Synthesis, structures, and magnetic properties of a family of 3d-4f [Na2Fe6Ln2] complexes (Ln = Y, Gd and Dy): effect of ligands on the connection of inorganic subunits.

Synthesis, structures, and magnetic properties of a family of 3d-4f [Na2Fe6Ln2] complexes (Ln = Y, Gd and Dy): effect of ligands on the connection of inorganic subunits.
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DOI:
10.1039/c2dt31050c
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发表时间:
2013-01
影响因子:
4
通讯作者:
Qi Zhou;Fen Yang;Dan Liu;Yu Peng;Guanghua Li;Zhan Shi;S. Feng
Qi Zhou;Fen Yang;Dan Liu;Yu Peng;Guanghua Li;Zhan Shi;S. Feng
中科院分区:
化学2区
文献类型:
--
作者:
Qi Zhou;Fen Yang;Dan Liu;Yu Peng;Guanghua Li;Zhan Shi;S. Feng

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一族 3d-4f 异金属化合物 [Na(2)Fe(III)(6)Dy(III)(2)(N(3))(4)(HL)(4)(CH(3)O)(4)(PhCO(2))(6)] (1, H(4)L = 2-{[(2-羟基-3-甲氧基苯基)亚甲基]氨基}-2-(羟甲基)-1,3-丙二醇), [Na(2)Fe(III)(6)Dy(III)(2)(N(3))(4)(L')(4)(CH(3)O)(4)(PhCO(2))(6)(H(2)O)] (2, H(3)L' = (E)-2-乙基-2-(2-羟基-3-甲氧基亚苄基氨基)丙烷-1,3-二醇), [Na(2)Fe(III)(6)Dy(III)(2)(N(3))(4)(L')(4)(CH(3)O)(4)(Bu(t)CO(2))(6)] (3) [Na(2)Fe(III)(6)Y(III)(2)(N(3))(4)(L')(4)(CH(3)O)(4)(PhCO(2))(6)(H(2)O)](4),和 [Na(2)Fe(III)(6)Gd(III)(2)(N(3))(4)(L')(4)(CH(3)O)(4)(PhCO(2))(6)(CH(3)OH)(2)](5) 使用希夫碱配体、三核铁前体配合物、叠氮化物和镧系元素硝酸盐作为反应物制备。在化合物1和2中,[Na(2)Fe(III)(6)Dy(III)(2)]簇的结构形成一对顺式、反式异构体,其中属于席夫碱配体的游离羟基被甲基取代。当使用新戊酸酯代替体积较大的苯甲酸酯时,反式-[Na(2)Fe(III)(6)Dy(III)(2)]簇在化合物2中形成菱形网格状层状结构时充当网络节点。化合物2、4和5具有相似的金属核,只是具有不同的晶体溶剂分子。所有化合物的磁性测量表明金属中心之间的主要反铁磁相互作用。
A family of 3d-4f heterometallic compounds [Na(2)Fe(III)(6)Dy(III)(2)(N(3))(4)(HL)(4)(CH(3)O)(4)(PhCO(2))(6)] (1, H(4)L = 2-{[(2-hydroxy-3-methoxyphenyl)methylene]amino}-2-(hydroxymethyl)-1,3-propanediol), [Na(2)Fe(III)(6)Dy(III)(2)(N(3))(4)(L')(4)(CH(3)O)(4)(PhCO(2))(6)(H(2)O)] (2, H(3)L' = (E)-2-ethyl-2-(2-hydroxy-3-methoxybenzylideneamino)propane-1,3-diol), [Na(2)Fe(III)(6)Dy(III)(2)(N(3))(4)(L')(4)(CH(3)O)(4)(Bu(t)CO(2))(6)] (3) [Na(2)Fe(III)(6)Y(III)(2)(N(3))(4)(L')(4)(CH(3)O)(4)(PhCO(2))(6)(H(2)O)] (4), and [Na(2)Fe(III)(6)Gd(III)(2)(N(3))(4)(L')(4)(CH(3)O)(4)(PhCO(2))(6)(CH(3)OH)(2)] (5) have been prepared using Schiff-base ligands, trinuclear iron precursor complexes, azides and lanthanide nitrates as reactants. In compounds 1 and 2, the structure of the [Na(2)Fe(III)(6)Dy(III)(2)] cluster forms a couple of cis,trans-isomers with substitution of methyl for a free hydroxyl group which belongs to the Schiff-base ligand. When the pivalates are employed instead of bulkier benzoates, the trans-[Na(2)Fe(III)(6)Dy(III)(2)] clusters act as network nodes in the formation of rhombic grid-like layered structures in compound 2. Compounds 2, 4 and 5 have similar metallic cores, only with different crystal solvent molecules. The magnetic measurements on all the compounds indicate dominant antiferromagnetic interactions between the metal centers.