نوع مقاله : مقاله پژوهشی
چکیده تصویری
موضوعات
عنوان مقاله English
نویسندگان English
In the present research, first, the synthesis and characterization of a magnetic covalent organic framework modified with sulfonic acid were done. Then, the catalytic application of the prepared magnetic covalent organic framework modified with sulfonic acid was investigated in the preparation of some heterocyclic compounds containing hexahydroquinoline and pyrazole. The structure of the prepared the prepared magnetic covalent organic framework modified with sulfonic acid was confirmed by several methods such as Fourier-transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), derivative thermogravimetry (DTG), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS), elemental mapping, transmission electron microscopy (TEM), nitrogen absorption and desorption and vibrating-sample magnetometer (VSM). Then, the prepared structure was used in the preparation of hexahydroquinoline and pyrazole derivatives. Among the advantages of this research, are the multicomponent preparation of hexahydroquinoline and pyrazole derivatives in solvent-free conditions, high yield, and short reaction time, as well as recyclability and reusability of the catalyst.
کلیدواژهها English
[1] A. P. Cote, A. I. Benin, N. W. Ockwig, M. OKeeffe, A. J. Matzger. O. M. Yaghi, Science, 310 (2005) 1166.
[2] K. Geng, T. He, R. Liu, S. Dalapati, K. Tian Tan, Z. Li, S. Tao, Y. Gong, Q. Jiang, D. Jiang, Chem. Rev., 120
(2020) 8814.
[3] R. K. Sharma, P. Yadav, M. Yadav, R. Gupta, P. Rana, A. Srivastava, R. Zboril, R. S. Varma, M. Antonietti, M. B. Gawande, Mater. Horiz., 7(2020) 411.
[4] K. Tian Tan, S. Ghosh, Z. Wang, F. Wen, D. Rodríguez-San-Miguel, J. Feng, N. Huang, W. Wang, F.
Zamora, X. Feng, A. Thomas, D. Jiang, Nat. Rev. Methods Primers, 3 (2023) 1.
[5] S. J. Lyle, P. J. Waller, O. M. Yaghi, Trends Chem., 1 (2019) 172.
[6] M. Yarie, Iran. J. Catal. Spotlight, 11 (2021) 89.
[7] X. Liu, D. Huang, C. Lai, G. Zeng, L. Qin, H. Wang, H. Yi, B. Li, S. Liu, M. Zhang, R. Deng, Y. Fu, L. Li,
[8] X. Zhao, P. Pachfule, A. Thomas, Chem. Soc. Rev., 50 (2021) 6871.
[9] B. S. Hote, T. A. Siddiqui and P. M. Pisal, Polycyclic Aromat. Compd., (2021) 1.
[10] P. Choudhury, P. Ghosh B. Basu, Mol. Divers., 24 (2020) 283.
[11] R. R. Raslan, S. A. Hessein, S. A. Fouad and N. A. Shmiess, J. Heterocycl. Chem., 59 (2021) 832.
[12] H. Aghahosseini, M. R. Ranjbar, A. Ramazani, Chemistry Select, 5 (2020) 8415.
[13] N. Hussain-Khil, A. Ghorbani-Choghamarani, M. Mohammadi, Sci. Rep., 11 (2021) 15657.
[14] F. Fazl, M. Torabi, M. Yarie, M. A. Zolfigol, RSC Adv., 12 (2022) 16342.
[15] M. Yarie, M. A. Zolfigol, Y. Bayat, A. Asgari, D. A. Alonso A. Khoshnood, RSC Adv., 6 (2016) 82842.
[16] S. Kalhor, M. Yarie, M. Rezaeivala, M. A. Zolfigol, Res. Chem. Intermed., 45 (2019) 3453.
[17] M.E.A. Zaki, H.A. Soliman, O.A. Hiekal, A.E. Rashad, Z. Naturforsch., 61 (2006) 1.
[18] N. Foloppe, L.M. Fisher, R. Howes, A. Potter, A.G. Robertson, A.E. Surgenor, Bioorg. Med. Chem., 14
(2006) 4792.
[19] N.R. Mohamed, N.Y. Khaireldin, A.F. Fahmy, A.A. El-Sayed, Der. Pharma. Chem., 2 (2010) 400.
[20] S. Noura, M. Ghorbani, M. A. Zolfigol, M. Narimani, M. Yarie, M. Oftadeh, J. Mol. Liq., 271
(2018) 778.
[21] M. Yarie, M. A. Zolfigol, S. Baghery, D. A. Alonso, A. Khoshnood, Y. Bayat, A. Asgari, J. Mol.
Liq., 271 (2018) 872.
[22] N. S. Kaminwar, S. U. Tekale, A. B. Chidrawar, L. Kótai, R. P. Pawar, Lett. Appl. NanoBioSci., 9 (2020)
[23] I.A. Khodja, A. Fisli, O. Lebhour, R. Boulcina, B. Boumoud, A. Debache, Lett. Org. Chem. 13 85 (2016).
[24] Y. Zhao, G. King, M. H. Kwan, A. J. Blacker, Org. Process Res. Dev., 20 (2016) 2012.
[25] N. Bu, W.Y. Wu, P. Jiang, Z.Y. Zhan, J.L. Wan, Z. J. Wu, R. Wan, Chem. Pap., 75 (2021) 4493.
[26] A. Khazaei, M. Tavasoli, V. Jamshidi, F. G. Ghalil, A. R. Moosavi‐Zare, Appl. Organomet. Chem., 32
(2018) e4368.
[27] S. T., Fardood, A., Ramazani, S. Moradi, J. Sol-Gel Sci. Technol., 82 (2017) 432.
[28] N. S. Kaminwar, S. U. Tekale, A. B. Chidrawar, L. Kótai, R. P. Pawar, Lett. Appl. NanoBioSci., 9 (2020)
[29] B. Eftekhari far, M. Nasr‐Esfahani, Appl. Organomet. Chem., 34 (2020) e5406.
[30] S. Nazari, M. Keshavarz, Russ. J. Gen. Chem., 87 (2017) 539.
[31] Z. Karimi-Jaberi, M. M. ReyazoShams, Heterocycl. Commun., 17 (2011) 5
