Cucurbit[7]uril limits the binding of coumarin bearing alkyl-acetoacetate with mercury and stimulates the desulphurisation reaction of its sulphur analog. Issue 12 (1st December 2020)

• Record Type: Journal Article
• Authors: Aliaga, Margarita E.; Pavez, Paulina; Quintero, Guillermo; Droguett, Kevin; Cañete, Álvaro; Santos, José G.
• Is Part Of: Supramolecular chemistry. Volume 32:Issue 12(2020)
• Page Start: 605
• Page End: 613
• Publication Date: 2020-12-01
• Subjects: Stabilisation keto form -- methyl β-ketodithioester framework -- competitive/cooperative approach -- coumarin derivatives -- CB7-promoted desulfurisation; Macromolecules -- Periodicals; Supramolecular chemistry -- Periodicals; 547.005
• DOI: 10.1080/10610278.2020.1856845
• Languages: English
• ISSNs: 1061-0278

Abstract

ABSTRACT: The inclusion of 7-diethylamino-coumarin derivatives, bearing an ethyl acetoacetate (CAM1 ) and a methyl β-ketodithioester moiety (CAM2 ) in the cavity of cucurbit[7]uril (CB7), leads to different interaction forms with mercuric ions (Hg 2+ ). The interaction between these ions and CAM1, in the presence of CB7, occurs through the lateral ethyl acetoacetate moiety of the keto form of CAM1, leading to the formation of binary assemblies such as Hg 2+ @CAM1 and Hg 2+ @CB7. As a consequence, the metal restricts the insertion of the dye into the CB7 cavity, decreasing the apparent binding constant between them. Interestingly, for the other derivative CAM2, a mercury-induced desulfurisation reaction of its β-ketodithioester moiety is kinetically accelerated by CB7 (by a factor ≈25), which subsequently leads to the generation of binary and ternary complexes among the analogue oxygenised from CAM2, metal and CB7. The later effect is a promising strategy that could be considered for the mercury sensing methodology. Graphic abstract: