首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >New tetranuclear metal carboxylate clusters with the [M-4(mu(3)-O)(2)](8+) (M = Mn-III or Fe-III) cores: crystal structures and properties of [Mn4O2Cl2(O2CC6H3F2-3,5)(6)(py)(4)], [Fe4O2Cl2(O2CMe)(6)(bpy)(2)] and [NBu4n][Fe4O2(O2CMe)(7)(pic)(2)]
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New tetranuclear metal carboxylate clusters with the [M-4(mu(3)-O)(2)](8+) (M = Mn-III or Fe-III) cores: crystal structures and properties of [Mn4O2Cl2(O2CC6H3F2-3,5)(6)(py)(4)], [Fe4O2Cl2(O2CMe)(6)(bpy)(2)] and [NBu4n][Fe4O2(O2CMe)(7)(pic)(2)]

机译:具有[M-4(mu(3)-O)(2)](8 +)(M = Mn-III或Fe-III)核的新四核金属羧酸盐簇:[Mn4O2Cl2(O2CC6H3F2- 3,5)(6)(py)(4)],[Fe4O2Cl2(O2CMe)(6)(bpy)(2)]和[NBu4n] [Fe4O2(O2CMe)(7)(pic)(2)]

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摘要

A variety of synthetic procedures have been employed that allow access to three new tetranuclear [M-4(mu(3)-O)(2)](8+) (M = Mn-III or Fe-III) complexes. The complex [Fe4O2Cl2(O2CMe)(6)(bpy)(2)] displays an unusual structural asymmetry in its core that can be described as a hybrid of the bent (butterfly) and planar dispositions of four M atoms seen previously in such compounds. Magnetochemical and Fe-57 Mossbauer studies on this compound showed that its structural asymmetry has little influence on these properties compared with the more symmetric types. The complex [NBu4n][Fe4O2(O2CMe)(7)(pic)(2)] has been prepared by an unusual chelate substitution in [NBu4n][Fe4O2(O2CMe)(7)(bpy)(2)] that does not disrupt the core or the bridging carboxylate groups. [References: 30]
机译:已经采用了各种合成程序,可以访问三个新的四核[M-4(mu(3)-O)(2)](8+)(M = Mn-III或Fe-III)复合物。配合物[Fe4O2Cl2(O2CMe)(6)(bpy)(2)]在其核中显示出异常的结构不对称性,可以描述为先前在此类化合物中看到的四个M原子的弯曲(蝴蝶状)和平面排列的混合体。对该化合物的磁化学和Fe-57 Mossbauer研究表明,与更对称的类型相比,其结构不对称对这些性质的影响很小。复合物[NBu4n] [Fe4O2(O2CMe)(7)(pic)(2)]是通过在[NBu4n] [Fe4O2(O2CMe)(7)(bpy)(2)]中进行不寻常的螯合取代制得的破坏核心或桥接羧酸酯基团。 [参考:30]

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