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首页> 外文期刊>New Journal of Chemistry >Design of 3-D europium(m)-organic frameworks based on pyridine carboxylate N-oxide and acyclic binary carboxylate: syntheses, structures, and luminescence properties
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Design of 3-D europium(m)-organic frameworks based on pyridine carboxylate N-oxide and acyclic binary carboxylate: syntheses, structures, and luminescence properties

机译:基于吡啶羧酸N-氧化物和无环二元羧酸的3-D euro(m)-有机骨架的设计:合成,结构和发光性质

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Four europium(III) complexes of 3-D open frameworks [Eu2(NNO)4(ox)(H2O)2]_n (1), [Eu2(INO)2(ox)2(H2O)2]_n (2), {[Eu2(INO)2(suc)2]·2.99H2O}_n (3) and {[Eu2(suc)3(H2O)2]·H2O}_n (4) (HNNO = nicotinic acid N-oxide, H2ox = oxalic acid, HINO = isonicotinic acid, H2suc = succinic acid) have been synthesized and characterized by IR, elemental analysis, TG/DTA and single-crystal X-ray diffraction analysis. Each of the four complexes has 1-D channels, and in 3 and 4 these are filled with solvent water molecules, making them bigger than in 1 and 2, where no lattice water molecules can reside. The formation of the four 3-D europium(III) frameworks of different molecular and crystal structures reflects the influence of the ligands' coordination modes, the length of the acyclic binary carboxylates, the ligand conformation as well as the molar ratio of reactants. At room temperature, all the complexes in the solid state exhibit typical red luminescence from Eu~(3+) ions, indicating effective energy transfer from the ligand to Eu~(3+) ion; however, their luminescence intensities are clearly different. The luminescence of 3 is the most intense due to the absence of coordinated water, while the complexes 1, 2 and 4 exhibit weaker luminescence due to oscillation of coordinated water molecules, which partially quenches their luminescence.
机译:3-D开放框架的四个euro(III)络合物[Eu2(NNO)4(ox)(H2O)2] _n(1),[Eu2(INO)2(ox)2(H2O)2] _n(2) ,{[Eu2(INO)2(suc)2]·2.99H2O} _n(3)和{[Eu2(suc)3(H2O)2]·H2O} _n(4)(HNNO =烟酸N-氧化物,已经合成了H2ox =草酸,HINO =异烟酸,H2suc =琥珀酸,并通过红外,元素分析,TG / DTA和单晶X射线衍射分析对其进行了表征。四个复合物中的每一个都有一维通道,在3和4中,这些通道充满了溶剂水分子,这使其比在其中没有晶格水分子存在的1和2中更大。四个不同分子和晶体结构的3-D((III)骨架的形成反映了配体配位方式,无环二元羧酸盐的长度,配体构象以及反应物摩尔比的影响。在室温下,所有固态的配合物都从Eu〜(3+)离子显示出典型的红色发光,表明从配体到Eu〜(3+)离子的有效能量转移。但是,它们的发光强度明显不同。由于不存在配位水,3的发光最强,而配合物1,2和4由于配位水分子的振荡而显示出较弱的发光,这部分消灭了它们的发光。

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