Huh Daniel N, Ziller Joseph W, Evans William J
Department of Chemistry, University of California, Irvine, California, 92697, USA.
Acta Crystallogr E Crystallogr Commun. 2020 Jun 23;76(Pt 7):1131-1135. doi: 10.1107/S2056989020008051. eCollection 2020 Jul 1.
The green compound poly[(tetra-hydro-furan)-tris-[μ-η:η-1-(tri-methyl-sil-yl)cyclo-penta-dien-yl]caesium(I)ytterbium(II)], [CsYb(CHSi)(CHO)] or [(THF)Cs(μ-η:η-Cp')Yb] was synthesized by reduction of a red THF solution of (CHSiMe)Yb with excess Cs metal and identified by X-ray diffraction. The compound crystallizes as a two-dimensional array of hexa-gons with alternating Cs and Yb ions at the vertices and cyclo-penta-dienyl groups bridging each edge. This, based off the six-electron cyclo-penta-dienyl rings occupying three coordination positions, gives a formally nine-coordinate tris-(cyclo-penta-dien-yl) coordination environment to Yb and the Cs is ten-coordinate due to the three cyclo-penta-dienyl rings and a coordinated mol-ecule of THF. The complex comprises layers of CsYb hexa-gons with THF ligands and MeSi groups in between the layers. The Yb-C metrical parameters are consistent with a 4 Yb electron configuration.
绿色化合物聚[(四氢呋喃)-三-[μ-η:η-1-(三甲基硅基)环戊二烯基]铯(I)镱(II)],[CsYb(CHSi)(CHO)]或[(THF)Cs(μ-η:η-Cp')Yb],通过用过量的铯金属还原(CHSiMe)Yb的红色四氢呋喃溶液合成,并通过X射线衍射鉴定。该化合物结晶为二维六边形阵列,顶点处交替排列着铯和镱离子,每个边由环戊二烯基桥连。基于占据三个配位位置的六电子环戊二烯基环,这为镱提供了形式上九配位的三(环戊二烯基)配位环境,由于三个环戊二烯基环和一个配位的四氢呋喃分子,铯是十配位的。该配合物由CsYb六边形层组成,层间有四氢呋喃配体和甲基硅基。镱-碳的度量参数与4个镱电子构型一致。