An efficient one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles at room temperature by green synthesized Cu NPs using Otostegia persica leaf extract

被引:40
|
作者
Nasrollahzadeh, Mahmoud [1 ,2 ]
Sajadi, S. Mohammad [3 ]
Mirzaei, Yousef [4 ]
机构
[1] Univ Qom, Dept Chem, Fac Sci, Qom 3716146611, Iran
[2] Univ Qom, Environm Res Ctr, Qom 3716146611, Iran
[3] Soran Univ, Fac Sci, Dept Petr Geosci, POB 624, Soran, Kurdistan Reg G, Iraq
[4] Soran Univ, Fac Sci, Dept Biol, POB 624, Soran, Kurdistan Reg G, Iraq
关键词
1,4-Substituted 1,2,3-triazoles; Green synthesis; Cu NPs; Otostegia persica; MAGNETICALLY SEPARABLE CATALYST; HETEROGENEOUS CATALYST; COPPER NANOPARTICLES; REDUCTIVE AMINATION; TERMINAL ALKYNES; HIGHLY EFFICIENT; SODIUM-AZIDE; HALIDES; CYCLOADDITION; NANOCOMPOSITE;
D O I
10.1016/j.jcis.2016.01.050
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, copper nanoparticles (Cu NPs) were synthesized using a rapid, single step and completely green biosynthetic method by reduction of CuCl2 center dot 2H(2)O solution with aqueous extract of leaves of Otostegia persica containing fiavonoid and other phenolics as a main factor which acts as reducing agent and efficient stabilizer. UV-vis spectra gave surface plasmon resonance (SPR) at 560 nm. The Cu NPs were characterized by transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). A possible synthesis mechanism of Cu NPs was presented. In addition, we investigated the catalytic activity of Cu NPs for the one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles under mild reaction conditions with good to excellent yields. The catalyst could be easily recovered by centrifugation and reused at least five recycles with no significant decreases in the yields. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:156 / 162
页数:7
相关论文
共 50 条
  • [31] Synthesis, Characterization, and Antioxidant and Anticancer Activity of 1,4-Disubstituted 1,2,3-triazoles
    Sahin, Irfan
    Ozgeris, Fatma Betul
    Kose, Muhammet
    Bakan, Ebubekir
    Tumer, Ferhan
    JOURNAL OF MOLECULAR STRUCTURE, 2021, 1232
  • [32] One-pot chemoenzymatic synthesis of chiral disubstituted 1,2,3-triazoles in aqueous media
    de Oliveira, Camila de Souza
    de Andrade, Kleber Tellini
    Omori, Alvaro Takeo
    JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 2013, 91 : 93 - 97
  • [33] An Efficient, One-Pot, Regioselective Synthesis of 1,4-Diaryl-1H-1,2,3-triazoles Using Click Chemistry
    Kumar, Dalip
    Reddy, Vaddula Buchi
    SYNTHESIS-STUTTGART, 2010, (10): : 1687 - 1691
  • [34] One-pot synthesis of 1,2,3-triazoles from α-oxonitriles
    Lakhan, R
    Sharma, BP
    JOURNAL OF THE INDIAN CHEMICAL SOCIETY, 2001, 78 (02) : 101 - 102
  • [35] Cu(I)-promoted one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from anti-3-aryl-2,3-dibromopropanoic acids and nitrobenzaldehydes
    Liu, Xia
    Su, Changhui
    SYNTHETIC COMMUNICATIONS, 2017, 47 (04) : 279 - 284
  • [36] Regioselective one-pot synthesis of 1,4-disubstituted 1,2,3-triazole derivatives
    Gumus, Aysegul
    Ucur, Sibel
    HETEROCYCLIC COMMUNICATIONS, 2014, 20 (06) : 361 - 364
  • [37] Synthesis of silver-graphene nanocomposite and its catalytic application for the one-pot three-component coupling reaction and one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles in water
    Salam, Noor
    Sinha, Arjyabaran
    Roy, Anupam Singha
    Mondal, Paramita
    Jana, Nikhil R.
    Islam, Sk Manirul
    RSC ADVANCES, 2014, 4 (20) : 10001 - 10012
  • [38] One-Pot Approach for the Synthesis of Bis-indole-1,4-disubstituted-1,2,3-triazoles
    Saehlim, Natthiya
    Kasemsuk, Teerapich
    Sirion, Uthaiwan
    Saeeng, Rungnapha
    JOURNAL OF ORGANIC CHEMISTRY, 2018, 83 (21): : 13233 - 13242
  • [39] Copper(II)-promoted regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles in water
    Reddy, KR
    Rajgopal, K
    Kantam, ML
    SYNLETT, 2006, (06) : 957 - 959
  • [40] Synthesis and antimicrobial evaluation of 1,4-disubstituted 1,2,3-triazoles with aromatic ester functionality
    Kaushik, C. P.
    Kumar, Krishan
    Singh, S. K.
    Singh, Dharmendra
    Saini, Sangita
    ARABIAN JOURNAL OF CHEMISTRY, 2016, 9 (06) : 865 - 871