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合成喹啉取代的吡唑、异噁唑和吡啶作为潜在的蓝色发光体。

Synthesis of quinolone substituted pyrazoles, isoxazoles and pyridines as a potential blue luminophors.

机构信息

Organic Chemistry Research Center, Department of Chemistry, K. T. H. M. College, Gangapur Road, Nashik, 422 002, MS, India.

出版信息

J Fluoresc. 2010 Sep;20(5):1129-37. doi: 10.1007/s10895-010-0654-9. Epub 2010 Mar 31.

Abstract

Series of quinolone C(3)-substituted pyrazolines, isoxazolines, pyridines and pyrimidines were synthesized in good yields by the cyclocondensation reactions of 1, 2-unsaturated ketones and hydrazines, hydroxylamine hydrochloride and dimedone respectively. The quinolone derivatives (3, 5 and 7) were synthesized and further studied for their photophysical properties. High absorption and quantum yield are found for N(1)-phenyl and C(3,4)-dimethoxy substituents on phenyl ring (3h). Energy optimization by PM6 methods showed high stability required for selection of suitable candidates to be use as future blue emitters.

摘要

通过 1,2-不饱和酮与腙、羟胺盐酸盐和二亚甲基酮的环缩合反应,以较高产率合成了一系列喹诺酮 C(3)-取代的吡唑啉、异噁唑啉、吡啶和嘧啶衍生物。合成了喹诺酮衍生物(3、5 和 7),并进一步研究了它们的光物理性质。在苯环上引入 N(1)-苯基和 C(3,4)-二甲氧基取代基(3h)可获得高吸收和量子产率。通过 PM6 方法进行的能量优化表明,所需的高稳定性可用于选择合适的候选物作为未来的蓝色发光体。

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