首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Spin-spin interactions in the oxides A(3)M ' MO6 (M = Rh, Ir; A = Ca, Sr; M ' = alkaline earth, Zn, Cd, Na) of the K4CdCl6 structure type examined by electronic structure calculations
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Spin-spin interactions in the oxides A(3)M ' MO6 (M = Rh, Ir; A = Ca, Sr; M ' = alkaline earth, Zn, Cd, Na) of the K4CdCl6 structure type examined by electronic structure calculations

机译:通过电子结构计算研究了K4CdCl6结构类型的氧化物A(3)M'MO6(M = Rh,Ir; A = Ca,Sr; M'=碱土金属,Zn,Cd,Na)中的自旋-自旋相互作用

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摘要

The oxides A(3)M'MO6 (M = Rh, Ir: A = Ca, Sr; M' = alkaline earth, Zn, Cd) of the K4CdCl6 structure type consist of isolated (MO6)(8-) octahedral anions and exhibit an antiferromagnetic ordering at low temperatures. The spin-spin interactions in these oxides, Ca3NaMO6 (M = Ir, Ru), and Sr3NaRuO6 were examined by calculating how strongly the t(2g)-block levels of adjacent (MO6)((6+n)-) (n = 1, 2) anions interact in the presence and absence of the intervening cations A(2+) and M' (n+) (n = I, 2). Our calculations show that the spin-spin interactions in these oxides are three-dimensional, and the superexchange interactions occur mainly through the short intrachain and interchain M-O ... O-M linkages. When the Mn+ cation is very small compared with the A(2+) cation, the intrachain interaction is substantially stronger than the interchain interaction. The opposite is found when the sizes of the Mn+ and A(2+) cations become similar. [References: 32]
机译:K4CdCl6结构类型的氧化物A(3)M'MO6(M = Rh,Ir:A = Ca,Sr; M'=碱土金属,Zn,Cd)由孤立的(MO6)(8-)八面体阴离子和在低温下表现出反铁磁有序性。通过计算相邻(MO6)((6 + n)-)(t = 2g)的t(2g)嵌段水平有多强,检查了这些氧化物Ca3NaMO6(M = Ir,Ru)和Sr3NaRuO6中的自旋-自旋相互作用。 1,2)阴离子在存在和不存在中间阳离子A(2+)和M'(n +)(n = I,2)的情况下相互作用。我们的计算表明,这些氧化物中的自旋-自旋相互作用是三维的,超交换相互作用主要通过短链内和链间M-O ... O-M键发生。当Mn +阳离子与A(2+)阳离子相比非常小时,链内相互作用明显强于链间相互作用。当Mn +和A(2+)阳离子的大小变得相似时,发现相反的情况。 [参考:32]

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