TY - JOUR
T1 - Application of palladium nanoparticles supported on ordered mesoporous oxides for C-N and C[triple bond, length as m-dash]C coupling reactions in water
AU - Maqunga, Nomathamsanqa Prudence
AU - Ndolomingo, Matumuene Joe
AU - Bingwa, Ndzondelelo
AU - Meijboom, Reinout
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025/7/25
Y1 - 2025/7/25
N2 - This study sought to synthesize supported palladium nanocatalysts that are, in general, convenient to synthesize, suitable for mild conditions, recyclable, and stable in water. The sol-gel procedure was successfully extended to synthesize mesoporous metal oxides with well-dispersed palladium nanoparticles. The resulting catalysts were extensively characterized using techniques such as TEM, powder XRD, SEM-EDX, thermogravimetric analysis, and BET surface area measurements. The catalytic activity of the prepared heterogeneous palladium nanoparticles supported on mesoporous oxides was investigated in terms of C-N and C C coupling reactions, yielding products of alkynes and N-arylamines. Specifically, alkynes were effectively cross-coupled with various aryl iodides and aryl bromides, yielding diaryl alkynes with high efficiency and minimal catalyst loss. Similarly, the Buchwald-Hartwig amination reaction produced its desired products with high selectivity and yield.
AB - This study sought to synthesize supported palladium nanocatalysts that are, in general, convenient to synthesize, suitable for mild conditions, recyclable, and stable in water. The sol-gel procedure was successfully extended to synthesize mesoporous metal oxides with well-dispersed palladium nanoparticles. The resulting catalysts were extensively characterized using techniques such as TEM, powder XRD, SEM-EDX, thermogravimetric analysis, and BET surface area measurements. The catalytic activity of the prepared heterogeneous palladium nanoparticles supported on mesoporous oxides was investigated in terms of C-N and C C coupling reactions, yielding products of alkynes and N-arylamines. Specifically, alkynes were effectively cross-coupled with various aryl iodides and aryl bromides, yielding diaryl alkynes with high efficiency and minimal catalyst loss. Similarly, the Buchwald-Hartwig amination reaction produced its desired products with high selectivity and yield.
UR - https://www.scopus.com/pages/publications/105012209499
U2 - 10.1039/d5ra02824h
DO - 10.1039/d5ra02824h
M3 - Article
AN - SCOPUS:105012209499
SN - 2046-2069
VL - 15
SP - 26981
EP - 26991
JO - RSC Advances
JF - RSC Advances
IS - 33
ER -