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trans-2-R-1,3-BIS(ANTHRACENE-9-YLMETHYL)OCTAHYDROBENZIMIDAZOLES. SYNTHESIS AND INVESTIGATION OF SPECTRAL PROPERTIES

И. Е. Толпыгин, К. С. Тихомирова, О. С. Попова, О. Г. Николаева, Ю. В. Ревинский, А. Д. Дубоносов, В. А. Брень
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Abstract


Through the interaction of (±)-trans-cyclohexane-1,2-diamine and anthracene-9-carbaldehyde with the following reduction of the condensation product N,N'-bis(anthracen-9-ylmethyl)cyclohexane-1,2-diamine was obtained. It was demonstrated that interaction of this diamine with aldehydes leads to the formation of octahydrobenzimidazoles. Investigation of the chemosensory properties of the obtained compounds revealed their high activity towards Zn2+ cations.

How to Cite
Tolpygin, I. E.; Tihomirova, K. S.; Popova, O. S.; Nikolaeva, O. G.; Revinskii, Yu. V.; Dubonosov, A. D.; Bren, V. A. Chem. Heterocycl. Compd. 2014, 50, 41. [Khim. Geterotsikl. Soedin. 2014, 47.]

For this article in the English edition see DOI 10.1007/s10593-014-1446-y


Keywords


cyclohexane-1,2-diamine; octahydrobenzimidazoles; cyclization; chemosensors; fluorescence

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