首页> 美国卫生研究院文献>Acta Crystallographica Section E: Crystallographic Communications >Crystal structure of μ-fluorido-bis­{(η4-cyclo­octa­diene)hexa­fluorido­anti­monato(V)platinum(II)} hexa­fluorido­anti­monate(V) hydrogen fluoride 0.75-solvate
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Crystal structure of μ-fluorido-bis­{(η4-cyclo­octa­diene)hexa­fluorido­anti­monato(V)platinum(II)} hexa­fluorido­anti­monate(V) hydrogen fluoride 0.75-solvate

机译:μ-氟代双­ {(η4-环­八­二烯)六氟代­抗­monato(V)铂(Ⅱ)}的晶体结构氟代­抗­酸盐(V)0.75溶剂化氢

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摘要

In the complex cation of the binuclear solvated title salt, [Pt2F(SbF6)2(C8H12)2]SbF6·0.75HF, an F atom bridges the two platinum(II) atoms with a bond angle of 123.3 (2)°. The corresponding Pt—F bond lengths are in the range of other fluorine-bridged binuclear platinum(II) complexes. Two of the three SbF6 anions each coordinate with one F atom to one platinum(II) atom. Including the η4-bound cyclo­octa­diene (COD) ligands, the overall coordination sphere of each platinum(II) atom is square-planar. The third SbF6 anion is not bound to the complex. Hydrogen fluoride is present in the crystal structure as a solvent disordered over three positions, each with an occupancy of 0.25. F⋯F distances of 2.5512 (7), 2.6076 (8) and 3.2215 (10) Å to surrounding SbF6 anions are indicative of F—H⋯F hydrogen-bonding inter­actions although no H atoms could be localized for the disordered solvent mol­ecules. The resulting hydrogen-bonded network is three-dimensional.
机译:在双核溶剂化标题盐[Pt2F(SbF6)2(C8H12)2] SbF6·0.75HF的复合阳离子中,F原子桥接两个铂(II)原子,其键角为123.3(2)°。相应的Pt-F键长度在其他氟桥联双核铂(II)配合物的范围内。三个SbF6 -阴离子中的两个分别与一个F原子与一个Platinum(II)原子配位。包括与η 4 结合的环八碳二烯(COD)配体,每个铂(II)原子的整体配位域为方形。第三个SbF6 -阴离子未与该复合物结合。氟化氢作为溶剂存在于晶体结构中,分布在三个位置,每个位置的占有率为0.25。到周围的SbF6 -阴离子的F⋯F距离为2.5512(7),2.6076(8)和3.2215(10)Å,表明F-H⋯F氢键相互作用,尽管没有H原子可以定位于无序的溶剂分子。所得的氢键网络是三维的。

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