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Reaction of thiourea S,S-dioxides with dyes containing carbonyl or azo groups

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Abstract

The kinetics of decomposition of thiourea and N-methylthiourea S,S-dioxides in alkaline aqueous medium and their reactions with oxygen, Indigo Carmine, and Acid Yellow 11 were studied. The decomposition of thiourea S,S-dioxides in weakly alkaline media was found to follow two pathways leading to the formation of ammonia and sulfoxylate ion, respectively. The second pathway predominates in strongly alkaline media. Thiourea S,S-dioxides can be used for selective reduction of azo compounds to the corresponding hydrazo derivatives.

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References

  1. Budanov, V.V., Khimiya i tekhnologiya vosstanovitelei na osnove sul’foksilovoi kisloty. Rongalit i ego analogi (Chemistry and Technology of Reducing Agents Based on Sulfoxylic Acid. Rongalite and Its Analogs), Moscow: Khimiya, 1984.

    Google Scholar 

  2. Polenov, Yu.V., Cand. Sci. (Chem.) Dissertation, Ivanovo, 1985.

  3. Davtyan, K.A. and Makarov, S.V., Izv. Vyssh. Uchebn. Zaved., Khim. Khim. Tekhnol., 2001, vol. 44, no. 3, p. 103.

    CAS  Google Scholar 

  4. Budanov, V.V. and Makarov, S.V., Khimiya serosoderzhashchikh vosstanovitelei (Chemistry of Sulfurcontaining Reducing Agents), Moscow: Khimiya, 1994.

    Google Scholar 

  5. Makarov, S.V., Usp. Khim., 2001, vol. 70, no. 10, p. 995.

    Google Scholar 

  6. Miller, A.E., Bischoff, J.J., and Pae, K., Chem. Res. Toxicol., 1988, vol. 1, no. 3, p. 169.

    Article  CAS  Google Scholar 

  7. Makarov, S.V., Kudrik, E.V., van Eldik, R., and Naidenko, E.V., J. Chem. Soc., Dalton Trans., 2002, no. 22, p. 4074.

  8. Huang, S.-L. and Chen, T.Y., J. Chin. Chem. Soc., 1975, vol. 22, no. 1, p. 91.

    CAS  Google Scholar 

  9. Louis-Andre, O. and Gelbard, G., Bull. Soc. Chim. Fr., 1986, no. 4, p. 565.

  10. Nesmeyanov, A.N. and Nesmeyanov, N.A., Nachala organicheskoi khimii (Principles of Organic Chemistry), Moscow: Khimiya, 1974, vol. 2.

    Google Scholar 

  11. Walter, W. and Randau, G., Justus Liebigs Ann. Chem., 1969, vol. 722, p. 80.

    CAS  Google Scholar 

  12. Stepanov, B.I., Vvedenie v khimiyu i tekhnologiyu organicheskikh krasitelei (Chemistry and Technology of Organic Dyes. An Introduction), Moscow: Khimiya, 1977, p. 279.

    Google Scholar 

  13. Tietze, L.-F. and Eicher, T., Reactions and Syntheses in the Organic Chemistry Laboratory, Mill Valley, CA: Univ. Science Books, 1989. Translated under the title Preparativnaya organicheskaya khimiya, Moscow: Mir, 1999, p. 389.

    Google Scholar 

  14. Svarovsky, S.A., Simoyi, R.H., and Makarov, S.V., J. Chem. Soc., Dalton Trans., 2000, no. 4, p. 511.

  15. Debš, D., Electrochemical Data, Budapest: Akad. Kiado, 1978.

    Google Scholar 

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Original Russian Text © S.V. Makarov, E.V. Kudrik, K.A. Davydov, 2006, published in Zhurnal Obshchei Khimii, 2006, Vol. 76, No. 10, pp. 1669–1673.

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Makarov, S.V., Kudrik, E.V. & Davydov, K.A. Reaction of thiourea S,S-dioxides with dyes containing carbonyl or azo groups. Russ J Gen Chem 76, 1599–1603 (2006). https://doi.org/10.1134/S1070363206100173

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  • DOI: https://doi.org/10.1134/S1070363206100173

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