首页> 外文期刊>Crystal Research and Technology: Journal of Experimental and Industrial Crystallography >Synthesis, crystal structure, magnetic characterization and spectroscopic properties of a new dinuclear iron(III) complex asymmetrically bridged by a phenoxo and methoxo groups
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Synthesis, crystal structure, magnetic characterization and spectroscopic properties of a new dinuclear iron(III) complex asymmetrically bridged by a phenoxo and methoxo groups

机译:新型不对称苯氧基和甲氧氧基桥联的双核铁(III)配合物的合成,晶体结构,磁性表征和光谱性质

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摘要

Dinuclear iron(III) derivative of Fe2L1(OCH3)Cl-2 (L-1=1,3-bis[N-(5-bromo-2-hydroxybenzylidene)-2-aminoethyl]-2-(5-bromo-2-hydroxyphenyl)imidazolidine) has been synthesized, its crystal structure determined and magnetically characterized. The title compound crystallizes in orthorhombic space group Pbcn with cell parameters a = 12.9770(10), 18.7930(10), 25.2950(10) angstrom, V = 6168.9(6)angstrom(3), Z = 8, D-cal = 1.951 Mg/m(3). The two iron(III) ions are asymmetrically bridged by a phenoxo and methoxo groups in the compound. The iron(III) centers are separated by 3.166(3) angstrom. Magnetic susceptibilities of the complex were measured over the range 5-298 K and the observed data were successfully simulated by the equation based on the spin-Hamiltonian operator. Magnetic susceptibility measurements indicate very weak antiferromagnetic coupling between the iron(III) ions with J = -11.5 cm(-1). The comparison of the magnetic and structural parameters of the investigated compound is given and the nature of the magnetic super-exchange interaction of the title compound is compared with similar dinuclear iron(III) complexes.
机译:Fe2L1(OCH3)Cl-2(L-1 = 1,3-双[N-(5-溴-2-羟基亚苄基)-2-氨基乙基] -2-(5-溴-2)的双核铁(III)衍生物-羟基苯基)咪唑烷)已经合成,其晶体结构已确定并经磁学表征。标题化合物在正交晶空间群Pbcn中结晶,单元参数为a = 12.9770(10),18.7930(10),25.2950(10)埃,V = 6168.9(6)埃(3),Z = 8,D-cal = 1.951 Mg / m(3)。两个铁(III)离子被化合物中的苯氧基和甲氧基不对称桥接。铁(III)中心相隔3.166(3)埃。在5-298 K范围内测量了复合物的磁化率,并通过基于自旋哈密顿算子的方程式成功地模拟了观测数据。磁化率测量结果表明,铁(III)离子之间的反铁磁耦合非常弱,J = -11.5 cm(-1)。给出了所研究化合物的磁性和结构参数的比较,并且将标题化合物的磁性超交换相互作用的性质与类似的双核铁(III)配合物进行了比较。

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