TY - JOUR
T1 - Immobilized Ni on TMEDA@βSiO2@αSiO2@Fe3O4
T2 - as a novel magnetic nanocatalyst for preparation of pyrido[2,3-d:6,5-d′]dipyrimidines
AU - Almajidi, Yasir Qasim
AU - Ubaidullah, Mohd
AU - Pandit, Bidhan
AU - Kareem, A. K.
AU - Romero-Parra, Rosario Mireya
AU - Bobirjon, Adizov
AU - Kadhum, Wesam R.
AU - AL-Erjan, Amran M.
AU - Abosaooda, Munther
AU - Mahmoud, Aisha Kamal
N1 - Funding Information:
The authors are grateful to acknowledge the Research Council of King Saud University, Riyadh, Saudi Arabia.
Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/4/14
Y1 - 2023/4/14
N2 - In the current body of research, a very quick and effectual procedure for the synthesis of pyrido[2,3-d:6,5-d′]dipyrimidines has been developed. This method is accomplished through the one-pot multi-component reaction of 2-thiobarbituric acid, NH4OAc and aldehydes utilizing Ni-TMEDA@βSiO2@αSiO2@Fe3O4 as a novel mesoporous nanomagnetic catalyst at room temperature. This protocol is one of the few reports of the preparation of these derivatives without the use of conventional heating as well as energies such as microwave and ultrasound radiation. The characterization of the prepared catalyst was well accomplished by different techniques such as FT-IR, ICP-OES, SEM, TEM, BET, XRD, VSM, TGA, EDX and Elemental mapping. This organometallic catalyst was reusable for seven times with negligible decrement in its catalytic performance. In addition, all of the products were produced with high TON and TOF values, which demonstrates that our catalyst has a very high level of activity in the preparation of pyrido[2,3-d:6,5-d′]dipyrimidines.
AB - In the current body of research, a very quick and effectual procedure for the synthesis of pyrido[2,3-d:6,5-d′]dipyrimidines has been developed. This method is accomplished through the one-pot multi-component reaction of 2-thiobarbituric acid, NH4OAc and aldehydes utilizing Ni-TMEDA@βSiO2@αSiO2@Fe3O4 as a novel mesoporous nanomagnetic catalyst at room temperature. This protocol is one of the few reports of the preparation of these derivatives without the use of conventional heating as well as energies such as microwave and ultrasound radiation. The characterization of the prepared catalyst was well accomplished by different techniques such as FT-IR, ICP-OES, SEM, TEM, BET, XRD, VSM, TGA, EDX and Elemental mapping. This organometallic catalyst was reusable for seven times with negligible decrement in its catalytic performance. In addition, all of the products were produced with high TON and TOF values, which demonstrates that our catalyst has a very high level of activity in the preparation of pyrido[2,3-d:6,5-d′]dipyrimidines.
UR - http://www.scopus.com/inward/record.url?scp=85156136917&partnerID=8YFLogxK
U2 - 10.1039/d3ra01720f
DO - 10.1039/d3ra01720f
M3 - Original Article
AN - SCOPUS:85156136917
SN - 2046-2069
VL - 13
SP - 11393
EP - 11405
JO - RSC Advances
JF - RSC Advances
IS - 17
ER -