Abstract
By the reaction of 1-imino-2-phenyl-1H-indene-3-amine with 1,4-naphthylenediamine and 1,4-diaminonaphthalenesulfonic acid linear products of 1 : 2 and 2 : 1 condensation as well as macrocyclic compounds were synthesized.
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Smirnov, R.P., Berezina, G.R., Kolesnikov, N.A., and Berezin, B.D., Izv. Vuzov, Ser. Khim. Khim. Tekhnol., 1986, vol. 29, no. 7, p.3.
Neustroeva, N.R., Berezina, G.R., Vorobjev, U.G., and Smirnov, R.P., Zh. Obshch. Khim, 1995, vol. 65, no. 10, p. 1726.
Berezin, B.D., Koordinatsionnye soedineniya porfirinov i ftalotsianina (Coordination Compounds of Porphyrins and Phthalocyanine), Moscow: Nauka, 1978.
Berezina, N.M., Bazanov, M.I., Semeykin, A.S., and Berezin, M.D., J. Phys. Chem., 2009, vol. 83, no. 5, p. 785. doi 10.1134/S0036024409050185
Berezina, G.R., Vorobjev, U.G., and Smirnov, R.P., Russ. J. Gen. Chem., 1998, vol. 68, no. 6, p.968.
Berezina, G.R., Vorobjev, U.G., and Smirnov, R.P., Russ. J. Org. Chem., 1999, vol. 35, no. 5, p.786.
Berezina, G.R., Vorobjev, Yu.G., Vorobjeva, S.M., and Andreikina, I.A., Russ. J. Gen. Chem., 2004, vol. 74, no. 8, p. 1254. doi 10.1007/s11176-005-0147-8
Berezina, G.R. and Fomina, I.S., Russ. J. Gen. Chem., 2014, vol. 84, no. 7, p. 1308. doi 10.1134/S107036321407010X
Berezina, G.R., Kuptsova, K.D., and Berezina, N.M., Russ. J. Gen. Chem., 2015, vol. 85, no. 3, p. 584. doi 10.1134/S1070363215030093
Tsiklicheskie β-diketony (Cyclic β-Diketones), Vanaga, G., Ed., Riga: Akad. Nauk Latv. SSR, 1961, p.41.
Bellamy, L.J., The Infrared Spectra of Complex Molecules, New York: Wiley, 1971.
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Original Russian Text © G.R. Berezina, 2018, published in Zhurnal Obshchei Khimii, 2018, Vol. 88, No. 6, pp. 958–961.
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Berezina, G.R. Macrocyclic Compounds with 2-Phenylindene Fragments. Synthesis and Properties. Russ J Gen Chem 88, 1138–1141 (2018). https://doi.org/10.1134/S1070363218060154
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DOI: https://doi.org/10.1134/S1070363218060154