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Pd-grafted porous metal–organic framework material as an efficient and reusable heterogeneous catalyst for C–C coupling reactions in water

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Palladium nanoparticles (Pd NPs) have been grafted at the surfaces of a Co-containing metal-organic framework material MCoS-1, which has been characterized by HR TEM, XPS and EPR spectroscopic analyses as discussed by the authors.
Abstract
Palladium nanoparticles (Pd NPs) have been grafted at the surfaces of a Co-containing metal–organic framework material MCoS-1. The Pd NPs grafted material Pd(0)/MCoS-1 has been characterized by HR TEM, XPS and EPR spectroscopic analyses. Pd(0)/MCoS-1 showed excellent catalytic activities in Suzuki–Miyaura cross-coupling reaction for the synthesis of a diverse range of biaryl organics in water. Sonogashira cross-coupling between terminal alkynes and aryl halides has also been carried out over this Pd-nanocatalyst in water without the addition of any Cu co-catalyst. In both reactions the catalyst is easily recoverable and can be reused for several times without appreciable loss of catalytic activity. No evidence of the leaching of Pd from the catalyst during the course of reaction has been observed, suggesting true heterogeneity in our catalytic systems.

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Catalysis and photocatalysis by metal organic frameworks

TL;DR: The present review summarizes the current state of the art in the use of MOFs as solid catalysts according to the type of site, making special emphasis on the more recent strategies to increase the population of these active sites and tuning their activity, either by adapting the synthesis conditions or by post-synthetic modification.
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Application of metal and metal oxide nanoparticles@MOFs

TL;DR: Nanoparticles@MOFs composites combine the tailorable porosity of MOFs with the versatile functionality of metal or metaloxide nanoparticles as mentioned in this paper, and have been shown to possess unique functional properties.
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Metal-organic frameworks catalyzed C-C and C-heteroatom coupling reactions.

TL;DR: The use of MOFs as catalysts to promote cross-coupling reactions involving organometallic reaction intermediates and catalysis by Lewis acid sites, which are of large synthetic utility due to the high yields achieved, mild conditions and compatibility with other functional groups.
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Pd-grafted open metal site copper-benzene-1,4-dicarboxylate metal organic frameworks (Cu-BDC MOF's) as promising interfacial catalysts for sustainable Suzuki coupling.

TL;DR: Recyclability test for the Pd@Cu-BDC/Py-SI catalyst showed a successful reusability for 7 runs, and the palladium ions was coordinated onto the Schiff base-decorated Cu-B DC pore cage, that this bifunctional Pd @Cu- BDC/ Py- SI catalyst was successfully applied for Suzuki cross-coupling reaction.
References
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Journal ArticleDOI

Palladium-catalyzed cross-coupling reactions of organoboron compounds

Norio Miyaura, +1 more
- 01 Nov 1995 - 
TL;DR: In this paper, a cross-coupling reaction is proposed for coupling 1 -Alkenylboron Derivatives: Synthesis of Conjugated Dienes 6.
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Engineering Metal Organic Frameworks for Heterogeneous Catalysis

TL;DR: In conclusion, MOFs as Host Matrices or Nanometric Reaction Cavities should not be considered as a source of concern in the determination of MOFs’ properties in relation to other materials.
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Nanoparticles as Recyclable Catalysts: The Frontier between Homogeneous and Heterogeneous Catalysis

TL;DR: The Review presents the recent developments and the use of NP catalysis in organic synthesis, for example, in hydrogenation and C--C coupling reactions, and the heterogeneous oxidation of CO on gold NPs.
Journal ArticleDOI

Palladium-Catalyzed Coupling Reactions of Aryl Chlorides

TL;DR: This review summarizes both the seminal early work and the exciting recent developments in the area of palladium-catalyzed couplings of aryl chlorides.
Journal ArticleDOI

Carbon-Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts

TL;DR: Pd on Modified Silica 159 4.5.1.
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