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首页> 外文期刊>Russian Journal of Coordination Chemistry >Synthesis, Crystal Structure, and Biological Activity of the Binuclear Complex [Pr2(C_(10)H9N2O4)2(C7H5O3)4(H2O)2]·2H2O~1
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Synthesis, Crystal Structure, and Biological Activity of the Binuclear Complex [Pr2(C_(10)H9N2O4)2(C7H5O3)4(H2O)2]·2H2O~1

机译:双核配合物[Pr2(C_(10)H9N2O4)2(C7H5O3)4(H2O)2]·2H2O〜1的合成,晶体结构和生物活性

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A novel binuclear praseodymium(III) complex with N-(2-propionyl)salicyloylhydrazone (C_(10)H_(10)N2O4, H3L) and p-hydroxybenzoic acid (C7H6O3, Phba) was prepared in a H2O-C2H5OH mixed solution, and the crystal structure of [Pr2(H2L)2(Phba)4(H26)2]·2H2O ( ) was determined by X-ray single crystal diffractometry. Complex crystallizes in the monoclinic system, space group P2_1/c, a = 1.1050(4), b = 1.9534(7), c = 1.2376(4) A, p = 94.955(7)°, and Z= 4. In the structure each Pr~(3)ion lies in a single capped square antiprism geometry coordinated by carboxyl O and acyl O atoms and azomethine N atom of one ligand (H2L~ form), which coordinates via the keto form, four carboxyl O atoms from two Phba, and O atoms of two water molecules. In each molecule, two tridentate ligands were coordinated by the H2L~- form, and each Pr~(3+) ion was chelated by the carboxyl group from Phba. The carboxyl groups of H2L~- and other two Phba were coordinated via μ2-bridging form and bidentate bridging form, respectively. Complex and ligands Phba and H3L were also searched for biological activity against Valsa mali by the growth rate method. The result showed that the inhibitory rate of ligands Phba and H3L is better than complex , especially Phba.
机译:在H2O-C2H5OH混合溶液中制备了新型的N-(2-丙酰基)水杨酰hydr(C_(10)H_(10)N2O4,H3L)和对羟基苯甲酸(C7H6O3,Phba)的双核(III)络合物,用X射线单晶衍射法测定[Pr2(H2L)2(Phba)4(H26)2]·2H2O()的晶体结构。复合物在单斜晶系空间群P2_1 / c,a = 1.1050(4),b = 1.9534(7),c = 1.2376(4)A,p = 94.955(7)°和Z = 4时结晶。每个Pr〜(3)离子的结构为一个封闭的方形反棱镜几何结构,该几何结构由一个配体(H2L〜形式)的羧基O和酰基O原子以及偶氮甲碱N原子配位,该配位基通过酮形式配位,来自两个配位基的四个羧基O原子Phba和两个水分子的O原子。在每个分子中,两个三齿配体通过H2L-配位,每个Pr_(3+)离子都被Phba的羧基螯合。 H2L〜-和其他两个Phba的羧基分别通过μ2-桥联形式和双齿桥联形式进行配位。还通过生长速率法研究了复合物和配体Phba和H3L的抗Valsa mali生物活性。结果表明,配体Phba和H3L的抑制率优于配合物,尤其是Phba。

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