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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis, photophysical properties, and antimicrobial activity of novel styryl colorants derived from 7-methoxy-1,4-diphenethyl-1,2,3,4- tetrahydroquinoxaline-6-carbaldehyde
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Synthesis, photophysical properties, and antimicrobial activity of novel styryl colorants derived from 7-methoxy-1,4-diphenethyl-1,2,3,4- tetrahydroquinoxaline-6-carbaldehyde

机译:衍生自7-甲氧基-1,4-二苯乙基-1,2,3,4-四氢喹喔啉-6-甲醛的苯乙烯基着色剂的合成,光物理性质和抗菌活性

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摘要

The novel 1,4-diphenethyl-1,2,3,4-tetrahydro-7-methoxyquinoxalin-6- carbaldehyde was synthesized by reductive alkylation of 6-methoxy quinoxaline with phenyl acetic acid and was further subjected to Knoevenagel condensation with various active methylene compounds to synthesize novel styryl colorants. Photophysical properties of styryl colorants were studied using UV-visible and fluorescence spectroscopy. These colorants displayed orange to violet hue and showed fluorescence emission maxima in the region of 560-640 nm, and displayed a large Stokes shift (85-104 nm). Compounds were subjected to thermogravimetric analysis which showed excellent stability up to 310°C. These styryl compounds were evaluated for their antimicrobial study as antifungal against Candida albicans C. albicans and Aspergillus niger and antibacterial against Escherichia coli and Staphylococcus aureus. The results revealed good antimicrobial activity against tested organisms. The synthesized chromophores were characterized using elemental analysis, FTIR, ~(13)C-NMR and ~1H-NMR spectroscopy and mass spectrometry.
机译:通过将6-甲氧基喹喔啉与苯基乙酸还原烷基化,合成新型的1,4-二苯乙基-1,2,3,4-四氢-7-甲氧基喹喔啉-6-甲醛,然后将其与各种活性亚甲基进行Knoevenagel缩合反应。合成新型苯乙烯基着色剂的化合物。使用紫外可见光和荧光光谱法研究了苯乙烯基着色剂的光物理性质。这些着色剂显示出橙色至紫色的色调,并在560-640 nm的范围内显示出最大的荧光发射,并显示出较大的斯托克斯位移(85-104 nm)。对化合物进行热重分析,显示出在高达310°C的稳定性。对这些苯乙烯基化合物进行了抗微生物研究,以评估其对白色念珠菌,白色念珠菌和黑曲霉的抗真菌作用以及对大肠杆菌和金黄色葡萄球菌的抗菌作用。结果表明对被测生物具有良好的抗菌活性。使用元素分析,FTIR,〜(13)C-NMR和〜1H-NMR光谱和质谱对合成的生色团进行表征。

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