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Citric acid as an efficient and green catalyst for the synthesis of hexabenzylhexaazaisowurtzitane (HBIW) | ||
Iranian Journal of Catalysis | ||
مقاله 8، دوره 6، شماره 1، خرداد 2016، صفحه 65-68 اصل مقاله (1.24 M) | ||
نوع مقاله: Articles | ||
نویسندگان | ||
Sahar Shokrollahi1؛ Ali Ramazani* 1؛ Seyed Jamal Tabatabaei Rezaei1؛ Asemeh Mashhadi Malekzadeh1؛ Pegah Azimzadeh Asiabi1؛ Sang Woo Joo* 2 | ||
1Department of Chemistry, University of Zanjan, P O Box 45195-313, Zanjan, Iran | ||
2School of Mechanical Engineering, Yeungnam University, Gyeongsan 712-749, Republic of Korea | ||
چکیده | ||
The condensation of benzylamine with glyoxal leads to Hexabenzylhexaazaisowurtzitane (HBIW) in acetonitrile solvent with citric acid as a green catalyst under both conventional stirring and ultrasonic irradiation conditions. The influence of four variables, including the amount of catalyst, solvent, reaction time and ultrasonic power, on the reaction yield was investigated. The results showed that the optimum parameters for synthesis of HBIW were 5% mol with respect to glyoxal for catalyst, acetonitrile-water as solvent, 5 minutes as reaction time and 150 W for ultrasonic power. In general, improvement in rates and yields were observed when the reactions were carried out under sonication in comparison with classic conditions. | ||
کلیدواژهها | ||
Hexabenzylhexaazaisowurtzitane (HBIW)؛ Citric acid؛ green chemistry؛ ultrasound irradiation | ||
مراجع | ||
[1] G. Centi, S. Perathoner, Catal. Today. 77 (2003) 287–297. [2] I. Lavilla, V. Romero, I. Costas, C. Bendicho, TrAC-Trend. Anal. Chem. 61 (2014) 1–10. [3] A. Richard, B. Poliakoff, M. Poliakoff, Mendeleev Commun. 21 (2011) 235–238. [4] G.J. Hutchings, Catal. Today. 122 (2007) 196–200. [5] C. Wen, A. Yin, W.L. Dai, Appl. Catal. B: Environ. 160 (2014) 730-741. [6] S. Sami, M. Norollahi, S. Miri, Iran. J. Catal. 4 (2014) 55-61. [7] S. Khodabakhshi, M. Baghernejad, Iran. J. Catal. 3 (2013) 67-71. [8] R. Mahesh, A.K. Dhar, T.S. TVNV, S. Thirunavukkarasu, T. Devadoss, Chin. Chem. Lett. 22 (2011), 389-392. [9] H. Zhang, D. Zhao, D. Tang, T. Zhang, Z. Shao, Int. J. Hydrogen Energy 39 (2014) 9467-9472. [10] C. Wehmer, Chem. Zentr. 2 (1893) 457–462. [11] H.A. Krebs, W.A. Johnson, Enzymologia 4 (1937) 148–156. [12] H.S. Grewal, K.L. Kalra, Biotechnol. Adv. 13 (1995) 209-234. [13] B.M. Yapo, Bioresource Technol. 100 (2009) 3147–3151. [14] M. Berovic, M. Legisa, Biotechnol. Annu. Rev. 13 (2007) 303-343. [15] K. Kirimura, Y. Honda, T. Hattori, Comprehensive Biotechnology. Second Edition, Elsevier, 2011, pp. 135-142. [16] M. Moresi, E. Parente, Encyclopedia of Food Microbiology. Second Edition, Elsevier, 2014, pp. 804-815. [17] J. Xu, Y.Q. Chen, H.J. Zhang, J.W. Bao, L. Tang, K. Wang, J.H. Zhang, X.S. Chen, Z.G. Mao, Bioresource Technol. 176 (2015) 121–128. [18] A.K. Sider, B.R. Nirmala Sikder, J.P. Gandhe, S. Agrawal, S. Haridwar, Def. Sci. J. 52 (2002) 135-146. [19] Y. Bayat, H. Ebrahimi, F. Fotouhi-Far, Org. Process Res. Dev. 16 (2012) 1733−1738. [20] A.T. Nielsen, R.A. Nissan, D.J. Vanderah, C.L. Coon, R.D. Gilardi, C.F. George, J. Flippen-Anderson, J. Org. Chem. 55 (1990) 1459-1466. [21] W. Qiu, Sh. Chen, Y. Yu, J. Chem. Crystallogr. 28 (1998) 593–596. [22] M.R. Crampton, J. Hamid, R. Millar, G. Ferguson, J. Chem. Soc. Perkin Trans. 2 (1993) 923–929. [23] M.A. Quraishi, F.A. Ansari, J. Appl. Electrochem. 33 (2003) 233–238. [24] S.K. Singh, A.K. Mukherjee, M.M. Singh, Indian J. Chem. Technol. 18 (2011) 291-300. [25] R. Arabian, A. Ramazani, B. Mohtat, V. Azizkhani, S.W. Joo, M. Rouhani, J. Energ. Mater. 32 (2014) 300-305. [26] J. Safari, Z. Zarnegar, S. Naseh, Z. Akbari, Iran. J. Catal. 4 (2014) 125-132. [27] M.R. Nabid, S.J. Tabatabaei Rezaei, R. Ghahremanzadeh, A. Bazgir, Ultrason. Sonochem. 17 (2010) 159-161. [28] S.J. Tabatabaei Rezaei, M.R. Nabid, A. Yari, S.W. Ng, Ultrason. Sonochem. 18 (2011) 49-53. [29] S.J. Tabatabaei Rezaei, Y. Bide, M.R. Nabid, Tetrahedron Lett. 53 (2012) 5123–5126. [30] M. Rouhani, A. Ramazani, S.W. Joo, Ultrason. Sonochem. 22 (2015) 391-396. [31] M. Rouhani, A. Ramazani, S.W. Joo, Ultrason. Sonochem. 21 (2014) 262–267. | ||
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