Calcined Layered Double Hydroxides: Catalysts for Xanthene, 1,4-Dihydropyridine, and Polyhydroquinoline Derivative Synthesis.


Journal

ACS omega
ISSN: 2470-1343
Titre abrégé: ACS Omega
Pays: United States
ID NLM: 101691658

Informations de publication

Date de publication:
30 Jun 2020
Historique:
received: 25 04 2020
accepted: 04 06 2020
entrez: 9 7 2020
pubmed: 9 7 2020
medline: 9 7 2020
Statut: epublish

Résumé

This work is generally focused on the synthesis of NiFeTi-layered double hydroxides (LDHs) using a hydrothermal route, which were calcined at various temperatures (varying from 200 to 600 °C). The synthesized materials were physicochemically characterized. X-ray diffraction results revealed the loss of the layered structure on calcination resulting in the formation of layered double oxides (LDOs) or mixed metal oxides, which was also supported by Fourier transform infrared studies. Scanning electron microscopy results also show loss of the layered structure and the creation of LDOs on increasing the temperature. These LDOs were tested as the catalysts for the synthesis of biologically significant xanthene, 1,4-dihydropyridine, and polyhydroquinoline derivatives. Among all, NiFeTi LDH calcined at 600 °C proved to be the best catalyst for the synthesis of these derivative compounds under optimized conditions. The advantages obtained were excellent yields in a lesser reaction time. Stability and reusability were also assessed; the catalyst was stable even after five cycles. Furthermore, the memory effect of the obtained NiFeTi CLDH calcined at 600 °C confirms that the material so formed is a calcined state of LDH itself. High catalytic efficiency, easy fabrication, and recycling ability of NiFeTi CLDH calcined at 600 °C make it a potential catalyst for the synthesis of xanthene, 1,4-dihydropyridine, and polyhydroquinoline derivatives.

Identifiants

pubmed: 32637842
doi: 10.1021/acsomega.0c01901
pmc: PMC7331214
doi:

Types de publication

Journal Article

Langues

eng

Pagination

15673-15680

Informations de copyright

Copyright © 2020 American Chemical Society.

Déclaration de conflit d'intérêts

The authors declare no competing financial interest.

Références

ACS Appl Mater Interfaces. 2009 Oct;1(10):2353-62
pubmed: 20355873
Water Res. 2008 Mar;42(6-7):1343-68
pubmed: 18061644
Sci Rep. 2019 Nov 7;9(1):16225
pubmed: 31700113
ACS Omega. 2018 Nov 30;3(11):16377-16385
pubmed: 31458273
ACS Omega. 2018 May 08;3(5):5012-5020
pubmed: 31458714
Chem Pharm Bull (Tokyo). 2006 Jan;54(1):111-3
pubmed: 16394561
Spectrochim Acta A Mol Biomol Spectrosc. 2005 Jul;61(9):1997-2003
pubmed: 15911383
J Nat Prod. 2009 Mar 27;72(3):527-39
pubmed: 19191562
Org Biomol Chem. 2010 Mar 7;8(5):1097-105
pubmed: 20165800
Biochem J. 1989 Mar 15;258(3):683-7
pubmed: 2471509

Auteurs

Garima Rathee (G)

Drug Discovery & Development Laboratory, Department of Chemistry, University of Delhi, Delhi 110007, India.

Sahil Kohli (S)

Drug Discovery & Development Laboratory, Department of Chemistry, University of Delhi, Delhi 110007, India.

Nidhi Singh (N)

Drug Discovery & Development Laboratory, Department of Chemistry, University of Delhi, Delhi 110007, India.

Amardeep Awasthi (A)

Drug Discovery & Development Laboratory, Department of Chemistry, University of Delhi, Delhi 110007, India.

Ramesh Chandra (R)

Drug Discovery & Development Laboratory, Department of Chemistry, University of Delhi, Delhi 110007, India.
Dr. B. R. Ambedkar Centre for Biomedical Research, University of Delhi, Delhi 110007, India.

Classifications MeSH