苯乙炔
化学
催化作用
苯乙烯
金属
单晶
甲烷氧化偶联
偶联反应
金属有机骨架
组合化学
物理化学
有机化学
结晶学
吸附
聚合物
共聚物
作者
Estefanía Tiburcio,Yongkun Zheng,Cristina Bilanin,Juan Carlos Hernández‐Garrido,Alejandro Vidal‐Moya,Judit Oliver–Meseguer,Nuria Martín,Marta Mon,Jesús Ferrando−Soria,Donatella Armentano,Antonio Leyva‐Pérez,Emilio Pardo
摘要
The combination of well-defined Fe3+ isolated single-metal atoms and Ag2 subnanometer metal clusters within the channels of a metal-organic framework (MOF) is reported and characterized by single-crystal X-ray diffraction for the first time. The resulting hybrid material, with the formula [Ag02(Ag0)1.34FeIII0.66]@NaI2{NiII4[CuII2(Me3mpba)2]3}·63H2O (Fe3+Ag02@MOF), is capable of catalyzing the unprecedented direct conversion of styrene to phenylacetylene in one pot. In particular, Fe3+Ag02@MOF─which can easily be obtained in a gram scale─exhibits superior catalytic activity for the TEMPO-free oxidative cross-coupling of styrenes with phenyl sulfone to give vinyl sulfones in yields up to >99%, which are ultimately transformed, in situ, to the corresponding phenylacetylene product. The results presented here constitute a paradigmatic example of how the synthesis of different metal species in well-defined solid catalysts, combined with speciation of the true metal catalyst of an organic reaction in solution, allows the design of a new challenging reaction.
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