scholarly journals Surfactant encapsulated palladium-polyoxometalates: controlled assembly and their application as single-atom catalysts

2016 ◽  
Vol 7 (2) ◽  
pp. 1011-1015 ◽  
Author(s):  
Peilei He ◽  
Biao Xu ◽  
Xiaobin Xu ◽  
Li Song ◽  
Xun Wang
Keyword(s):  
Catalytic Activity ◽  
Coupling Reaction ◽  
Single Atom ◽  
High Catalytic Activity ◽  
Controlled Assembly

Two kinds of assembly structures (nanorolls and hollow spindles) based on the palladium substituted Wells–Dawson polyoxometalate (Pd-POM) were synthesised and showed high catalytic activity for both the Suzuki–Miyaura coupling reaction and semihydrogenation reaction.

Catalytic activity of palladium-doped silver dilute nanoalloys for formate oxidation from a theoretical perspective

2019 ◽  
Vol 21 (40) ◽  
pp. 22598-22610 ◽  
Author(s):  
Nan Zhang ◽  
Fuyi Chen ◽  
Longfei Guo
Keyword(s):  
Catalytic Activity ◽  
Oxidation Reaction ◽  
Theoretical Perspective ◽  
Single Atom ◽  
High Catalytic Activity ◽  
Formate Oxidation ◽  
First Time ◽  
Single Atom Alloys

We demonstrate for the first time that the Pd1Ag single-atom alloys exhibit a high catalytic activity for formate oxidation reaction.

High Catalytic Activity of Pd Nanoparticles Synthesized from Green Alga Chlorella vulgaris in Buchwald-hartwig Synthesis of N-Aryl Piperazines

2019 ◽  
Vol 7 (1) ◽  
pp. 23-33
Author(s):  
Vaibhav Mishra ◽  
Anju Arya ◽  
Tejpal Singh Chundawat
Keyword(s):  
Catalytic Activity ◽  
Green Alga ◽  
Chlorella Vulgaris ◽  
Direct Synthesis ◽  
Coupling Reaction ◽  
Pd Nanoparticles ◽  
High Catalytic Activity ◽  
Pd Nanoparticle ◽  
Green Algal ◽  
Green Alga Chlorella

Background: The N-aryl piperazines are an important component of many drug products used for the treatment of malaria, depression, anxiety and Parkinson diseases. Buchwald-Hartwig amination is the latest and well-known reaction for Pd catalyzed direct synthesis of N-aryl piperazine from aryl halides. Although several Pd-ligand systems have already been discovered for this conversion, Pd nanoparticles are recently being used for this useful coupling reaction due to their recyclability and durability. Metal nanoparticles show enhanced catalytic activity compared to their bulk counterparts due to increased surface area at the edges and corners. The use of green algal extract in place of chemical ligands makes this process more environment-friendly and cost-effective. In this research, Pd nanoparticles synthesized using green alga C. Vulgaris were utilized as an alternative approach for the coupling reaction during the preparation of N-aryl piperazines. Methods: Synthesized Pd nanoparticles from C. Vulgaris were characterized by FTIR, SEM and XRD techniques. The catalytic activity of the synthesized nanoparticles was monitored for the synthesis of N-aryl piperazines by Buchwald-Hartwig reaction. The synthesized N-aryl piperazines were characterized by NMR, FTIR and mass analysis. Results: A very good catalytic activity of the synthesized Pd nanoparticles from green alga Chlorella vulgaris extract was observed. The green alga not only reduces the size of the Pd metal to nanoparticles but also acts as a green ligand for reduction of Pd(II) to Pd(0) during nanoparticle synthesis. Using this Pd nanoparticles-green ligand system, several N-aryl piperazines were synthesized in good to excellent yields. Reaction conditions for better conversion were optimized. The comparative advantage of the catalytic system with recently published works on Buchwald-Hartwig C-N coupling reaction is given. Recyclability and durability of the catalyst were explored and the results were found to be promising. A plausible mechanism of Pd nanoparticle catalyzed reaction is also proposed. Conclusion: Catalytic activity of the Pd nanoparticle synthesized from Chlorella vulagris in the synthesis of N-aryl piperazines by Buchwald-Hartwig reaction is reported first time to the best of our knowledge and understanding. The green approach of Pd catalyst to facilitate the reaction and its environmental impact is the main characteristic of the process.

scholarly journals Palladium/phosphorus-functionalized porous organic polymer with tunable surface wettability for water-mediated Suzuki–Miyaura coupling reaction

RSC Advances ◽  
2019 ◽  
Vol 9 (63) ◽  
pp. 36600-36607 ◽  
Author(s):  
Yizhu Lei ◽  
Zaifei Chen ◽  
Guangxing Li
Keyword(s):  
Catalytic Activity ◽  
Coupling Reaction ◽  
Surface Wettability ◽  
Organic Polymer ◽  
High Catalytic Activity ◽  
Aryl Chlorides ◽  
Porous Organic Polymer

A palladium/phosphorus-functionalized porous organic polymer with tunable surface wettability was successfully prepared. The catalyst displayed high catalytic activity for the water-mediated Suzuki–Miyaura coupling reaction of aryl chlorides.

Single-atom transition metals supported on black phosphorene for electrochemical nitrogen reduction

Nanoscale ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 4903-4908 ◽  
Author(s):  
Kang Liu ◽  
Junwei Fu ◽  
Li Zhu ◽  
Xiaodong Zhang ◽  
Hongmei Li ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Transition Metals ◽  
Reduction Reaction ◽  
Single Atom ◽  
High Catalytic Activity ◽  
Nitrogen Reduction ◽  
Mild Conditions ◽  
Black Phosphorene

Electrochemical nitrogen reduction reaction (NRR) is a promising route to produce ammonia under mild conditions. Single-atom W supported on BP was screened as a promising electrocatalyst with high catalytic activity, stability, and selectively for NRR.

A tailored oxide interface creates dense Pt single-atom catalysts with high catalytic activity

2020 ◽  
Vol 13 (4) ◽  
pp. 1231-1239 ◽  
Author(s):  
Mi Yoo ◽  
Young-Sang Yu ◽  
Hyunwoo Ha ◽  
Siwon Lee ◽  
Jin-Seok Choi ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Single Atom ◽  
High Catalytic Activity ◽  
Oxide Interface ◽  
Single Atoms

Catalytic supremacy of Pt-single atoms achieved by CeOx–TiO2 interfaces.

scholarly journals N,N-Dimethylformamide-stabilized copper nanoparticles as a catalyst precursor for Sonogashira–Hagihara cross coupling

RSC Advances ◽  
2017 ◽  
Vol 7 (37) ◽  
pp. 22869-22874 ◽  
Author(s):  
Hideo Oka ◽  
Katsuya Kitai ◽  
Takeyuki Suzuki ◽  
Yasushi Obora
Keyword(s):  
Catalytic Activity ◽  
Copper Nanoparticles ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
High Catalytic Activity ◽  
Catalyst Precursor ◽  
Cross Coupling Reaction

We found that DMF-stabilized Cu NPs have high catalytic activity in the Sonogashira cross-coupling reaction at low catalyst loadings (0.2 mol%).

Colloidal Co single-atom catalyst: a facile synthesis strategy and high catalytic activity for hydrogen generation

2020 ◽  
Vol 22 (4) ◽  
pp. 1269-1274 ◽  
Author(s):  
Junkai Wang ◽  
Zhenxia Huang ◽  
Lilin Lu ◽  
Quanli Jia ◽  
Liang Huang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Catalytic Activity ◽  
Hydrogen Generation ◽  
Single Atom ◽  
High Catalytic Activity ◽  
Mixing Process ◽  
Facile Synthesis ◽  
On Demand ◽  
Synthesis Strategy ◽  
Facile Route

A facile route for on-demand hydrogen production via simply controlling the mixing process of a KBH4 solution and an aqueous solution of ISOBAM-104 stabilized Co2+ ions.

Molecule-level graphdiyne coordinated transition metals as a new class of bifunctional electrocatalysts for oxygen reduction and oxygen evolution reactions

2019 ◽  
Vol 21 (35) ◽  
pp. 19651-19659 ◽  
Author(s):  
Zhen Feng ◽  
Renyi Li ◽  
Yaqiang Ma ◽  
Yi Li ◽  
Dong Wei ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Transition Metals ◽  
Oxygen Reduction ◽  
Oxygen Evolution ◽  
Single Atom ◽  
High Catalytic Activity ◽  
New Class ◽  
Bifunctional Electrocatalysts

Graphdiyne (GDY) could provide a unique platform for synthesizing uniform single-atom catalysts (SACs) with high catalytic activity toward oxygen reduction (ORR) and oxygen evolution (OER) reactions.

scholarly journals Facile Synthesis and Characterization of Palladium@Carbon Catalyst for the Suzuki-Miyaura and Mizoroki-Heck Coupling Reactions

2021 ◽  
Vol 11 (11) ◽  
pp. 4822
Author(s):  
Hamed M. Alshammari ◽  
Obaid F. Aldosari ◽  
Mohammad Hayal Alotaibi ◽  
Raja L. Alotaibi ◽  
Mosaed S. Alhumaimess ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Activated Carbon ◽  
Coupling Reaction ◽  
Aryl Halides ◽  
High Catalytic Activity ◽  
Coupling Reactions ◽  
Heck Coupling ◽  
Efficient Catalyst ◽  
X Ray ◽  
Suzuki Reactions

Palladium-based carbon catalysts (Pd/C) can be potentially applied as an efficient catalyst for Suzuki–Miyaura and Mizoroki–Heck coupling reactions. Herein, a variety of catalysts of palladium on activated carbon were prepared by varying the content of ‘Pd’ via an in situ reduction method, using hydrogen as a reducing agent. The as-prepared catalysts (0.5 wt % Pd/C, 1 wt % Pd/C, 2 wt % Pd/C and 3 wt % Pd/C) were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and Brunauer–Emmett–Teller (BET) analyses. The catalysts were tested as a coupling catalyst for Suzuki–Miyaura coupling reactions involving aryl halides and phenyl boronic acid. The optimization of the catalyst by varying the palladium content on the activated carbon yielded Pd/C catalysts with very high catalytic activity for Suzuki reactions of aryl halides and a Mizoroki–Heck cross-coupling reaction of 4-bromoanisol and acrylic acid in an aqueous medium. A high ‘Pd’ content and uniform ‘Pd’ impregnation significantly affected the activity of the catalysts. The catalytic activity of 3% Pd/C was found to make it a more efficient catalyst when compared with the other synthesized Pd/C catalysts. Furthermore, the catalyst reusability was also tested for Suzuki reactions by repeatedly performing the same reaction using the recovered catalyst. The 3% Pd/C catalyst displayed better reusability even after several reactions.

Sign in / Sign up

Export Citation Format

Share Document