Abstract
Vertical S 1–S 0 electronic transitions of the highly solvent-sensitive fluorescence label 2-propionyl-6-dimethylamino naphthalene (PRODAN) are modeled by semiempirical CISD AM1 and TD DFT calculations in a large number of solvents of different polarity and hydrogen donating ability. Calculations correctly reproduce the observed solvent induced shifts of the emission maxima. The fluorescence Frank-Condon transition energies in solvent can be predicted quantitatively at the AM1 SM5.42 OPEN(2,2) C.I. = 5 CISD level. For the planar PRODAN emitting state at the latter level we obtain a regression with practically unit slope and zero intercept for aprotic solvents. The respective relationship for the O-twisted S 1 state has a slope of 0.59 and intercept of 9100 cm −1. These results support the concept that no geometry twist in the S 1 state of PRODAN is necessary to explain the observed solvent effects on fluorescence.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
