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

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(OH(2))(6)][AuBr(4)][Image: see text](α-cyclodextrin)(2)}(n) chain superstructure formed during the rapid co-precipitation of α-cyclodextrin and KAuBr(4) 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 KAuBr(4) and KAuCl(4), we hypothesize that a perfect match in molecular recognition between α-cyclodextrin and [AuBr(4)](−) 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 [AuBr(4)](−) and [K(OH(2))(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.