UiO-67 Metal-organic framework immobilized Fe3+ catalyst for efficient Morita-Baylis-Hillman reaction

2022 ◽  
Author(s):  
Yuzhen Zhao ◽  
Min Zhu ◽  
Hailing Shang ◽  
Xiang Cheng ◽  
Daniele Ramella ◽  
...  
Keyword(s):  
Active Sites ◽  
Metal Organic Framework ◽  
Solvothermal Technique ◽  
Modification Method ◽  
Metal Organic ◽  
Organic Framework

A solvothermal technique was used to prepare UiO-67, a metal-organic framework based on Zirconium; immobilized Fe3+ active sites were added using a facile post-synthetic modification method. The as-synthesized catalyst UiO-67@Fe...

Atomic regulation of metal-organic framework derived carbon-based single-atom catalysts for electrochemical CO2 reduction reaction

2021 ◽  
Author(s):  
Danni Zhou ◽  
Xinyuan Li ◽  
Huishan Shang ◽  
Fengjuan Qin ◽  
Wenxing Chen
Keyword(s):  
Active Sites ◽  
Metal Organic Framework ◽  
Co2 Reduction ◽  
Carbon Dioxide Reduction ◽  
Reduction Reaction ◽  
Single Atom ◽  
Electrochemical Co2 Reduction ◽  
Metal Organic ◽  
Co2 Reduction Reaction ◽  
Organic Framework

Metal-organic framework (MOF) derived single-atom catalysts (SACs), featured unique active sites and adjustable topological structures, exhibit high electrocatalytic performance on carbon dioxide reduction reactions (CO2RR). By modulating elements and atomic...

scholarly journals Photo-generated dinuclear {Eu(II)}2 active sites for selective CO2 reduction in a photosensitizing metal-organic framework

2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Zhi-Hao Yan ◽  
Ming-Hao Du ◽  
Junxue Liu ◽  
Shengye Jin ◽  
Cheng Wang ◽  
...  
Keyword(s):  
Active Sites ◽  
Metal Organic Framework ◽  
Co2 Reduction ◽  
Metal Organic ◽  
Organic Framework

scholarly journals A Zirconium Metal-Organic Framework with SOC Topological Net for Catalytic Peptide Bond Hydrolysis

2021 ◽  
Author(s):  
Sujing Wang ◽  
Antoine Tissot ◽  
Guillaume Maurin ◽  
Tatjana Parac-Vogt ◽  
Christian Serre ◽  
...  
Keyword(s):  
Active Sites ◽  
Metal Organic Framework ◽  
Cost Effective ◽  
Peptide Bond ◽  
Catalytic Performance ◽  
Wide Range ◽  
Horse Heart Myoglobin ◽  
Metal Organic ◽  
Effective Synthesis ◽  
Organic Framework

<div>The discovery of nanozymes for selective cleavage of proteins would boost the emerging areas of modern proteomics, however, the development of efficient and reusable artificial catalysts for peptide bond hydrolysis is challenging. Here we report the detailed catalytic properties of a microporous zirconium carboxylate metal-organic framework, MIP-201, in promoting peptide bond hydrolysis in a simple dipeptide, as well as in horse-heart myoglobin (Mb) protein that consists of 153 amino acids. We demonstrate that MIP-201 features an excellent catalytic activity and selectivity, a good tolerance toward reaction conditions covering a wide range of different pH values, and importantly, an exceptional recycling ability associated with easy regeneration process. Taking into account the excellent catalytic performance of MIP-201 and its other advantages such as 6-connected Zr6 cluster active sites, the green, scalable and cost-effective synthesis, and an outstanding chemical and architectural stability, our finding suggests that MIP-201 may be a promising and practical alternative to the current commercially available catalysts for peptide bond hydrolysis.</div>

scholarly journals A Zirconium Metal-Organic Framework with SOC Topological Net for Catalytic Peptide Bond Hydrolysis

2021 ◽  
Author(s):  
Sujing Wang ◽  
Antoine Tissot ◽  
Guillaume Maurin ◽  
Tatjana Parac-Vogt ◽  
Christian Serre ◽  
...  
Keyword(s):  
Active Sites ◽  
Metal Organic Framework ◽  
Cost Effective ◽  
Peptide Bond ◽  
Catalytic Performance ◽  
Wide Range ◽  
Horse Heart Myoglobin ◽  
Metal Organic ◽  
Effective Synthesis ◽  
Organic Framework

<div>The discovery of nanozymes for selective cleavage of proteins would boost the emerging areas of modern proteomics, however, the development of efficient and reusable artificial catalysts for peptide bond hydrolysis is challenging. Here we report the detailed catalytic properties of a microporous zirconium carboxylate metal-organic framework, MIP-201, in promoting peptide bond hydrolysis in a simple dipeptide, as well as in horse-heart myoglobin (Mb) protein that consists of 153 amino acids. We demonstrate that MIP-201 features an excellent catalytic activity and selectivity, a good tolerance toward reaction conditions covering a wide range of different pH values, and importantly, an exceptional recycling ability associated with easy regeneration process. Taking into account the excellent catalytic performance of MIP-201 and its other advantages such as 6-connected Zr6 cluster active sites, the green, scalable and cost-effective synthesis, and an outstanding chemical and architectural stability, our finding suggests that MIP-201 may be a promising and practical alternative to the current commercially available catalysts for peptide bond hydrolysis.</div>

scholarly journals A Porphyrinic Zirconium Metal–Organic Framework for Oxygen Reduction Reaction: Tailoring the Spacing between Active-Sites through Chain-Based Inorganic Building Units

2020 ◽  
Vol 142 (36) ◽  
pp. 15386-15395 ◽  
Author(s):  
Magdalena Ola Cichocka ◽  
Zuozhong Liang ◽  
Dawei Feng ◽  
Seoin Back ◽  
Samira Siahrostami ◽  
...  
Keyword(s):  
Oxygen Reduction Reaction ◽  
Oxygen Reduction ◽  
Active Sites ◽  
Metal Organic Framework ◽  
Reduction Reaction ◽  
Metal Organic ◽  
Zirconium Metal ◽  
Organic Framework

An Efficient and Reusable Multifunctional Composite Magnetic Nanocatalyst for Knoevenagel Condensation

Synlett ◽  
2019 ◽  
Vol 30 (06) ◽  
pp. 699-702 ◽  
Author(s):  
Yu Hu ◽  
Nan Yao ◽  
Jin Tan ◽  
Yang Liu
Keyword(s):  
Active Sites ◽  
Heterogeneous Catalysts ◽  
Knoevenagel Condensation ◽  
Metal Organic Framework ◽  
Catalytic Performance ◽  
Significant Loss ◽  
Magnetic Nanocatalyst ◽  
Metal Organic ◽  
Nife2o4 Nanoparticles ◽  
Organic Framework

A range of multifunctional magnetic metal–organic framework nanomaterials consisting of various mass ratios of the metal–organic framework MIL-53(Fe) and magnetic SiO2@NiFe2O4 nanoparticles were designed, prepared, characterized, and evaluated as heterogeneous catalysts for the Knoevenagel condensation. The as-fabricated nanomaterials, especially the nanocatalyst MIL-53(Fe)@SiO2@NiFe2O4(1.0), showed good catalytic performance in the Knoevenagel condensation at room temperature as a result of synergistic interaction between the Lewis acid iron sites of MIL-53(Fe) and the active sites of the magnetic SiO2@NiFe2O4 nanoparticles. In addition, the heterogeneous catalyst was readily recovered and a recycling test showed that it could be reused for five times without significant loss of its catalytic activity, making it economical and environmentally friendly.

scholarly journals Study of the adsorption of an organic pollutant onto a microporous metal organic framework

2020 ◽  
Author(s):  
Mansouri Taki Eddine Mohammed ◽  
Nibou Djamel ◽  
Trari Mohamed ◽  
Samira Amokrane
Keyword(s):  
Methyl Orange ◽  
Adsorption Capacity ◽  
Active Sites ◽  
Physical Adsorption ◽  
Metal Organic Framework ◽  
Specific Interaction ◽  
Maximum Adsorption Capacity ◽  
Film Diffusion ◽  
Metal Organic ◽  
Organic Framework

Abstract In this study, the microporous Metal Organic Framework-5 (MOF-5) has been synthesized to be used to remove methyl orange by adsorption. The adsorption experiments exhibit a good adsorption capacity at a catalyst dose of 0.1 g L−1 and for an initial concentration of 200 mg L−1, whereas the performance is stable over a wide pH range. The equilibrium adsorption data showed a sigmoidal course, which is well fitted by the Dubinin-Astakhov model applicable for physical adsorption processes (E = 0.055 kJ mol−1) onto heterogeneous surfaces and a more homogeneous pore structure (n = 9.9), with a maximum adsorption capacity of 1248.35 mg g−1. As can be observed from the evaluation of the kinetic data, the surface of the adsorbent is heterogeneous with different active sites for Methyl Orange (MO) adsorption. Moreover, based on the rate constant, it can be suggested that there is a specific interaction like electrostatic interaction between MO and the adsorbent for rapid and high uptake of the dye, whereas the adsorption phenomenon is reversible. According to the adsorption mechanisms, intra-particle and film diffusion models simultaneously controlled the rate sorption, which was confirmed by the calculated intra-particle diffusion and the film diffusion coefficients. The evaluation of the thermodynamic parameters revealed that the MO adsorption is spontaneous, endothermic and the randomness increases with the adsorption of MO.

scholarly journals Electro-reduction of carbon dioxide at low over-potential at a metal–organic framework decorated cathode

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Xinchen Kang ◽  
Lili Li ◽  
Alena Sheveleva ◽  
Xue Han ◽  
Jiangnan Li ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Formic Acid ◽  
Active Sites ◽  
Metal Organic Framework ◽  
Computational Modelling ◽  
Structural Defects ◽  
Resonance Spectroscopy ◽  
Faradaic Efficiency ◽  
Metal Organic ◽  
Organic Framework

Abstract Electrochemical reduction of carbon dioxide is a clean and highly attractive strategy for the production of organic products. However, this is hindered severely by the high negative potential required to activate carbon dioxide. Here, we report the preparation of a copper-electrode onto which the porous metal–organic framework [Cu2(L)] [H4L = 4,4′,4″,4′′′-(1,4-phenylenebis(pyridine-4,2,6-triyl))tetrabenzoic acid] can be deposited by electro-synthesis templated by an ionic liquid. This decorated electrode shows a remarkable onset potential for reduction of carbon dioxide to formic acid at −1.45 V vs. Ag/Ag+, representing a low value for electro-reduction of carbon dioxide in an organic electrolyte. A current density of 65.8 mA·cm−2 at −1.8 V vs. Ag/Ag+ is observed with a Faradaic efficiency to formic acid of 90.5%. Electron paramagnetic resonance spectroscopy confirms that the templated electro-synthesis affords structural defects in the metal–organic framework film comprising uncoupled Cu(II) centres homogenously distributed throughout. These active sites promote catalytic performance as confirmed by computational modelling.

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