[Nb2Cl8(Me2Te)4], [Nb2Cl8(Me2S)2] and [Nb2Cl8(Me2Se)2]. The complexes are very sensitive to moisture and dioxygen, and some also readily undergo C–E bond cleavage. Two ligand fragmentation products were identified –[Nb2Cl4(μ-S)2MeS(CH2)3SMe}2] and [Nb2Cl4(μ-Se)2o-C6H4(CH2)2Se}4]. X-ray crystal structures are also reported for the oxidation/hydrolysis products [NbOCl3(Me2S)] and [NbOCl3MeS(CH2)2SMe}].
NbCl 4与二
硫醚MeS(CH 2)n SMe(n = 2或3),i PrS(CH 2)2 S i Pr或o -C 6 H 4(CH 2
SEt)2以1:1摩尔比反应数天之内在CH 2 Cl 2或
甲苯中的比例,得到红色或橙色顺磁性配合物[NbCl 4(二
硫醚)]。它们的X射线晶体结构证实了螯合二
硫醚的八面体几何形状失真。单独的MeS(CH 2)2 SMe也会形成[NbCl4 MeS(CH 2) 2 SMe} 2 ]络合物基于方形反棱柱几何中的八坐标Nb( IV)。由Me
SE(CH 2) n
SEMe( n = 2或3)和n Bu
SE(CH 2) 3
SE n Bu形成相似的六坐标顺式-[NbCl 4(二
硒醚)]。单齿
配体Me 2 S,Me 2
SE和n Bu 2
SE形成[NbCl 4(R 2 E) 2](E = S,
SE)在溶液中不稳定,失去R 2 E形成
化学计量比为1:1的配合物,显示为抗磁性二聚体,[(Me