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Synthesis and electronic spectra of 3-hetaryl substituted coumarin derivatives 7-hydroxy-2H-chromen-2-on and 9-hydroxy-2H-benzo(f)chromen-2-on

机译:3-杂芳基取代的香豆素衍生物7-羟基-2H-铬2--2-和9-羟基-2H-苯并(f)铬-2--2-的合成及电子光谱

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摘要

The synthesis of 3-hetaryl substituted coumarin derivatives [7-hydroxy-2H-chromen-2-o.n and 9-hydroxy-2H-benzo(f)chromen-2-on] containing a hydroxyl group by reacting 2,4-dihydroxybenzaldehyde and 2,4-dihydroxynaphtaldehydes with 2-cyanomethylbenzothiazole, 2-cyanomethylbenzimidazole, 1-methyl-2-cyanomethylbenzimidazole and 2-cyanomethyl-4-phenylthiazole is presented. The absorption and steady-state fluorescence characteristics of the synthesised 3-hetaryl substituted 7-hydroxy-2H-chromen-2-on and 9-hydroxy-2H-benzo(f)chromen-2-on in a solution of ethanol and at different pH values are studied to assess their possible application as fluorescent probes for use in molecular biology and medicine.
机译:通过2,4-二羟基苯甲醛与2-羟基苯甲醛的反应合成具有羟基的3-杂芳基香豆素衍生物[7-羟基-2H-铬-2--2-和9-羟基-2H-苯并(f)铬-2--2-]。提出了具有2-氰基甲基苯并噻唑,2-氰基甲基苯并咪唑,1-甲基-2-氰基甲基苯并咪唑和2-氰基甲基-4-苯基噻唑的2,4-二羟基萘醛。合成的3-杂芳基取代的7-羟基-2H-chromen-2-on和9-羟基-2H-苯并(f)chromen-2-on在乙醇溶液中的吸收和稳态荧光特性对pH值进行了研究,以评估其在分子生物学和医学中用作荧光探针的可能应用。

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