通过 "Dangler "中间体进行金属-金属氧化还原反应生成异金属锰钴氧化立方体。

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Journal of the American Chemical Society Pub Date : 2024-07-24 Epub Date: 2024-07-08 DOI:10.1021/jacs.4c05367
T Alexander Wheeler, T Don Tilley
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引用次数: 0

摘要

与杂环丁烷结合的附着金属是众所周知的酶活性位点的组成部分,它们介导着困难的化学转化。这些金属离子有时被称为 "悬金属",其具体作用的研究一直受到缺乏适当模型结构的合理合成路线的阻碍。为了生成通过羧酸桥与氧化立方烷结合的悬垂金属离子,立方烷 Co4(μ3-O)4(OAc)4(t-Bupy)4(OAc = 乙酸酯,t-Bupy = 4-叔丁基吡啶)与各种金属醋酸盐络合物发生了反应。与 Cu(OAc)2 反应生成了具有结构特征(通过 X 射线衍射)的二氯化铜当体 Cu2Co4(μ4-O)2(μ3-O)2(OAc)6(Cl)2(t-Bupy)4。与此相反,与 Mn(OAc)2 的类似反应通过金属-金属交换产生了含 MnIV 的立方阳离子[MnCo3(μ3-O)4(OAc)4(t-Bupy)4]+,副产物为 Co(OAc)2 和[CoIII(μ-OH)(OAc)]n 低聚物。此外,形式上为 CoIV 的立方烷复合物[Co4(μ3-O)4(OAc)4(t-Bupy)4][PF6]与 Mn(OAc)2 反应生成了相应的含锰立方烷,产率为 80%。通过紫外-可见(UV-vis)光谱对 Co4(μ3-O)4(OBz)4(py)4(OBz = 苯甲酸盐)和[Mn(acac)2(py)2][PF6]之间的相关金属-金属交换反应进行的机理研究,为涉及反应物的速率决定性结合以及通过加成中间体中的μ-氧桥进行电子转移的过程提供了支持。交换的速率与立方烷吡啶和苯甲酸配体取代基的供体强度相关;电子供体较多的吡啶配体可加速金属-金属交换,而电子供体和抽电子的苯甲酸配体均可加速交换。这些实验表明,立方烷氧化配体的碱性促进了金属-金属交换反应性。锰和立方烷起始材料的氧化还原电位以及同位素标记研究表明,当体中间体具有内球电子转移机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Metal-Metal Redox Exchange to Produce Heterometallic Manganese-Cobalt Oxo Cubanes via a "Dangler" Intermediate.

Metal-Metal Redox Exchange to Produce Heterometallic Manganese-Cobalt Oxo Cubanes via a "Dangler" Intermediate.

Pendent metals bound to heterocubanes are components of well-known active sites in enzymes that mediate difficult chemical transformations. Investigations into the specific role of these metal ions, sometimes referred to as "danglers", have been hindered by a paucity of rational synthetic routes to appropriate model structures. To generate pendent metal ions bonded to an oxo cubane through a carboxylate bridge, the cubane Co43-O)4(OAc)4(t-Bupy)4 (OAc = acetate, t-Bupy = 4-tert-butylpyridine) was exposed to various metal acetate complexes. Reaction with Cu(OAc)2 gave the structurally characterized (by X-ray diffraction) dicopper dangler Cu2Co44-O)23-O)2(OAc)6(Cl)2(t-Bupy)4. In contrast, the analogous reaction with Mn(OAc)2 produced the MnIV-containing cubane cation [MnCo33-O)4(OAc)4(t-Bupy)4]+ by way of a metal-metal exchange that gives Co(OAc)2 and [CoIII(μ-OH)(OAc)]n oligomers as byproducts. Additionally, reaction of the formally CoIV cubane complex [Co43-O)4(OAc)4(t-Bupy)4][PF6] with Mn(OAc)2 gave the corresponding Mn-containing cubane in 80% yield. A mechanistic examination of the related metal-metal exchange reaction between Co43-O)4(OBz)4(py)4 (OBz = benzoate) and [Mn(acac)2(py)2][PF6] by ultraviolet-visible (UV-vis) spectroscopy provided support for a process involving rate-determining association of the reactants and electron transfer through a μ-oxo bridge in the adduct intermediate. The rates of exchange correlate with the donor strength of the cubane pyridine and benzoate ligand substituents; more electron-donating pyridine ligands accelerate metal-metal exchange, while both electron-donating and -withdrawing benzoate ligands can accelerate exchange. These experiments suggest that the basicity of the cubane oxo ligands promotes metal-metal exchange reactivity. The redox potentials of the Mn and cubane starting materials and isotopic labeling studies suggest an inner-sphere electron-transfer mechanism in a dangler intermediate.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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