0000000000889782

AUTHOR

Sandra Monti

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Structure and Photochemical Behavior of the Cyclodextrin Inclusion Complexes of the Benzoylthiophene-Derived Drugs Tiaprofenic Acid (=5-Benzoyl-α-met…

2001

The effect of β-cyclodextrin (β-CD) on the excited-state reactivity of the two benzoylthiophene derivatives, tiaprofenic acid (TPA; 2) and suprofen (SPF; 3) in their carboxylate forms is studied. The presence of β-cyclodextrin does not affect the nature of the photoproduced transients and the photoproducts, but increases the photodegradation quantum yields of both drugs. The efficiency of the photodecarboxylation process is enhanced. This effect is rationalized in the light of the inclusion of 2 and 3 in the β-CD cavity, affecting the energy of the lowest excited states of the drugs. The structure of the complexes is determined by induced circular dichroism, and molecular-mechanics and dyna…

chemistry.chemical_classificationCircular dichroismCyclodextrinOrganic ChemistrySuprofenPhotochemistryBiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundAcetic acidchemistryDrug DiscoverymedicineReactivity (chemistry)CarboxylatePhysical and Theoretical ChemistryPhotodegradationTiaprofenic acidmedicine.drugHelvetica Chimica Acta
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