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- W2319810461 endingPage "4516" @default.
- W2319810461 startingPage "4503" @default.
- W2319810461 abstract "Multinuclear (1H, 77Se, and 199Hg) NMR spectroscopy demonstrates that 1-methyl-1,3-dihydro-2H-benzimidazole-2-selone, H(sebenzimMe), a structural analogue of the selenoamino acid, selenoneine, binds rapidly and reversibly to the mercury centers of HgX2 (X = Cl, Br, I), while X-ray diffraction studies provide evidence for the existence of adducts of composition [H(sebenzimMe)]xHgX2 (X = Cl, x = 2, 3, 4; X = I, x = 2) in the solid state. H(sebenzimMe) also reacts with methylmercury halides, but the reaction is accompanied by elimination of methane resulting from protolytic cleavage of the Hg–C bond, an observation that is of relevance to the report that selenoneine demethylates CysHgMe, thereby providing a mechanism for mercury detoxification. Interestingly, the structures of [H(sebenzimMe)]xHgX2 exhibit a variety of different hydrogen bonding patterns resulting from the ability of the N–H groups to form hydrogen bonds with chlorine, iodine, and selenium." @default.
- W2319810461 created "2016-06-24" @default.
- W2319810461 creator A5025133309 @default.
- W2319810461 creator A5072093741 @default.
- W2319810461 date "2015-03-30" @default.
- W2319810461 modified "2023-10-18" @default.
- W2319810461 title "Protolytic Cleavage of Hg–C Bonds Induced by 1-Methyl-1,3-dihydro-2<i>H</i>-benzimidazole-2-selone: Synthesis and Structural Characterization of Mercury Complexes" @default.
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