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  • Time resolved spectroscopy of 2-(dimethylamine)fluorene. Solvent effects and photophysical behavior.

Time resolved spectroscopy of 2-(dimethylamine)fluorene. Solvent effects and photophysical behavior.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy (2011-09-17)
Francisco G Sánchez, Aurora N Díaz, Manuel Algarra, Josefa Lovillo, Alfonso Aguilar
ABSTRACT

The effect of different solvents on the fluorescent properties of 2-(dimethylamine)fluorene (DAF) were studied. In aprotic solvents we detected a strongly emissive intramolecular charge transfer (ICT) state that decayed by intersystem crossing to triplet. In proton-accepting solvents DAF exhibits in the excited state an intramolecular proton transfer. An ionized species is postulated, which simultaneously twists to a rotated conformation in the excited state. Thus, the specific solvent interactions supplement but do not replace the twist mechanism and accompany the charge transfer accepted as the prerequisite for twisted intramolecular charged transfer (TICT) state formation.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Dimethylamine solution, purum, 33% in absolute ethanol (~5.6 M)
Sigma-Aldrich
Dimethylamine solution, 2.0 M in methanol
Sigma-Aldrich
Dimethylamine hydrochloride, 99%
Sigma-Aldrich
Dimethylamine solution, 2.0 M in THF
Sigma-Aldrich
Dimethylamine hydrochloride, purum, ≥98.0% (AT)
Sigma-Aldrich
Dimethylamine solution, 40 wt. % in H2O