scholarly journals Effect of Substrates on Catalytic Activity of Biogenic Palladium Nanoparticles in C–C Cross-Coupling Reactions

ACS Omega ◽  
2019 ◽  
Vol 4 (2) ◽  
pp. 3329-3340 ◽  
Author(s):  
Manashi Sarmah ◽  
Arindom B. Neog ◽  
Purna K. Boruah ◽  
Manash R. Das ◽  
Pankaj Bharali ◽  
...  
ChemCatChem ◽  
2016 ◽  
Vol 9 (3) ◽  
pp. 451-457 ◽  
Author(s):  
Beau Van Vaerenbergh ◽  
Jeroen Lauwaert ◽  
Wim Bert ◽  
Joris W. Thybaut ◽  
Jeriffa De Clercq ◽  
...  

2017 ◽  
Vol 95 (10) ◽  
pp. 1073-1080 ◽  
Author(s):  
Ramin Ghorbani-Vaghei ◽  
Narges Sarmast

Poly and mono sulfonamide ligands were successfully used for the stabilization of palladium nanoparticles. The prepared nano catalysts that appeared to be heterogeneous and novel were characterized with various analytical tools. To establish the catalytic activity of the prepared catalysts, they were used in the Suzuki–Miyaura and Sonogashira–Hagihara coupling reactions of aryl halides under low palladium loading conditions. The catalysts showed good stability and could be recovered and reused for seven reaction cycles without significant loss of catalytic activity.


2008 ◽  
Vol 61 (8) ◽  
pp. 610 ◽  
Author(s):  
Guozhi Fan ◽  
Hanjun Zhang ◽  
Siqing Cheng ◽  
Zhandong Ren ◽  
Zhijun Hu ◽  
...  

Palladium chloride anchored on polystyrene modified by 5-amino-1,10-phenanthroline was prepared and used as an efficient recoverable catalyst for Suzuki cross-coupling reactions. The heterogeneous catalysts can be easily separated from the reaction mixture and reused for five cycles without significant Pd leaching and loss of catalytic activity. Rate enhancement in the Suzuki reaction by Lewis acids was also studied.


2014 ◽  
Vol 38 (9) ◽  
pp. 4267-4274 ◽  
Author(s):  
Manoj Trivedi ◽  
Sanjeev kumar Ujjain ◽  
Raj Kishore Sharma ◽  
Gurmeet Singh ◽  
Abhinav Kumar ◽  
...  

A cyano-bridged Cu(ii)–Cu(i) complex was synthesized and transformed into CuO nanoparticles. Their catalytic activity in C–N, C–O, and C–S cross-coupling reactions was explored.


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