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Organometallic Compounds of the Lanthanides. LIII. (C5H5Gd)52-OCH3)43-OCH3)45-O) and [Na2(tC4H9OGd)43-OtC4H9)86-O)], two New Alkoxi Gadolinium Clusters with Interstitial Oxygen Gadolinium trichloride reacts in tetrahydrofurane with cyclopentadienyl sodium and two equivalents of sodium methoxide with formation of (C5H5Gd)52-OCH3)43-OCH3)45-O) ( 1 ), and with potassium tert-butoxide with formation of [Na2(tC4H9OGd)43-OtC4H9)86-O)] ( 2 ). The X-ray structure of 1 shows a tetragonal pyramide build up by five gadolinium atoms, containing an oxygen atom in the center of the base and eight bridging methoxo groups. The structure of 2 consists of an oxygen centered octahedron build up by two sodium and four gadolinium atoms, connected by eight bridging tert-butoxy groups and four terminal butoxides. The monoclinic crystals of 1 , space group I2/a have the following crystallographic data: a = 2 276.9(5) pm, b = 2 063.1(6) pm, c = 3 152.2(3) pm, β = 90.7(1)°, Z = 12, Dcalcd 1.85 g · cm?3, R = 0.0519. 2 crystallizes tetragonal, space group I4/mmm with a = 1 728.5(4) pm, b = 1 031.0(3) pm, Z = 2, Dcalcd 1.69 g · cm?3, R = 0.0682.  相似文献   

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The three title compounds, namely 4‐phenyl‐1H‐imidazolium hexa‐μ2‐chloro‐chloro‐μ4‐oxo‐tris­(4‐phenyl‐1H‐imidazole‐κN1)­tetra­copper(II) monohydrate, (C9H9N2)[Cu4Cl7O(C9H8N2)3]·H2O, hexa‐μ2‐chloro‐μ4‐oxo‐tetra­kis­(pyridine N‐oxide‐κO)tetra­copper(II), [Cu4Cl6O(C5H5NO)4], and hexa‐μ2‐chloro‐tetra­kis(2‐methyl‐1H‐imidazole‐κN1)‐μ4‐oxo‐tetra­copper(II) methanol trisolvate, [Cu4Cl6O(C4H6N2)4]·3CH4O, exhibit the same Cu4OCl6 framework, where the O atom at the centre of an almost regular tetra­hedron bridges four copper cations at the corners. This group is in turn surrounded by a Cl6 octa­hedron, leading to a rather globular species. This special arrangement of the CuII cations results in a diversity of magnetic behaviours.  相似文献   

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The largest multinuclear zinc framework synthesized is in the title compound (see picture), which contains structural features closely related to the motifs found in layered and three‐dimensional zincophosphates and zincophosphonates. The reactive centers make this zincophosphonate a viable precursor for the synthesis of porous zincophosphonate materials.  相似文献   

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Synthesis and Crystal Structures of the Phosphaneimine Complexes [Cu(μ-HNPEt3)]4(O3S–CF3)4 and [Pt2Me6(μ-I)2(μ-HNPMe3)] The title compounds have been prepared by the reaction of copper(I)triflate with [NiBr(NPEt3)]4 in CH2Cl2 suspension in the presence of water, and by the reaction of [PtMe3I]4 with Me3SiNPMe3 in boiling toluene in the presence of cesium fluoride, respectively. According to the crystal structure determinations the cation of the copper complex forms tetrameric units [Cu(HNPEt3)]44+ with S4 symmetry with Cu–N bond lengths of 191.6 and 192.1 pm. In the platinum complex the platinum atoms are linked by two μ-I bridging atoms as well as by the μ-N atom of the HNPMe3 ligand with Pt–N bond lengths of 228.1 and 229.5 pm.  相似文献   

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Crystal Structures of [Ti(NPh2)4] and [Ti2(μ-O)(NPh2)6] [Ti(NPh2)4] has been prepared from TiCl3(THF)3 and LiNPh2, the μ-oxo complex [Ti2(μ-O)(NPh2)6] results from partial hydrolysis of [Ti(NPh2)4] in toluene solution. Both complexes are characterized by crystal structure determinations. In [Ti(NPh2)4] the titanium atom is coordinated by the four nitrogen atoms in a distorted tetrahedral fashion with Ti–N bond lengths of 193.8 pm in average. In [Ti22-O)(NPh2)6] the μ-oxo ligand forms a linear symmetric TiOTi bridge with rTiO = 181.2 pm and TiN = 193.4 pm in average.  相似文献   

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