Zhou Liying, Wang Junfeng, Zhang Yong, Yao Yingming, Shen Qi
Key Laboratory of Organic Synthesis, Jiangsu Province, Department of Chemistry and Chemical Engineering, Suzhou University, Suzhou 215123, PR China.
Inorg Chem. 2007 Jul 9;46(14):5763-72. doi: 10.1021/ic070162x. Epub 2007 Jun 7.
The synthesis and structures of a series of lanthanide(II) and lanthanide(III) complexes supported by the amido ligand N(SiMe3)Ar were described. Several lanthanide(III) amide chlorides were synthesized by a metathesis reaction of LnCl3 with lithium amide, including {[(C6H5)(Me3Si)N]2YbCl(THF)}2.PhCH3 (1), [(C6H3-iPr2-2,6)(SiMe3)N]2YbCl(mu-Cl)Li(THF)3.PhCH3 (4), [(C6H3-iPr2-2,6)(SiMe3)N]YbCl2(THF)3 (6), and [(C6H3-iPr2-2,6)(SiMe3)N]2SmCl3Li2(THF)4 (7). The reduction reaction of 1 with Na-K alloy afforded bisamide ytterbium(II) complex [(C6H5)(Me3Si)N]2Yb(DME)2 (2). The same reaction for Sm gave an insoluble black powder. An analogous samarium(II) complex [(C6H5)(Me3Si)N]2Sm(DME)2 (3) was prepared by the metathesis reaction of SmI2 with NaN(C6H5)(SiMe3). The reduction reaction of ytterbium chloride 4 with Na-K alloy afforded monoamide chloride {[(C6H3-iPr2-2,6)(SiMe3)N]Yb(mu-Cl)(THF)2}2 (5), which is the first example of ytterbium(II) amide chloride, formed via the cleavage of the Yb-N bond. The same reduction reaction of 7 gave a normal bisamide complex [(C6H3-iPr2-2,6)(SiMe3)N]2Sm(THF)2 (8) via Sm-Cl bond cleavage. This is the first example for the steric effect on the outcome of the reduction reaction in lanthanide(II) chemistry. 5 can also be synthesized by the Na/K alloy reduction reaction of 6. All of the complexes were fully characterized including X-ray diffraction for 1-7.
描述了一系列由酰胺配体N(SiMe3)Ar支撑的镧系元素(II)和镧系元素(III)配合物的合成及结构。通过LnCl3与氨基锂的复分解反应合成了几种镧系元素(III)酰胺氯化物,包括{[(C6H5)(Me3Si)N]2YbCl(THF)}2.PhCH3(1)、[(C6H3-iPr2-2,6)(SiMe3)N]2YbCl(μ-Cl)Li(THF)3.PhCH3(4)、[(C6H3-iPr2-2,6)(SiMe3)N]YbCl2(THF)3(6)和[(C6H3-iPr2-2,6)(SiMe3)N]2SmCl3Li2(THF)4(7)。用钠钾合金还原1得到双酰胺镱(II)配合物[(C6H5)(Me3Si)N]2Yb(DME)2(2)。对钐进行相同反应得到一种不溶性黑色粉末。通过SmI2与NaN(C6H5)(SiMe3)的复分解反应制备了类似的钐(II)配合物[(C6H5)(Me3Si)N]2Sm(DME)2(3)。用钠钾合金还原氯化镱4得到单酰胺氯化物{[(C6H3-iPr2-2,6)(SiMe3)N]Yb(μ-Cl)(THF)2}2(5),它是通过Yb-N键断裂形成的镱(II)酰胺氯化物的首个实例。对7进行相同的还原反应通过Sm-Cl键断裂得到正常的双酰胺配合物[(C6H3-iPr2-2,6)(SiMe3)N]2Sm(THF)2(8)。这是镧系元素(II)化学中空间效应影响还原反应结果的首个实例。5也可以通过6的钠/钾合金还原反应合成。所有配合物都经过了全面表征,包括对1 - 7进行X射线衍射分析。