深铬移
离子液体
乙腈
斯托克斯位移
化学
量子产额
溶剂
荧光
激发态
光化学
分子
有机化学
量子力学
物理
催化作用
核物理学
作者
Stella Schmode,Andranik Petrosyan,Franziska Fennel,Alexander Villinger,Stefan Lochbrunner,Ralf Ludwig
标识
DOI:10.1002/anie.201703832
摘要
We have incorporated the dye N-methyl-6-oxyquinolone [6MQz] in its protonated form as a cation into an ionic liquid (IL) and thus to synthesize an IL dye. The IL dye N-methyl-6-hydroxyquinolinium bis(trifluoromethylsulfonyl) imide [6MQc][NTf2 ] was characterized by NMR, ATR IR spectroscopy and X-ray crystallography. The fluorescence of the IL dye has a large Stokes shift of Δλ=116 nm and a quantum yield of φF =0.56 in acetonitrile. Characteristic solvent dependent shifts can be detected in the emission spectra. In other ILs, acetonitrile and THF we observe a bathochromic shift of up to 28 nm compared to the pure IL dye at 467 nm. For stronger polar solvents the fluorescence signals are strongly red-shifted to 650 nm indicating proton transfer to the solvent molecules in the excited state. This underlines the importance of the IL building block [MQc]+ as photo acid.
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