Bockman, T. M. published the artcileTime-resolved spectroscopy and charge-transfer photochemistry of aromatic EDA complexes with X-pyridinium cations, COA of Formula: C6H5F4NO3S, the publication is Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) (1992), 1581-94, database is CAplus.
Direct photoexcitation of 1:1 aromatic EDA complexes with various N-substituted X-pyridinium cations (X = nitro, fluoro, methoxy and acetoxy) is achieved by the specific irradiation of their charge-transfer (CT) absorption bands. Time-resolved picosecond spectroscopy refers to charge-transfer activation by the identification of the aromatic cation radical as the initial transient (T1) formed in a photoinduced electron-transfer together with the X-pyridinyl radical. The homolytic fragmentation of the latter varies with the X-substituent in the order X = NO2 > F > AcO > CH3O, and the addition of Xâ?/sup> to the aromatic donors leads to a series of cyclohexadienyl adducts that are identified as longer-lived transients (T2) by time-resolved (nanosecond/μs) spectroscopy. The phototransients T1 and T2 together account for the different types of aromatic product (resulting from ring substitution, side-chain substitution and dimerization) that are generated by steady-state CT photochem. of the aromatic EDA complexes with X-pyridinium cations.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) published new progress about 107263-95-6. 107263-95-6 belongs to pyridine-derivatives, auxiliary class Fluorination reagent, name is 1-Fluoropyridiniumtriflate, and the molecular formula is C6H5F4NO3S, COA of Formula: C6H5F4NO3S.
Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem