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Preparation and characterization of cationic organolanthanides with less bulky ligands

机译:配体体积较小的阳离子有机镧系元素的制备与表征

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摘要

The cationic complexes stabilized by methylcyclopentadienyl (MeCp ligands, i.e.[(MeCp)2Ln(THF)z][BPh4]?2THF (1, Ln=Sm; 2, Ln=Yb) have been preparedby oxidation of (MeCp)2Ln(THF) with AgBPH4 in tetrahydrofuran(THF) and characterized by elemental analyses, IR spectra, molarconductivities and TGDTA measurements. 2 was characterized byX-ray. The two centroids of methylcyclopentadienyl rings and thetwo oxygen atoms of THF molecules form a distorted tetrahedronaround the ytterbium atom with an average Yb-C(ring) bonddistance of 2.55? and Cen(1)-Yb-Cen(2) angle of 127.6°.Thestructural analysis indicates that the cationic complex with lessbulky ligands has a more open coordination environment aroundthe metal atom than that with bulky ligands. The results alsoconfirm that the stabilization of the cationic lanthanocenes can beachieved no matter how big or small the ligand is.
机译:通过氧化(MeCp)2Ln(THF)制备了由甲基环戊二烯基(MeCp配体,即[(MeCp)2Ln(THF)z] [BPh4]?2THF(1,Ln = Sm; 2,Ln = Yb)稳定的阳离子配合物)在四氢呋喃(THF)中用AgBPH4进行元素分析,红外光谱,摩尔电导率和TGDTA测量.2用X射线表征。甲基环戊二烯基环的两个质心和THF分子的两个氧原子在with原子周围形成扭曲的四面体, Yb-C(环)平均键距为2.55?,Cen(1)-Yb-Cen(2)角为127.6°。结构分析表明,配体少的阳离子络合物在金属原子周围的配位环境更开放。结果还证实,无论配体多大或少,阳离子镧系元素的稳定都可以实现。

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