Plant mediated synthesis of flower-like Cu2O microbeads from Artimisia campestris L. extract for the catalyzed synthesis of 1,4-disubstituted 1,2,3-triazole derivatives

被引:3
|
作者
Abdelbaki, Halla [1 ,2 ]
Djemoui, Amar [3 ]
Souli, Lahcene [3 ]
Souadia, Ahmed [4 ]
Ouahrani, Mohammed Ridha [1 ,2 ]
Djemoui, Brahim [5 ]
Lahrech, Mokhtar Boualem [3 ]
Messaoudi, Mohammed [6 ]
Ben Amor, Ilham [7 ]
Benarfa, Adel [8 ,9 ]
Alsalme, Ali [10 ]
Bechelany, Mikhael [11 ,12 ]
Barhoum, Ahmed [13 ]
机构
[1] Univ El Oued, Fac Exact Sci, Dept Chem, El Oued, Algeria
[2] Univ El Oued, Fac Nat Sci & Life, Lab Biodivers & Applicat Biotechnol Agr Field, El Oued, Algeria
[3] ZIANE Achour Univ, Fac Exact Sci & Comp Sci, Dept Chem, Lab Organ Chem & Nat Subst, Djelfa, Algeria
[4] ZIANE Achour Univ, Fac Exact Sci & Comp Sci, Dept Chem, Lab Physicochem Mat & Environm, Djelfa, Algeria
[5] Oran Univ 1, Fac Exact & Appl Sci FSEA, Dept Chem, Oran, Algeria
[6] Nucl Res Ctr Birine CRNB, Djelfa, Algeria
[7] Univ El Oued, Fac Technol, Dept Proc Engn & Petrochem, El Oued, Algeria
[8] Univ Amar Telidji Laghouat, Lab Sci Fondamentales LSF, Laghouat, Algeria
[9] Ctr Rech Sci & Tech Anal Physico Chim CRAPC PTAPC, Laghouat, Algeria
[10] King Saud Univ, Coll Sci, Dept Chem, Riyadh, Saudi Arabia
[11] Univ Montpellier, Inst Europeen Membranes IEM, CNRS, UMR 5635,ENSCM, Pl Eugene Bataillon, Montpellier, France
[12] Gulf Univ Sci & Technol, GUST, Mubarak Al Abdullah, Kuwait
[13] Helwan Univ, Fac Sci, Chem Dept, NanoStruc Res Grp, Cairo, Egypt
来源
FRONTIERS IN CHEMISTRY | 2024年 / 11卷
关键词
cuprous oxide; flower-like nanostructures; Artimisia Campestris L. extract; green synthesis; 1,4-disubstituted 1,2,3-triazoles; CUPROUS-OXIDE NANOPARTICLES; ANTIMICROBIAL ACTIVITY; BIOLOGICAL EVALUATION; GREEN SYNTHESIS; EFFICIENT; DEGRADATION;
D O I
10.3389/fchem.2023.1342988
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study presents a novel method for synthesizing 1,4-disubstituted 1,2,3-triazole derivatives through a one-pot, multi-component addition reaction using flower-like Cu2O microbeads as a catalyst. The flower-like Cu2O microbeads were synthesized using an aqueous extract of Artimisia Campestris L. This extract demonstrated the capability to reduce and stabilize Cu2O particles during their initial formation, resulting in the formation of a porous flower-like morphology. These Cu2O microbeads exhibit distinctive features, including a cubic close-packed (ccp) crystal structure with an average crystallite size of 22.8 nm, bandgap energy of 2.7 eV and a particle size of 6 mu m. Their catalytic activity in synthesizing 1,4-disubstituted 1,2,3-triazole derivatives was investigated through systematic exploration of key parameters such as catalyst quantity (1, 5, 10, 15, 20, and 30 mg/mL), solvent type (dimethylformamide/H2O, ethanol/H2O, dichloromethane/H2O, chloroform, acetone, and dimethyl sulfoxide), and catalyst reusability (four cycles). The Cu2O microbeads significantly increased the product yield from 20% to 85.3%. The green synthesis and outstanding catalytic attributes make these flower-like Cu2O microbeads promising, efficient, and recyclable catalysts for sustainable and effective chemical transformations.
引用
收藏
页数:16
相关论文
共 50 条
  • [41] Copper(I)-Catalyzed Synthesis of 1,4-Disubstituted 1,2,3-Triazoles from Azidoformates and Aryl Terminal Alkynes
    Lee, Heejin
    Lee, Jae Kyun
    Min, Sun-Joon
    Seo, Hyeonglim
    Lee, Youngbok
    Rhee, Hakjune
    JOURNAL OF ORGANIC CHEMISTRY, 2018, 83 (08): : 4805 - 4811
  • [42] Synthesis of novel 1,4-disubstituted-1,2,3-triazole semi synthetic analogues of forskolin by click reaction
    Reddy, M. Koteswara
    Kumar, K. Santosh
    Sreenivas, P.
    Krupadanam, G. L. David
    Reddy, K. Janardhan
    TETRAHEDRON LETTERS, 2011, 52 (49) : 6537 - 6540
  • [43] Synthesis of 1,2,3-Triazole Derivatives from 2,3-Dienoates of Methyl Maleopimarate
    Malikova, R. N.
    Sakhautdinov, I. M.
    Abdullin, M. F.
    Mukhamet'yanova, A. F.
    Yunusov, M. S.
    CHEMISTRY OF NATURAL COMPOUNDS, 2017, 53 (02) : 341 - 344
  • [44] Synthesis of 1,2,3-Triazole Derivatives from 2,3-Dienoates of Methyl Maleopimarate
    R. N. Malikova
    I. M. Sakhautdinov
    M. F. Abdullin
    A. F. Mukhamet’yanova
    M. S. Yunusov
    Chemistry of Natural Compounds, 2017, 53 : 341 - 344
  • [45] One-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from nitrobenzenes
    Fen Zhao
    Zhen Chen
    Kai Xie
    Rui Yang
    Yu-Bo Jiang
    ChineseChemicalLetters, 2016, 27 (01) : 109 - 113
  • [46] One-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from nitrobenzenes
    Zhao, Fen
    Chen, Zhen
    Xie, Kai
    Yang, Rui
    Jiang, Yu-Bo
    CHINESE CHEMICAL LETTERS, 2016, 27 (01) : 109 - 113
  • [47] Design, synthesis, structural characterization and in vitro evaluation of new 1,4-disubstituted-1,2,3-triazole derivatives against glioblastoma cells
    da Silva, Veronica D.
    de Faria, Bruna M.
    Colombo, Eduardo
    Ascari, Lucas
    Freitas, Gabriella P. A.
    Flores, Leona S.
    Cordeiro, Yraima
    Romao, Luciana
    Buarque, Camilla D.
    BIOORGANIC CHEMISTRY, 2019, 83 : 87 - 97
  • [48] Synthesis of novel 1,2,3-triazole tethered 1,3-disubstituted β-carboline derivatives and their cytotoxic and antibacterial activities
    Salehi, Peyman
    Babanezhad-Harikandei, Kosar
    Bararjanian, Morteza
    Al-Harrasi, Ahmed
    Esmaeili, Mohammad-Ali
    Aliahmadi, Atousa
    MEDICINAL CHEMISTRY RESEARCH, 2016, 25 (09) : 1895 - 1907
  • [49] Regioselective Synthesis and Molecular Docking Studies of 1,5-Disubstituted 1,2,3-Triazole Derivatives of Pyrimidine Nucleobases
    Algieri, Vincenzo
    Costanzo, Paola
    Tallarida, Matteo Antonio
    Olivito, Fabrizio
    Jiritano, Antonio
    Fiorani, Giulia
    Peccati, Francesca
    Jimenez-Oses, Gonzalo
    Maiuolo, Loredana
    De Nino, Antonio
    MOLECULES, 2022, 27 (23):
  • [50] Synthesis of novel 1,2,3-triazole tethered 1,3-disubstituted β-carboline derivatives and their cytotoxic and antibacterial activities
    Peyman Salehi
    Kosar Babanezhad-Harikandei
    Morteza Bararjanian
    Ahmed Al-Harrasi
    Mohammad-Ali Esmaeili
    Atousa Aliahmadi
    Medicinal Chemistry Research, 2016, 25 : 1895 - 1907