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多组氨酸环肽与两个金属结合中心的配位能力——电位和光谱研究。

The coordination abilities of the multiHis-cyclopeptide with two metal-binding centers--potentiometric and spectroscopic investigation.

机构信息

Department of Inorganic Chemistry, Wroclaw Medical University, Szewska 38, 50-139 Wroclaw, Poland.

出版信息

Dalton Trans. 2012 Oct 21;41(39):12114-20. doi: 10.1039/c2dt31224g.

Abstract

In this paper we present the formation of mono- and binuclear complexes by the octapeptide (c(HKHPHKHP)) with copper(II) ions. The ligand was synthesized manually by the solid-phase method. Its characteristic cyclic structure significantly influences the coordination abilities. The studied peptide has two Pro amino acid residues in the sequence. This causes the formation of two independent centres able to undertake metal ion binding. The potentiometric and spectroscopic (UV-vis, CD and EPR) studies were carried out in aqueous solutions in the pH range 2.5-11.0 at 298 K, HNO(3) was used as the solvent with KNO(3), where the ionic strength was 0.1 M. The analysis of the potentiometric together with spectroscopic studies have shown that the investigated peptide forms only mono-nuclear complexes when the metal-to-ligand molar ratio is 1 : 1. When the concentration of Cu(ii) ions increases and the ligand-to-metal molar ratio is 1 : 2 the formation of binuclear complexes is preferred in the system.

摘要

本文介绍了八肽(c(HKHPHKHP))与铜(II)离子形成单核和双核配合物的情况。配体通过固相法人工合成。其特征环状结构显著影响配位能力。研究的肽在序列中有两个脯氨酸氨基酸残基。这导致形成两个独立的中心,能够进行金属离子结合。在 298 K 下,在 pH 值为 2.5-11.0 的水溶液中进行了电位和光谱(UV-vis、CD 和 EPR)研究,使用 HNO(3)作为溶剂,并用 KNO(3)保持离子强度为 0.1 M。电位分析与光谱研究的结合表明,当金属与配体的摩尔比为 1:1 时,所研究的肽仅形成单核配合物。当 Cu(ii)离子的浓度增加,配体与金属的摩尔比为 1:2 时,体系中优先形成双核配合物。

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