Comprehensive exploration of the optical and biological properties of new quinoline based cellular probes. (September 2017)

• Record Type: Journal Article
• Authors: Czaplinska, Barbara; Maron, Anna; Malecki, Jan Grzegorz; Szafraniec-Gorol, Grazyna; Matussek, Marek; Malarz, Katarzyna; Mrozek-Wilczkiewicz, Anna; Danikiewicz, Witold; Musiol, Robert; Slodek, Aneta
• Is Part Of: Dyes and pigments. Volume 144(2017)
• Page Start: 119
• Page End: 132
• Publication Date: 2017-09
• Subjects: Quinoline -- Optical properties -- Solvatochromism -- DFT study -- Intracellular probe; Dyes and dyeing -- Periodicals; Pigments -- Periodicals; 667.2
• DOI: 10.1016/j.dyepig.2017.05.029
• Languages: English
• ISSNs: 0143-7208

Abstract

Abstract: A series of quinoline derivatives containing bithiophene and N -octyl-carbazole moieties and a variety of substituents in the quinoline core were synthesized and characterized. The influence of bithienyl and N -octyl-carbazyl substituents on the photophysical properties of novel quinolines were thoroughly investigated and supported by DFT calculations. The absorption and emission maxima of quinolines are located at 373-412 and 410–606 nm, respectively, which considerably red-shifts when an electron-withdrawing substituent (NO2 ) is introduced to the quinoline ring. The quantum yield and lifetime for carbazyl-substituted quinolines are considerably higher (Φem = 9–70%, τ = 0.83–5.72 ns) compared to their bithiophene substituted counterparts (Φem = 18–53%, τ = 0.61–1.46 ns) resulting from greater planarity of carbazyl-substituted quinolines as proved by theoretical calculations. The carbazyl functional group in quinolines has immense impact on values of Δμ (13.83–15.50 D) indicating that the electron-donating ability of carbazole moiety relative to bithiophene motif (Δμ = 9.16–13.83) in studied quinolines is more predisposed to intramolecular charge transfer (ICT). The capability of the novel compounds for cellular staining was investigated. All examined quinoline derivatives penetrate cell organelles quickly and efficiently with good overall fluorescence and signal to noise ratio. Relative lack of toxicity make them useful in such applications. Graphical abstract: Highlights: Quinoline derivatives substituted by bithiophene and carbazole moieties were examined. Photophysical properties of the obtained compounds were studied in details and compared with DTF calculations. The effect of substituents in examined compounds on optical properties was discussed. Imaging of quinoline derivatives in cells was tested.