Synthesis and properties of azo compounds based on nitroanilines - 2,4,6-trinitrotoluene derivatives and 1,3,5-trinitrobenzene

Кобраков, К. И.; Kuznetsov, D. N.; Ruchkina, A. G.; Sharpar, N. M.

doi:10.31044/1684-5811-2019-20-10-440-444

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“…Проводя в течение последних 10 лет систематические исследования по выявлению возможностей и перспектив превращения ТНТ в продукты мирного назначения, мы показали, что МФГ является высокореакционноспособным субстратом в синтезе азокрасителей и азопигментов, обладающих высокими эксплуатационными, а также фунгицидными и хелатирующими свой-ствами [2][3][4][5]. В серии работ [6][7][8][9] нами описаны синтезы на основе МФГ 2H-1-бензопиран-2-онов и акридинов -аналогов природных полициклических соединений, перспективных для изучения в качестве химико-фармацевтических препаратов или прекурсоров в схемах фрагментарно-ориентированного дизайна лекарственных средств.…”

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Spectral-Luminescent Properties of Some New Dihydroxy-2h-1-Benzopyran-2-Ones Synthesized Based on 2,4,6-Trihydroxytoluene

Kuznetsov¹,

Кобраков²,

Bobylev³

2020

IVKKT

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2,4,6-trihydroxytoluene (methylphloroglucinol) is a promising reagent in organic synthesis, after development out getting it from 2,4,6-trinitrotoluene. We previously synthesized of derivatives of 5,7-dihydroxy-2H-1-benzopyran-2-ones by the interaction of 2,4,6-trihydroxytoluene and 2,4,6 -trihydroxy-3-methylbenzoic acid with polyfunctional carbonyl compounds. The first time, a detailed analysis of the electronic absorption and fluorescence spectra of derivatives of 5,7-dihydroxy-2H-1-benzopyran-2-ones is carried out. In the electronic absorption spectra of the studied compounds, the absorption in the long-wavelength region of the spectrum is determined by electronic transitions with intramolecular charge carry. The possibility of controlling the bathochromic or hypsochromic shift of the long-wavelength absorption band by introducing substituents of various electronic nature into the molecule has been revealed. It was shown that some of the studied compounds have pronounced luminescence in the blue-green region of the spectrum (390–508 nm) with a quantum yield of 9–40%. The highest quantum yield (38%) was achieved when the 5,7-dihydroxy-2H-1-benzopyran-2-one carboxyl group was introduced into position 6. The bromination of this compound leads to a decrease in the quantum yield to 9.5 % The introduction into the 3 position of 5,7-dihydroxy-4,8-dimethylchromen-2-one phenyl substituted fragment along with O-acylation leads to a sharp decrease in the quantum yield. It is concluded that the studied objects are promising as basic structures for the search for new biosensors.

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