethylcy-clopentadienyl) yttrium and ytterbium tetrahydroborates[J]. Acta Chimica Sinica, 1992, 50(10): 1024-1032.
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