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串联高价金属三氟甲磺酸酯+负载钯催化剂促进的快速醚和醇 C-O 键氢解。

Rapid ether and alcohol C-O bond hydrogenolysis catalyzed by tandem high-valent metal triflate + supported Pd catalysts.

机构信息

Department of Chemistry, Northwestern University , 2145 Sheridan Road, Evanston, Illinois 60208, United States.

出版信息

J Am Chem Soc. 2014 Jan 8;136(1):104-7. doi: 10.1021/ja411546r. Epub 2013 Dec 26.

Abstract

The thermodynamically leveraged conversion of ethers and alcohols to saturated hydrocarbons is achieved efficiently with low loadings of homogeneous M(OTf)n + heterogeneous Pd tandem catalysts (M = transition metal; OTf = triflate; n = 4). For example, Hf(OTf)4 mediates rapid endothermic ether ⇌ alcohol and alcohol ⇌ alkene equilibria, while Pd/C catalyzes the subsequent, exothermic alkene hydrogenation. The relative C-O cleavage rates scale as 3° > 2° > 1°. The reaction scope extends to efficient conversion of biomass-derived ethers, such as THF derivatives, to the corresponding alkanes.

摘要

通过使用低负载的均相 M(OTf)n 和多相 Pd 串联催化剂,实现了醚和醇的热力学上有利的转化为饱和烃。例如,Hf(OTf)4 介导快速的吸热醚 ⇌ 醇和醇 ⇌ 烯烃平衡,而 Pd/C 则催化随后的放热烯烃加氢反应。相对的 C-O 断裂速率为 3° > 2° > 1°。该反应范围扩展到有效转化生物质衍生的醚,如 THF 衍生物,为相应的烷烃。

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