首页> 外文期刊>Chemistry: A European journal >Could redox-switched binding of a redox-active ligand to a copper(II) centie drive a conformational proton pump gale? A synthetic model study
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Could redox-switched binding of a redox-active ligand to a copper(II) centie drive a conformational proton pump gale? A synthetic model study

机译:氧化还原活性配体与铜(II)的氧化还原转换结合能驱动构象质子泵大风吗?综合模型研究

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A proposal for a redox-linked conformational gate to proton translocation-a proton pump gate-based upon a transition-metal redox-switch-able hemilabile ligand (RHL) system is made. Consideration of the requirements for such a system reveals copper(II) to be the ideal metal centre. To test the proposal and, thereby, to provide an artificial proton pump gate, the copper coordination chemistry of three tris(pyridylmethyl)amine (tpa) ligands with one "leg" (PY*) substituted at the 6-position of the pyridine ring by a dimethoxyphenyl (L-1), a hydroquinone (H2L2) or a quinone (L-3) substituent has been investigated. Crystal structures of sp-[Cu(kappa(4)N-L-1)Cl]Cl.3H(2)O (sp = square pyramidal), sp-[Cu(kappa(3)N-H2L2)-Cl-2] and tbp-[Cu(kappa(4)N,kappaO-HL2)] [PF6] (tbp = trigonal bipyramidal) have been determined. The Cut complexes [Cu(L)(MeCN)(n)](+) (L=L-1, H2L2) display physicochemical properties consistent with a "dangling" PY* leg; from the NMR spectra, the barriers to inversion of the ligand amine donor for the Cut complexes are estimated to be within the range of about 30-45 kJmol(-1). In the Cu-II complexes, coordination of the PY* leg is finely balanced and critically depends on the nature of the PY* substituent and the availability of potential co-ligand(s). For example, tbp-[Cu(kappa(4)N-L-1)Cl](+) reacts cleanly with Cl- ions to afford sp-[Cu(kappa(3)N-L-1)Cl-2]; Vis/NIR spectrophotometric titrations suggest the affinity of tbp-[Cu(kappa(4)N-L-1)Cl](+) for Cl- ion in dichloromethane is 9.7 X 10(2) and is at least 10(4)-fold greater than that of tbp-[Cu(kappa(4)N-L-3)Cl](+). The complex sp-[Cu(kappa(3)N-(HL2)-L-2)Cl-2] has a "dangling" PY* leg, in which an intramolecular OH(hydroquinone)...N(pyridine) hydrogen bond "ties-up" the pyridyl nitrogen atom, and reacts with Bronsted bases to give tbp-[Cu(kappa(4)N,kappaO-HL2)](+). Two-electron oxidation of sp-[Cu(kappa(3)N-H2L2)Cl-2] is linked to loss of two protons and a conformational change, and affords tbp-[Cu(kappa(4)N-L-3)Cl](+). The [Cu(kappa(3)N-H2L2)Cl-2]-[Cu(kappa(4)N-L-3)Cl](+) system provides a first demonstration of the critical step in the proposed proton pumping cycle, namely a redox-driven and proton-linked conformational change. The possible biological relevance of this work to proton pumping in cytochrome c oxidase is mentioned. [References: 79]
机译:提出了一种基于氧化还原的构象门质子易位的方法-基于可过渡金属氧化还原转换的半不稳定配体(RHL)系统的质子泵门。对这种系统的要求的考虑表明,铜(II)是理想的金属中心。为了测试该建议并由此提供一种人造质子泵门,需要对三个三(吡啶甲基)胺(tpa)配体进行铜配位化学反应,在吡啶环的6位上取代一个“支腿”(PY *)已经研究了通过二甲氧基苯基(L-1)对苯二酚(H2L2)或醌(L-3)取代基。 sp- [Cu(kappa(4)NL-1)Cl] Cl.3H(2)O(sp =方锥),sp- [Cu(kappa(3)N-H2L2)-Cl-2]的晶体结构并确定了tbp- [Cu(kappa(4)N,kappaO-HL2)] [PF6](tbp =三角双锥体)。 Cut复合物[Cu(L)(MeCN)(n)](+)(L = L-1,H2L2)具有与“悬挂”的PY *腿一致的理化性质;从NMR光谱中,Cut配合物的配体胺供体的转化障碍估计在约30-45 kJmol(-1)的范围内。在Cu-II络合物中,PY *支链的协调非常精细,并且关键取决于PY *取代基的性质和潜在共配体的可用性。例如,tbp- [Cu(kappa(4)N-L-1)Cl](+)与Cl-离子干净反应,得到sp- [Cu(kappa(3)N-L-1)Cl-2];可见/近红外分光光度滴定表明,tbp- [Cu(kappa(4)NL-1)Cl](+)对二氯甲烷中Cl离子的亲和力是9.7 X 10(2),至少是10(4)倍大于tbp- [Cu(kappa(4)NL-3)Cl](+)。复杂的sp- [Cu(kappa(3)N-(HL2)-L-2)Cl-2]具有“悬垂”的PY *腿,其中分子内的OH(氢醌)... N(吡啶)氢键“绑定”吡啶氮原子,并与布朗斯台德碱反应,得到tbp- [Cu(k(a)(4)N,kα-O-HL2)](+)。 sp- [Cu(kappa(3)N-H2L2)Cl-2]的双电子氧化与两个质子的损失和构象变化有关,并提供tbp- [Cu(kappa(4)NL-3)Cl ](+)。 [Cu(kappa(3)N-H2L2)Cl-2]-[Cu(kappa(4)NL-3)Cl](+)系统提供了在所提出的质子泵送循环中关键步骤的第一个证明,即氧化还原驱动和质子相关的构象变化。提到了这项工作与质子泵入细胞色素c氧化酶的可能生物学相关性。 [参考:79]

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