Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur 208016, India.
Inorg Chem. 2021 Sep 6;60(17):12870-12882. doi: 10.1021/acs.inorgchem.1c01215. Epub 2021 Aug 9.
Diheme cytochromes, the simplest members in the multiheme family, play substantial biochemical roles in enzymatic catalysis as well as in electron transfer. A series of diiron(III) porphyrin dimers have been synthesized as active site analogues of diheme cytochromes. The complexes contain six-coordinated iron(III) having thiophenol and imidazole at the fifth and sixth coordination sites, respectively. The iron centers in the complexes have been found to be in a low-spin state, as confirmed through solid-state Mössbauer and electron paramagnetic resonance (EPR) spectroscopic investigations. Mössbauer quadrupole splitting of complexes having mixed ligands is substantially larger than that observed when both axial ligands are the same. Rhombic types of EPR spectra with narrow separation between , , and clearly distinguish heme thiolate coordination compared to bis(imidazole)-ligated low-spin heme centers. The redox potential in diheme cytochromes has been found to be tuned by interheme interactions along with the nature of axial ligands. The effect of mixed-axial ligation within the diiron(III) porphyrin dimers is demonstrated by a positive shift in the Fe(III)/Fe(II) redox couple upon thiophenolate coordination compared to their bis(imidazole) analogues. The p of the imidazole also decides the extent of the shift for the Fe(III)/Fe(II) couple, while the potential of the mixed-ligated diiron(III) porphyrin dimer is more positive compared to their monomeric analogue. A variation of around 1.1 V for the Fe(III)/Fe(II) redox potential in the diiron(III) porphyrin dimer can be achieved with the combined effect of axial ligation and a metal spin state, while such a large variation in the redox potential, compared to their monomeric analogues, is attributed to the heme-heme interactions observed in dihemes. Moreover, theoretical calculations also support the experimental shifts in the redox potential values.
双铁细胞色素是多血红素家族中最简单的成员,在酶催化以及电子转移中发挥着重要的生化作用。一系列二铁(III)卟啉二聚体已被合成,作为双铁细胞色素的活性位点类似物。这些配合物含有六配位的铁(III),其第五和第六配位位分别为硫酚和咪唑。通过固态穆斯堡尔和电子顺磁共振(EPR)光谱研究证实,配合物中的铁中心处于低自旋状态。具有混合配体的配合物的穆斯堡尔四极分裂明显大于两个轴向配体相同时观察到的分裂。菱形类型的 EPR 谱, 和 之间的分离很窄,与双(咪唑)配低自旋血红素中心相比,清楚地区分了血红素硫醇配位。在双铁细胞色素中,发现通过沿轴向配体的性质的亚铁血红素相互作用来调节亚铁血红素的氧化还原电势。二铁(III)卟啉二聚体中混合轴向配体的影响通过硫酚配位时相对于其双(咪唑)类似物的 Fe(III)/Fe(II)氧化还原对的正移来证明。咪唑的 p 也决定了 Fe(III)/Fe(II) 配合物的位移程度,而混合配体的二铁(III)卟啉二聚体的电势比其单体类似物更正。通过轴向配体和金属自旋态的组合效应,在二铁(III)卟啉二聚体中可以实现 Fe(III)/Fe(II) 氧化还原电势的约 1.1 V 的变化,而与单体类似物相比,这种氧化还原电势的大变化归因于在双铁细胞色素中观察到的血红素血红素相互作用。此外,理论计算也支持实验中氧化还原电势值的变化。