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Synthesis, photophysical and antioxidant properties of pyrrolo[3,2-c]carbazole and dipyrrolo[3,2-c:2,3-g]carbazole compounds

机译:Pyrrolo [3,2-C]咔唑和二吡咯的合成,光药和抗氧化性能[3,2-C:2,3-G]咔唑化合物

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The synthesis of (6-ethyl-1,6-dihydropyrrolo[3,2-c]carbazol-2-yl)methanol 5 and (6-ethyl-6,11-dihydro-1H-dipyrrolo[3,2-c:2,3-g]carbazole-2,10-diyl)dimethanol 6 were achieved via the reduction of methyl pyrrolo carbazole carboxylate 3 and methyl dipyrrolo carbazole carboxylate 4, respectively. The structures of hydroxymethyl-pyrrolocarbazoles 5 and 6 were supported by FT-IR, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, H-1 and C-13 NMR spectroscopy. The photophysical properties of the targeted compounds 3-6 were investigated by employing absorption and fluorescence spectroscopy in different common organic solvents. Also, the fluorescence lifetime ((F)) of the compounds was measured utilizing a time-correlated single-photon counting technique in tetrahydrofuran. Antioxidant activities of compounds 3-6 were determined by employing three different assays, namely DPPH radical scavenging, ABTS cation radical decolarization and cupric reducing antioxidant capacity. The results revealed that the ABTS cationic scavenging activity assay was found to be the most sensitive method for the determination of inhibition values.
机译:(6-乙基-1,6-二氢吡咯醇[3,2-C]咔唑-2-基)甲醇5和(6-乙基-6,11-二氢-1H-DIPyrrolo [3,2-C:通过减少甲基吡咯咔唑羧酸甲酸甲酯3和甲基双溴罗甲咔唑羧酸甲酯4,实现二甲醇6。通过FT-IR,基质辅助激光解吸/电离飞行时间质谱,H-1和C-13 NMR光谱来支持羟甲基 - 吡咯烷咔唑5和6的结构。通过在不同常见的有机溶剂中使用吸收和荧光光谱来研究靶向化合物3-6的光物理性质。而且,使用在四氢呋喃中的时间相关的单光子计数技术测量化合物的荧光寿命((f))。通过采用三种不同的测定来确定化合物3-6的抗氧化活性,即DPPH自由基清除,ABTS阳离子自由基沥青和降低抗氧化能力。结果显示,ABTS阳离子清除活性测定是最敏感的抑制值的方法。

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