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Single crystals of two new modifications of [P(C6H5)4]2[Cu2I4] were obtained by reaction of granulated copper with iodine and [P(C6H5)4]I in dry acetone under nitrogen atmosphere. They crystallise monoclinically, space group P21/n (No. 14), a = 11.550(6), b = 7.236(2), c = 27.232(13) Å, β = 98.13(3)°, V = 2253(2) Å3, and Z = 2 ([P(C6H5)4]2[Cu2I4]-C), and space group Cc (No. 9), a = 17.133(5), b = 15.941(5), c = 18.762 (6) Å, β = 114.02(1)°, V = 4681(3) Å3, and Z = 4 ([P(C6H5)4]2[Cu2I4]-D), respectively. In these compounds the [CuI2]? anions form dimers di-μ-iodo-diiodocuprate(I), which are either planar ( C ) or folded ( D ).  相似文献   

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[μ-Ni(C5H5)P(C6H5)3] [μ-C5H5]2 [ZnC5H5]2 has been obtained from the reaction of Cp2Zn with Ni(COD)2 in the presence of Ph3P and its structure determined by X-ray crystallography. It consists of two cyclopentadienylzinc moieties bridged by the Ni atom of a CpNiPPh3 group and by a Cp group. A possible mechanism for the formation of the compound is discussed.  相似文献   

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Preparation and Crystal Structure of Tetraphenylphosphonium Hexathiocyanatorhodate(III), [P(C6H5)4]3[Rh(SCN)6] By treatment of RhCl3 · n H2O with KSCN in water a mixture of the linkage isomers [Rh(NCS)n(SCN)6–n]3?, n = 0–2 is formed which is separated by ion exchange chromatography on diethylaminoethyl cellulose. The X-ray structure determination on a single crystal of [P(C6H5)4]3[Rh(SCN)6] (monoclinic, space group C1c1, a = 13.620(5), b = 22.929(13), c = 22.899(9) Å, β = 98.55(3)°, Z = 4) confirms the coordination of all ligands via S with the middle Rh? S distance of 2.372 Å and Rh? S? C angles of 109°. The SCN groups are nearly linear with 175° and averaged bondlengths S? C 1.63 and C? N 1.14 Å. The crystal lattice is build up by layers of complex anions and voluminous cations with no specific interactions but which are closely connected by thiocyanate ligands and phenyl rings.  相似文献   

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