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Counterion and steric effects in self-assembled HgX _2-thioether coordination polymers

机译:自组装的HgX _2-硫醚配位聚合物的抗衡离子和空间效应

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A series of mercury dithioether coordination polymers were synthesized from mercury dihalides and rigid xylyl dithioethers containing methyl, t-butyl, and benzyl pendant groups (ligands 3a-c). The resulting coordination polymers were examined by X-ray crystallography. Changes in sterics surrounding mercury result in structures ranging from one-dimensional polymers (e.g., (3a?HgI _2) _∞, (3b?Hg _2Cl _4) _∞, (3b?HgBr _2) _∞) to two-dimensional sheets (e.g., (3c?HgCl _2) _∞) and three-dimensional extended networks (e.g., [(3c) _2(HgBr _2) _3] _∞) from crystallizations which were conducted under identical conditions with the same 1:1 stoichiometry. Bridging mercury-halide bonds were found to play a surprisingly large role in governing the final structures.
机译:由二卤化汞和含有甲基,叔丁基和苄基侧基(配体3a-c)的硬质二甲苯基二硫醚合成了一系列汞二硫醚配位聚合物。通过X射线晶体学检查所得的配位聚合物。汞周围空间的空间变化导致结构从一维聚合物(例如(3a?HgI _2)_∞,(3b?Hg _2Cl _4)_∞,(3b?HgBr _2)_∞)到二维薄片(例如((3c?HgCl _2)_∞)和三维扩展网络([[(3c)_2(HgBr _2)_3]_∞),这些结晶是在相同的条件下以相同的1:1化学计量进行的。发现桥联卤化氢键在控制最终结构中起着惊人的巨大作用。

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