scholarly journals The societal significance of catalysis and the growing practical importance of single-site heterogeneous catalysts

Author(s):  
John Meurig Thomas

The concept of single-site heterogeneous catalysis, herein defined and extensively illustrated, offers a strategy for the design of new solid catalysts. By capitalizing on the opportunities presented by nanoporous materials to assemble a wide range of new, well-defined, catalytically active centres, it is possible to bring about numerous environmentally benign processes that can replace traditional methods of chemical production. The latter often employs aggressive, corrosive or hazardous reagents. By using both microporous (less than 20 Å diameter) and mesoporous solids (20–500 Å diameter), abundant scope exists for the construction and application of shape-selective, regio-selective and enantioselective catalysts.

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1445
Author(s):  
Francisco G. Cirujano ◽  
Rafael Luque ◽  
Amarajothi Dhakshinamoorthy

Metal–organic frameworks (MOFs) have become one of the versatile solid materials used for a wide range of applications, such as gas storage, gas separation, proton conductivity, sensors and catalysis. Among these fields, one of the more well-studied areas is the use of MOFs as heterogeneous catalysts for a broad range of organic reactions. In the present review, the employment of MOFs as solid catalysts for the Henry reaction is discussed, and the available literature data from the last decade are grouped. The review is organized with a brief introduction of the importance of Henry reactions and structural properties of MOFs that are suitable for catalysis. The second part of the review discusses the use of MOFs as solid catalysts for the Henry reaction involving metal nodes as active sites, while the third section provides data utilizing basic sites (primary amine, secondary amine, amides and urea-donating sites). While commenting on the catalytic results in these two sections, the advantage of MOFs over other solid catalysts is compared in terms of activity by providing turnover number (TON) values and the structural stability of MOFs during the course of the reaction. The final section provides our views on further directions in this field.


Author(s):  
Vladimiro Dal Santo ◽  
Matteo Guidotti ◽  
Rinaldo Psaro ◽  
Leonardo Marchese ◽  
Fabio Carniato ◽  
...  

The main methods for the design and preparation of single-site heterogeneous catalysts on inorganic oxide supports are described and reviewed. Catalytically active metal sites can be either introduced into the framework of porous materials via direct synthesis or added to a pre-existing support by post-synthesis techniques. Particular attention is paid to selected examples where the geometry, the nature and the chemical surroundings of the active single site is a key factor to obtain catalytic systems with enhanced chemo-, regio- and stereoselectivity. The ever-increasing capabilities of ‘nanoarchitecture’ at molecular level enable chemists to build ideal catalysts for the sustainable transformation of bulky and high added-value molecules.


2021 ◽  
Author(s):  
Yuen Wu ◽  
Haoran Zhang ◽  
Xiaoqian Wang ◽  
Fan Wu ◽  
Xiao-Kang Liu ◽  
...  

Abstract Solid catalysts play vital roles as heterogeneous catalysts in numerous applications in the chemical, petrochemical, pharmaceutical, energy, food and automobile industries, facilitating large-scale production and facile product separation. However, conventional heterogeneous catalysts possess three major shortcomings that hinder their wide-spread application, including i) inferior catalytic activity and selectivity caused by a diversity of active sites, ii) tendency towards deactivation caused by agglomeration of catalyst particles, and iii) undesired carbon deposition in transformation of hydrocarbons. 1-4 In this research, we present a new kind of heterogeneous catalyst that consists of a liquid metal with dissolved catalytically active metal atoms, denoted as a heterogeneous droplet catalyst (HDC). Taking galinstan as the liquid metal with Cu as catalytically active metal solute (denoted as Cu-HDC) as an example, we demonstrate that the dissolved Cu atoms promote selective oxidation of methane into primary oxygenates at room temperature with a superb activity of 1940 mmol·gCu-1·h-1 and a selectivity of over 90%, outperforming state-of-the-art industrial catalysts. The liquid metal solvent ensures a high, entropically driven dispersion of the Cu atoms and prevents carbon deposition. The highly promising Cu-HDC catalyst shows a stable operation over 240 hours. By employing in-situ X-ray absorption spectroscopy (XAS), near ambient-pressure X-ray photoelectron spectroscopy (NAP-XPS) and density functional theory (DFT), we show that the narrow d-orbital of the dissolved Cu atoms in HDC facilitates formation of adsorbed methyl radicals *CH3 and impedes their transformation into *CH2 (where the * notation is used to denote an adsorption site) 5,6. These features enhance the selectivity towards primary oxygenates and prevent over-oxidization and formation of C2+ products. As the phase of the HDC is different from those of gas, aqueous and organic solution phases its separation is as facile as that of solid catalysts. Unlike conventional supported catalysts that are designed with well-defined crystal structures, crystal facets and defects, HDCs are characterized by weak interactions between the liquid metal support and the active metal solute, by having mobile surfaces and by dynamic catalytically active centers. These unprecedented features endow HDCs unique adsorption behavior and adaptive activation of molecules. For this reason, HDCs have the potential to become a major category of catalysts in the field of heterogeneous catalysis.


Author(s):  
Urbano Díaz ◽  
Mercedes Boronat ◽  
Avelino Corma

Catalyst selectivity is associated with well-defined homogeneous active sites. Transition metal complexes and organocatalysts are highly active and selective in the homogeneous phase, and their heterogenization by incorporating them into inorganic solid materials allows combining their excellent catalytic activity with improved separation, recovering and recycling properties. In this article, we present the structural characteristics and catalytic properties of hybrid organic–inorganic materials in which the molecular catalysts are part of the inorganic structure, emphasizing the possibilities of periodic mesoporous hybrid materials and coordination polymers as single-site solid catalysts.


Author(s):  
Michel Che ◽  
Kohsuke Mori ◽  
Hiromi Yamashita

This study concerns single-site heterogeneous photocatalysts, composed of isolated transition metals ions (single-sites) dispersed on silica-based supports, which can be used as photocatalysts. The first part gives the definition of single-site heterogeneous catalysts. The main difficulty to prepare the latter resides in the speciation of the key elements (metal of the catalytically active phase and oxygen of the solid support) and other species (notably counter ions and ligands) the presence of which depends on the synthesis method adopted. The best preparation methods as well as the ideal features of single-site heterogeneous photocatalysts are discussed before the study focuses on single-site heterogeneous photocatalysts. Case studies are presented with photocatalysts involving titanium and chromium, and their photocatalytic reactions such as CO 2 reduction with H 2 O, degradation of organic pollutants diluted in water, NO decomposition and selective oxidation of propane are also described.


2020 ◽  
Vol 24 ◽  
Author(s):  
Ghodsi Mohammadi Ziarani ◽  
Shima Roshankar ◽  
Fatemeh Mohajer ◽  
Alireza Badiei

Abstract:: Mesoporous silica nanomaterials provide an extraordinary advantage for making new and superior heterogeneous catalysts because of their surface silanol groups. The functionalized mesoporous SBA-15, such as acidic, basic, BrÖnsted, lewis acid, and chiral catalysts, are used for a wide range of organic synthesis. The importance of the chiral ligands, which were immobilized on the SBA-15, was mentioned in this review to achieve chiral products as valuable target molecules. Herein, their synthesis and application in different organic transformations are reviewed from 2016 till date 2020.


Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1259
Author(s):  
Ana Franco ◽  
Rafael Luque ◽  
Carolina Carrillo-Carrión

Biomass-derived materials are put forward as eco-friendly alternatives to design heterogeneous catalysts. To contribute in this field, we explored the potential of mesoporous biogenic silica (RH-Silica) obtained from lignocellulosic waste, in particular from rice husk, as an inorganic support to prepare heterogenized iron oxide-based catalysts. Mechanochemistry, considered as a green and sustainable technique, was employed to synthetize iron oxide nanoparticles in pure hematite phase onto the biosilica (α-Fe2O3/RH-Silica), making this material a good candidate to perform catalyzed organic reactions. The obtained material was characterized by different techniques, and its catalytic activity was tested in the selective oxidation of styrene under microwave irradiation. α-Fe2O3/RH-Silica displayed a good catalytic performance, achieving a conversion of 45% under optimized conditions, and more importantly, with a total selectivity to benzaldehyde. Furthermore, a good reusability was achieved without decreasing its activity after multiple catalytic cycles. This work represents a good example of using sustainable approaches and green materials as alternatives to conventional methods in the production of high-added value products.


1992 ◽  
Vol 277 ◽  
Author(s):  
Geoffrey A. Ozin ◽  
Carol L. Bowes ◽  
Mark R. Steele

ABSTRACTVarious MOCVD (metal-organic chemical vapour deposition) type precursors and their self-assembled semiconductor nanocluster products [1] have been investigated in zeolite Y hosts. From analysis of in situ observations (FTIR, UV-vis reflectance, Mössbauer, MAS-NMR) of the reaction sequences and structural features of the precursors and products (EXAFS and Rietveld refinement of powder XRD data) the zeolite is viewed as providing a macrospheroidal, multidendate coordination environment towards encapsulated guests. By thinking about the α- and β-cages of the zeolite Y host effectively as a zeolate ligand composed of interconnected aluminosilicate “crown ether-like” building blocks, the materials chemist is able to better understand and exploit the reactivity and coordination properties of the zeolite internal surface for the anchoring and self-assembly of a wide range of encapsulated guests. This approach helps with the design of synthetic strategies for creating novel guest-host inclusion compounds having possible applications in areas of materials science such as nonlinear optics, quantum electronics, and size/shape selective catalysis.


2016 ◽  
Vol 138 (32) ◽  
pp. 10232-10237 ◽  
Author(s):  
Robert J. Comito ◽  
Keith J. Fritzsching ◽  
Benjamin J. Sundell ◽  
Klaus Schmidt-Rohr ◽  
Mircea Dincă

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