scholarly journals Ruthenium(0) Nanoclusters Stabilized by a Nanozeolite Framework: Isolable, Reusable, and Green Catalyst for the Hydrogenation of Neat Aromatics under Mild Conditions with the Unprecedented Catalytic Activity and Lifetime

2010 ◽  
Vol 132 (18) ◽  
pp. 6541-6549 ◽  
Author(s):  
Mehmet Zahmakıran ◽  
Yalçın Tonbul ◽  
Saim Özkar
Keyword(s):  
Catalytic Activity ◽  
Green Catalyst ◽  
Mild Conditions

scholarly journals Ultra-Small Pd(0) Nanoparticles into a Designed Semisynthetic Lipase: An Efficient and Recyclable Heterogeneous Biohybrid Catalyst for the Heck Reaction under Mild Conditions

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2358 ◽  
Author(s):  
David Lopez-Tejedor ◽  
Blanca de las Rivas ◽  
Jose M. Palomo
Keyword(s):  
Catalytic Activity ◽  
Protein Structure ◽  
Heck Reaction ◽  
Catalytic Performance ◽  
Reducing Agent ◽  
Chemically Modified ◽  
Mild Conditions ◽  
In Situ Formation ◽  
Geobacillus Thermocatenulatus

A novel heterogeneous enzyme-palladium (Pd) (0) nanoparticles (PdNPs) bionanohybrid has been synthesized by an efficient, green, and straightforward methodology. A designed Geobacillus thermocatenulatus lipase (GTL) variant genetically and then chemically modified by the introduction of a tailor-made cysteine-containing complementary peptide- was used as the stabilizing and reducing agent for the in situ formation of ultra-small PdNPs nanoparticles embedded on the protein structure. This bionanohybrid was an excellent catalyst in the synthesis of trans-ethyl cinnamate by Heck reaction at 65 °C. It showed the best catalytic performance in dimethylformamide (DMF) containing 10–25% of water as a solvent but was also able to catalyze the reaction in pure DMF or with a higher amount of water as co-solvent. The recyclability and stability were excellent, maintaining more than 90% of catalytic activity after five cycles of use.

The Effect of Ni Precursor Salts on Diatomite Supported Ni-Mg Catalysts in Methanation of CO2

2021 ◽  
Vol 1016 ◽  
pp. 1417-1422
Author(s):  
Chao Sun ◽  
Jugoslav Krstic ◽  
Vojkan Radonjic ◽  
Miroslav Stankovic ◽  
Patrick da Costa
Keyword(s):  
Catalytic Activity ◽  
Atmospheric Pressure ◽  
Textural Properties ◽  
Catalytic Performance ◽  
Nickel Salt ◽  
Nitrate Salt ◽  
Efficient Catalyst ◽  
Mild Conditions ◽  
The Difference ◽  
Supported Ni

This study is aimed to investigate the effect of Ni precursor salts on the properties (textural, phase-structural, reducibility, and basicity), and catalytic performance of diatomite supported Ni-Mg catalyst in methanation of CO2. The NiMg/D-X catalysts derived from various nickel salts (X = S-sulfamate, N-nitrate or A-acetate) were synthesized by the precipitation-deposition (PD) method. The catalysts were characterized by N2-physisorption, XRD, TPR-H2, and TPD-CO2 techniques. The different catalytic activity (conversion) and selectivity, observed in CO2 methanation carried out under relatively mild conditions (atmospheric pressure; temperatures: 250-450 °C) are related and explained by the difference in textural properties, metallic Ni-crystallite size, reducibility, and basicity of studied catalysts. The results showed that catalyst derived from Ni-nitrate salt (NiMg/D-N) is more suitable for the preparation of efficient catalyst for CO2 methanation than its counterparts derived from sulfamate (NiMg/D-S) or acetate (NiMg/D-A) nickel salt. The NiMg/D-N catalyst showed the highest specific surface area and total basicity, and the best catalytic performance with CO2 conversion of 63.3 % and CH4 selectivity of 80.9 % at 450 °C.

A highly efficient catalyst for Suzuki–Miyaura coupling reaction of benzyl chloride under mild conditions

RSC Advances ◽  
2014 ◽  
Vol 4 (69) ◽  
pp. 36437-36443 ◽  
Author(s):  
Zhenhong Guan ◽  
Buyi Li ◽  
Guoliang Hai ◽  
Xinjia Yang ◽  
Tao Li ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Benzyl Chloride ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Efficient Catalyst ◽  
Microporous Polymers ◽  
Mild Conditions ◽  
Highly Efficient ◽  
Cross Coupling Reactions

Microporous polymers with built-in triphenylphosphine palladium exhibit highly efficient catalytic activity for cross-coupling reactions of benzyl chloride under mild conditions.

Ce3+ self-doped CeOx/FeOCl: an efficient Fenton catalyst for phenol degradation under mild conditions

2019 ◽  
Vol 48 (10) ◽  
pp. 3476-3485 ◽  
Author(s):  
Jian Zhang ◽  
Mengxue Yang ◽  
Ye Lian ◽  
Mingliang Zhong ◽  
Jingquan Sha ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Room Temperature ◽  
Phenol Degradation ◽  
Natural Light ◽  
Neutral Solution ◽  
Mild Conditions ◽  
Fenton Catalyst ◽  
First Time

Herein, a novel Ce3+ self-doped CeOx/FeOCl composite was successfully prepared by a facile method for the first time, which showed remarkable catalytic activity as a Fenton catalyst in the degradation of phenol under the conditions of a neutral solution, room temperature and natural light.

Efficient hydrogenolysis of aryl ethers over Ce-MOF supported Pd NPs under mild conditions: mechanistic insight using density functional theoretical calculations

2020 ◽  
Vol 10 (20) ◽  
pp. 6892-6901
Author(s):  
Ashish Kumar Kar ◽  
Surinder Pal Kaur ◽  
T. J. Dhilip Kumar ◽  
Rajendra Srivastava
Keyword(s):  
Catalytic Activity ◽  
Adsorption Energy ◽  
Density Functional ◽  
Theoretical Calculations ◽  
Desorption Energy ◽  
Mild Conditions ◽  
Mechanistic Insight ◽  
Aryl Ethers ◽  
Benzyl Phenyl Ether ◽  
Supported Pd

The significant Pd0 content and optimum bonding of the reactant & product (higher adsorption energy of benzyl phenyl ether and lower desorption energy for phenol) are responsible for the exceptional catalytic activity of Pd/Ce-MOF.

scholarly journals Catalytic Activity of Polynuclear vs. Dinuclear Aroylhydrazone Cu(II) Complexes in Microwave-Assisted Oxidation of Neat Aliphatic and Aromatic Hydrocarbons

Molecules ◽  
2018 ◽  
Vol 24 (1) ◽  
pp. 47 ◽  
Author(s):  
Manas Sutradhar ◽  
Tannistha Barman ◽  
Armando Pombeiro ◽  
Luísa Martins
Keyword(s):  
Catalytic Activity ◽  
Aromatic Hydrocarbons ◽  
Catalytic Performance ◽  
Antiproliferative Agents ◽  
One Dimensional ◽  
X Ray ◽  
X Ray Crystallography ◽  
Mild Conditions ◽  
Microwave Assisted ◽  
Aliphatic And Aromatic Hydrocarbons

One-dimensional (1D) polynuclear Cu(II) complex (1) derived from (5-bromo-2-hydroxybenzylidene)-2-hydroxybenzohydrazide (H2L) is synthesized and characterized by elemental analysis, IR spectroscopy, ESI-MS, and single crystal X-ray crystallography. Its catalytic performance towards the solvent-free microwave-assisted peroxidative oxidation of aliphatic and aromatic hydrocarbons under mild conditions is compared with that of dinuclear Cu(II) complexes (2 and 3) of the same ligand, previously reported as antiproliferative agents. Polymer 1 exhibits the highest activity, either for the oxidation of cyclohexane (leading to overall yields, based on the alkane, of up to 39% of cyclohexanol and cyclohexanone) or towards the oxidation of toluene (selectively affording benzaldehyde up to a 44% yield), after 2 or 2.5 h of irradiation at 80 or 50 °C, respectively.

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