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2(SeO 3)(Te 3O 7) (M?=?Co 2+, Ni 2+)]]>

机译:<![CDATA [新型混合阴离子组化合物的结构和磁性M 2 (SEO 3 )(TE 3 O 7 )(m?=?:supplace =“post”> 2 + ,ni 2 + )]]]>

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AbstractNovel mixed-anionic-group compounds M2(SeO3)(Te3O7) (M?=?Co2+, Ni2+) are successfully synthesized by a conventional hydrothermal method. Two compounds are isostructural which crystallize in the orthorhombic system of a space groupPnma. The framework shows a (MO6)chain structure along theb-axis, while SeO3groups are isolated and Te3O7groups form the (Te3O7)chains running along thea-axis. This is the first time to realize transition-metal compounds coexisting with Se4+and Te4+anionic groups. Magnetic measurements show that Co2(SeO3)(Te3O7) possesses an antiferromagnetic ordering at ~11?K, while Ni2(SeO3)(Te3O7) exhibits a similar antiferromagnetic ordering at ~31?K. Also, the fitting of magnetic susceptibility using a spin-chain model gives the exchange couplingJ/kB?=??1.515?K for Co2(SeO3)(Te3O7) andJ/kB?=??8.963?K for Ni2(SeO3)(Te3O7), respectively.Graphical abstractDisplay OmittedHighlights?Two new compounds M2(SeO3)(Te3O7) (M?=?Co and Ni) were synthesized by a conventional hydrothermal method.?The compounds exhibit a linear spin chain structure.?The first transition-metal compounds coexist with Se4+and Te4+anionic groups.]]>
机译:<![CDATA [ 抽象 新型混合阴离子基团物M 2 (SEO 3 )(TE 3 0 7 )(M = CO 2 + ,镍 2 + )被成功地通过传统的水热法合成。两种化合物是同构的,其结晶中的空间群的斜方晶系晶Pnma 。该框架示出了(MO 6 沿该链结构 b'/ CE:斜体>轴,而的SeO 3 组被分离和Te 3 0 7 基团形成(TE 3 0 7 链沿轴。这是第一次实现具有硒共存的过渡金属化合物 4 + 和Te 4 + 的阴离子基团。磁性测量表明,钴 2 (SEO 3 )(TE 3 0 7 )在〜11k上具有反铁磁性有序,而镍 2 (SEO 3 )(TE 3 0 < CE:INF LOC = “POST”> 7 )在〜31ķ表现出类似的反铁磁性有序。另外,使用旋链模型磁化率的嵌合给出了交换耦合Ĵ / K ?= ?? 1.515 K中钴α2 (SEO 3 )(TE 3 0 7 )和Ĵ / K =&8.963 K中的Ni 2 (SEO 3 /:INF>)(TE ):交 “> 3 0 7 图形抽象 显示中省略 亮点 两个新物M 2 (SEO 3 )(TE 3 0 7 )(M = Co和Ni)通过常规水热法合成 该化合物表现出的线性自旋链结构 第一过渡金属化合物共存与硒 4 + 和Te 4 +。阴离子基团 ]]>

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