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Chemosensor properties of mono- and bisthioureas based on 9-anthrylmethyl-substituted alkylamines and diamines

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Abstract

Mono- and bisthioureas were synthesized based on N-(9-anthrylmethyl)-substituted alkylamines and diamines. Their luminescent and complexing properties were studied by the electronic, IR, and NMR 1H spectroscopy. N-(9-Anthrylmethyl)-N-(6-{9-anthrylmethyl[(phenylamino)carbothioyl]amino}hexyl)-N′-phenylthiourea was shown to be a highly effective fluorescent chemosensor for Hg2+ cations.

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Correspondence to A. D. Dubonosov.

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Original Russian Text © I.E. Tolpygin, E.N. Shepelenko, Yu.V. Revinskii, A.V. Tsukanov, A.D. Dubonosov, V.A. Bren’, V.I. Minkin, 2010, published in Zhurnal Obshchei Khimii, 2010, Vol. 80, No. 4, pp. 603–608.

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Tolpygin, I.E., Shepelenko, E.N., Revinskii, Y.V. et al. Chemosensor properties of mono- and bisthioureas based on 9-anthrylmethyl-substituted alkylamines and diamines. Russ J Gen Chem 80, 765–770 (2010). https://doi.org/10.1134/S1070363210040146

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  • DOI: https://doi.org/10.1134/S1070363210040146

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