Synthesis, Computational and cytotoxicity studies of aryl hydrazones of β-diketones: Selective Ni metal Responsive fluorescent chemosensors.

A new fluorescent sensor 2-(2-(3-chloro-4-fluorophenyl)hydrazono)-5,5-dimethyl cyclohexane-1,3-dione (A) and 2-(2-(4-chloro-2-nitrophenyl)hydrazono)-5,5-dimethyl cyclohexane-1,3-dione (B) composed of a β-diketones of aryl hydrazones synthesized by simple and cost-effective method. Various analytical tools analyzed the structural investigations of the synthesized substituted β-diketones of aryl hydrazones like FT-IR, H, C NMR and UV-Vis techniques, Single-crystal X-ray diffraction studies (SCXRD) (for A), Scanning electron microscopy (SEM), and fluorescence spectroscopy. SEM also investigates surface morphology modifications of aryl hydrazones and Ni complex.

Synthesis, electronic structure investigation of 3-pentyl-2,6-di(furan-2-yl)piperidin-4-one by FT-IR, FT-Raman and UV-Visible spectral studies and ab initio/DFT calculations.

FT-IR and FT-Raman spectra of 3-pentyl-2,6-di(furan-2-yl) piperidin-4-one (3-PFPO) were recorded in the solid phase. The structural and spectroscopic analyses of 3-PFPO were made by using B3LYP/HF level with 6-311++G(d, p) basis set. The fundamental vibrations are assigned on the basis of the total energy distribution (TED) of the vibrational modes, calculated with scaled quantum mechanics (SQM) method and PQS program.

Electronic spectral studies of some fluorescent probes: a comparison of two approaches.

Schiff base derivatives were synthesized and characterized by NMR spectra, mass and CHN analysis. The fluorescence properties of these dyes are strongly solvent dependent and the wavelength of maximum fluorescence emission shifts to red. The Kamlet-Taft and Catalan's solvent scales were found to be the most suitable for describing the solvatochromic shifts of the absorption and fluorescence emission.

Physico-chemical studies on some fluorescence sensors: DFT based ESIPT process.

A group of novel heterocyclic Schiff base derivatives were synthesized and characterized by NMR spectra, mass and CHN analysis. Excited state intramolecular proton transfer (ESIPT) processes in o-hydroxy Schiff base have been studied using electronic spectral studies. Experimental and FT studies support that trans enol form predominates over the cis enol form.