Theoretical and experimental study of the ground and excited states of 1,4-dihydropyridine based hexahydroquinoline derivatives achieved by microwave irradiation

被引:11
|
作者
Gunduz, Miyase Gozde [1 ]
da Silva, Claudia de Brito [2 ]
Zanotto, Gabriel Modernell [3 ]
Toldo, Josene Maria [3 ]
Simsek, Rahime [1 ]
Safak, Cihat [1 ]
Bruno Goncalves, Paulo Fernando [3 ]
Rodembusch, Fabian Severo [2 ]
机构
[1] Hacettepe Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey
[2] Univ Fed Rio Grande do Sul, Grp Pesquisa Fotoquim Organ Aplicada, Inst Quim, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Inst Quim, Grp Quim Teor, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
关键词
MOLECULAR-ORBITAL METHODS; PHOTODEGRADATION PRODUCTS; MEDICINAL CHEMISTRY; ELECTRON-TRANSFER; BASIS-SET; PHOTOCHEMISTRY; FLUORESCENCE; PHOTOPHYSICS; CHANNELS; SCAFFOLD;
D O I
10.1039/c7nj02226c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this article, the photophysical characterisation in solution of a series of hexahydroquinoline derivatives is described using UV-Vis absorption and steady-state fluorescence emission spectroscopies. The compounds were obtained from one-pot four component synthesis via Hantzsch reaction using microwave irradiation. These compounds present absorption maxima located at around 350 nm and fluorescence emission maxima in the UV-violet-blue region. The Lippert-Mataga correlation indicates an ICT character in the excited state for the studied compounds since a linear relation of the fluorescence maxima versus the solvent polarity function was found. Theoretical calculations were also performed in order to study the geometry and charge distribution of these compounds in their ground and excited electronic states. No significant changes in absorption and emission maximum wavelength were found by changing the solvent or substituent groups attached to the hexahydroquinoline structure.
引用
收藏
页码:11686 / 11694
页数:9
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