Core-shell structured Fe3O4@MgO: magnetically recyclable nanocatalyst for one-pot synthesis of polyhydroquinoline derivatives under solvent-free conditions

被引:8
作者
Shinde, Gayatree [1 ]
Thakur, Jyotsna [1 ]
机构
[1] CK Thakur ACS Coll, Raigad 410206, Maharashtra, India
关键词
Fe3O4@MgO; core-shell nanostructures; magnetically separable; polyhydroquinoline; green approach; RECOVERABLE NANOCATALYST; FE3O4; NANOPARTICLES; EFFICIENT CATALYST; 1,4-DIHYDROPYRIDINES; ANTIBACTERIAL; MICROWAVE; MGO;
D O I
10.1007/s12039-023-02134-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Core-shell nanostructured Fe3O4@MgO catalyst was synthesized using a two-fold co-precipitation technique. High-resolution transmission electron microscopy (HR-TEM) images demonstrated that the catalyst had a core-shell framework with spherical morphology. In present study, Fe3O4@MgO is successfully used as an effective, novel, and recoverable nanocatalyst in an easy-to-follow, affordable, environment-friendly, and productive process for the synthesis of polyhydroquinoline derivatives via one-pot four-component Hantzsch condensation reaction. Importantly, magnetically retrievable Fe3O4@MgO nanoparticles provides high catalytic efficiency in solvent-free condition and can be used repeatedly up to six cycles without significant loss of catalytic activity. The study provides a greener route to yield 82-94% of polyhydroquinoline in a short reaction time under ultrasonication.
引用
收藏
页数:11
相关论文
共 43 条
  • [1] Fe3O4@B-MCM-41: A new magnetically recoverable nanostructured catalyst for the synthesis of polyhydroquinolines
    Abdollahi-Alibeik, Mohammad
    Rezaeipoor-Anari, Ali
    [J]. JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 2016, 398 : 205 - 214
  • [2] Magnetic nickel ferrite nanoparticles as an efficient catalyst for the preparation of polyhydroquinoline derivatives under microwave irradiation in solvent-free conditions
    Ahankar, Hamideh
    Ramazani, Ali
    Joo, Sang Woo
    [J]. RESEARCH ON CHEMICAL INTERMEDIATES, 2016, 42 (03) : 2487 - 2500
  • [3] Ultrasound and Nano-Catalysts: An Ideal and Sustainable Combination to Carry out Diverse Organic Transformations
    Banerjee, Bubun
    [J]. CHEMISTRYSELECT, 2019, 4 (08): : 2484 - 2500
  • [4] A review on multi-component green synthesis of N-containing heterocycles using mixed oxides as heterogeneous catalysts
    Bhaskaruni, Sandeep V. H. S.
    Maddila, Suresh
    Gangu, Kranthi Kumar
    Jonnalagadda, Sreekantha B.
    [J]. ARABIAN JOURNAL OF CHEMISTRY, 2020, 13 (01) : 1142 - 1178
  • [5] Chaudhary RG., 2016, J. Chin. Adv. Mater. Soc., V4, P110, DOI 10.1080/22243682.2016.1164618
  • [6] Magnetic nanocatalysts: Synthesis and application in multicomponent reactions
    Chen, Meng-Nan
    Mo, Li-Ping
    Cui, Zhen-Shui
    Zhang, Zhan-Hui
    [J]. CURRENT OPINION IN GREEN AND SUSTAINABLE CHEMISTRY, 2019, 15 : 27 - 37
  • [7] Catalytic applications of layered double hydroxides: recent advances and perspectives
    Fan, Guoli
    Li, Feng
    Evans, David G.
    Duan, Xue
    [J]. CHEMICAL SOCIETY REVIEWS, 2014, 43 (20) : 7040 - 7066
  • [8] Synthetic and theoretical studies on the reduction of electron withdrawing group conjugated olefins using the Hantzsch 1,4-dihydropyridine ester
    Garden, SJ
    Guimaraes, CRW
    Corréa, MB
    de Oliveira, CAF
    Pinto, AD
    de Alencastro, RB
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (23) : 8815 - 8822
  • [9] S-Benzylisothiourea complex of palladium on magnetic nanoparticles: A highly efficient and reusable nanocatalyst for synthesis of polyhydroquinolines and Suzuki reaction
    Ghorbani-Choghamarani, Arash
    Tahmasbi, Bahman
    Moradi, Zahra
    [J]. APPLIED ORGANOMETALLIC CHEMISTRY, 2017, 31 (08)
  • [10] MoO2Cl2 catalyzed efficient synthesis of functionalized 3,4-dihydropyrimidin-2(1H)-ones/thiones and polyhydroquinolines: recyclability, fluorescence and biological studies
    Guggilapu, Sravanthi Devi
    Prajapti, Santosh Kumar
    Nagarsenkar, Atulya
    Lalita, Guntuku
    Vegi, Ganga Modi Naidu
    Babu, Bathini Nagendra
    [J]. NEW JOURNAL OF CHEMISTRY, 2016, 40 (01) : 838 - 843