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Selective isolation of gold facilitated by second-sphere coordination with α-cyclodextrin

机译:第二球与α-环糊精配位促进金的选择性分离

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摘要

Gold recovery using environmentally benign chemistry is imperative from an environmental perspective. Here we report the spontaneous assembly of a one-dimensional supramolecular complex with an extended {[K(OH2)6][AuBr4](α-cyclodextrin)2}n chain superstructure formed during the rapid co-precipitation of α-cyclodextrin and KAuBr4 in water. This phase change is selective for this gold salt, even in the presence of other square-planar palladium and platinum complexes. From single-crystal X-ray analyses of six inclusion complexes between α-, β- and γ-cyclodextrins with KAuBr4 and KAuCl4, we hypothesize that a perfect match in molecular recognition between α-cyclodextrin and [AuBr4] leads to a near-axial orientation of the ion with respect to the α-cyclodextrin channel, which facilitates a highly specific second-sphere coordination involving [AuBr4] and [K(OH2)6]+ and drives the co-precipitation of the 1:2 adduct. This discovery heralds a green host–guest procedure for gold recovery from gold-bearing raw materials making use of α-cyclodextrin—an inexpensive and environmentally benign carbohydrate.
机译:从环境的角度出发,使用环境友好的化学方法回收金是必不可少的。在这里,我们报告一维超分子复合物的自发组装,该复合物具有在α-环糊精和KAuBr4快速共沉淀过程中形成的扩展的{[K(OH2)6] [AuBr4](α-环糊精)2} n链超结构。在水里。即使存在其他方平面钯和铂络合物,该相变对于该金盐也是选择性的。通过对α-,β-和γ-环糊精与KAuBr4和KAuCl4的六个包合物的单晶X射线分析,我们假设α-环糊精与[AuBr4] -导致离子相对于α-环糊精通道的近轴取向,这有助于涉及[AuBr4] -和[K(OH2)6]的高度特定的第二球配位 + 并推动1:2加合物的共沉淀。这一发现预示着一种绿色的主客程序,该程序利用α-环糊精(一种廉价且对环境无害的碳水化合物)从含金原料中回收金。

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