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RESEARCH PRODUCT
Adducts of free-base meso-tetraarylporphyrins with trihaloacetic acids: Structure and photostability
Gabriela DyrdaMałgorzata A. BrodaZbigniew HnatejkoTomasz PedzinskiRudolf Słotasubject
Meso-tetraarylporphyrinsSinglet oxygenGeneral Chemical EngineeringGeneral Physics and AstronomyFree baseProtonation02 engineering and technologyGeneral ChemistryChromophore010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryDFT calculations01 natural sciencesPorphyrinTrihaloacetic acids0104 chemical sciencesAdductPorphyrin protonationchemistry.chemical_compoundAcetic acidchemistry0210 nano-technologyPhotodegradationPyrroledescription
Abstract Four diverse meso-tetraarylporphyrins in the form of diprotonated adducts with trifluoro-, trichloro-, tribromoacetic acids and acetic acid were investigated in benzene solution. Despite similar structural distortion of the chromophore system due to protonation, the respective adducts demonstrated different photostability when exposed to UV irradiation. The trifluoro- and trichloroacetic adducts, and the acetic acid one, showed some common features both molecular and in the mechanism of photodegradation. However, the tribromo-derivative decayed according to a different kinetic scheme, revealing a considerable impact of the bromine atoms upon the pyrrole units of the porphyrin macrocycle, which led to extremely low UV resistance. Singlet molecular oxygen generated by the studied species was confirmed to contribute to the photolysis of the porphyrin system.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2020-04-01 | Journal of Photochemistry and Photobiology A-Chemistry |