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- W2110488557 abstract "The conformational flexibility and programmed assembly of a dumbbell-shaped polyoxometalate–organic hybrid molecule comprising two Dawson-type polyoxometalates linked by a 2,2′-bipyridine unit, which can be coordinate to metal ions, in this case of Zn2+, are described. SAXS, UV/vis, and NMR spectroscopic techniques confirm that the hybrid molecules exist as the trans dumbbell in metal-ion-free solutions and can be reversibly transformed into the cis dumbbell through coordination upon the addition of ZnCl2 into a DMSO solution containing the hybrid. Subsequent addition of EDTA reverses the switching process by extracting the Zn2+ cations from the hybrid. During the interchange process between trans and cis dumbbells, a further reorganization of the hybrid molecules occurs through bond rotation to minimize steric clashes between the polyoxometalate subunits, in order to stabilize the corresponding dumbbell conformation. The Zn2+-controlled conformational transformation of the hybrid can be further utilized to manipulate the hybrid’s solvophobic interaction-driven self-assembly behavior in the metal-ion driven reversible formation of 140 nm sized vesicles, studied by laser light scattering techniques." @default.
- W2110488557 created "2016-06-24" @default.
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- W2110488557 date "2013-08-29" @default.
- W2110488557 modified "2023-10-12" @default.
- W2110488557 title "Exploring the Programmable Assembly of a Polyoxometalate–Organic Hybrid via Metal Ion Coordination" @default.
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- W2110488557 doi "https://doi.org/10.1021/ja404777g" @default.
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