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Novel Mn(III) Porphyrins and Prospects of Their Application in Catalysis

  • Coordination Compounds
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Abstract

Four novel Mn(III) porphyrins have been synthesized and characterized by UV-Vis, IR, ESI-mass spectroscopy, elemental analysis, magnetic susceptibility studies, TLC, and conductivity measurements. The tentative structure has been proposed. Depolymerization of coal using the synthesized Mn(III) porphyrins have been demonstrated by the optical density method using humic acid as a model of coal. The synthesized complexes have shown excellent depolymerization activity based on comparative studies. Complexes have been successfully applied for the catalytic oxidation of benzyl alcohol, aniline, benzoin, and benzaldehyde into benzaldehyde, nitrobenzene, benzil, and benzoic acid, respectively, at room temperature and pressure.

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References

  1. P. Souza, M. A. Mandiola, A. Arquero, et al., Naturforsch. Z. B 49, 263 (1994).

    Article  CAS  Google Scholar 

  2. N. R. Champness, C. S. Frampton, G. Reid, et al., J. Chem. Soc. Dalton Trans., 3031 (1994). doi https://doi.org/10.1039/DT9940003031

  3. J. T. Groves, J. Porphyrins Phthalocyanines, 4, 350 (2000). doi

    Article  CAS  Google Scholar 

  4. S. Nimri and E. Keinan, J. Am. Chem. Soc. 121, 8978 (1999). doi https://doi.org/10.1021/ja990314q

    Article  CAS  Google Scholar 

  5. M. V. Vinodu and M. Padmanabhan, Proc. Indian Acad. Sci. (Chem. Sci.) 113, 1 (2001).

    Article  CAS  Google Scholar 

  6. M. M. Q. Simos, M. G. P. M. S. Neves, and J. A. S. Cavaleiro, Jord. J. Chem. 1, 1 (2006).

    Google Scholar 

  7. I. Batinic-Haberle, I. Spasojevic, R. D. Stevens et al., Dalton Trans., 617 (2006). doi https://doi.org/10.1039/B513761F

  8. M. Biesaga, K. Pyrzynska, M. Trojanowicz, Talanta, 51, 209 (2000). doi https://doi.org/10.1016/S0039-9140(99)00291-X

    Article  CAS  PubMed  Google Scholar 

  9. L. F. Lauffer, Chem. Rev. 87, 901 (1987). doi https://doi.org/10.1021/cr00081a003

    Article  CAS  Google Scholar 

  10. M. Ravikanth and T. K. Chandrashekhar, Structure-Bond. 82, 105 (1995). doi https://doi.org/10.1007/BFb0036827

    Article  CAS  Google Scholar 

  11. Biotechnology in Pulp and Paper Industry, Eds. by P. S. Skerker, R. L. Farrell, D. Dolphin, F. Cui, and T. Wijesekera (Butterworth-Heinemann, Boston, 1990), Ch. 18.

    Google Scholar 

  12. D. L. Crawfold and R. L. Crawfold, Enz. Microb. Technol. 2, 11 (1980). doi https://doi.org/10.1016/0141-0229(80)90003-4

    Article  Google Scholar 

  13. S. B. Pointing, A. L. Pelling, G. J. D. Smith, et al., Mycol Res. 109, 115 (2005). doi https://doi.org/10.1017/S0953756204001376

    Article  CAS  PubMed  Google Scholar 

  14. V. Shanmugam and K. D. S. Yadav, Indian J. Exp. Biol. 34, 116 (1996).

    Google Scholar 

  15. M. Hofrichter, Enz. Microbiol. Technol. 30, 454 (2002). doi https://doi.org/10.1016/S0141-0229(01)00528-2

    Article  CAS  Google Scholar 

  16. M. Yadav, P. Yadav, K. D. S. Yadav, Biochemistry (Moscow) 74, 1125 (2009). doi https://doi.org/10.1134/S0006297909100083

    Article  CAS  Google Scholar 

  17. T. Murashima, S. Tsujimoto, T. Yamada, et al., Tetrahed. Lett. 46, 113 (2005). doi https://doi.org/10.1016/j.tetlet.2004.11.024

    Article  CAS  Google Scholar 

  18. J. M. Pedrosa, M. Perez, I. Prieto, Phys. Chem. Chem. Phys. 4, 2329 (2002). doi https://doi.org/10.1039/B108360K

    Article  CAS  Google Scholar 

  19. R. J. Errington, Advanced Practical Inorganic and Metalloorganic Chemistry, 1st Ed. (Chapman and Hall, London, 1997).

    Google Scholar 

  20. W. L. F. Armarego, D. D. Perrin, Purification of Laboratory Chemicals, 4th Ed. (Butterworth-Heinemann, Oxford, 1997).

    Google Scholar 

  21. B. S. Furniss, A. J. Hannaford, V. Rogers, et al., Vogel’s Text Book of Practical Organic Chemistry, 4th Ed. (ELBS, London, 1984).

    Google Scholar 

  22. G. H. Jeffery, J. Bassett, J. Mendham, et al., Vogel’s Text Book of Quantitative Chemical Analysis, 5th Ed. (ELBS, London, 1996).

    Google Scholar 

  23. S. Yadava and S. L. Bharati, J. Coord. Chem. 64, 3950 (2011). doi. https://doi.org/10.1080/958972.2011.632412

    Article  CAS  Google Scholar 

  24. S. L. Bharati and S. Yadava, J. Coord. Chem. 65, 3492 (2012). doi. https://doi.org/10.1080/00958972.2012.718763

    Article  CAS  Google Scholar 

  25. A. D. Adler, F. R. Longo, J. D. Finarelli, et al., J. Org. Chem. 32, 476 (1967). doi https://doi.org/10.1021/jo01288a053

    Article  CAS  Google Scholar 

  26. E. B. Fleischer, J. M. Palmer, T. S. Srivastava, et al., J. Am. Chem. Soc. 93, 3162 (1971). doi https://doi.org/10.1021/ja00742a012

    Article  CAS  PubMed  Google Scholar 

  27. B. R. Stults, V. W. Day, E. L. Tassett, et al., Inorg. Nucl. Chem. Lett. 9, 1259 (1973). doi https://doi.org/10.1016/0020-1650(73)80007-8

    Article  CAS  Google Scholar 

  28. B. R. Stults, V. W. Day, R. S. Marianelli, and V. B. Day, Inorg. Chem. 14, 722 (1975). doi https://doi.org/10.1021/ic50146a004

    Article  CAS  Google Scholar 

  29. B. Bahramian, V. Mirkhani, M. Moghadam, et al., Appl. Catal. A: Gen. 315, 52 (2006). doi https://doi.org/10.1016/j.apcata.2006.08.037

    Article  CAS  Google Scholar 

  30. S. L. H. Rebelo, M. M. Q Simoes, M. G. P. M. S. Neves, et al., J. Mol. Catal. A: Chem., 201, 9 (2003). doi https://doi.org/10.1016/S1381-1169(03)00149-3

    Article  CAS  Google Scholar 

  31. S. F. A. Kettle, Coordination Compounds (Pitman Press, London, 1975)

    Google Scholar 

  32. D. W. Thomas and A. E. Martell, J. Am. Chem. Soc. 78, 1338 (1956). doi https://doi.org/10.1021/ja01588a021

    Article  CAS  Google Scholar 

  33. R. J. H. Clark and C. S. Williams, Spectrochim. Acta 22, 1081 (1966). doi https://doi.org/10.1016/0371-1951(66)80198-4

    Article  CAS  Google Scholar 

  34. R. J. Dyer, Applications of Absorption Spectroscopy of Organic Compounds (Prentice-Hall of India, New Delhi, 1969).

    Google Scholar 

  35. T. N. Lomova and B. D. Berezin, Russ. J. Coord. Chem. 27, 85 (2001). doi https://doi.org/10.1023/A:1009523115380

    Article  CAS  Google Scholar 

  36. G. Wilkinson, R. D. Gillard, and J. A. McCleverty, Comprehensive Coordination Chemistry (Pergamon, Oxford, 1987).

    Google Scholar 

  37. I. Gamo, Bull. Chem. Soc. Jpn. 34, 760 (1961). doi https://doi.org/10.1246/bcsj.34.760

    Article  CAS  Google Scholar 

  38. A. D. Allen and C. V. Senoff, Canad. J. Chem. 43, 888 (1965). doi https://doi.org/10.1139/v65-115

    Article  Google Scholar 

  39. J. W. Buchler, W. Kokisch, and P. Smith, Struct. Bond. (Berlin) 34, 79 (1978).

    Article  CAS  Google Scholar 

  40. H. Sckeno and H. Kobayashi, J. Chem. Phys. 75, 283 (1981).

    Google Scholar 

  41. E. Fagadar-Cosma, M. C. Mirica, I. Balcu, et al., Molecules 14, 1370 (2009). doi https://doi.org/10.3390/molecules14041370

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Y. Lamamoto, M. D. Assis, K. J. Ciuffi, et al., J. Mol. Catal. A: Chem. 116, 365 (1997). doi https://doi.org/10.1016/S1381-1169(96)00343-3

    Article  Google Scholar 

  43. H. A. O. Hill, A. J. Macfarlane, and R. J. P. Williams, J. Chem. Soc. A, 1704 (1969). doi https://doi.org/10.1039/J19690001704

  44. J. E. Huheey, E. A. Keiter, and R. L. Keiter, Inorganic Chemistry, Principles of Structure and Reactivity (Pearson, Singapore, 2005), p. 445.

    Google Scholar 

  45. S. L. Bharati, P. K. Chaurasia, and S. Yadava, J. Coord. Chem. 61, 232 (2016). doi https://doi.org/10.1134/S0036023616020212

    CAS  Google Scholar 

  46. I. Batinic-Haberle, I. Spasojevic, R. D. Stevens, et al., J. Chem. Soc. Dalton Trans., 2689 (2002). doi https://doi.org/10.1039/B201057G

    Google Scholar 

  47. I. Batinic-Haberle, I. Spasojevic, R. D. Stevens, et al., Dalton Trans., 1696 (2004). doi https://doi.org/10.1039/B400818A

    Google Scholar 

  48. D. V. Behere and S. Mitra, Inorg. Chem. 19, 992 (1980). doi https://doi.org/10.1021/ic50206a039

    Article  CAS  Google Scholar 

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Correspondence to S. L. Bharati or P. K. Chaurasia.

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Bharati, S.L., Sarma, C., Hazarika, P.J. et al. Novel Mn(III) Porphyrins and Prospects of Their Application in Catalysis. Russ. J. Inorg. Chem. 64, 335–341 (2019). https://doi.org/10.1134/S0036023619030045

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