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三齿配体钌配合物的合成、结构和性质:含有{RuNO}5 部分的罕见的钌亚硝酰配合物的分离和表征。

Syntheses, structures and properties of ruthenium complexes of tridentate ligands: isolation and characterization of a rare example of ruthenium nitrosyl complex containing {RuNO}5 moiety.

机构信息

Department of Chemistry, Indian Institute of Technology, Roorkee, Roorkee-247667, Uttarakhand, India.

出版信息

Dalton Trans. 2013 Oct 7;42(37):13444-52. doi: 10.1039/c3dt00027c. Epub 2013 Jul 29.

Abstract

Novel ruthenium complexes [Ru(L(1))(NO)Cl2] (1), [Ru(L(2))(PPh3)Cl2] (2), [Ru(L(2))(PPh3)(NO2)Cl] (3) and Ru(L(2))(PPh3)(NO)Cl2 (4) (where L(1)H = N'-phenyl-N'-(pyridin-2-yl)picolinohydrazide and L(2) = (1-phenyl-1-(pyridin-2-yl)-2-(pyridin-2-ylmethylene)hydrazine) were synthesized. These complexes were characterized by using IR, UV-Vis, elemental analysis, electrochemical and NMR spectral studies. The molecular structures of nitrosyl complexes 1 and 4 were determined by X-ray crystallographic studies. Complexes 1 and 4 readily released NO under visible and ultraviolet light and free NO was transferred to reduced myoglobin. The amount of photoreleased NO was estimated using Griess reagent assay. During photolysis of NO, the generation of reactive nitrogen or/and reactive oxygen species was determined by DPPH (2,2-diphenyl-1-picrylhydrazine) radical quenching studies under aerobic conditions. A paramagnetic complex Ru(L(2))(PPh3)(NO)Cl3 (5) was synthesized via chemical oxidation of 4 with an excess of ceric ammonium nitrate (CAN) in acetonitrile. Complex 5 was characterized by UV-Vis, IR, elemental analysis and EPR spectral studies which authenticated the presence of the {RuNO}(5) moiety in 5. Theoretical investigation by DFT calculation supported the oxidation of complex 4 having {RuNO}(6) species and the formation of 5 containing {RuNO}(5).

摘要

新型钌配合物[Ru(L(1))(NO)Cl2](1)、[Ru(L(2))(PPh3)Cl2](2)、[Ru(L(2))(PPh3)(NO2)Cl](3)和Ru(L(2))(PPh3)(NO)Cl2(4)(其中 L(1)H = N'-苯基-N'-(吡啶-2-基)吡啶甲酰肼,L(2) = (1-苯基-1-(吡啶-2-基)-2-(吡啶-2-基亚甲基)肼)被合成。这些配合物通过红外、紫外可见、元素分析、电化学和 NMR 光谱研究进行了表征。通过 X 射线晶体学研究确定了亚硝酰配合物 1 和 4 的分子结构。配合物 1 和 4 在可见光和紫外光下容易释放 NO,并且游离的 NO 被转移到还原的肌红蛋白中。通过格里试剂测定法估计光解产生的 NO 量。在 NO 的光解过程中,通过 DPPH(2,2-二苯基-1-苦基肼)自由基淬灭研究在有氧条件下确定了活性氮和/或活性氧物质的生成。通过过量硝酸铈铵(CAN)在乙腈中的化学氧化,合成了顺磁性配合物Ru(L(2))(PPh3)(NO)Cl3(5)。通过 UV-Vis、IR、元素分析和 EPR 光谱研究对 5 进行了表征,这些研究证实了 5 中存在{RuNO}(5)部分。通过 DFT 计算的理论研究支持了具有{RuNO}(6)物种的配合物 4 的氧化和含有{RuNO}(5)的 5 的形成。

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