| تعداد نشریات | 48 |
| تعداد شمارهها | 1,235 |
| تعداد مقالات | 10,619 |
| تعداد مشاهده مقاله | 21,478,479 |
| تعداد دریافت فایل اصل مقاله | 14,458,383 |
Nanomagnetic organic-inorganic hybrid (CuFe2O4@Si-Imid-PMo): an efficient green catalyst for the synthesis of 2,4,5-trisubstituted imidazoles | ||
| Iranian chemical communication | ||
| مقاله 2، دوره 7، Issue 3, pp. 160-229, Serial No. 24، مهر 2019، صفحه 174-185 اصل مقاله (1.11 M) | ||
| نوع مقاله: Original Research Article | ||
| شناسه دیجیتال (DOI): 10.30473/icc.2018.41914.1468 | ||
| نویسندگان | ||
| Ebrahim Teymoori1؛ Abolghasem Davoodnia* 1؛ Amir Khojastehnezhad* 2؛ Nasrinsadat Hosseininasab1 | ||
| 1Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran | ||
| 2Department of Chemistry, Ferdowsi University, Mashhad, Iran | ||
| چکیده | ||
| In this research, a new magnetic nanocatalyst CuFe2O4@Si-Imid-PMo containing acidic ionic liquid based on imidazolium cation and phosphomolybdic acid anion immobilized on CuFe2O4@SiO2 magnetic nanoparticles was prepared and characterized using FT-IR, EDX, SEM, and VSM techniques. Then, the catalytic activity of CuFe2O4@Si-Imid-PMo was evaluated in the synthesis of 2,4,5-trisubstituted imidazoles. The results showed that the catalyst has high activity and the desired products were obtained in high yields within short reaction times. The best result was obtained at 120 °C in the presence of 0.02 g of the catalyst under solvent-free conditions. The catalyst was also readily recovered by a external magnetic and can be used for several times without substantial reduction in its catalytic activity. | ||
| کلیدواژهها | ||
| CuFe2O4@Si-Imid-PMo؛ immobilized ionic liquid؛ Magnetic nanoparticles؛ magnetically separable؛ imidazoles | ||
| مراجع | ||
|
[1] (a) R.N. Grass, E.K. Athanassiou, W.J. Stark, Angew. Chem. Int., 2007, 46, 4909-4912; (b) P.D. Stevens, G. Li, J. Fan, M. Yen, Y. Gao, Chem. Comm., 2005, 4435-4437; (c) A.H. Lu, W. Schmidt, N. Matoussevitch, H. Bönnemann, B. Spliethoff, B. Tesche, E. Bill, W. Kiefer, F. Schüth, Angew. Chem. Int., 2004, 43, 4303-4306; (d) M.M. Heravi, H. Hamidi, N. Karimi, A. Amouchi, Adv. J. Chem. A, 2018, 1, 1-6.http://www.ajchema.com/article_78187.html; (e) M.M. Heravi, H. Abdi Oskooie, Z. Latifi, H. Hamidi, Adv. J. Chem. A, 2018, 1, 7-11. http://www.ajchema.com/article_79156.html; (f) A, Moghimi, M. Yari, J. Chem. Rev., 2019, 1, 1-18. http://www.jchemrev.com/article_77437.html
[2] (a) S. Wittmann, A. Schätz, R.N. Grass, W. J. Stark, O. Reiser, Angew. Chem. Int., 2010, 49, 1867-1870; (b) B. Kaboudin, R. Mostafalu, T. Yokomatsu, Green Chem., 2013, 15, 2266-2274. [3] Y. Wang, J.-K. Lee, J. Mol. Catal. A Chem., 2007, 263, 163-168. [4] V. Polshettiwar, R. S. Varma, Org. Biomol. Chem., 2009, 7, 37-40. [5] (a) T. Zeng, L. Yang, R. Hudson, G. Song, A. R. Moores, C.-J. Li, Org. Lett., 2010, 13, 442-445; (b) B. Karimi, E. Farhangi, Adv. Synth. Catal., 2013, 355, 508-516. [6] (a) E.F. Kozhevnikova, E.G. Derouane, I.V. Kozhevnikov, Chem. Comm., 2002, 1178-1179; (b) S. Roberts, I. Kozhevnikov, E. Derouane, in Catalysts for Fine Chemical Synthesis, Wiley Chichester, 2002. [7] X. Zheng, L. Zhang, J. Li, S. Luo, J.-P. Cheng, Chem. Comm., 2011, 47, 12325-12327. [8] (a) H. Hamadi, M. Kooti, M. Afshari, Z. Ghiasifar, N. Adibpour, J. Mol. Catal. A: Chem., 2013, 373, 25-29; (b) H. Eshghi, A. Khojastehnezhad, F. Moeinpour, M. Bakavoli, S.M. Seyedi, M. Abbasi, RSC Adv., 2014, 4, 39782-39789; (c) H. Eshghi, A. Javid, A. Khojastehnezhad, F. Moeinpour, F.F. Bamoharram, M. Bakavoli, M. Mirzaei, Chin. J. Catal., 2015, 36, 299-307. [9] S.A. Laufer, W. Zimmermann, K.J. Ruff, J. Med. Chem., 2004, 47, 6311-6325. [10] J.A. Murry, Curr. Opin. Drug. Discov. Dev., 2003, 6, 945-965. [11] A.K. Takle, M.J. Brown, S. Davies, D.K. Dean, G. Francis, A. Gaiba, A.W. Hird, F.D. King, P.J. Lovell, A. Naylor, Bioorg. Med. Chem. Lett., 2006, 16, 378-381. [12] A.R. Karimi, Z. Alimohammadi, M.M. Amini, Mol. Divers., 2010, 14, 635-641. [13] S.D. Sharma, P. Hazarika, D. Konwar, Tetrahedron Lett., 2008, 49, 2216-2220. [14] A. Olyaei, Z. Derikvand, F. Noruzian, M. Sadeghpour, Iran. Chem. Comm., 2016, 4, 337-346. [15] H. Ramezanalizadeh, Iran. Chem. Comm., 2018, 6, 160-176. [16] R. Sharma, C. Sharma, Catal. Commun. 2011, 12, 327-331. [17] R.S. Joshi, P.G. Mandhane, M.U. Shaikh, R.P. Kale, C.H. Gill, Chin. Chem. Lett., 2010, 21, 429-432. [18] A.A. Mohammadi, M. Mivechi, H. Kefayati, Monatsh. Chem., 2008, 139, 935-937. [19] B. Das, J. Kashanna, R.A. Kumar, P. Jangili, Monatsh. Chem., 2013, 144, 223-226. [20] L.-M. Wang, Y.-H. Wang, H. Tian, Y.-F. Yao, J.-H. Shao, B. Liu, J. Fluorine Chem., 2006, 127, 1570-1573. [21] S. Samai, G.C. Nandi, P. Singh, M. Singh, Tetrahedron, 2009, 65, 10155-10161. [22] M.A. Zolfigol, A. Khazaei, A.R. Moosavi-Zare, A. Zare, Z. Asgari, V. Khakyzadeh, A. Hasaninejad, J. Ind. Eng. Chem., 2013, 19, 721-726. [23] A. Khazaei, A.R. Moosavi‐Zare, F. Gholami, V. Khakyzadeh, Appl. Organometal. Chem., 2016, 30, 691-694. [24] M.A. Zolfigol, S. Baghery, A.R. Moosavi-Zare, S.M. Vahdat, RSC Adv., 2015, 5, 32933-32940. [25] M. Ashrafi, A. Davoodnia, N. Tavakoli-Hoseini, Bull. Korean Chem. Soc., 2013, 34, 1508-1512. [26] A.Y. Usyatinsky, Y.L. Khmelnitsky, Tetrahedron Lett., 2000, 41, 5031-5034. [27] J. Safari, S.D. Khalili, S.H. Banitaba, H. Dehghani, J. Korean Chem. Soc., 2011, 55, 787-793. [28] (a) A. Davoodnia, M. Khashi, N. Tavakoli-Hoseini, R. Moloudi, H. A. Zamani, Monatsh. Chem., 2013, 144, 677-680; (b) M. Khashi, A. Davoodnia, J. Chamani, Phosphorus Sulfur Silicon Relat. Elem., 2014, 189, 839-848; (c) S. Ameli, A. Davoodnia, M. Pordel, H. Behmadi, J. Heterocycl. Chem., 2017, 54, 1437-1441. [29] (a) H. Eshghi, A. Khojastehnezhad, F. Moeinpour, S. Rezaeian, M. Bakavoli, M. Teymouri, A. Rostami, K. Haghbeen, Tetrahedron, 2015, 71, 436-444; (b) B. Maleki, N. Nasiri, R. Tayebee, A. Khojastehnezhad, H. A. Akhlaghi, RSC Adv., 2016, 6, 79128-79134; (c) B. Maleki, E. Sheikh, E.R. Seresht, H. Eshghi, S.S. Ashrafi, A. Khojastehnezhad, H. Veisi, Org. Prep. Proced. Int., 2016, 48, 37-44; (d) F. Tajfirooz, A. Davoodnia, M. Pordel, M. Ebrahimi, A. Khojastehnezhad, Appl. Organomet. Chem., 2018, 32, e3930. [30] A. Bazgir, G. Hosseini, R. Ghahremanzadeh, ACS Comb. Sci., 2013, 15, 530-534. [31] S. Swami, A. Agarwala, R. Shrivastava, New J. Chem., 2016, 40, 9788-9794. [32] D.A. Kotadia, S.S. Soni, J. Mol. Catal. A: Chem., 2012, 353, 44-49. [33] F. Nemati, A. Elhampour, H. Farrokhi, M. B. Natanzi, Catal. Commun., 2015, 66, 15-20. | ||
|
آمار تعداد مشاهده مقاله: 1,670 تعداد دریافت فایل اصل مقاله: 873 |
||