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Rotamerism in (2-anthryl)ethylenes. Evidence from fluorescence lifetimes and quenching studies

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j150650a029· OSTI ID:5896045

The fluorescence decay of trans (2-anthryl)ethylenes containing phenyl, 2-naphthyl, and 2-thienyl groups as the second substituent is biexponential. The decay profiles in benzene are analyzable in terms of two lifetimes in the ranges 6-11 and 17-30 ns, respectively. The complex decay behavior as well as the observation of excitation wavelength dependence of fluorescence spectra, quantum yields, exciplex emission maxima, and fluorescence quenching constants (with oxygen, ethyl iodide (EtI), and N,N-dimethylaniline (DMA) as quenchers) is attributed to the existence of quasi-energetic rotamers in solutions of (2-anthryl)ethylenes. Exciplex lifetimes and transient absorption spectra of radical anions obtained by nanosecond laser flash photolysis in the presence of N,N-dimethylaniline are also presented. 17 references, 6 figures, 6 tables.

Research Organization:
Univ. of Notre Dame, IN
OSTI ID:
5896045
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 88:6; ISSN JPCHA
Country of Publication:
United States
Language:
English