光降解
化学
阿米必利
舒必利
光激发
光化学
磺胺
卤素
降级(电信)
光解
药物化学
立体化学
乙草胺
反应中间体
氢键
过氧化氢酶
激进的
苯甲酸
反应中间体
苯甲酰胺
异构化
反应机理
超纯水
转化(遗传学)
作者
Chuanguang Wang,Changsheng Guo,Ruonan Guo,Yanghui Deng,Hailong Yin,Jian Xu
标识
DOI:10.1021/acs.est.5c13185
摘要
Amisulpride (AMI) and sulpiride (SUL), two structurally related benzamide antipsychotics frequently detected in aquatic environments, differ in whether a primary amino group (−NH 2 ) is directly attached to the benzoyl ring, a minor variation that leads to striking differences in their photoreactivity and environmental fate. AMI undergoes rapid direct photodegradation ( t 1/2 = 14.5 min at pH 8.0), whereas SUL degrades 28 times more slowly ( t 1/2 = 407.7 min). Theoretical calculations revealed that the disparity originates from their primary photoexcitation mechanisms. AMI retains planarity and exhibits a strong π→π* transition, while torsional distortion in SUL results in a weak, partially forbidden n→π* transition, making SUL far more dependent on the photodegradation involving • OH, CO 3 •–, and self-sensitized 3 SUL*. Experiments with NO 3 –, HCO 3 –, and Br – demonstrated pronounced acceleration of SUL photodegradation in natural and simulated waters, confirming the key role of indirect pathways for SUL and their minimal contribution to AMI. Six AMI and four SUL transformation products (TPs) were identified exclusively from direct photodegradation, arising from sulfone cleavage, ring oxidation, and N-dealkylation. Toxicity predictions showed that SUL photodegradation leads to detoxification, whereas AMI produces multiple transformation products with higher predicted toxicity. These findings demonstrate that −NH 2 positional isomerism governs photoexcitation, indirect photoreactivity, and environmental risk.
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