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新型双(吡唑)-2,2'-联吡啶混合配体铜(II)配合物的合成、表征及高效超氧化物歧化酶样活性

Synthesis, characterization and potent superoxide dismutase-like activity of novel bis(pyrazole)-2,2'-bipyridyl mixed ligand copper(II) complexes.

作者信息

Potapov Andrei S, Nudnova Evgenia A, Domina Galina A, Kirpotina Liliya N, Quinn Mark T, Khlebnikov Andrei I, Schepetkin Igor A

机构信息

Department of Chemistry, Altai State Technical University, Barnaul 656038, Russia.

出版信息

Dalton Trans. 2009 Jun 21(23):4488-98. doi: 10.1039/b900869a. Epub 2009 Apr 7.

Abstract

Eleven new complexes of Cu(II) chloride and nitrate with bis(pyrazol-1-yl)propane and bis[2-(pyrazol-1-yl)ethyl]ether ligands were prepared and characterized by spectral and electrochemical methods. X-Ray crystal structure determination of bis[2-(3,5-dimethylpyrazol-1-yl)ethyl]etherdinitratocopper revealed a hepta-coordinated structure with the bis(pyrazole) ligand coordinated in a tridentate NNO-fashion and both of the nitrate ions in a bidentate fashion. Reaction of Cu(II) nitrate complexes with 2,2'-bipyridyl led to the displacement of one of the nitrate ions into the outer sphere and the formation of mixed-ligand complexes. Mixed-ligand bipyridyl Cu(II) complexes demonstrated the highest superoxide dismutase (SOD)-like activity in a chemical superoxide anion-generating system, with IC(50) values in the low micromolar range. Density functional theory calculations showed that introduction of a bipypidyl ligand into the complexes dramatically lowered the lowest unoccupied molecular orbital (LUMO) energy level, which explains the increased SOD-like activity of these complexes compared to non-bipy species. These bipy complexes were also effective scavengers of reactive oxygen species generated by phagocytes (human neutrophils and murine bone marrow leukocytes) ex vivo. Thus, these bipy mixed-ligand complexes represent a promising class of SOD mimetics for future development.

摘要

制备了11种氯化铜(II)和硝酸铜与双(吡唑-1-基)丙烷和双[2-(吡唑-1-基)乙基]醚配体的新配合物,并通过光谱和电化学方法对其进行了表征。双[2-(3,5-二甲基吡唑-1-基)乙基]醚二硝酸铜的X射线晶体结构测定显示,其为七配位结构,双(吡唑)配体以三齿NNO方式配位,两个硝酸根离子均以双齿方式配位。硝酸铜(II)配合物与2,2'-联吡啶反应导致其中一个硝酸根离子位移到外层球,形成混合配体配合物。混合配体联吡啶铜(II)配合物在化学超氧阴离子生成系统中表现出最高的超氧化物歧化酶(SOD)样活性,IC(50)值在低微摩尔范围内。密度泛函理论计算表明,在配合物中引入联吡啶配体显著降低了最低未占据分子轨道(LUMO)能级,这解释了与非联吡啶物种相比,这些配合物的SOD样活性增加的原因。这些联吡啶配合物也是体外吞噬细胞(人中性粒细胞和小鼠骨髓白细胞)产生的活性氧的有效清除剂。因此,这些联吡啶混合配体配合物代表了一类有前途的用于未来开发的SOD模拟物。

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