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

机译:交换 S -乙酰化,六配位N 2 S 2 O 2 络合物中的金属的配体解缠/解缠途径

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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: S -乙酰化在MN 2 S 2 配合物中对金属交换的影响在一系列MN 2 S 2 O 2 复合体。虽然对于MN 2 S 2 衍生物不会发生干净的交换过程,其中 S < / em>-桥联的聚集体占主导地位,乙酰化使金属的交换遵循第一行过渡金属的Irving–Williams稳定性系列: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',从而支持一种交换机制,该机制涉及如早先由Margerum等人针对M(EDTA)系统定义的配体解缠/缠结过程。源自 S -乙酰化的增强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,并突出了其新的作用。 S -乙酰化。

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