Abstract
The earlier unknown organosilicon polyiodides of 2-thiobenzimidazolium have been synthesized basing on the three-component reaction of 2-thiobenzimidazole, bis(iodomethyl) derivatives of siloxanes or silanes, and molecular iodine; the products have been identified by means of NMR, IR, and UV spectroscopy.
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Foreman, K.W., Nguyen, H.N., Ofori, L.O., Wanner, J., and Werner, D., WO Patent 183359 Al, 2016.
Zniber, R., Moussaif, A., Achour, R., El Ghoul, M., Maltouf, A.F., Mekkak, A.I., and Harrata, A., Rev. Roumaine Chim., 2009, vol. 54, p. 643.
Gatta, L., Perna, F., Figura, N., Ricci, C., Holton, J., D’Anna, L., Miglioli, M., and Vaira, D., J. Antimicrob. Chemother., 2003, vol. 51, p. 439. doi https://doi.org/10.1093/jac/dkg085
De Almeida, M.V., Cardoso, S.H., De Assis, J.V., and De Souza, M.V.N., J. Sulfur Chem., 2007, vol. 28, p. 17. doi https://doi.org/10.1080/17415990601055291
El Ouasif, L., Bouyahya, A., Zniber, R., El Ghoul, M., Achour, R., Chakchak, H., Talbaoui, A., El Boury, H., Dakka, N., Bakri, Y., and Mediterr., J. Chem., 2017, vol. 6, p. 77. doi https://doi.org/10.13171/mjc61/01704011035
Mavrova Ts., Yancheva, D., Anastassova, N., Anichina, K., Zvezdanovic, J., Djordjevic, A., Markovic, D, and Smelcerovic, A., Bioorg. Med. Chem., 2015, vol. 23, no. 19, p. 6317. doi https://doi.org/10.1016/j.bmc.2015.08.029
Andrzejewska, M., Yepez-Mulia, L., Tapia, A., Cedillo-Rivera, R., Laudy, A.E., Starósciak, B.J., and Kazimierczuk, Z., Eur. J. Pharm. Sci., 2004, vol. 21, nos. 2–3, p. 323. doi https://doi.org/10.1016/j.ejps.2003.10.024
Yiğit, B., Gök, Y., Özdemir, I., and Günal, S., J. Coord. Chem., 2012, vol. 65, p. 371. doi https://doi.org/10.1080/00958972.2012.654469
Radha, Y., Manjula, A., Reddy, M.B., and Vittal, R.B., Ind. J. Chem. (B), 2011, vol. 50, no. 12, p. 1762. doi 123456789/13216
Mor, M., Bordi, F., Silva, C., Rivara, S., Zuliani, V., Vacondio, F., Rivara, M., Barocelli, E., Bertoni, S., Ballabeni, V., Magnanini, F., Impicciatore, M., and Vincenzo Plazzi, P., Bioorg. Med. Chem., 2004, vol. 12, no. 4, p. 663. doi https://doi.org/10.1016/j.bmc.2003.11.030
Anand, A., Kulkarni, M.V., Joshi, S.D., and Dixit, S.R., Bioorg. Med. Chem. Lett., 2016, vol. 26, no. 19, p. 4709. doi https://doi.org/10.1016/j.bmcl.2016.08.045
Hosamani, K.M. and Shingalapur, R.V., Arch. Pharm., 2011, vol. 344, no. 5, p. 311. doi https://doi.org/10.1002/ardp.200900291
Mahdavian, M. and Ashhari, S., Electrochim. Acta, 2010, vol. 55, p. 1720. doi https://doi.org/10.1016/j.electacta.2009.10.055
Finšgar, M., Corros. Sci., 2013, vol. 72, p. 90. doi https://doi.org/10.1016/j.corsci.2013.03.011
El Achaby, M., Ennajih, H., Arrakhiz, F.Z., El Kadib, A., Bouhfid, R., Essassi, E., and Qaiss, A., Composites (B), 2013, vol. 51, p. 310. doi https://doi.org/10.1016/j.compositesb.2013.03.009
Cai, G., Feng, J., Zhu, J., Wilkie, C.A., Polymer Degrad. Stab., 2014, vol. 99., P., 204. doi https://doi.org/10.1016/j.polymdegradstab.2013.11.004
Zhong, B., Dong, H., Lin, J., Jia, Z., Luo, Y., Jia, D., and Liu F., Ind. Eng. Chem. Res., 2017, vol. 56, no. 32, p. 9135. doi https://doi.org/10.1021/acs.iecr.7b02250
Voronkov, M.G., Chernov, N.F., Trofimova, O.M., and Aksamentova, T.N., Russ. Chem. Bull., 1993, p. 1965.
Pourreza, N. and Ghanemi, K., J. Hazard Mater., 2009, vol. 161, nos. 2–3, p. 982. doi https://doi.org/10.1016/j.jhazmat.2008.04.043
Iwamoto, K., Kimura, H., Oike, M., and Sato, M., Org. Biomol. Chem., 2008, vol. 6, p. 912. doi 610.1039/B719430G
Iqbal, M.A., Haque, R.A., Ahamed, M.B.K., Majid, A.M.S., and Al-Rawi, S.S., Med. Chem. Res., 2013, vol. 22, p. 2455. doi https://doi.org/10.4172/2161-1009.1000147
Lal, A.K. and Milton, M.D., Tetrahedron Lett., 2014, vol. 55, no. 10, p. 1810. doi https://doi.org/10.1016/j.tetlet.2014.01.127
Lee, J.P. Yoo, B., Suresh, T., Kang, M.S., Vital, R., and Kim, K.J., Electrochim. Acta, 2009, vol. 54, no. 18, p. 4365. doi https://doi.org/10.1016/j.electacta.2009.03.006
Zeng, W. and Jiang, J., Crystals, 2017, vol. 7, p. 303. doi https://doi.org/10.3390/cryst7100303
Voronkov, M.G., Trofimova, O.M., Bolgova, Yu.I., and Chernov, N.F., Chem. Heterocycl. Compd., 2001, vol. 37, no. 11, p. 1358. doi https://doi.org/10.1023/A:1017994916574
Abele, E., Abele, R., Arsenyan, P., Belyakov, S., Veveris, M., and Lukevics, E., Chem. Heterocycl. Compd., 2007, vol. 43, no. 2, p. 220. doi https://doi.org/10.1007/s10593-007-0034-9
Funding
The authors thank L.I. Larina (Irkutsk Institute of Chemistry, Siberian Branch of Russian Academy of Sciences) for recording the 15N NMR spectra. This study was performed using of equipment of the Baikal Center for Collective Usage, Siberian Branch of Russian Academy of Sciences.
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Russian Text © The Author(s), 2019, published in Zhurnal Obshchei Khimii, 2019, Vol. 89, No. 8, pp. 1239–1244.
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Zhilitskaya, L.V., Yarosh, N.O., Shagun, L.G. et al. New Organosilicon Bis-Derivatives of 2-Thiobenzimidazole. Russ J Gen Chem 89, 1625–1629 (2019). https://doi.org/10.1134/S1070363219080127
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DOI: https://doi.org/10.1134/S1070363219080127