TY - JOUR
T1 - Green Approach for the Synthesis of 2-Phenyl-2H-indazoles and Quinazoline Derivatives Using Sustainable Heterogeneous Copper Oxide Nanoparticles Supported on Activated Carbon and OER Study
AU - Thrilokraj, R.
AU - Kumar, Maruboina Hemanth
AU - Ankalgi, Vishwanath
AU - Shaikh, Shoyebmohamad F.
AU - Al-Enizi, Abdullah M.
AU - Małecki, Jan Grzegorz
AU - Kshirsagar, Umesh A.
AU - Rout, Chandra Sekhar
AU - Dateer, Ramesh B.
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/10/29
Y1 - 2024/10/29
N2 - This research work reports the synthesis of copper oxide (CuO) nanoparticles supported on activated carbon by a simple impregnation method using 2-propanol as a green solvent, followed by calcination. The synthesized CuO@C is used as an efficient heterogeneous nanocatalyst for the synthesis of 2H-indazoles and quinazolines utilizing commercially available 2-bromobenzaldehydes, primary amines, and sodium azide under ligand-free and base-free conditions. The present methodology demonstrates the formation of new N-N, C-N, and C═N bonds under one-pot reaction conditions using PEG-400 as a green solvent. The reaction pathways are supported by control experiments and mechanistic elucidation. Further, the synthesized catalyst was characterized by a range of microscopic and spectroscopic techniques such as powdered X-ray diffraction, fourier transform infrared spectroscopy, field emission scanning electron microscopy, energy-dispersive X-ray, UV-vis, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy, and BET-BJH analysis. Importantly, the study focused on the recyclability of the catalyst and successfully showed gram-scale production.
AB - This research work reports the synthesis of copper oxide (CuO) nanoparticles supported on activated carbon by a simple impregnation method using 2-propanol as a green solvent, followed by calcination. The synthesized CuO@C is used as an efficient heterogeneous nanocatalyst for the synthesis of 2H-indazoles and quinazolines utilizing commercially available 2-bromobenzaldehydes, primary amines, and sodium azide under ligand-free and base-free conditions. The present methodology demonstrates the formation of new N-N, C-N, and C═N bonds under one-pot reaction conditions using PEG-400 as a green solvent. The reaction pathways are supported by control experiments and mechanistic elucidation. Further, the synthesized catalyst was characterized by a range of microscopic and spectroscopic techniques such as powdered X-ray diffraction, fourier transform infrared spectroscopy, field emission scanning electron microscopy, energy-dispersive X-ray, UV-vis, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy, and BET-BJH analysis. Importantly, the study focused on the recyclability of the catalyst and successfully showed gram-scale production.
UR - https://www.scopus.com/pages/publications/85206629534
U2 - 10.1021/acs.langmuir.4c03054
DO - 10.1021/acs.langmuir.4c03054
M3 - Article
C2 - 39410783
AN - SCOPUS:85206629534
SN - 0743-7463
VL - 40
SP - 22918
EP - 22930
JO - Langmuir
JF - Langmuir
IS - 43
ER -