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The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated hexacoordinate N2S2O2 complexes

机译:在S-乙酰化六配位N2S2O2络合物中交换金属的配体解缠/解缠途径

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摘要

The effect of S-acetylation in MN2S2 complexes on metal exchange reactivity was examined in a series of MN2S2O2 complexes. While clean exchange processes do not occur for the MN2S2 derivatives where formation of S-bridged aggregates predominate, acetylation permits the metal exchange with hierarchy that follows the Irving–Williams series of stability for first row transition metals: Fe2+ < Co2+ < Ni2+ < Cu2+ > Zn2+. The rate determining step consistent with kinetic parameters depends on both M and M′, supporting a mechanism of exchange that involves ligand unwrapping/rewrapping process as earlier defined by Margerum et al. for M(EDTA) systems. The enhanced metal exchange deriving from S-acetylation is of significance to probes and detection of cysteine-S metallo-proteins and metallo-enzyme active sites, and highlights a new role for S-acetylation.
机译:在一系列MN2S2O2络合物中检查了MN2S2络合物中S-乙酰化对金属交换反应性的影响。对于主要形成S桥骨的MN2S2衍生物而言,不会发生干净的交换过程,而乙酰化可使金属交换的层级遵循Irving–Williams系列第一行过渡金属的稳定性:Fe 2 + 2 + 2 + 2 + 2 + 。与动力学参数一致的速率确定步骤取决于M和M',这支持了一种交换机制,该机制涉及如Margerum等人先前定义的配体解缠/缠结过程。适用于M(EDTA)系统。源自S-乙酰化的增强的金属交换对于探测和检测半胱氨酸-S金属蛋白和金属酶活性位点具有重要意义,并突出了S-乙酰化的新作用。

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