Evans William J, Lee David S, Ziller Joseph W
Department of Chemistry, University of California, Irvine, California 92697-2025, USA.
J Am Chem Soc. 2004 Jan 21;126(2):454-5. doi: 10.1021/ja036923m.
The reaction of Ln[N(SiMe3)2]3 with K under N2 in THF forms the dinitrogen complexes {[(Me3Si)2N]2(THF)Ln}2(mu-eta2:eta2-N2) (Ln = Y, Ho, Tm, and Lu) previously available only for lanthanides with highly reducing divalent states, that is, Tm, Dy, and Nd. The Y and Lu complexes are the first diamagnetic complexes of this type. The Ln2N2 moiety is planar, and the 1.268(3) and 1.285(4) A NN distances in these complexes are consistent with the presence of (N2)2-.
Ln[N(SiMe3)2]3在氮气氛围下于四氢呋喃中与钾反应,生成二氮配合物{[(Me3Si)2N]2(THF)Ln}2(μ-η2:η2-N2)(Ln = Y、Ho、Tm和Lu),这类配合物之前仅在具有高还原二价态的镧系元素(即Tm、Dy和Nd)中出现过。Y和Lu的配合物是此类中的首个抗磁性配合物。Ln2N2部分呈平面结构,这些配合物中1.268(3) Å和1.285(4) Å的NN距离与(N2)2-的存在相符。