Khanna Radhika, Kumar Ramesh, Dalal Aarti, Kamboj Ramesh C
Department of Chemistry, Kurukshetra University, Kurukshetra, 136119, Haryana, India.
J Fluoresc. 2015 Sep;25(5):1159-63. doi: 10.1007/s10895-015-1623-0. Epub 2015 Jul 16.
The synthesis and spectral studies of variously substituted 3-hydroxychromones have been carried out. A key relationship between the structural motif of synthesized 3-hydroxychromones (3-HCs) and their fluorescent properties was found. The chromones substituted with electron-donating group at 4'-position expressed the red shift of the N() and T() band and also exhibited the increased fluorescent intensity ratio while the chromones with electron-withdrawing group showed the blue shift of the N() and T() band. Therefore, these 3-HCs may behave as the possible fluorescent probes.
已开展了各种取代的3-羟基色酮的合成及光谱研究。发现了合成的3-羟基色酮(3-HCs)的结构基序与其荧光性质之间的关键关系。在4'-位被供电子基团取代的色酮表现出N()和T()带的红移,并且荧光强度比也增加,而带有吸电子基团的色酮则表现出N()和T()带的蓝移。因此,这些3-HCs可能用作潜在的荧光探针。