{"title":"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。","authors":"T Alexander Wheeler, T Don Tilley","doi":"10.1021/jacs.4c05367","DOIUrl":null,"url":null,"abstract":"<p><p>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 Co<sub>4</sub>(μ<sub>3</sub>-O)<sub>4</sub>(OAc)<sub>4</sub>(<i>t</i>-Bupy)<sub>4</sub> (OAc = acetate, <i>t</i>-Bupy = 4-<i>tert</i>-butylpyridine) was exposed to various metal acetate complexes. Reaction with Cu(OAc)<sub>2</sub> gave the structurally characterized (by X-ray diffraction) dicopper dangler Cu<sub>2</sub>Co<sub>4</sub>(μ<sub>4</sub>-O)<sub>2</sub>(μ<sub>3</sub>-O)<sub>2</sub>(OAc)<sub>6</sub>(Cl)<sub>2</sub>(<i>t</i>-Bupy)<sub>4</sub>. In contrast, the analogous reaction with Mn(OAc)<sub>2</sub> produced the Mn<sup>IV</sup>-containing cubane cation [MnCo<sub>3</sub>(μ<sub>3</sub>-O)<sub>4</sub>(OAc)<sub>4</sub>(<i>t</i>-Bupy)<sub>4</sub>]<sup>+</sup> by way of a metal-metal exchange that gives Co(OAc)<sub>2</sub> and [Co<sup>III</sup>(μ-OH)(OAc)]<i><sub>n</sub></i> oligomers as byproducts. Additionally, reaction of the formally Co<sup>IV</sup> cubane complex [Co<sub>4</sub>(μ<sub>3</sub>-O)<sub>4</sub>(OAc)<sub>4</sub>(<i>t</i>-Bupy)<sub>4</sub>][PF<sub>6</sub>] with Mn(OAc)<sub>2</sub> gave the corresponding Mn-containing cubane in 80% yield. A mechanistic examination of the related metal-metal exchange reaction between Co<sub>4</sub>(μ<sub>3</sub>-O)<sub>4</sub>(OBz)<sub>4</sub>(py)<sub>4</sub> (OBz = benzoate) and [Mn(acac)<sub>2</sub>(py)<sub>2</sub>][PF<sub>6</sub>] 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.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":" ","pages":"20279-20290"},"PeriodicalIF":15.6000,"publicationDate":"2024-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11273651/pdf/","citationCount":"0","resultStr":"{\"title\":\"Metal-Metal Redox Exchange to Produce Heterometallic Manganese-Cobalt Oxo Cubanes via a \\\"Dangler\\\" Intermediate.\",\"authors\":\"T Alexander Wheeler, T Don Tilley\",\"doi\":\"10.1021/jacs.4c05367\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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 Co<sub>4</sub>(μ<sub>3</sub>-O)<sub>4</sub>(OAc)<sub>4</sub>(<i>t</i>-Bupy)<sub>4</sub> (OAc = acetate, <i>t</i>-Bupy = 4-<i>tert</i>-butylpyridine) was exposed to various metal acetate complexes. Reaction with Cu(OAc)<sub>2</sub> gave the structurally characterized (by X-ray diffraction) dicopper dangler Cu<sub>2</sub>Co<sub>4</sub>(μ<sub>4</sub>-O)<sub>2</sub>(μ<sub>3</sub>-O)<sub>2</sub>(OAc)<sub>6</sub>(Cl)<sub>2</sub>(<i>t</i>-Bupy)<sub>4</sub>. In contrast, the analogous reaction with Mn(OAc)<sub>2</sub> produced the Mn<sup>IV</sup>-containing cubane cation [MnCo<sub>3</sub>(μ<sub>3</sub>-O)<sub>4</sub>(OAc)<sub>4</sub>(<i>t</i>-Bupy)<sub>4</sub>]<sup>+</sup> by way of a metal-metal exchange that gives Co(OAc)<sub>2</sub> and [Co<sup>III</sup>(μ-OH)(OAc)]<i><sub>n</sub></i> oligomers as byproducts. Additionally, reaction of the formally Co<sup>IV</sup> cubane complex [Co<sub>4</sub>(μ<sub>3</sub>-O)<sub>4</sub>(OAc)<sub>4</sub>(<i>t</i>-Bupy)<sub>4</sub>][PF<sub>6</sub>] with Mn(OAc)<sub>2</sub> gave the corresponding Mn-containing cubane in 80% yield. A mechanistic examination of the related metal-metal exchange reaction between Co<sub>4</sub>(μ<sub>3</sub>-O)<sub>4</sub>(OBz)<sub>4</sub>(py)<sub>4</sub> (OBz = benzoate) and [Mn(acac)<sub>2</sub>(py)<sub>2</sub>][PF<sub>6</sub>] 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.</p>\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\" \",\"pages\":\"20279-20290\"},\"PeriodicalIF\":15.6000,\"publicationDate\":\"2024-07-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11273651/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/jacs.4c05367\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/7/8 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c05367","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/8 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
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 Co4(μ3-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 Cu2Co4(μ4-O)2(μ3-O)2(OAc)6(Cl)2(t-Bupy)4. In contrast, the analogous reaction with Mn(OAc)2 produced the MnIV-containing cubane cation [MnCo3(μ3-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 [Co4(μ3-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 Co4(μ3-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.
期刊介绍:
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