Premium
Multifaceted Photoreactivity of 6‐Fluoro‐7‐aminoquinolones from the Lowest Excited States in Aqueous Media: A Study by Nanosecond and Picosecond Spectroscopic Techniques
Author(s) -
Monti Sandra,
Sortino Salvatore,
Fasani Elisa,
Albini Angelo
Publication year - 2001
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/1521-3765(20010518)7:10<2185::aid-chem2185>3.0.co;2-u
Subject(s) - intersystem crossing , chemistry , photochemistry , excited state , singlet state , triplet state , nanosecond , singlet fission , picosecond , lomefloxacin , electron transfer , molecule , organic chemistry , norfloxacin , laser , biochemistry , physics , ciprofloxacin , nuclear physics , optics , antibiotics
Nanosecond and picosecond absorption and emission spectroscopic techniques were applied to the investigation of the reactivity from the lowest excited states of some 6‐fluoro‐7‐piperazino‐4‐quinolone‐3‐carboxylic acids (FQs) in aqueous media at neutral pH, in the absence and presence of different sodium salts. Following the detection of various transients, we proposed a mechanism for the cleavage of the carbon−fluorine bond that proceeded through different reaction pathways, dependent on the molecular structure and the characteristics of the medium. The drug lomefloxacin (LOM), a 6,8‐difluoroquinolone derivative, underwent heterolytic cleavage of the C8−F bond from the excited singlet state. With the 6‐monofluoroquinolone norfloxacin (NOR) and the corresponding 1,8‐naphthyridinone enoxacin (ENX), the lowest singlet state was not significantly reactive and an important deactivation channel was intersystem crossing (ISC) to the triplet manifold. The lowest triplet state underwent cleavage of the C6−F bond through a solvent mediated process possibly via a cyclohexadienyl anionic adduct. In the presence of sulfite or phosphate buffer a novel defluorination mechanism, induced by electron transfer from the inorganic anions to the FQ triplet state, was observed. The correlation between the transients observed and the final photoproducts in the different media was elucidated.