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Chemphyschem. 2003 Oct 17;4(10):1084-94.

A theoretical study of the UV/visible absorption and emission solvatochromic properties of solvent-sensitive dyes.

Author information

1
Department of Molecular Biology, TPC-15, Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA. wengehan@scripps.edu

Abstract

Using the density-functional vertical self-consistent reaction field (VSCRF) solvation model, incorporated with the conductor-like screening model (COSMO) and the self-consistent reaction field (SCRF) methods, we have studied the solvatochromic shifts of both the absorption and emission bands of four solvent-sensitive dyes in different solutions. The dye molecules studied here are: S-TBA merocyanine, Abdel-Halim's merocyanine, the rigidified amino-coumarin C153, and Nile red. These dyes were selected because they exemplify different structural features likely to impact the solvent-sensitive fluorescence of "push-pull", or merocyanine, fluorophores. All trends of the blue or red shifts were correctly predicted, comparing with the experimental observations. Explict H-bonding interactions were also considered in several protic solutions like H2O, methanol and ethanol, showing that including explicit H-bonding solvent molecule(s) in the calculations is important to obtain the correct order of the excitation and emission energies. The geometries, electronic structures, dipole moments, and intra- and intermolecular charge transfers of the dyes in different solvents are also discussed.

PMID:
14596006
DOI:
10.1002/cphc.200300801
[Indexed for MEDLINE]

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