Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Greener synthesis of 1,2,3-triazoles using a copper(i)-exchanged magnetically recoverable beta-zeolite as catalyst

Full text
Author(s):
Costa, Elizama R. [1] ; Andrade, Floyd C. D. [1] ; de Albuquerque, Danilo Yano [1] ; Ferreira, Luanne E. M. [2] ; Lima, Thiago M. [2] ; Lima, Carolina G. S. [3] ; Silva, Domingos S. A. [4] ; Urquieta-Gonzalez, Ernesto A. [4] ; Paixao, Marcio W. [1] ; Schwab, Ricardo S. [1]
Total Authors: 10
Affiliation:
[1] Univ Fed Sao Carlos UFSCar, Ctr Excellence Res Sustainable Chem CERSusChem, Dept Quim, Rodovia Washington Luis, Km 235 SP-310, BR-13565905 Sao Carlos, SP - Brazil
[2] Univ Fed Fluminense, Dept Quim Inorgan, Campus Valonguinho, Outeiro Sao Joao Batista S-N, BR-24020150 Niteroi, RJ - Brazil
[3] Univ Fed Fluminense, Dept Quim Organ, Campus Valonguinho, Outeiro Sao Joao Batista S-N, BR-24020150 Niteroi, RJ - Brazil
[4] Univ Fed Sao Carlos DEQ, Res Ctr Adv Mat & Energy, C Postal 676, BR-13565905 Sao Carlos, SP - Brazil
Total Affiliations: 4
Document type: Journal article
Source: NEW JOURNAL OF CHEMISTRY; v. 44, n. 35, p. 15046-15053, SEP 21 2020.
Web of Science Citations: 0
Abstract

Herein, we describe the preparation and thorough characterization of a novel magnetically recoverable copper(i)-exchanged beta-zeolite and its use as an efficient catalyst for the synthesis of 1,2,3-triazolesviathe one-pot three-component reaction of organic halides, terminal acetylenes, and sodium azide in water. The magnetically recoverable beta-zeolite could be easily separated from the reaction mixture with the aid of a magnet and reused in several consecutive reactions. Importantly, a series of characterizations studies allowed us to disclose the mechanism for the deactivation of the catalyst, and therefore to propose a method for its reactivation. (AU)

FAPESP's process: 14/50249-8 - Green chemistry: sustainable synthetic methods employing benign solvents, safer reagents, and bio-renewable feedstock
Grantee:Arlene Gonçalves Corrêa
Support Opportunities: Research Grants - Research Centers in Engineering Program
FAPESP's process: 13/06558-3 - Asymmetric catalysis: preparation of chiral alcohols and their derivatives from highly functionalized organozinc reagents and application of new chiral ligands supported on magnetic nanoparticles
Grantee:Ricardo Samuel Schwab
Support Opportunities: Regular Research Grants