Visible light-driven photocatalytic Heck reaction over carbon nanocoil supported Pd nanoparticles

2016 ◽  
Vol 6 (21) ◽  
pp. 7738-7743 ◽  
Author(s):  
Xiao-Wei Guo ◽  
Cai-Hong Hao ◽  
Cheng-Yu Wang ◽  
Sarina Sarina ◽  
Xiao-Ning Guo ◽  
...  

This paper presents a carbon nanocoil supported Pd nanoparticle system (Pd/CNCs) as a photocatalyst for coupling reaction of aryl halides and alkenes (Heck reaction) at 40 °C.

2019 ◽  
Vol 43 (37) ◽  
pp. 14674-14677 ◽  
Author(s):  
Shunmin Ding ◽  
Baihong Qu ◽  
Yuan Li ◽  
Ling Sun ◽  
Shaohua Wu ◽  
...  

Herein, a meso–macroporous organic polymer-supported Pd nanoparticle catalyst (Pd/MOP-I) with homogeneously dispersed small Pd NPs (ca. 2.4 nm) was synthesized by a simple ion-exchange approach.


2019 ◽  
Vol 2019 ◽  
pp. 1-7 ◽  
Author(s):  
Linda Zh. Nikoshvili ◽  
Nadezhda A. Nemygina ◽  
Tatiana E. Khudyakova ◽  
Irina Yu. Tiamina ◽  
Alexey V. Bykov ◽  
...  

This paper describes the synthesis of Pd-containing catalysts based on nonfunctionalized hypercrosslinked polystyrene via impregnation with Pd acetate. Developed Pd nanoparticulate catalyst allowed achieving conversion of aryl halide up to 90% in Suzuki cross-coupling reaction under mild conditions and at the absence of phase-transfer agents. During the selective hydrogenation of triple C-C bond of 2-methyl-3-butyn-2-ol, up to 96% selectivity with respect to corresponding olefinic alcohol was found at 95% conversion. The influences of the procedure of catalyst synthesis like precursor decomposition and reductive activation method on Pd nanoparticle formation are discussed.


2017 ◽  
Vol 2 (4) ◽  
pp. 472-478 ◽  
Author(s):  
M. Obst ◽  
R. S. Shaikh ◽  
B. König

A novel reactor for solvent-free, visible-light-driven photocatalytic transformations was developed.


2013 ◽  
Vol 91 (5) ◽  
pp. 348-351 ◽  
Author(s):  
Suresh B. Waghmode ◽  
Sudhir S. Arbuj ◽  
Bina N. Wani ◽  
C.S. Gopinath

PdCl2 catalyzed carbon–carbon bond formation (Heck reaction) between substituted aryl halides and olefins was carried out without a ligand, under irradiation with UV–visible light. The results demonstrated that UV–visible light accelerated the rate of the reaction, leading to an excellent yield of corresponding products. The recovered palladium nanoparticles could be thermally recycled several times. PdCl2 gave excellent conversion up to the fifth addition of substrate.


2019 ◽  
Vol 7 (1) ◽  
pp. 23-33
Author(s):  
Vaibhav Mishra ◽  
Anju Arya ◽  
Tejpal Singh Chundawat

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.


2020 ◽  
Vol 41 (2) ◽  
pp. 357-363 ◽  
Author(s):  
Zhi-Feng Jiao ◽  
Ji-Xiao Zhao ◽  
Xiao-Ning Guo ◽  
Xiang-Yun Guo

RSC Advances ◽  
2015 ◽  
Vol 5 (5) ◽  
pp. 3512-3520 ◽  
Author(s):  
Debojeet Sahu ◽  
Pankaj Das

Highly dispersed silica-supported Pd nanoparticles were synthesizedviaa simple strategy. The material showed excellent catalytic activity for Suzuki–Miyaura reactions and could be reused several times.


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