The photochemistry of propranolol (PR), 1-isopropylamino-2-(1-naphthyloxy)propan-2-ol, has been studied by combining laser-flash photolysis and steady-state measurements. Like other compounds bearing the naphthalene chromophore, the triplet state is produced quite efficiently (Phi(isc) = 0.35) and it is able to transfer its energy to oxygen, sensitizing singlet oxygen formation with Phi(Delta) = 0.24. PR photodecomposition takes place in an aerated aqueous medium and leads to 6-hydroxy-1,4-naphtphthoquinone as the sole stable photoproduct. This seems to be consistent with the intermediary formation of the highly photolabile 1,4-naphthoquinone. It is demonstrated that photodegradation occurs via a type II mechanism involving irreversible trapping of self-photogenerated singlet molecular oxygen. RI Sortino, Salvatore/E-4684-2011
Irreversible photo-oxidation of propranolol triggered by self-photogenerated singlet molecular oxygen
SORTINO, Salvatore;Petralia S;
2002-01-01
Abstract
The photochemistry of propranolol (PR), 1-isopropylamino-2-(1-naphthyloxy)propan-2-ol, has been studied by combining laser-flash photolysis and steady-state measurements. Like other compounds bearing the naphthalene chromophore, the triplet state is produced quite efficiently (Phi(isc) = 0.35) and it is able to transfer its energy to oxygen, sensitizing singlet oxygen formation with Phi(Delta) = 0.24. PR photodecomposition takes place in an aerated aqueous medium and leads to 6-hydroxy-1,4-naphtphthoquinone as the sole stable photoproduct. This seems to be consistent with the intermediary formation of the highly photolabile 1,4-naphthoquinone. It is demonstrated that photodegradation occurs via a type II mechanism involving irreversible trapping of self-photogenerated singlet molecular oxygen. RI Sortino, Salvatore/E-4684-2011I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
