首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Facile synthesis of a new Cu(II) complex with an unsymmetrical ligand and its use as an O-3 donor metalloligand in the synthesis of Cu(II)-Mn(II) complexes: structures, magnetic properties, and catalytic oxidase activities
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Facile synthesis of a new Cu(II) complex with an unsymmetrical ligand and its use as an O-3 donor metalloligand in the synthesis of Cu(II)-Mn(II) complexes: structures, magnetic properties, and catalytic oxidase activities

机译:容易合成具有非对称配体的新型Cu(II)络合物及其用作Cu(II)-MN(II)复合物的合成中的O-3供体金属溶胶剂:结构,磁性和催化氧化酶活性

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摘要

A new, facile Cu(II) template method has been employed for the unsymmetrical dicondensation of 1,2-ethylenediamine with salicylaldehyde and o-vanillin. The mononuclear complex, [CuL] (1), thus obtained, has been used as an O-3 donor metalloligand for the synthesis of four new Cu(II)-Mn(II) complexes, [(CuL)MnCl2] (2), [(CuL)Mn(NO3)(2)(CH3OH)](n) (3), {[(CuL)Mn(benz)(H2O)](2)center dot(CuL)(2)(ClO4)(2)} (4) and [(CuL)Mn(benz)Cl](2) (5) (where benz = benzoate). Single-crystal structural analyses reveal that 2 is a dinuclear complex while complex 3 is polymeric with a repeating dinuclear [(CuL)Mn(NO3)(2)(CH3OH)] unit, linked via the nitrate ion. Both 4 and 5 are discrete tetranuclear complexes, where the dinuclear units [(CuL)Mn(benz)(H2O)] and [(CuL)Mn(benz)Cl] are connected by double benzoate and double chloride bridges, respectively. In complex 4, two monomeric [CuL] units are cocrystallized with the tetranuclear complex. An important difference in the structure of 4 from the other three complexes is that one solvent water molecule is coordinated to each Mn(II) ion, which makes complex 4 catalytically very active towards mimicking catecholase and phenoxazinone synthase-like oxidation reactions. The turnover numbers (k(cat)) for the aerial oxidation of 3,5-di-tert-butylcatechol and o-aminophenol are 399 h(-1) and 230 h(-1), respectively. The evidence of the intermediate species in the mass spectra indicates possible heterometallic cooperation where the Mn(II) center helps in substrate binding and Cu(II) participates in the oxidation reactions with molecular oxygen. Cyclic voltammetry measurements suggest the reduction of Cu(II) to Cu(I) during the catalytic process. Temperature-dependent dc molar magnetic susceptibility measurements reveal that complexes 2-5 are antiferromagnetically coupled with the exchange coupling constants (J) of J = -13.5 cm(-1) and J = -13.5 cm(-1) for 2 and 3, respectively, J(1) = -12.6 cm(-1) and J(2) = -1.20 cm(-1) for complex 4 and J(1) = -13.24 cm(-1) and J(2) = 0.36 cm(-1) for complex 5 as is expected from the Cu-O-Mn bridging angles.
机译:一种新的容易Cu(II)模板方法已经用于1,2-乙二胺与水杨醛和O-香草蛋白的不对称二染色。由此获得的单核复合物[CUL](1)已被用作O-3供体金属化物标配合,用于合成四种新的Cu(II)-MN(II)配合物,[(CUL)MnCl2](2) ,[(CUL)Mn(NO 3)(2)(2)(2)(3)(3),{[(CUL)Mn(苯兹)(H2O)](2)中心点(CUL)(2)(CLO4) (2)}(4)和[(CUL)Mn(苯兹)Cl](2)(5)(其中苯子=苯甲酸盐)。单晶结构分析显示,2是正核复合物,而复合物3是聚合物,其具有通过硝酸根离子连接的重复的二核[(NO 3)(2)(2)(2)(2)(2)(2)(2))单元。图4和5均为离散的四核复合物,其中二核单元[(CUL)Mn(苯所述苯)(H2O)]和[(CUL)Mn(Benz)Cl]分别通过双苯甲酸和双氯化物桥连接。在复合物4中,两种单体[CUL]单位是通过四核络合物的CoCry化。来自其他三个络合物的4的结构的重要差异是,对每个Mn(II)离子配位的一个溶剂水分子,其使复合物4催化非常活跃地朝向模拟的儿茶酚酶和苯氧嗪酮合成酶样氧化反应。用于3,5-二叔丁基基丙醇和O-氨基苯酚的空中氧化的周转数(K(猫))分别为399h(-1)和230h(-1)。质谱中中间物质的证据表明了可以在底物结合和Cu(II)中有助于用分子氧的氧化反应参与氧化反应的可能的杂动机合作。循环伏安法测量表明在催化过程中,Cu(II)在Cu(I)中的降低。温度依赖性DC摩尔磁化率测量显示,复合物2-5与J = -13.5cm(-1)和J = -13.5cm(-1)的交换耦合常数(j)进行反式磁极耦合2和3,分别,j(1)= -12.6cm(-1)和j(2)= -1.20cm(-1)用于复合4和j(1)= -13.24cm(-1)和j(2)= 0.36从Cu-O-Mn桥接角度预期的复合物5的Cm(-1)。

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