تعداد نشریات | 418 |
تعداد شمارهها | 10,005 |
تعداد مقالات | 83,621 |
تعداد مشاهده مقاله | 78,331,441 |
تعداد دریافت فایل اصل مقاله | 55,377,740 |
Tungstophosphoric acid embedded magnetic chitosan as a green catalyst for the synthesis of N-cyclohexyl-3-aryl quinoxaline-2-amines | ||
Iranian Journal of Catalysis | ||
مقاله 3، دوره 7، شماره 3، آذر 2017، صفحه 193-199 اصل مقاله (1.33 M) | ||
نوع مقاله: Articles | ||
نویسندگان | ||
Ali Ayati1؛ Mansoureh Daraie2؛ Majid M. Heravi* 2؛ Bahareh Tanhaei1 | ||
1Department of Chemical Engineering, Quchan University of Advanced Technology, Quchan, Iran. | ||
2Department of Chemistry, School of Sciences, Alzahra University, Vanak, Tehran, Iran. | ||
چکیده | ||
In the present study, a novel catalyst was well designed by incorporating the tungstophosphoric acid into the magnetic chitosan, as highly stable composite, in which the iron oxides were used the strong super-magnetic core. The prepared composite was characterized by several methods, including FTIR, XRD, SEM, TEM and EDS and its catalytic activity was examined in a facile, green and highly efficient one-pot reaction for the synthesis of N-cyclohexyl-3-aryl-quinoxaline-2-amines with o-phenylenediamine, benzaldehyde and cyclohexyl isocyanide in water, under reflux conditions. This heterogeneous catalytic system was separated easily by an external magnet and was reused at least in four runs without pre-activation and appreciable loss in its activity. | ||
کلیدواژهها | ||
Magnetic Chitosan؛ Heteropolyacid؛ Multicomponent reactions؛ Green synthesis | ||
مراجع | ||
[1] M.M. Heravi, G. Rajabzadeh, F.F. Bamoharram, N. Seifi, J. Mol. Catal. A: Chem. 256 (2006) 238-241. [2] A. Ayati, A. Ahmadpour, F.F. Bamoharram, M.M. Heravi, H. Rashidi, Chin. J. Catal. 32 (2011) 978-982. [3] M.M. Heravi, V. Zadsirjan, K. Bakhtiari, H.A. Oskooie, F.F. Bamoharram, Catal. Commun. 8 (2007) 315-318. [4] F.F. Bamoharram, M.M. Heravi, S. Mehdizadeh, Synth. React. Inorg. Met.-Org. Nano-Met. Chem. 39 (2009) 746-750. [5] A. Ayati, A. Ahmadpour, F.F. Bamoharram, M.M. Heravi, M. Sillanpää, Gold Bull. 45 (2012) 145-151. [6] M.M. Heravi, S. Sadjadi, J. Iran. Chem. Soc. 6 (2009) 1-54. [7] S. Sadjadi, M.M. Heravi, Curr. Org. Chem. 20 (2016) 1404-1444. [8] M.M. Heravi, H. Alinejhad, K. Bakhtiari, Z. Daroogheha, F.F. Bamoharram, F. Derikvand, B. Alimadadi, Synthetic Communications 40 (2010) 2191-2200. [9] M.M. Heravi, E. Hashemi, Y.S. Beheshtiha, K. Kamjou, M. Toolabi, N. Hosseintash, J. Mol. Catal. A: Chem. 392 (2014) 173-180. [10] L.T.A. Sofia, A. Krishnan, M. Sankar, N.K.K. Raj, P. Manikandan, P.R. Rajamohanan, T.G. Ajithkumar, J. Phys Chem. C 113 (2009) 21114-21122. [11] M.M. Heravi, V. Rasmi, F.F. Bamoharram, S. Sadjadi, L. Fotouhi, S. Sadjadi, M. Bakavoli, Synth. Commun. 39 (2009) 4109-4116. [12] A. Micek-Ilnicka, E. Bielanska, L. Litynska-Dobrzynska, A. Bielanski, Appl. Catal. A 421- 422 (2012) 91- 98. [13] N. Toutounchian, A. Ahmadpour, M.M. Heravi, F.F. Bamoharram, A. Ayati, F. Deymeh, Res. Chem. Intermed. 42 (2016) 3283-3301. [14] T. Alishiri, H.A. Oskooei, M.M. Heravi, Synt. Commun. 43 (2013) 3357-3362. [15] F. Nemati, M.M. Heravi, A. Elhampour, RSC Adv. 5 (2015) 45775-45784. [16] M. Feyen, C. Weidenthaler, F. Schüth, A.H. Lu, Chem. Mater. 22 (2010) 2955-2961. [17] J. Safari, L. Javadian, Ultrason. Sonochem. 22 (2015) 341-348. [18] A. Naghipour, A. Fakhri, Catal. Commun. 73 (2016) 39-45. [19] M. Bodnar, J.F. Hartmann, J. Borbely, Biomacromolecule 6 (2005) 2521-2527. [20] W. Li, L. Xiao, C. Qin, J. Macromol. Sci. A Pure. Appl. Chem. 48 (2010) 57-64. [21] B. Tanhaei, A. Ayati, M. Lahtinen, M. Sillanpää, Chem. Eng. J. 259 (2015) 1-10. [22] A. Ayati, B. Tanhaei, M. Sillanpää, J. Appl. Polym. Sci. 134 (2017) 44360. [23] A. Ayati, M.M. Heravi, M. Daraie, B. Tanhaei, F.F. Bamoharram, M. Sillanpää, J. Iran Chem. Soc. 13 (2016) 2301–2308. [24] A. Kong, P. Wang, H. Zhang, F. Yang, S.P. Huang, Y. Shan, App. Phys. A: Gen. 417- 418 (2012) 183-189. [25] H.E. Blackwell, Curr. Opin. Chem. Biol. 10 (2006) 203-212. [26] B.B. Toure, D.G. Hall, Chem. Rev. 109 (2009) 4439-4486. [27] M.M. Heravi, B. Talaei, Adv. Heterocycl. Chem. 114 (2015) 147-225. [28] S. Brauch, S.S.v. Berkel, B. Westermann, Chem. Soc. Rev. 42 (2013) 4948-4962. [29] A. Domling, Chem. Rev. 106 (2006) 17-89. [30] S. Sadjadi, M.M. Heravi, Tetahedron 67 (2011) 2707-2752. [31] K. Toshima, R. Takano, T. Ozawa, S. Matsumura, Chem. Commun. 3 (2002) 212-213 [32] F. Zaragoza, H. Stephensen, J. Org. Chem. 64 (1999) 2555-2557. [33] S.A. Raw, C.D. Wilfred, R.J.K. Taylor, Chem. Commun. 18 (2003) 2286-2287. [34] K.R.J. Thomas, M. Velusamy, J.T. Lin, C.-H. Chuen, Y.-T. Tao, Chem. Mater. 17 (2005) 1860-1866. [35] S. Dailey, W.J. Feast, R.J. Peace, I.C. Sage, S. Till, E.L. Wood, J. Mater. Chem. 11 (2001) 2238-2243. [36] J.L. Sessler, H. Maeda, T. Mizuno, V.M. Lynch, H. Furuta, Chem. Commun. 8 (2002) 862-863. [37] M.M. Heravi, B. Baghernejad, H.A. Oskooie, Tetrahedron Lett. 50 (2009) 767-769. [38] R. Mirsafaei, M.M. Heravi, S. Ahmadi, M.H. Moslemin, T. Hosseinnejad, J. Mol. Catal. A: Chem. 402 (2015) 100-108. [39] E. Hashemi, Y.S. Beheshtiha, S. Ahmadi, M.M. Heravi, Trans. Met. Chem. 39 (2014) 593-601. [40] B. Zhao, Y. Wang, H. Guo, J. Wang, Y. He, Z. Jiao, M. Wu, Mater. Sci. Poland 25 (2007) 1143-1148. [41] M. Monier, D.M. Ayad, Y. Wei, A.A. Sarhan, React. Funct. Polym. 70 (2010) 257-266. [42] A. Ayati, B. Tanhaei, F.F. Bamoharram, A. Ahmadpour, P. Maydannik, M. Sillanpää, Sep. Pur. Technol. 171 (2016) 62-68. [43] F.F. Bamoharram, Molecules 14 (2009) 3124-3221. [44] B. Tanhaei, A. Ayati, M. Lahtinen, B.M. Vaziri, M. Sillanpää, J. Appl. Polym. Sci. 133 (2016) 43466. [45] B. Tanhaei, A. Ayati, F.F. Bamoharram, M. Lahtinen, M. Sillanpää, J. Chem. Technol. Biotechnol. 91 (2016) 1452-1460. [46] E.L. Mogilevskaya, T.A. Akopova, A.N. Zelenetskii, A.N. Ozerin, Polym. Sci. Series A 48 (2006) 116-123. | ||
آمار تعداد مشاهده مقاله: 612 تعداد دریافت فایل اصل مقاله: 538 |