Rubbi Alessandro, Tanini Damiano, Capperucci Antonella, Orian Laura
Dipartimento di Scienze Chimiche, Università degli Studi di Padova, Via Marzolo 1, 35131 Padova, Italy.
Dipartimento di Chimica "Ugo Schiff", Università di Firenze, Via della Lastruccia 3-13, 50019 Sesto Fiorentino, Italy.
Inorg Chem. 2025 May 26;64(20):10022-10031. doi: 10.1021/acs.inorgchem.5c00581. Epub 2025 May 9.
The recent synthesis of a series of diorganotellurides as glutathione peroxidase mimics has prompted our in silico investigation on their oxidation mechanism by HO at the ZORA-M06/TZ2P-ae//ZORA-OLYP/TZ2P level of theory. The role of the chalcogen (S and Se vs Te) on the energetics of the reactions has been elucidated within the framework of density functional theory and activation strain analysis. It emerges that the nature of the β-substituent plays a role in the catalytic activity that is found also when tellurium is replaced by its lighter siblings (S or Se). Our results provide general and useful insight for the development of small chalcogen-based organic molecules for the catalytic activation of HO.
最近合成了一系列作为谷胱甘肽过氧化物酶模拟物的二有机碲化物,这促使我们在ZORA-M06/TZ2P-ae//ZORA-OLYP/TZ2P理论水平上对它们被HO氧化的机制进行计算机模拟研究。在密度泛函理论和活化应变分析的框架内,阐明了硫族元素(S、Se与Te)对反应能量学的作用。结果表明,β-取代基的性质在催化活性中起作用,当碲被其较轻的同族元素(S或Se)取代时也会发现这种作用。我们的结果为开发用于HO催化活化的小型硫族元素基有机分子提供了全面而有用的见解。