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1.
Pol J Pharmacol Pharm ; 29(2): 137-42, 1977.
Article in English | MEDLINE | ID: mdl-16254

ABSTRACT

The rate and type of the photochemical degradation of perazine derivatives in acidic aqueous solutions depends upon the nature of the substituent at C2 atom. Free perazine degrades by two parallel reactions, namely a fast reversible first-order photooxidation and a slow zero-order photolysis. An introduction of the substituent in the C2 position results frequently in the elimination of one of these reactions.


Subject(s)
Antipsychotic Agents/radiation effects , Perazine/radiation effects , Ultraviolet Rays , Drug Stability , Kinetics , Oxidation-Reduction , Perazine/analogs & derivatives , Photochemistry , Photolysis , Time Factors
2.
Pol J Pharmacol Pharm ; 29(2): 143-9, 1977.
Article in English | MEDLINE | ID: mdl-16255

ABSTRACT

A quantum yield phi of photooxidation of perazine derivatives estimated actinometrically and the pKa, values were used for the correlation with the substituent volumes. The Hammett type plots of phi= f(sigma) and phi= f(pKa10--pKa1) are discussed.


Subject(s)
Antipsychotic Agents/radiation effects , Perazine/radiation effects , Ultraviolet Rays , Chemical Phenomena , Chemistry , Drug Stability , Hydrogen-Ion Concentration , Oxidation-Reduction , Perazine/analogs & derivatives , Photochemistry
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