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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Synthesis, Structures, and Luminescence Properties of Lanthanide Complexes with Structurally Related New Tetrapodal Ligands Featuring Salicylamide Pendant Arms
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Synthesis, Structures, and Luminescence Properties of Lanthanide Complexes with Structurally Related New Tetrapodal Ligands Featuring Salicylamide Pendant Arms

机译:具有水杨酰胺侧链的结构相关新四脚体配体的镧系元素配合物的合成,结构和发光性质

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To explore the relationships between the structures of ligands and their complexes, we have synthesized and characterized a series of lanthanide complexes with two structurally related ligands, 1,1,1,1-tetrakis{[(2'-(2-benzylaminoformyl))phenoxyl]methyl)methane (L-I) and 1,1,1,1-tetrakis([(2'-(2-picolyaminoformyl))phenoxyl]methyl)methane (L-II). A series of zero- to three-dimensional lanthanide coordination complexes have been obtained by changing the substituents on the Pentaerythritol. Our results revealed that, complexes of the L-I ligand, {Ln(4)L(3)(I)(NO3)(12) center dot nC(4)H(10)O}(infinity) (Ln = Nd, Eu, Tb, Er, n = 3 or 6)] show the binodal 3,4-connected three-dimensional interpenetration coordination polymers with topology of a (83)4(86)3 notation. Compared to L-I, complexes of L-II present a cage-like homodinuclear [Ln(2)L(2)(II)(NO3)(6) center dot 2H(2)O) center dot nH(2)O (Ln = Nd, Tb, Dy, n = 0 or 1) or a helical one-dimensional coordination {[ErLII(NO3)(3) center dot H2O] center dot H2O}(infinity) polymer. The luminescence properties of the resulting complexes formed with ions used in fluoroimmunoassays (Ln = Eu, Tb) are also studied in detail. It is noteworthy that subtle variation of the terminal group from benzene to pyridine not only sensibly affects the overall molecular structures but also the luminescence properties as well.
机译:为了探索配体的结构与其配合物之间的关系,我们合成并表征了具有两个与结构相关的配体1,1,1,1-tetrakis {[((2'-(2-苄氨基甲酰基))苯氧基]甲基)甲烷(LI)和1,1,1,1-四([((2'-(2-picolyaminoformyl))苯氧基]甲基)甲烷(L-II)。通过改变季戊四醇上的取代基获得了一系列的零至三维镧系配位络合物。我们的研究结果表明,LI配体的复合物{Ln(4)L(3)(I)(NO3)(12)中心点nC(4)H(10)O}(无穷大)(Ln = Nd,Eu ,Tb,Er,n = 3或6)]显示具有(83)4(86)3表示法拓扑的双斜体3,4-连接的三维互穿配位聚合物。与LI相比,L-II的络合物呈笼状同核[Ln(2)L(2)(II)(NO3)(6)中心点2H(2)O)中心点nH(2)O(Ln = Nd,Tb,Dy,n = 0或1)或螺旋一维配位{[ErLII(NO3)(3)中心点H2O]中心点H2O}(无穷大)聚合物。还详细研究了与用于氟免疫测定法(Ln = Eu,Tb)的离子形成的络合物的发光特性。值得注意的是,末端基团从苯到吡啶的细微变化不仅明显影响了整体分子结构,而且还影响了发光性能。

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