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MOF-Triggered Synthesis of Subnanometer Ag02 Clusters and Fe3+ Single Atoms: Heterogenization Led to Efficient and Synergetic One-Pot Catalytic Reactions

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URI: http://hdl.handle.net/10498/29603

DOI: 10.1021/jacs.3c02155

ISSN: 0002-7863

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Author/s
Tiburcio, Estefanía; Zheng, Yongkun; Bilanin, Cristina; Hernández Garrido, Juan CarlosAuthority UCA; Vidal Moya, Alejandro; Oliver-Meseguer, Judit; Martín, Nuria; Mon, Marta; Ferrando Soria, Jesús; Armentano, Donatella; Leyva-Pérez, Antonio; Pardo, Emilio
Date
2023-04-28
Department
Ciencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica
Source
Journal of the American Chemical Society. Vol. 145, nº 18, 10 May 2023, pp. 10342 - 10354
Abstract
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.
Subjects
Aromatic hydrocarbons; Catalysis; Catalyst activity; Hybrid materials; Organic polymers; Organometallics; Single crystals
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  • Artículos Científicos [12009]
  • Artículos Científicos IMEYMAT [578]
Atribución 4.0 Internacional
This work is under a Creative Commons License Atribución 4.0 Internacional

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