Spotlight: Porphyrin-based catalysts

Document Type: Spotlights

Author

Faculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838683, Iran.

Abstract

< p>Mohammad Dashteh was born in 1994 in Dashteh/ Hamedan, Iran. Having graduated in the field of Pure Chemistry (2016) from Bu-Ali Sina University, Hamedan, Iran, he continued his M.Sc. in 2018 in Organic Chemistry under the supervision of Professor Mohammad Ali Zolfigol. He is currently working towards his Ph.D. under the supervision of Professor Mohammad Ali Zolfigol and Professor Ardeshir Khazaei in the department of chemistry at Bu-Ali Sina University, Hamedan, Iran. His research interest is the design, synthesis, and characterization of task-specific biological-based catalysts and their applications in organic transformations.

Keywords


[1] (a) J. T. Groves, J. Inorg. Biochem. 100 (2006) 434-447; (b) L.Que Jr, W. B. Tolman. Nature. 455 (2008) 333; (c) J. P.Collman, J. I. Brauman, T. R. Halbert, K. S. Suslick, Proc.Natl. Acad. Sci. U.S.A. 73 (1976) 3333-3337; (d) D. Dolphin. Biochem.7 (2012) 33.
[2] Harper, Douglas, Buglione, Drew Carey, "porphyrian., The Online Etymology Dictionary, Retrieved 14 September 2014.
[3] A.S. Ivanov, A.I. Boldyrev. Org. Bio. chem. 12 (2014) 6145-50.
[4] T.D. Lash. J. Porphyr. Phthalocyanines.15 (2011) 1093-115.
[5] T. Tanaka, A. Osuka. Chem. Soc. Rev. 44 (2015) 943-69.
[6] S. Hiroto, Y. Miyake, H. Shinokubo. Chem. Rev. 117 (2017) 2910-3043.
[7] M. Costas. Chem. Rev. 255 (2011) 2912–2932.
[8] P. Le Maux, H.F. Srour, G. Simonneaux. Tetrahedron. 68 (2012) 5824-5828.
[9] H. Srour, P. Le Maux, G. Simonneaux. Inorg. Chem. 51 (2012) 5850–5856.
[10] P. Le Maux, G. Simonneaux. Chem. Commun. 47 (2011) 6957–6959.
[11] J. Cossy, D. Belotti. Tetrahedron Lett. 42 (2001) 4329–4331.
[12] B. Whittney, Sh. Lindsey, Sh. Mark. Handbook of Porphyrins: Chemistry, Properties and Applications. 2014.
[13] L. Feng, K. Wang, E. joseph, H-C. Zhou. Trends in Chemistry. Article in Press (2020), Review.
[14] C.F. Pereira, M.Q. Simoes, J.P.C. Tome, F.A.A. Paz. Molecules. 21 (2016) A126.
[15] J.C. Barona-Castano, C.C. Carmona-Vargas, T.J. Oliveira, K.T. Graca, M. Neves, P.M.S. Amparo, F. Faustino. Molecules. 21 (2016) no.310.
[16] A.B. Sorokin. Inorg. React. Mech. 8 (2012) 89-84.
[17] M.P. Doyle. Angew. Chem. Int. Edit. 48 (2009) 850-852.    
[18] B. Boitrel, V. Baveux-Chambenoit, P. Richard. Helv. Chim. Acta. 87 (2004) 2447-2464.
[19] A. B. Solovieva, S.F. Timashev. Russ. Chem. Rev. 72 (2003) 965-984.
[20] G.B. Maravin, M.V. Avdeev, E.I. Bagrii. Pet. Chem. 40 (2000) 1-18.
[21] F. Bedioui. Coord Chem Rev. 144 (1995) 39-68.
[22] S. Mondal, K. Sahu, B. Patra, S. Jena, H.S. Biswal, S. Kar. Dalton Trans. 49 (2020) 1424-1432.
[23] L.M. Mateo, Q. Sun, S.X. Liu, J.J. Bergkamp, K. Eimre, C.A. Pignedoli, P. Ruffieux, S. Decurtins, G. Bottari, R. Fasel, T. Torres. Angew. Chem. Int. Ed. 59 (2020) 1334-9.
[24] P. Kar, T. K. Maji, P. K. Sarkar, P. Lemmens, S. K. Pal. J. Mater. Chem. A. 6 (2018) 3674–3683.
[25] A. R. McDonald, N. Franssen, G. P. M. van Klink, G. van Koten. J. Organomet. Chem. 694 (2009) 2153-2162.
[26] H. Y. Wang, K. Y. Pu, S. Huang, F. Liu, B. Peng, W. Wei. Funct. Polym. 69 (2009) 117–123.
[27] X.X. Guo, J. Jiang, Q. Han, X.H. Liu, X.T. Zhou, H.B. Ji. Appl. Catal. A. 590 (2020) 117352.
[28] K. Rybicka-Jasińska, W. Shan, K. Zawada, K.M Kadish, D. Gryko. J. Am. Chem. Soc. 138 (2016) 15451-8.
[29] S. Nakagaki, G. Ferreira, G. Ucoski, K. Dias de Freitas Castro. Molecules. 18 (2013) 7279–7308.
[30] B. Akagah, A.T. Lormier, A. Fournet, B. Figadère, Org. Biomol. Chem. 6 (2008) 4494–4497
[31] Q.G. Ren, S.Y. Chen, X.T. Zhou, H.B. Ji. Bioorg. Med. Chem. 18 (2010) 8144-8149.
[32] F. Burg, S. Breitenlechner, C. Jandl, T. Bach. J. Chem. Sci. 2020.
[33] S. Takaishi, Chem. Sci. 4 (2013) 1509–1513.
[34] N. Wojaczy, E. Wojaczy. Chem. Rev. 110 (2010) 4303–4356.
[35] E. Baciocchi, M.F. Gerini, A. Lapi. J. Org. Chem. 69 (2004) 3586-3589.