Spotlight: Porphyrin-based catalysts

Subject Areas : Iranian Journal of Catalysis

Mohammad Dashteh ¹

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

Received: 2020-03-30 Accepted : 2020-07-13 Published : 2020-09-01

Keywords:

References:

[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.