Here, the synthesis and catalytic activities of benzoimidazole-derived organoselenium compounds have been explored. The synthesized bis(2-benzoimidazolyl) diselenide, having increased Lewis acidity on the selenium center, outperforms simple phenyl and -phenyl benzamide-based diselenides when compared for thiol peroxidase hydrogen peroxide decomposing antioxidant activity with a reduction rate of 18.6 ± 1.
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