scholarly journals Poly(o-aminothiophenol)-stabilized Pd nanoparticles as efficient heterogenous catalysts for Suzuki cross-coupling reactions

RSC Advances ◽  
2017 ◽  
Vol 7 (74) ◽  
pp. 47104-47110 ◽  
Author(s):  
Yuan Chen ◽  
Minggui Wang ◽  
Long Zhang ◽  
Yan Liu ◽  
Jie Han

Poly(o-aminothiophenol)-stabilized Pd nanoparticles have been obtained through a facile one-step route, which exhibit excellent catalytic performance in Suzuki cross-coupling reactions.

2018 ◽  
Vol 42 (8) ◽  
pp. 419-423
Author(s):  
Li-Jie Zhang ◽  
Xian Yao ◽  
Ying-xin Sun ◽  
Jia-wei Zhang ◽  
Chun Cai

Pd–Ni bimetallic nanoparticles (BMNPs) supported on ZrO2 were prepared by an impregnation–reduction method. The BMNPs showed excellent catalytic performance in Suzuki carbon–carbon cross-coupling reactions and almost quantitative conversion of the substrates was obtained under mild conditions in the absence of ligand. The excellent catalytic performance of the bimetallic catalyst could be a result of the synergistic effect between the two metal components. The catalyst showed outstanding recyclability during the reaction process; no obvious decrease in catalytic performance was observed after five cycles.


2015 ◽  
Vol 13 (17) ◽  
pp. 4953-4959 ◽  
Author(s):  
Roberto Ricciardi ◽  
Jurriaan Huskens ◽  
Willem Verboom

Dendrimer-encapsulated Pd nanoparticles anchored within continuous flow microreactors are efficient for C–C cross-coupling reactions. This is witnessed by the good catalytic performance for the Heck–Cassar and Suzuki–Miyaura couplings.


2020 ◽  
Author(s):  
Baojian Xiong ◽  
Yue Li ◽  
Yin Wei ◽  
Søren Kramer ◽  
Zhong Lian

Cross-coupling between substrates that can be easily derived from phenols is highly attractive due to the abundance and low cost of phenols. Here, we report a dual nickel/palladium-catalyzed reductive cross-coupling between aryl tosylates and aryl triflates; both substrates can be accessed in just one step from readily available phenols. The reaction has a broad functional group tolerance and substrate scope (>60 examples). Furthermore, it displays low sensitivity to steric effects demonstrated by the synthesis of a 2,2’disubstituted biaryl and a fully substituted aryl product. The widespread presence of phenols in natural products and pharmaceuticals allow for straightforward late-stage functionalization, illustrated with examples such as Ezetimibe and tyrosine. NMR spectroscopy and DFT calculations indicate that the nickel catalyst is responsible for activating the aryl triflate, while the palladium catalyst preferentially reacts with the aryl tosylate.


2019 ◽  
Vol 4 (17) ◽  
pp. 5019-5032 ◽  
Author(s):  
Astha Shukla ◽  
Rajib K. Singha ◽  
Takehiko Sasaki ◽  
Vemulapalli V. D. N. Prasad ◽  
Rajaram Bal

2018 ◽  
Vol 9 (46) ◽  
pp. 8673-8681 ◽  
Author(s):  
Petr Slavík ◽  
Dustin W. Kurka ◽  
David K. Smith

From waste to wealth – a self-assembled hydrogel remediates palladium from solution down to sub-ppm levels, and the resulting gel, which has embedded Pd nanoparticles, acts as a green and efficient catalyst for Suzuki–Miyaura cross-coupling reactions.


2014 ◽  
Vol 38 (9) ◽  
pp. 4622-4627 ◽  
Author(s):  
Xiaohang Zhu ◽  
Jianrui Niu ◽  
Fengwei Zhang ◽  
Jinghui Zhou ◽  
Xinzhe Li ◽  
...  

We report on the synthesis, characterization and catalytic performance of a palladium-based superparamagnetic catalyst of Fe3O4@polyaniline core/shell microspheres (Fe3O4@PANI–PdII).


2015 ◽  
Vol 44 (37) ◽  
pp. 16592-16601 ◽  
Author(s):  
Yinle Li ◽  
Zhuqing Zhang ◽  
Jianfeng Shen ◽  
Mingxin Ye

The novel multifunctional Fe3O4@C–Pd@CeO2 nanospheres show excellent catalytic performance in the Suzuki–Miyaura cross-coupling reaction and the reduction of 4-nitrophenol.


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