Mialane Pierre, Dolbecq Anne, Marrot Jérôme, Rivière Eric, Sécheresse Francis
Institut Lavoisier, IREM, UMR 8637, Université de Versailles Saint-Quentin, 45 Avenue des Etats-Unis, 78035 Versailles cedex, France.
Chemistry. 2005 Mar 4;11(6):1771-8. doi: 10.1002/chem.200400769.
Reaction of Cu(II), [gamma-SiW10O36]8-, and N3- affords three azido polyoxotungstate complexes. Two of them have been characterized by single-crystal X-ray diffraction. Complex KNaCs10[{gamma-SiW10O36Cu2(H2O)(N3)2}2].26H2O (1) is obtained as crystals in few hours after addition of CsCl. This linear tetranuclear Cu(II) complex consists in two [gamma-SiW10O36Cu2(H2O)(N3)2]6- units connected through two W=O bridges. When the filtrate is left to stand for one night, a new complex is obtained. From both elemental analysis and IR spectroscopy, it has been postulated that this compound could be formulated K(1.5)Cs(5.5)[SiW10O37Cu2(H2O)2(N3)].14 H2O (1 a), showing the loss of one azido ligand per polyoxometalate unit. Finally, when no cesium salt is added to the reaction medium, the nonanuclear complex K12Na7[{SiW8O31Cu3(OH)(H2O)2(N3)}3(N3)].24 H2O (2) is obtained after three days. Compound 2 crystallizes in the R3c space group and consists in three {Cu3} units related by a C3 axis passing through the exceptional mu-1,1,1,3,3,3-azido bridging ligand. Each trinuclear Cu(II) unit is embedded in the [gamma-SiW8O31]10- ligand, an unprecedented tetravacant polyoxometalate, showing that partial decomposition of the [gamma-SiW10O36]8- precursor occurs with time in such experimental conditions. Magnetically, complex 1 behaves as two isolated {Cu2(mu(1,1)-N3)2} pairs in which the metal centers are strongly ferromagnetically coupled (J = +224 cm(-1), g = 2.20), the coupling through the W=O bridges being negligible. The magnetic behavior of complex 2 has also been studied. Relatively weak ferromagnetic couplings (J1 = +1.0 cm(-1), J2 = +20.0 cm(-1), g=2.17) have been found inside the {Cu3} units, while the intertrimeric magnetic interactions occurring through the hexadentate azido ligand have been found to be antiferromagnetic (J3 = -5.4 cm(-1)) and ferromagnetic (J4 = +1.3 cm(-1)) with respect to the end-to-end and end-on azido-bridged Cu(II) pairs, respectively.
铜(II)、[γ-SiW₁₀O₃₆]⁸⁻和N₃⁻反应生成三种叠氮基多金属氧酸盐配合物。其中两种已通过单晶X射线衍射进行了表征。在加入CsCl后数小时内,得到配合物KNaCs₁₀[{γ-SiW₁₀O₃₆Cu₂(H₂O)(N₃)₂}₂]·26H₂O(1)晶体。这种线性四核铜(II)配合物由两个通过两个W=O桥连接的[γ-SiW₁₀O₃₆Cu₂(H₂O)(N₃)₂]⁶⁻单元组成。当滤液静置一晚后,得到一种新的配合物。通过元素分析和红外光谱推测,该化合物可能的化学式为K₁.₅Cs₅.₅[SiW₁₀O₃₇Cu₂(H₂O)₂(N₃)]·14H₂O(1a),表明每个多金属氧酸盐单元损失了一个叠氮配体。最后,当反应介质中不添加铯盐时,三天后得到九核配合物K₁₂Na₇[{SiW₈O₃₁Cu₃(OH)(H₂O)₂(N₃)}₃(N₃)]·24H₂O(2)。化合物2结晶于R3c空间群,由三个{Cu₃}单元组成,这些单元通过一个穿过特殊的μ-1,1,1,3,3,3-叠氮桥连配体的C₃轴相关联。每个三核铜(II)单元嵌入在[γ-SiW₈O₃₁]¹⁰⁻配体中,这是一种前所未有的四空位多金属氧酸盐,表明在这种实验条件下,[γ-SiW₁₀O₃₆]⁸⁻前体随时间发生了部分分解。在磁性方面,配合物1表现为两个孤立的{Cu₂(μ(1,1)-N₃)₂}对,其中金属中心强烈铁磁耦合(J = +224 cm⁻¹,g = 2.20),通过W=O桥的耦合可忽略不计。也对配合物2的磁性行为进行了研究。在{Cu₃}单元内发现相对较弱的铁磁耦合(J₁ = +1.0 cm⁻¹,J₂ = +20.0 cm⁻¹,g = 2.17),而通过六齿叠氮配体发生的三聚体间磁相互作用对于端对端和端对叠氮桥连的铜(II)对分别为反铁磁(J₃ = -5.4 cm⁻¹)和铁磁(J₄ = +1.3 cm⁻¹)。