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Journal of Rare Earths
Administrated by CAST
Sponsored by CSRE and GRINM
Published by Elsevier B.V.
Editor-in-Chief: XU Guang xian
Journal of Rare Earths
(monthly, Since 1990)
ISSN 1002-0721 CODEN: JREAE6
Journal of the Chinese Society of Rare Earths
(Bimonthly, Since 1983)
ISSN 1000-4343 CODEN: ZXXUE5
 
Journal of Rare Earths Issue
Journal of Rare Earths 2011 Year Vol.29 NO.1 Page: 24-27
Synthesis and crystal structure of [Y(C5Me4SiMe3){-O(CH2)3CH3}{N(SiHMe2)2}]2
LUO Yunjie1, FENG Xiaoying1,2
(1. Organometallic Chemistry Laboratory, Ningbo Institute of Technology, Zhejiang University, Ningbo 315100, China; 2. Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, China)
Abstract:

A dimeric yttrium complex [Y(C5Me4SiMe3){-O(CH2)3CH3}{N(SiHMe2)2}]2 (1) was isolated as one of the byproducts from the reaction of Y{N(SiHMe2)3}3(THF)2 with C5Me4HSiMe3 in 1:1.1 molar ratio in toluene at 100 C for 2 d. Complex 1 was characterized by elemental analysis, NMR spectroscopy, FT-IR spectroscopy, and X-ray single crystal structure analysis. X-ray diffractions revealed that complex 1 was a symmetric dimer, and the center metal Y3+ was six-coordinated by one nitrogen atom from the amide group, two bridging oxygen atoms from the O(CH2)3CH3 groups, and one cyclopentadienyl ring in 5-fashion to adopt a distorted tetrahedron geometry. The formation of complex 1 was postulated to be a result from C–O bond cleavage reaction of THF.

Key word:yttrium amide complex; ring-opening reaction of THF; synthesis; crystal structure; rare earths
    
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