Skip to main content
Log in

NO2-induced synthesis of nitrato-iron(III) porphyrin with diverse coordination mode and the formation of isoporphyrin

  • Published:
Journal of Chemical Sciences Aims and scope Submit manuscript

Abstract

Two nitrato-iron(III) porphyrinates [Fe(4-Me-TPP)(NO3)] 1 and [Fe(4-OMe-TPP)(NO3)] 2 are reported. Interestingly, [Fe(4-Me-TPP)(NO3)] 1 has nitrate ion coordinated as monodentate (by single oxygen atom), while [Fe(4-OMe-TPP)(NO3)] 2 has nitrate coordination through bidentate mode. Compound 1 was found serendipitously in the reaction of [Fe(4-Me-TPP)Cl] with nitrous acid, which was performed for the synthesis of nitro-iron(III) porphyrin, [Fe(4-Me-TPP)NO2]. The compound 2 was synthesized by passing NO2 gas through a solution of [Fe(4-OMe-TPP)]2O. Upon passing NO2 gas through a solution of a μ-oxo-dimer, [Fe(4-Me-TPP)]2O also produces 1. It is interesting that in more electron-rich porphyrin 2, binding of the nitrate in a symmetrical bidentate way while in less electron-rich porphyrin 1, binding of the anion is unidentate by a terminal oxygen atom. However, it is expected that the energy difference between the monodentate and bidentate coordination mode is very small and the interchange between these coordination is possible. Upon passing NO2 gas through a solution of \(\upmu \)-oxo-dimeric iron(III) porphyrin, the nitrato-iron(III) porphyrin forms first, that later gets oxidized to π-cation radical to yield hydroxy-isoporphyrin in the presence of trace amount of water. These nitrato-iron(III) porphyrinates in moist air slowly converted back to their respective \(\upmu \)-oxo-dimeric iron(III) porphyrins.

[Fe(4-Me-TPP)]2O and [Fe(4-OMe-TPP)]2O react with NO2 to produce nitratoiron( III) porphyrin with monodentate and bidenate nitrate coordination, respectively. Further passage of NO2 oxidized these to π-cation radical to yield hydroxy-isoporphyrin in the presence of moisture. But nitrato-iron(III) porphyrinates in moist air slowly converted back to their respective μ-oxodimeric iron(III) porphyrins.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Scheme 1
Figure 1
Figure 2
Figure 3
Figure 4

Similar content being viewed by others

References

  1. (a) Wyllie G R A and Scheidt W R 2002 Chem. Rev. 102 1067; (b) Scheidt W R and Ellison M K 1999 Acc. Chem. Res. 32 350; (c) Ford P C 2010 Inorg. Chem. 49 6226; (d) Lehnert N, Berto T C, Galinato M G I and Goodrich L E 2011 The handbook of porphyrin, K M Kadish, K M Smith and R Guilard (eds) World Scientific Vol. 14, 1–247

  2. (a) Kumar M R, Zapata A, Ramirez A J, Bowen S K, Francisco W A and Farmer P J 2011 Proc. Natl. Acad. Sci. USA 108 18926; (b) Paolocci N, Saavedra W F, Miranda K M, Martignani C, Isoda T, Hare J M, Espey M G, Fukuto J M, Feelisch M, Wink D A and Kass D A 2001 Proc. Natl. Acad. Sci. USA 98 10463

    Google Scholar 

  3. (a) Cheng L and Richter-Addo G B 2000 The porphyrin handbook, K M Kadish, K M Smith and R Guilard (eds) Academic Press, San Diego, Vol. 4, pp 2590–260; (b) Doyle M P and Hoekstra J W 1981 J. Inorg. Biochem. 14 351; (c) Eich R F, Li T, Lemon D D, Doherty D H, Curry S R, Aitken J F, Mathews A J, Johnson K A, Smith R D, Phillips G N and Oleson J S 1996 Biochemistry 35 6976

  4. (a) Koropatkin N M, Pakras H B and Smith T J 2006 PNAS 103 9820; (b) Bhuyan J, Sarkar R and Sarkar S 2011 Angew. Chem. Int. Ed. 50 10604

  5. (a) Harischandra D N, Zhang R and Newcomb M J 2005 J. Am. Chem. Soc. 127 13776; (b) Pan Z, Zhang R, Fung L W M and Newcomb M 2007 Inorg. Chem. 46 1517

  6. Van Driel G J, Driessen W L and Reedjik J 1985 Inorg. Chem. 24 2919

    Article  Google Scholar 

  7. (a) Wyllie G R A, Munro O Q, Schulz C E and Scheidt W R 2007 Polyhedron 26 4664; (b) Phillippi M A, Baenziger N and Goff H M 1981 Inorg. Chem. 20 3904; (c) Ellison M K, Shang M, Kim J and Scheidt W R 1996 Acta Crystallogr. Sect. C 52 3040

  8. (a) Guzinski J A and Felton R H 1973 J. Chem. Soc., Chem. Commun. 715; (b) Barkigia K M, Renner M W, Xie H, Smith K M and Fajer J 1993 J. Am. Chem. Soc. 115 7894

  9. Cong Z, Kurahashi T and Fujii H 2012 J. Am. Chem. Soc. 134 4469

    Article  CAS  Google Scholar 

  10. (a) Woodward R B 1960 Angew. Chem. 72 651; (b) Woodward R B 1961 Pure Appl. Chem. 2 383; (c) Woodward R B 1967 Ind. Chim. Belge 27 1293

  11. Dolphin D, Felton R H, Borg D C and Fajar J 1970 J. Am. Chem. Soc. 92 743

    Article  CAS  Google Scholar 

  12. (a) Gold A, Ivey W, Toney G E, Sangaiah R 1984 Inorg. Chem. 23 2932; (b) Takeda Y, Tskshara S, Kobyashi Y, Miswa H, Sauragi H and Tokumaru K 1990 Chem. Lett. 11 2103; (c) Felton R H, Owen G S, Dolphin D, Forman A, Borg D C and Fajer J 1973 Ann. N.Y. Acad. Sci. 206 504; (d) Harriman A, Porter G and Walters P 1983 J. Chem. Soc., Faraday Trans. 1 79 1335; (e) Kadish K M and Rhodes R K 1981 Inorg. Chem. 20 2961; (f) Shine H J, Padilla A G and Wu S M 1979 J. Org. Chem. 44 4069; (g) Fawcett W R, Fedurco M, Smith K M and Xie H 1993 J. Electroanal. Chem. 354 281

  13. (a) Abhilash G J, Bhuyan J, Singh P, Maji S, Pal K and Sarkar S 2009 Inorg. Chem. 48 1790; (b) Bhuyan J and Sarkar S 2010 Chem. Eur. J. 16 10649

  14. Catalano M M, Crossley M J, Harding M M 1984 J. Chem. Soc. Chem. Commun. 1535

  15. Kumar A, Maji S, Dubey P, Abhilash G J, Pandey S and Sarkar S 2007 Tetrahedron Lett. 48 7287

    Article  CAS  Google Scholar 

  16. Altomare A, Burla M C, Camalli M, Cascarano G L, Giacovazzo C, Guagliardi A, Moliterni A G G, Polidori G and Spagna R 1999 J. Appl. Crystallogr. 32 115

    Article  CAS  Google Scholar 

  17. Sheldrick G M SHELX97 Programs for crystal structure analysis (Release 97-2); University of Göttingen: Göttingen, Germany 1997

  18. Bag N, Chern S, Peng S and Chang C K 1995 Tetrahedron Lett. 36 6409

    Article  CAS  Google Scholar 

  19. Nakamoto K 1986 Infrared and Raman spectra of inorganic and coordination compounds, John Wiley & Sons, New York, 4th Ed. pp 254–257

  20. Finnegan M G, Lappin A G and Scheidt W R 1990 Inorg. Chem. 29 181

    Article  CAS  Google Scholar 

  21. Bhuyan J and Sarkar S 2012 Chem. Asia. J. 7 2690

    Article  CAS  Google Scholar 

  22. (a) Khin C, Heinecke J and Ford P C 2008 J. Am. Chem, Soc. 130 13830; (b) Castro C E 1996 J. Am. Chem. Soc. 118 3984; (c) O’shea S K, Wang W, Wade R S and Castro C E 1996 J. Org. Chem. 61 6388; (d) Singh P, Saltsmana I, Mahammeda A, Goldbergb I, Tumanskiia B and Gross Z 2012 J. Porphyrins Phthalocyanines 16 663

  23. (a) Desiraju G 1991 Acc. Chem. Res. 24 290; (b) Bernstein J 2013 Cryst. Growth Des. 13 961; (c) Jin Y Z, Zhang R, Fu D and Lv Y 2011 Acta Crystallogr. E67 o1594; (d) Mazika M, Bläserb D and Boeseb R 2001 Tetrahedron 57 5791

Download references

Acknowledgements

JB acknowledges Doctoral Research Fellowships from the Council of Scientific and Industrial Research (CSIR), New Delhi and SS thanks the Department of Science and Technology (DST) New Delhi for funding the project.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to SABYASACHI SARKAR.

Additional information

Supplementary material

CCDC 890195 and 890196 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via http://www.ccdc.cam.ac.uk/data_request/cif. For supplementary figures S1S5, see the journal website (www.ias.ac.in/chemsci).

Dedicated in memory of Prof. P T Narasimhan

Electronic supplementary material

Below is the link to the electronic supplementary material.

(DOC 1.55 MB)

Rights and permissions

Reprints and permissions

About this article

Cite this article

BHUYAN, J., SARKAR, S. NO2-induced synthesis of nitrato-iron(III) porphyrin with diverse coordination mode and the formation of isoporphyrin . J Chem Sci 125, 707–714 (2013). https://doi.org/10.1007/s12039-013-0447-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12039-013-0447-1

Keywords

Navigation