Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
Dalton Trans. 2009 Aug 7(29):5766-72. doi: 10.1039/b903863a. Epub 2009 Jun 10.
Four new methylmercury-selenoamino acid complexes were synthesized, including methylmercury-L-selenoglutathionate, methylmercury-D,L-selenopenicillaminate, and two methylmercury-L-selenomethioninate complexes (one via a Hg-Se bonding and the other Hg-N bonding). All the complexes were characterized by NMR ((1)H, (13)C, (77)Se and (199)Hg), FT-IR and mass spectra. Their molecular structures were established by single crystal X-ray crystallography (for the Hg-N bonding methylmercury-L-selenomethioninate) and by quantum mechanical calculations using Gaussian-03 with the hybrid functional B3LYP/SDD. All four complexes were found to chemically and structurally resemble their sulfur analogues, with a slightly stronger binding affinity of Hg to Se than to S, suggesting chemical and structural mimicry might play a role in methylmercury-selenium antagonism in biological systems.
四种新的甲基汞-硒代氨基酸配合物被合成,包括甲基汞-L-谷胱甘肽、甲基汞-D,L-青霉胺酸、以及两种甲基汞-L-硒代蛋氨酸配合物(一种通过 Hg-Se 键合,另一种通过 Hg-N 键合)。所有配合物均通过 NMR ((1)H、(13)C、(77)Se 和 (199)Hg)、FT-IR 和质谱进行了表征。它们的分子结构通过单晶 X 射线晶体学(对于 Hg-N 键合的甲基汞-L-硒代蛋氨酸)和使用 Gaussian-03 程序中带有杂化泛函 B3LYP/SDD 的量子力学计算得到确定。所有四种配合物都被发现具有类似于其硫类似物的化学和结构特征,Hg 与 Se 的结合亲和力略强于与 S 的结合亲和力,这表明化学和结构模拟可能在生物系统中的甲基汞-硒拮抗作用中发挥作用。