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Coordination of 5,10,15,20-tetraphenyl-21H,23H-porphin by rhenium in various oxidation states

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Abstract

A method was developed for the synthesis of three rhenium complexes, (5,10,15,20-tetraphenyl-21H,23H-porphinato)(phenoxo)rhenium(III) (PhO)ReTPP, (5,10,15,20-tetraphenyl-21H,23H-porphi-nato)(chloro)rhenium(III) (Cl)ReTPP, and μ-oxo-bis[(oxo)-(5,10,15,20-tetraphenyl-21H,23H-porphi-nato)rhenium(V)] [O=ReTPP]2O, by one reaction between porphyrin H2TPP and H2ReCl6 in boiling phenol. In the complex formation reaction accompanied by the redox process, only the metal cation is involved in the transformation. Rhenium(IV) as chlororhenic acid dispropoportionates without participation of solvent or porphyrin to give Re(III) and Re(V) complexes. The chemical structures of the products were established by spectral and elemental analysis. Characteristics of the UV, Vis, IR, and 1H NMR spectra, the chromatographic mobility, and stability of the complexes were determined.

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References

  1. V. P. Solov’ev, M. S. Stuklova, E. V. Koltunova, et al., Koord. Khim. 29(9), 711 (2003).

    Google Scholar 

  2. N. T. Kuznetsov, Yu. G. Gorbunova, L. A. Lapkina, et al., Targeted Synthesis of Cyclic Tetrapyrrole Compounds for Technical Purposes (Nauka, Moscow, 2002) [in Russian].

    Google Scholar 

  3. The Porphyrin Handbook, Ed. by K. M. Kadish, K. M. Smith, and R. V. Guilard, vol. 3 (Academic Press, 2000), Handbook of Porphyrin Science, vol. 2 (World Scientific, 2010).

  4. K. J. C. Van Bommel, W. Verbom, H. Kooijman, et al., Inorg. Chem. 37, 4197 (1998).

    Article  Google Scholar 

  5. Zhi-yun Jia, Hou-fu Deng Man-fei Pu, Shun-zhong Luo, Eur. J. Nucl. Med. Mol. Imaging 35, 734 (2008).

    Article  CAS  Google Scholar 

  6. J. P. Collman, J. M. Garner, K. Kim, and J. A. Ibers, Inorg. Chem. 27, 4513 (1988).

    Article  CAS  Google Scholar 

  7. J. P. Collman, J. M. Garner, and L. K. Woo, J. Am. Chem. Soc. 111, 8141 (1989).

    Article  CAS  Google Scholar 

  8. J. P. Collman and H. J. Arnold, Acc. Chem. Res. 26, 586 (1993).

    Article  CAS  Google Scholar 

  9. K. E. Splan, M. H. Keefe, A. M. Massari, et al., Inorg. Chem. 41, 619 (2002).

    Article  CAS  Google Scholar 

  10. J. W. Buchler, A. Cian, J. Fischer, et al., Chem. Ber. 123, 2247 (2006).

    Article  Google Scholar 

  11. M. Toganoh, S. Ikeda, and H. Furuta, Inorg. Chem. 46, 10003 (2007).

    Article  CAS  Google Scholar 

  12. T. N. Lomova and B. D. Berezin, Koord. Khim. 27(2), 96 (2001).

    Google Scholar 

  13. M. Gouterman, The Porphyrins, Ed. by D. V. Dolphin, (Academic Press, New York, 1978), vol. III, p. 463.

    Google Scholar 

  14. T. N. Lomova, N. I. Volkova, and B. D. Berezin, Zh. Neorg. Khim. 28, 2514 (1983).

    CAS  Google Scholar 

  15. T. N. Lomova, B. D. Berezin, L. V. Oparin, and V. V. Zvezdina, Zh. Neorg. Khim. 27, 683 (1982).

    CAS  Google Scholar 

  16. T. N. Lomova, N. I. Volkova, and B. D. Berezin, Zh. Neorg. Khim. 32, 969 (1987).

    CAS  Google Scholar 

  17. T. N. Lomova, E. V. Motorina, E. Yu. Tyulyaeva, et al., in Advances in Porphyrin Chemistry (NII khimii SPbGU, St. Petersburg, 2007), vol. 5, p. 114 [in Russian].

    Google Scholar 

  18. E. Yu. Tyulyaeva, T. N. Lomova, and L. G. Andrianova, Zh. Neorg. Khim. 46, 432 (2001).

    CAS  Google Scholar 

  19. T. N. Lomova, L. P. Shormanova, and B. D. Berezin, Zh. Neorg. Khim. 32, 2489 (1987).

    CAS  Google Scholar 

  20. J. W. Buchler, L. Puppe, K. Rohbock, and H. H. Schneehage, Chem. Ber. 106, 2710 (1973).

    Article  CAS  Google Scholar 

  21. O. V. Molodkina, T. N. Lomova, and E. G. Mozhzhukhina, Izv. Akad. Nauk, Ser. Khim., No. 10, 2052 (1998).

  22. T. N. Lomova, in Advances in Porphyrin Chemistry (Izd. S. PbGU, St. Petersburg, 2001), vol. 3, p. 233 [in Russian].

    Google Scholar 

  23. S. K. Ghosh, R. Datra, and S. P. Rath, Inorg. Chem. 49, 3449 (2010).

    Article  CAS  Google Scholar 

  24. H. J. Ledon, M. C. Bonnet, Y. Brigandat, and F. Varescon, Inorg. Chem. 19, 3488 (1980).

    Article  CAS  Google Scholar 

  25. K. J. C. Van Bommel, W. Verbom, P. Hulst, et al., Inorg. Chem. 39, 4099 (2000).

    Article  Google Scholar 

  26. J. W. Buchler, W. Kokish, and P. D. Smith, Struct. Bond 34, 79 (1978).

    Article  CAS  Google Scholar 

  27. I. M. Cheremisina, Zh. Strukt. Khim. 19(2), 336 (1978).

    CAS  Google Scholar 

  28. A. Gordon and R. Ford, The Chemist’s Companion, A Handbook of Practical Data. Techniques and References (Wiley, New York, 1972).

    Google Scholar 

  29. P. A. Stuzhin, Doctoral (Chem.) Dissertation (Ivanovo, 2004).

  30. E. Gallo, A. Casell, F. Ragaini, et al., Inorg. Chem. 44, 2039 (2005).

    Article  CAS  Google Scholar 

  31. D. R. Evans and C. A. Reed, J. Am. Chem. Soc. 122, 4660 (2000).

    Article  CAS  Google Scholar 

  32. K. Shantha and A. L. Verma, Inorg. Chem. 35, 2723 (1996).

    Article  CAS  Google Scholar 

  33. D. E. Lansky, B. Mandimutsira, B. Ramdhanie, et al., Inorg. Chem. 44, 4485 (2005).

    Article  CAS  Google Scholar 

  34. M. L. Merlau, So-Hye Cho, Shih-Sheng Sun, et al., Inorg. Chem. 44, 5523 (2005).

    Article  CAS  Google Scholar 

  35. E. Yu. Tyulyaeva, T. N. Lomova, and E. G. Mozhzhukhina, Koord. Khim. 29, 605 (2003).

    Google Scholar 

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Original Russian Text © E.Yu. Tyulyaeva, N.G. Bichan, T.N. Lomova, E.G. Mozhzhukhina, 2012, published in Zhurnal Neorganicheskoi Khimii, 2012, Vol. 57, No. 9, pp. 1378–1384.

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Tyulyaeva, E.Y., Bichan, N.G., Lomova, T.N. et al. Coordination of 5,10,15,20-tetraphenyl-21H,23H-porphin by rhenium in various oxidation states. Russ. J. Inorg. Chem. 57, 1295–1301 (2012). https://doi.org/10.1134/S0036023612090203

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  • DOI: https://doi.org/10.1134/S0036023612090203

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