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首页> 外文期刊>European journal of inorganic chemistry >Encouraging chromium(III) ions to form larger clusters: Syntheses, structures, magnetic properties and theoretical studies of di- and octametallic Cr clusters
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Encouraging chromium(III) ions to form larger clusters: Syntheses, structures, magnetic properties and theoretical studies of di- and octametallic Cr clusters

机译:鼓励铬(III)离子形成更大的簇:双金属和八金属铬簇的合成,结构,磁性和理论研究

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Reaction of anhydrous CrCl2 with the tripodal ligands 1,1,1-tris(hydroxymethyl)ethane (H(3)thme), 1,1,1-tris(hydroxymethyl)propane (H(3)tmp) and pentaerythritol (H(4)peol) produces three new Crib clusters that have been structurally and magnetically characterised. The dimeric complex [Cr-2(H(2)tmp)(2)-Cl-4]center dot 2MeOH (1.2MeOH) is generated under reflux. An analogous reaction, but under solvothermal conditions produces the octametallic species [Cr8O2(thme)(2)(Hthme)(4)Cl-6]center dot 2MeOH (2.2MeOH) and [Cr8O2(Hpeol)(2)(H(2)peol)(4)Cl-6]center dot 3MeOH (3.3MeOH). Complex 1 is a simple dimeric species whereas the structures of 2 and 3 are based on the decametallate {M10O28}(26-) ion. Variable-temperature direct-current (dc) magnetic susceptibility data were collected for complexes 1 and 2 in the 1.8-300 K temperature range in fields up to 5.0 T. Complex 1 has a ground state of S = 0 with the best-fit parameters J = -12.30 +/- 0.04 cm(-1) and g = 1.990 +/- 0.003. Electronic structure calculations based on density functional theory (DFT) on 1 and 2 have been carried out and good agreement with the experimental data was found for 1. For 2, the theoretical results have been used as starting point to fit the J values to the experimental data, revealing the presence of competing antiferromagnetic (J(4,7) = -39.0 cm(-1); J(3,7) = J(4,6) = +1.1 cm(-1), J(4,5) = J(3,4) = -20.0 cm(-1), J(3,6) = -16.0 cm(-1) and J(1,3) = J(1,6) = J(1,4) = J(1,7) = -4.8 cm(-1)) exchange interactions between the Cr-III centres that suggests a singlet ground state with very close S = 1, 2, 3 and 4 excited states. Magneto-structural correlations developed on a model complex based on 1 show a strong dependence of J with Cr-O-Cr angle. A similar magneto-structural correlation is found for the J values obtained by theoretical calculations on 2. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
机译:无水CrCl2与三脚架配体1,1,1-三(羟甲基)乙烷(H(3)thme),1,1,1-三(羟甲基)丙烷(H(3)tmp)和季戊四醇(H( 4)peol)产生了三个新的Crib团簇,这些团簇在结构和磁学上都有特征。在回流下生成二聚体[Cr-2(H(2)tmp)(2)-Cl-4]中心点2MeOH(1.2MeOH)。发生类似反应,但在溶剂热条件下产生八金属物种[Cr8O2(thme)(2)(Hthme)(4)Cl-6]中心点2MeOH(2.2MeOH)和[Cr8O2(Hpeol)(2)(H(2 )peol)(4)Cl-6]中心点3MeOH(3.3MeOH)。配合物1是一个简单的二聚体物种,而2和3的结构则基于十金属离子{M10O28}(26-)离子。在温度高达1.5 T的磁场中,在1.8-300 K的温度范围内收集了配合物1和2的可变温度直流(dc)磁化率数据。配合物1的基态S = 0,具有最佳拟合参数J = -12.30 +/- 0.04 cm(-1),g = 1.990 +/- 0.003。进行了基于密度泛函理论(DFT)的1和2的电子结构计算,发现与1的实验数据吻合良好。对于2,将理论结果用作起点,以使J值适合于实验数据,揭示存在竞争性反铁磁(J(4,7)= -39.0 cm(-1); J(3,7)= J(4,6)= +1.1 cm(-1),J(4 ,5)= J(3,4)= -20.0 cm(-1),J(3,6)= -16.0 cm(-1)和J(1,3)= J(1,6)= J( Cr-III中心之间的1,4)= J(1,7)= -4.8 cm(-1))交换相互作用,表明具有非常接近的S = 1、2、3和4激发态的单重基态。在基于1的模型复合体上开发的磁结构相关性显示J与Cr-O-Cr角的强烈依赖性。对于在2上通过理论计算获得的J值,发现了类似的磁结构相关性。((c)Wiley-VCH Verlag GmbH&Co. KGaA,69451 Weinheim,德国,2006年)

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