Abstract
The reaction of dichloroglyoxime with sulfanilamide affords new glyoxime: disulfanilamide glyoxime (DsamH2, L). Two coordination compounds are synthesized from DsamH2: [Ni(DsamH)2]·2H2O (I) and [Cu(DsamH2)3]SO4·5H2O (II). Their compositions and structures are determined by elemental analysis and IR, UV, and NMR spectroscopy. Compounds L and II are studied by XRD (CIF files CCDC nos. 2080777 and 2080778, respectively). Both bis(ligand) and tris(ligand) complexes with L are synthesized depending on the synthesis conditions. The different degrees of deprotonation of the DsamH2 ligand in complexes I and II cause the formation of both molecular and ionic complexes. Complex II taken in optimum concentrations exerts a stimulating effect on the protease synthesis of the biotechnologically significant micromycete strains Fusarium gibbosum CNMN FD 12 and Trichoderma koningii Oudemans CNMN FD 15.
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REFERENCES
Janiak, Ch., Dalton Trans., 2003, p. 2781.
Bourosh, P.N., Coropceanu, E.B., Siminov, Yu.A., et al., Russ. J. Coord. Chem., 2002, vol. 28, no. 9, p. 647. https://doi.org/10.1023/A:1020095101054
Melnic, E., Coropceanu, E.B., Forni, A., et al., Cryst. Growth Des., 2016, vol. 16, no. 11, p. 6275.
Croitor, L., Coropceanu, E.B., Chisca, D., et al., Cryst. Growth Des., 2014, vol. 14, no. 6, p. 3015.
Coropceanu, E.B., Croitor, L., and Fonari, M.S., Polyhedron, 2012, vol. 38, no. 1, p. 68.
Coropceanu, E., Croitor, L., Gdaniec, M., et al., Inorg. Chim. Acta, 2009, vol. 362, no. 7, p. 2151.
Coropceanu, E.B., Croitor, L., Botoshansky, M.M., et al., Polyhedron, 2011, vol. 30, no. 15, p. 2592.
Coropceanu, E., Rija, A., Lozan, V., et al., Cryst. Growth Des., 2016, vol. 16, no. 2, p. 814.
Croitor, L., Coropceanu, E.B., Siminel, A.V., et al., CrystEngComm, 2012, vol. 14, no. 10, p. 3750.
Coropceanu, E.B., Croitor, L., Siminel, A.V., et al., Polyhedron, 2016, vol. 109, p. 107.
Bresciani Pahor, N., Farcolin, M., Marzilli, L.G., et al., Coord. Chem. Rev., 1985, vol. 63, p. 1.
Randaccio, L., Bresciani Pahor, N., Zangrando, E., and Marzilli, L.G., Chem. Soc. Rev., 1989, vol. 18, p. 225.
Desyatnik, A.A., Gerbeleu, N.V., Koropchanu, E.B., et al., Russ. J. Coord. Chem, 2002, vol. 28, no. 2, p. 135. https://doi.org/10.1023/A:1014240303176
Bourosh, P.N., Koropchanu, E.B., Ciloci, A.A., et al., Russ. J. Coord. Chem, 2009, vol. 35, no. 10, p. 751. https://doi.org/10.1134/S1070328409100078
Mokhir, A., Krämer, R., Voloshin, Y.Z., and Varzatskii, O.A., Bioorg. Med. Chem. Lett., 2004, vol. 14, no. 11, p. 2927.
Coropceanu, E.B., Bulhac, I.I., Shtefyrtse, A.A., et al., Russ. J. Coord. Chem., 2017, vol. 43, no. 3, p. 164. https://doi.org/10.1134/S1070328417030046
Ocak, U., Kantekin, H., Gok, Y., and Misir, M.N., New J. Chem., 2003, vol. 27, p. 1251.
Gumus, G., Ahsen, V., Lebrun, C., et al., New J. Chem., 2004, vol. 28, p. 177.
Ureche, D., Rija, A., Bulhac, A., et al., Russ. J. Inorg. Chem., 2020, vol. 65, no. 12, p. 1838. https://doi.org/10.1134/S0036023620120189
Bourosh, P.N., Coropceanu, E.B., Ciloci, A.A., et al., Russ. J. Coord. Chem., 2013, vol. 39, no. 11, p. 777. https://doi.org/10.1134/S107032841311002X
Yuksel, F., Gurek, G., Durmus, M., et al., Inorg. Chim. Acta, 2008, vol. 361, no. 8, p. 2225.
Rija, A., Bulhac, I., Coropceanu, E., et al., http://www.cjm.asm.md/sites/default/files/article_files/Rija%20016%20.pdf.
CrysAlis RED, O.D.L. Version 1.171.34.76. Data Collection and Processing Software for Agilent X-ray Diffractometers, 2003.
Sheldrick, G.M., Acta Crystallogr., Sect. A: Found. Crystallogr., 2008, vol. 64, no. 1, p. 112.
Deseatnic-Ciloci, A., Tiurina, J., Lupascu, G., et al., Brevet MD 4186, BOPI 2012, no. 11.
Deseatnic-Ciloci, A., Tiurina, J., Lupascu, G., et al., Brevet MD 4285, BOPI 2014, no. 5.
Gracheva, I.M., Grachev, Yu.P., Mosichev, M.S., et al., Laboratornyi praktikum po tekhnologii fermentnykh preparatov (Laboratory Works on the Technology of Enzyme Preparations), Moscow: Legkaya i pishch. Prom., 1982.
Dospekhov, B. Planirovanie polevogo opyta i staticheskaya obrabotka dannykh (Planning of Field Experiment and Statistical Data Treatment), Moscow: Kolos, 1985.
Bellamy, L.J., The Infrared Spectra of Complex Molecules, New York: Wiley, 1958.
Gordon, A. and Ford, R., The Chemist’s Companion: A Handbook of Practical Data, Techniques, and References, New York: Wiley, 1972.
Tarasevich, B.N., IK spektry osnovnykh klassov organicheskikh soedinenii. Spravochnye materialy (IR Spectra of the Main Classes of Organic Compounds), Moscow, 2012.
Nakamoto, K., Infrared Spectra and Raman Spectra of Inorganic and Coordination Compounds, New York: Wiley, 1986.
Coropceanu, E.B., Ureche, D., Rija, A.P., et al., Russ. J. Coord. Chem., 2021, vol. 47, no. 1, p. 17. https://doi.org/10.1134/S1070328421010024
Allen, F.H., Acta Crystallogr., Sect. B: Struct. Sci., 2002, vol. 58, nos. 3–1, p. 380.
Durmus, M., Ahsen, V., Luneau, D., and Pecaut, J., Inorg. Chim. Acta, 2004, vol. 357, p. 588.
Kakanejadifard, A. and Amani, V., Acta Crystallogr., Sect. E: Struct. Rep. Online, 2008, vol. 64, p. o1512.
Endres, H. and Schendzielorz, M., Acta Crystallogr., Sect. C: Struct. Struct. Commun., 1984, vol. 40, p. 453.
Ureche, D., Bulhac, I., Rija, A., et al., Russ. J. Coord. Chem., 2019, vol. 45, no. 12, p. 843. https://doi.org/10.1134/S107032841912008X
Belombe, M.M., Nenwa, J., Kammoe, A.L., and Poudeu, P.F.P., Acta Crystallogr., Sect. E: Struct. Rep. Online, 2006, vol. 62, p. m2583.
Belombe, M.M., Nenwa, J., Mbiangue, Y.A., et al., Acta Crystallogr., Sect. E: Struct. Rep. Online., 2008, vol. 64, p. m1440.
Endres, H. and Jannack, T., Acta Crystallogr., Sect. B: Struct. Crystallogr. Cryst. Chem., 1980, vol. 36, p. 2136.
Nenwa, J., Djonwouo, P.L., Belombe, M.M., et al., ScienceJet, 2013, vol. 2, p. 43.
Belombe, M.M., Nenwa, J., Mbiangue, Y.A., et al., Dalton Trans., 2009, p. 4519.
Belombe, M.M., Nenwa, J., Bebga, G., et al., Acta Crystallogr., Sect. E: Struct. Rep. Online., 2007, vol. 63, p. m2037.
Bekaroglu, O., Sarisaban, S., Koray, A.R., et al., Acta Crystallogr., Sect. B: Struct. Crystallogr. Cryst. Chem., 1978, vol. 34, p. 3591.
Belombe, M.M., Nenwa, J., Lonnecke, P., and Hey-Hawkins, E., Z. Anorg. Allg. Chem., 2009, vol. 635, p. 420.
Kawata, S., Kitagawa, S., Machida, H., et al., Inorg. Chim. Acta, 1995, vol. 229, p. 211.
Endres, H., Genc, N., and Nothe, D., Z. Naturforsch., A: Phys. Sci., vol. 38, p. 90.
Endres, H., Nothe, D., Rossato, E., and Hatfield, W.E., Inorg. Chem., 1984, vol. 23, p. 3467.
Endres, H. and Genc, N., Acta Crystallogr., Sect. C: Cryst. Struct. Commun., 1983, vol. 39, p. 704.
Nenwa, J., Djonwouo, P.L., Nfor, E.N., et al., Z. Naturforsch., B: J. Chem. Sci., 2014, vol. 69, p. 321.
Endres, H., Z. Anorg. Allg. Chem., 1984, vol. 513, p. 78.
Tommasino, J.-B., Pilet, G., Renaud, F.N.R., et al., Polyhedron, 2012, vol. 37, p. 27.
Xiao, B., Gong, T.-J., Xu, J., et al., J. Am. Chem. Soc., 2011, vol. 133, p. 1466.
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This work was carried out in terms of state assignments (projects nos. 20.80009.5007.15 and 20.80009.5007.28) of the National Agency for Research and Development of Republic of Moldova.
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Translated by E. Yablonskaya
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Bourosh, P.N., Coropceanu, E.B., Rija, A.P. et al. Synthesis and Structures of Disulfanilamide Glyoxime and Ni(II) and Cu(II) Complexes with This Ligand Stimulating the Proteolytic Properties of [Cu(DsamH2)3]SO4·5H2O. Russ J Coord Chem 48, 41–51 (2022). https://doi.org/10.1134/S1070328422010018
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DOI: https://doi.org/10.1134/S1070328422010018