Abstract
An approach for the synthesis of new organic ligands combining in their structure pyridine, benzothiazole, and polyethylene glycol fragments was developed, proceeding from 6-hydroxy-2-(pyridin-2-yl)benzothiazole and mono- or ditosyl-substituted polyethylene glycols. The ligand 2-(2-{[2-(pyridin-2-yl)benzothiazol-6-yl]oxy}ethoxy)ethanol (L) in the reaction with Cu(ClO4)2•6 H2O and CuCl2•2 H2O formed coordination compounds of the composition L2Cu(ClO4)2•7 H2O and LCuCl2•0.5 H2O, respectively.
Article PDF
Avoid common mistakes on your manuscript.
References
Sh. Oka, K. Ogino, Sh. Matsuura, S. Yosbimura, K. Yamarnoto, Yu. Okazaki, T. Takemotol, N. Kato, T. Uda, Clin. Chim. Acta, 182, 1989, 209.
A. E. G. Cass, P. M. Harrison, Verlag Chemie: Basel, 1985, 1, 121.
R. Gr. Alscher, N. Erturk, L. S. Heath, J. Exp. Bot., 2002, 372, 1331.
J. A. Tainer, E. D. Getzoff, J. S. Richardson, D. C. Richardson, Nature, 1983, 306, 284.
W. R. Rypniewski, S. Mangani, B. Bruni, P. L. Orioli, M. Casati, K. S. J. Wilson, Mol. Biol., 1995, 3, 411.
B. S. P. Costa, R. M. Totaro, E. G. Ferrer, P. A. M. Williams, J. Trace Elem. Med. Biol., 2002, 16, 183.
J. R. J. Sorenson, Prog. Med. Chem., 1989, 26, 437.
D. P. Riley, W. J. Rivers, R. H. Weis, Anal. Biochem., 1991, 196, 344.
D. Klug-Roth, J. J. Rabani, Phys. Chem., 1976, 80, 588.
R. N. Patel, K. B Pandeya, J. Inorg. Biochem., 1998, 72, 109.
R. N. Patel, S. Kumar, K. B. Pandeya, Spectrochim. Acta, A, 2000, 56, 2791.
G. Facchin, M. H. Torre, E. Kremer, O. E. Piro, E. E. Castellano, E. J. Baran, J. Inorg. Biochem., 2002, 89, 174.
S. Kubota, J. T. Yang, Proc. Nat. Acad. Sci. USA, 1984, 81, 3283.
P. Deschamps, P. P. Kulkarni, B. Sarkar, Inorg. Chem., 2004, 43, 3338.
R. N. Patel, N. Singh, R. P. Shrivastava, S. Kumar, J. Mol. Liq., 2000, 89, 207.
R. N. Patel, S. Kumar, K. B. Pandeya, P. V. Khadikar, Spectrochim. Acta, A, 2002, 58, 2961.
R. N. Patel, N. Singh, K. K. Shukla, U. K. Chauhan, Spectrochim. Acta, A, 2005, 61, 287.
O. V. Pryma, S. R. Petrusenko, V. N. Kokozay, B. W. Skelton, O. V. Shiskin, T. S. Teplystka, Eur. J. Inorg. Chem., 2003, 7, 1426.
K. Skorda, S. P. Perlepes, R. Keuleers, A. Terzis, C. P. Raptopoulou, J. C. Plakatouras, Trans. Met. Chem., 1999, 24, 541.
A. L. Abuhijleh, C. Woods, Inorg. Chem. Commun., 2002, 5, 269.
I. Szilágyi, I. Labádi, K. Hernadi, I. Pálinkó, I. L. Fekete, L. Korecz, A. Rockenbauer, T. Kiss, New J. Chem., 2005, 29, 740.
A. Barik, B. Mishra, L. Shen, H. Mohan, R. M. Kadam, S. Dutta, H. Y. Zhang, K. I. Priyadarsini, Free Rad. Biol. Med., 2005, 39, 811.
F. Bellia, D. La Mendola, G. Maccarrone, P. Mineo, D. Vitalini, E. Scamporrino, S. Sortino, G. Vecchio, E. Rizzarelli, Inorg. Chim. Acta, 2007, 360, 945.
Y. H. Zhou, W. Q. Wan, D. L. Sun, J. Tao, L. Zhang, X. W. Wei, Z. Anorg. Allg. Chem., 2014, 640, 249.
I. S. Antipin, M. A. Kazymova, M. A. Kuznetsov, A. V. Vasilyev, M. A. Ishchenko, A. A. Kiryushkin, L. M. Kuznetsova, S. V. Makarenko, V. A. Ostrovskii, M. L. Petrov, O. V. Solod, Yu. G. Trishin, I. P. Yakovlev, V. G. Nenaidenko, E. K. Beloglazkina, I. P. Beletskaya, Yu. A. Ustynyuk, P. A. Solov’ev, I. V. Ivanov, E. V. Malina, N. V. Sivova, V. V. Negrebetskii, Yu. I. Baukov, N. A. Pozharskaya, V. F. Traven’, A. E. Shchekotikhin, A. V. Varlamov, T. N. Borisova, Yu. A. Lesina, E. A. Krasnokutskaya, S. I. Rogozhnikov, S. N. Shurov, T. P. Kustova, M. V. Klyuev, O. G. Khelevina, P. A. Stuzhin, A. Yu. Fedorov, A. V. Gushchin, V. A. Dodonov, A. V. Kolobov, V. V. Plakhtinskii, V. Yu. Orlov, A. P. Kriven’ko, O. V. Fedotova, N. V. Pchelintseva, V. N. Charushin, O. N. Chupakhin, Yu. N. Klimochkin, A. Yu. Klimochkina, V. N. Kuryatnikov, Yu. A. Malinovskaya, A. S. Levina, O. E. Zhuravlev, L. I. Voronchikhina, A. S. Fisyuk, A. V. Aksenov, N. A. Aksenov, I. V. Aksenova, Russ. J. Org. Chem., 2017, 53, 1257.
E. K. Beloglazkina, I. V. Yudin, A. G. Majouga, A. A. Moiseeva, A. I. Tursina, N. V. Zyk, Russ. Chem. Bull., 2006, 55, 1803.
H. Ohtsu, Y. Shimazaki, A. Odani, O. Yamauchi, W. Mori, S. Itoh, S. Fukuzumi, J. Am. Chem. Soc., 2000, 122, 5733.
G. M. Sheldrick, Acta Crystallogr., 2008, A64, 112.
K. Brandenburg, DIAMOND, Release 2.1d; Crystal Impact GbR, Bonn, Germany, 2000.
K. Serdons, T. Verduyckt, D. Vanderghinste, P. Borghgraef, J. Cleynhens, F. Van Leuven, H. Kung, G. Bormans, A. Verbruggen, Eur. J. Med. Chem., 2009, 44, 1415.
N. K. Downer-Riley, Y. A. Jackson, Tetrahedron, 2008, 64, 7741.
F. Kazemi, A. R. Massah, M. Javaherian, Tetrahedron, 2007, 63, 5083.
Author information
Authors and Affiliations
Corresponding author
Additional information
Based on the materials of the V All-Russian Organic Chemistry Conference (ROCC-V) (September 10–14, 2018, Vladikavkaz, Russia).
Rights and permissions
About this article
Cite this article
Barskaya, E.S., Shorokhov, V.V., Rzheutsky, A.V. et al. New 2-(2-pyridyl)-substituted benzothiazoles with polyethylene glycol substituents. Russ Chem Bull 68, 638–643 (2019). https://doi.org/10.1007/s11172-019-2468-5
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11172-019-2468-5