Manganese porphyrin supported on activated carbon as a new catalyst for epoxidation of alkenes with hydrogen peroxide

Subject Areas : Iranian Journal of Catalysis

Saeed Rayati ¹ , Makan Etefagh ² , Majid Masteri-Farahani ³

1 - Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 16315‐1618, Tehran 15418, Iran.
2 - Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 16315‐1618, Tehran 15418, Iran.
3 - Faculty of Chemistry, Kharazmi University, P.O. Box 15719-14911, Tehran, Iran.

Received: 2022-11-29 Accepted : 2023-06-17 Published : 2023-07-01

Keywords:

References:

[1] F.P. Ballistreri, R.M. Toscano, M.E. Amato, A. Pappalardo, C. Gangemi, S. Spidalieri, R. Puglisi, G. Trusso Sfrazzetto, Catalysts.8 (2018) 129.

[2] S.E. Denmark, D.C. Forbes, D.S. Hays, J.S. DePue, R. Wilde, J. Org. chem. 60 (1995) 1391-1407.

[3] W. Wang, C. Li, Y. Pi, J. Wang, R. Tan, D. Yin, Catal. Sci. Technol. 9 (2019) 5626-5635.

[4] T. Ma, C. Xu, F. Liu, Y. Feng, W. Zhang, W. Tang, H. Zhang, X. Li, Y. Nie, S. Zhao, Y. Li, D. Ji, Z. Fang, W. He, K. Guo, Mol. Catal. 541 (2023) 113074.

[5] G. Grigoropoulou, J.H. Clark, J.A. Elings, Green Chem. 5 (2003) 1-7.

[6] P. Zhou, X. Wang, B. Yang, F. Hollmann, Y. Wang, RSC adv.7 (2017) 12518-12523.

[7] B. Rezazadeh, A.R. Pourali, A. Banaei, H. Behniafar, J. Coord. Chem. 72 (2019) 3401-3416.

[8] X.T. Ma, X.H. Lu, C.C. Wei, Z.S. Zhao, H.J. Zhan, D. Zhou, Q.H. Xia, Catal. Commun. 67 (2015) 98-102.

[9] J. Jiang, J.X. Wang, X.T. Zhou, H.Y. Chen, H.B. Ji, Eur. J. Inorg. Chem. 2018 (2018) 2666-2674.

[10] X.T. Zhou, Q.H. Tang, H.B Ji, Tetrahedron Lett. 50 (2009) 6601-6605.

[11] L. Li, H.J. Song, X.G. Meng, R.Q. Yang, N. Zhang, Tetrahedron Lett. 59 (2018) 2436-2439.

[12] K. Maljutenko, V. Borovkov, D. Kananovich, I. Järving, M. Lopp, Tetrahedron. 74 (2018) 661-664.

[13] S. Rayati, F. Nejabat, F. Panjiali, Catal. Commun. 122 (2019) 52-57.

[14] S. Rayati, F. Nejabat, S. Zakavi, Inorg. Chem. Commun. 40 (2014) 82-86.

[15] S. Rayati, P. Nafarieh, Appl. Organomet. Chem. 33 (2019) e4789.

[16] A. Rezaeifard, M. Jafarpour, S. Rayati, R. Shariati, Dyes Pigm. 80 (2009) 80-85.

[17] S. Zakavi, A.G. Mojarrad, S. Rayati, J. Mol. Catal. A. Chem. 363 (2012) 153-158.

[18] R. Marcos da Silva Junior, E. Henrique dos Santos, S. Nakagaki, Mol. Cat. 541 (2023) 113080.

[19] A.S. Estrada-Montaño, V. Gómez-Benítez, A. Camacho-Dávila, E. Rivera, D. Morales-Morales, G. Zaragoza-Galán, J. Porphyr. Phthalocyanines. 26 (2022) 821-836.

[20] V.S. Da Silva, S. Nakagaki, G.M. Ucoski, Y.M. Idemori, G. DeFreitas-Silva, RSC adv. 5 (2015) 106589-106598.

[21] J.T. Groves, T.E. Nemo, R.S. Myers, J. Am. Chem. Soc. 101 (1979) 1032-1033.

[22] J.T. Groves, Y. Watanabe, Inorg. Chem. 25 (1986) 4808-4810.

[23] D. Mohajer, G. Karimipour, M. Bagherzadeh, New. J. Chem. 28 (2004) 740-747.

[24] Z.L. Magnuson, R.W. Larsen, Inorganica. Chim. Acta. 552 (2023) 121483.

[25] A. Bahuguna, A. Kumar, V. Krishnan, Asian J. Org. Chem. 8 (2019) 1263-1305.

[26] A.R. Silva, C. Freire, B. De Castro, Carbon. 14 (2004) 3027-3030.

[27] M. Sadiq, M. Khan, M. Numan, R. Aman, S. Hussain, M. Sohail Ahmad, S. Sadiq, M. Abid Zia, H. Ur Rashid, R. Ali, Journal. Chem. 2017 (2017) 5732761.

[28] J.S. Choi, T.H. Kim, K.Y. Choo, J.S. Sung, M.B. Saidutta, S.D. Song, Y.W. Rhee, J. Porous Mater. 12 (2005) 301-310.

[29] E.I. El-Shafey, S.N. Ali, S. Al-Busafi, H.A. Al-Lawati, J. Environ, Chem. Eng. 4 (2016) 2713-2724.

[30] S. Rayati, E. Bohloulbandi, C. R. Chim. 17 (2014) 62-68.

[31] S. Rayati, E.K. Chegini, Macroheterocycles. 9 (2016) 151-155.

[32] S. Rayati, F. Nejabat, C. R. Chim. 20 (2017) 967-974.

[33] F. Nejabat, S. Rayati, J. Ind. Eng. Chem. 69 (2019) 324-330.

[34] S. Rayati, N. Pournaser, F. Nejabat, P. Nafarieh, Inorg. Chem. Commun. 107 (2019) 107447.

[35] S. Rayati, Z. J. Sheybanifard, Porphyr. Phthalocyanines. 19 (2015) 622-630.

[36] S. Rayati, S. Malekmohammadi, J. Exp. Nanosci. 11 (2016) 872-883.

[37] A. Mavrogiorgou, M. Papastergiou, Y. Deligiannakis, M. Louloudi, J. Mol. Catal. A. Chem. 393 (2014) 8-17.

[38] A. Simaioforidou, M. Papastergiou, A. Margellou, D. Petrakis, M. Louloudi, J. Mol. Catal. A. Chem. 426 (2017) 516-525.

[39] E. Assady, B. Yadollahi, M. Riahi Farsani, M. Moghadam, Appl. Organomet. Chem. 29 (2015) 561-565.

[40] S.S. Tareq, M.I. Saiman, T.Y.Y. Hin, A.H. Abdullah, U. Rashid, Bull. Chem. React. Eng. Catal. 13 (2018) 373-385.

[41] A.D. Adler, F.R. Longo, W. Shergalis, J. Am. Chem. Soc. 86 (1964) 3145-3149.

[42] J.W. Buchler, G. Eikelmann, L. Puppe, K. Rochbock, H.H. Schneehage, D. Weck, Lieb. Ann. Chem. 745 (1971) 135-151.

[43] M. Masteri-Farahani, M.K. Alavijeh, M.S. Hosseini, React. Kinet. Mech. Catal. 130 (2020) 303-315.

[44] A. Paradisi, E.M. Johnston, M. Tovborg, C.R. Nicoll, L. Ciano, A. Dowle, J. McMaster, Y. Hancock, G. Davies, P.H. Walton, J. Am. Chem. Soc. 141 (2019) 18585-18599.

[45] S. Rayati, D. Moradi, F. Nejabat, New J. Chem. 44 (2020) 19385-19392.