AI Article Synopsis

  • A new series of 1,3,5-triaryl-2-pyrazolines with varying alkyloxy chain lengths (1b-12b) was created and analyzed using IR, NMR, and GC-MS techniques.
  • The study explored how the length of the alkyloxy chains influences the absorption and fluorescence properties, revealing that all compounds fluoresced in the blue region but their emission intensity was notably affected.
  • The absorption and emission maxima were found to fall within the ranges of 337-364nm and 454-464nm, respectively, and the impact of a fluorine substituent on the aryl ring at the 3-position was also examined for its effect

Article Abstract

A series of new 1,3,5-triaryl-2-pyrazolines (1b-12b) having one to twelve carbon alkyloxy side chains were synthesized and characterized on the basis of their spectral (IR, (1)H &(13)C NMR and GC-MS) and microanalytical data. The UV-Vis and emission spectroscopy was used to study the effect of alkyloxy chain length on absorption and fluorescence properties of 1b-12b. All the compounds showed fluorescence in the blue region of the visible spectrum. Interestingly, the alkyloxy chain length strongly affects the emission intensity of 1,3,5-triaryl-2-pyrazoline framework without causing any major blue- or red-shift in the emission wavelength (λmax(em)). The absorption and emission maxima (λmax(abs) &λmax(em)) for compounds (1b-12b) were observed in the range of 337-364nm and 454-464nm, respectively. Furthermore, the effect of fluorine substituent on aryl ring present at 3-position of pyrazoline moiety on fluorescence properties is also discussed.

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http://dx.doi.org/10.1016/j.saa.2014.02.025DOI Listing

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