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Proton mediated spin state transition of cobalt heme analogs

机译:质子介导的钴血红素类似物的自旋态转变

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摘要

The spin state transition from low spin to high spin upon substrate addition is one of the key steps in cytochrome P450 catalysis. External perturbations such as pH and hydrogen bonding can also trigger the spin state transition of hemes through deprotonated histidine (e.g. Cytochrome c). In this work, we report the isolated 2-methylimidazole Cobalt(II) [Co(TPP)(2-MeHIm)] and [Co(TTP)(2-MeHIm)], and the corresponding 2-methylimidazolate derivatives where the N−H proton of axial 2-MeHIm is removed. Interestingly, various spectroscopies including EPR and XAFS determine a high-spin state (S = 3/2) for the imidazolate derivatives, in contrast to the low-spin state (S = 1/2) of all known imidazole analogs. DFT assisted stereoelectronic investigations are applied to understand the metal-ligand interactions, which suggest that the dramatically displaced metal center allowing a promotion eg(dπ) → b1g(dx2-y2) is crucial for the occurrence of the spin state transition.
机译:加入底物后,从低自旋到高自旋的自旋态转变是细胞色素P450催化的关键步骤之一。 pH和氢键等外部干扰也可以通过去质子化的组氨酸(例如细胞色素c)触发血红素的自旋态转变。在这项工作中,我们报告了分离的2-甲基咪唑钴(II)[Co(TPP)(2-MeHIm)]和[Co(TTP)(2-MeHIm)],以及相应的2-甲基咪唑化物衍生物,其中N-轴向2-MeHIm的H质子被去除。有趣的是,与所有已知的咪唑类似物的低旋态(S = 1/2)相比,包括EPR和XAFS在内的各种光谱学确定了咪唑酸酯衍生物的高旋态(S = 3/2)。 DFT辅助的立体电子学研究被用于理解金属-配体之间的相互作用,这表明金属中心发生了剧烈的位移,从而促进了例如(dπ)→b1g( d x 2 - y 2 )对于自旋状态转变的发生至关重要。

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