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Modulating the electron-transfer properties of a mixed-valence system through host-guest chemistry.


ABSTRACT: Metal directed self-assembly has become a much-studied route towards complex molecular architectures. Although studies on mixed valence, MV, systems accessible through this approach are almost non-existent, the potential applications of such systems are very exciting as MV states provide the basis of a number of molecular-scale devices, including single electron wires and switches. Furthermore, while many novel hosts for guest ions and molecules have been developed through metal directed self-assembly, as these products tend to be kinetically labile, very few electrochemical studies have been reported. Herein, we report that the interplay between the binding properties and redox activity of a self-assembled trinuclear RuII macrocycle leads to an hitherto unreported phenomenon, in which access to specific MV states can be gated by host-guest chemistry. Thus, this system is the first in which MV states and the extent of electron delocalisation are switched by an ion without any change in electrochemical potential.

SUBMITTER: Zubi A 

PROVIDER: S-EPMC5811089 | biostudies-other | 2015 Feb

REPOSITORIES: biostudies-other

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Modulating the electron-transfer properties of a mixed-valence system through host-guest chemistry.

Zubi Ahmed A   Wragg Ashley A   Turega Simon S   Adams Harry H   Costa Paulo J PJ   Félix Vítor V   Thomas Jim A JA  

Chemical science 20141126 2


Metal directed self-assembly has become a much-studied route towards complex molecular architectures. Although studies on mixed valence, MV, systems accessible through this approach are almost non-existent, the potential applications of such systems are very exciting as MV states provide the basis of a number of molecular-scale devices, including single electron wires and switches. Furthermore, while many novel hosts for guest ions and molecules have been developed through metal directed self-as  ...[more]

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