新型香豆素-苯并吡啶衍生物的光谱和生成特性

Slavamir S. Anufrik, V. Tarkovsky, Sergey N. Anuchin
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引用次数: 0

摘要

研究了香豆素苯并吡啶衍生物在乙醇和乙腈中相干激发的光谱和生成参数。结果表明,所研究化合物的吸收光谱存在几个极大值,光谱的结构与它们的双显色结构有关。结果表明,这些有机染料是双色性化合物。香豆素碱基的6、7位和苯并吡啶核心的6′、7′位取代基的性质决定了它们的光谱发光和激光性质。结果表明,取代基在香豆素碱和苯并吡啶核的某些位置的存在改变了分子的构象,从而改变了偶极矩和跃迁的振子强度。这类香豆素的生成能力只有在7位存在最强的给体取代基(例如,Et2N和OH),在6 '和7 '位存在足够强的受体时才能表现出来。染料苯并吡啶衍生物在730 ~ 740 nm的光谱范围内得到了激光。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spectral and generation properties of new coumarins – benzopyrylium derivatives
The spectral and generation parameters of coumarins, benzopyrylium derivatives, in ethanol and acetonitrile under coherent excitation were studied. It was found that the absorption spectra of the investigated compounds contain several maxima and the structuredness of the spectra is associated with their bichromophoric structure. It is shown that these organic dyes are bichromophoric compounds. It is noted that the nature of the substituents in positions 6 and 7 of the coumarin base and positions 6′ and 7′ of the benzopyrylium core determines their spectral-luminescent and lasing properties. It is demonstrated that the presence of substituents in certain positions of the coumarin base and the benzopyrylium core changes the conformation of the molecule and, accordingly, the dipole moments and oscillator strengths of the transition. The generation ability of coumarins of this class manifests itself only in the presence of the strongest donor substituents (for example, Et2N and OH) in position 7, and sufficiently strong acceptors in positions 6′ and 7′. Lasing was obtained in the spectral region of 730 –740 nm on dyes – benzopyrylium derivatives.
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