Synthesis, characterization and fluorescence studies of 3,5-diaryl substituted 2-pyrazolines

Spectrochim Acta A Mol Biomol Spectrosc. 2011 Mar;78(3):1075-9. doi: 10.1016/j.saa.2010.12.053. Epub 2010 Dec 22.

Abstract

A series of 2-pyrazolines have been synthesized from α, β unsaturated ketones and hydrazine hydrate with acetic/formic acid in ethanol/DMSO. The structures of 2-pyrazolines have been established by spectroscopic techniques i.e. UV, IR, (1)H NMR, (13)C NMR and micro element analysis. Fluorescence spectra were recorded in the solution at fixed concentration and same excitation wavelength at 290 nm. The absorption band positions of all the compounds broadly lie between 280 and 336 nm and fluorescence band positions in the range between 300 and 370 nm, the near ultraviolet region.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ketones / chemistry
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Pyrazoles / chemical synthesis*
  • Pyrazoles / chemistry*
  • Spectrometry, Fluorescence / methods*
  • Spectrophotometry, Infrared

Substances

  • Ketones
  • Pyrazoles