Abstract
The absorption and fluorescence spectra of Rose Bengal dye were studied in various solvents. It was found that solvent effects on the absorption wavelength are consistent with the solvatochromic model of Kamlet, Abboud and Taft. The solvent polarizability value π* was found to have a linear relationship with the absorption wavelength of the dye in various solvents. Additionally, the normalized transition energy value (ETN) showed some scattering when plotted versus Δνaf. Density functional calculations were used to assign the absorption in the region 540-570 nm to a π-π* transition between the HOMO and LUMO of the anion. Experimental ground state and excited state dipole moments were calculated by using the solvatochromatic shifts of absorption and fluorescence spectra as a function of the dielectric constant (ε) and refractive index (n). The dipole moment for Rose Bengal was found to be 1.72 Debye in the ground state, whereas this value was 2.33 Debye in the excited state.
Original language | English |
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Pages (from-to) | 133-137 |
Number of pages | 5 |
Journal | Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy |
Volume | 72 |
Issue number | 1 |
DOIs | |
Publication status | Published - Feb 2009 |
Keywords
- Absorption
- Density functional theory
- Dipole moments
- Dyes
- Fluorescence
- Rose Bengal
ASJC Scopus subject areas
- Analytical Chemistry
- Atomic and Molecular Physics, and Optics
- Instrumentation
- Spectroscopy