Nickel stabilized by triazole-functionalized carbon nanotubes as a novel reusable and efficient heterogeneous nanocatalyst for the Suzuki–Miyaura coupling reaction

RSC Advances ◽  
2016 ◽  
Vol 6 (112) ◽  
pp. 110622-110628 ◽  
Author(s):  
Abdol. R. Hajipour ◽  
Parisa Abolfathi

The synthesis of a MWCNT-grafted nickel catalyst through “click” reaction of azide-functionalized carbon nanotubes with propargyl alcohol, for the Suzuki–Miyaura coupling reaction.

2002 ◽  
Vol 01 (03n04) ◽  
pp. 285-293 ◽  
Author(s):  
M. CROSTON ◽  
J. LANGSTON ◽  
G. TAKACS ◽  
T. C. MORRILL ◽  
M. MIRI ◽  
...  

Aniline is oxidized to nitrosobenzene as the initial product, which undergoes further oxidation to nitrobenzene. The nitrosobenzene formation is catalyzed by functionalized multiwalled carbon nanotubes (CNT) followed by a coupling reaction between nitrosobenzene and aniline to produce azobenzene. This coupling requires close proximity of the reactants. It proceeds rapidly resulting in the UV-VIS absorption spectrum showing maxima at 327 nm and 425 nm. The nitrosobenzene yield in the presence of CNTs is controlled by the amount present in the medium. As the reaction is not catalyzed by unfunctionalized CNTs or graphitic particles, the uniqueness of the functionalized multiwalled CNTs in this catalysis suggests a nanodimensional reaction pathway.


2019 ◽  
Vol 77 ◽  
pp. 105912 ◽  
Author(s):  
Sufang Chen ◽  
Liang Chen ◽  
Yimei Wang ◽  
Cunwen Wang ◽  
Menghe Miao ◽  
...  

2013 ◽  
Vol 85 (17) ◽  
pp. 8391-8396 ◽  
Author(s):  
Jing Pan ◽  
Hanyu Zhang ◽  
Tae-Gon Cha ◽  
Haorong Chen ◽  
Jong Hyun Choi

ACS Nano ◽  
2021 ◽  
Author(s):  
Yu Zheng ◽  
Younghee Kim ◽  
Andrew C. Jones ◽  
Gabrielle Olinger ◽  
Eric R. Bittner ◽  
...  

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