Tathe Abhinav B, Sekar Nagaiyan
Tinctorial Chemistry Group, Department of Dyestuff Technology, Institute of Chemical Technology, N. P. Marg, Matunga, Mumbai, MH, India, 400019.
J Fluoresc. 2016 Mar;26(2):471-86. doi: 10.1007/s10895-015-1733-8. Epub 2015 Dec 11.
The red emitting dyes were synthesized by employing coumarin core as a donor and boron-bonded coumarin as an acceptor. 7-(N,N-Diethylamino)-coumarin 3-aldehyde was reacted with 3-acetyl-4-hydroxy-coumarin, 7-(N,N-diethylamino)-3-acetyl-4-hydroxy-coumarin and 3-acetyl-4-hydroxy-1-methyl-quinolone to form the corresponding chalcones. The synthesized chalcones were though red shifted as compared to the parent coumarin, and were not emitting in red region. The BF2-complexation was used as a tool to introduce a red shift in the molecules. The BF2-complexes synthesized were found to be red emitting and show higher one photon absorption cross section. The solvatochromism shown by these dyes was studied in the light of solvent polarity parameters. DFT calculations were used to understand the photophysical properties of the synthesized dyes. NLO properties of the dyes were estimated by solvatochromic and computational methods. All the molecules synthesized were characterised with the HRMS and NMR spectral Analysis.
通过使用香豆素核心作为供体和硼键合香豆素作为受体来合成红色发射染料。7-(N,N-二乙氨基)-香豆素-3-醛与3-乙酰基-4-羟基香豆素、7-(N,N-二乙氨基)-3-乙酰基-4-羟基香豆素和3-乙酰基-4-羟基-1-甲基喹诺酮反应形成相应的查耳酮。尽管合成的查耳酮与母体香豆素相比发生了红移,但在红色区域不发光。BF₂络合用作在分子中引入红移的工具。发现合成的BF₂络合物发出红色光并显示出更高的单光子吸收截面。根据溶剂极性参数研究了这些染料表现出的溶剂化显色现象。使用密度泛函理论(DFT)计算来理解合成染料的光物理性质。通过溶剂化显色和计算方法估计了染料的非线性光学(NLO)性质。合成的所有分子都通过高分辨率质谱(HRMS)和核磁共振(NMR)光谱分析进行了表征。