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      Exploiting redox activity in metal–organic frameworks: concepts, trends and perspectives

      Chemical Communications
      Royal Society of Chemistry (RSC)

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          Abstract

          This feature article highlights latest developments in experimental, theoretical and computational concepts relevant to redox-active metal–organic Frameworks.

          Abstract

          Of the many thousands of new metal–organic frameworks (MOFs) that are now discovered each year, many possess potential redox activity arising from the constituent metal ions and/or organic ligands, or the guest molecules located within their porous structures. Those redox states that can be accessed via postsynthetic redox modulation often possess distinct physical properties; if harnessed, these provide a basis for applications including microporous conductors, electrocatalysts, energy storage devices and electrochemical sensors, amongst others. This feature article highlights the latest developments in experimental, theoretical and computational concepts relevant to redox-active MOFs, including new solid state electrochemical and spectroelectrochemical techniques that have great utility in this field. A particular emphasis is on current and emerging trends at the fundamental level which underscore the importance of this promising class of electroactive materials for a wide range of technologically- and industrially-relevant applications.

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          Most cited references142

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          Metal-organic framework materials as chemical sensors.

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            Synthesis of metal-organic frameworks (MOFs): routes to various MOF topologies, morphologies, and composites.

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              On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer. I

              R Marcus (1956)
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                Author and article information

                Journal
                CHCOFS
                Chemical Communications
                Chem. Commun.
                Royal Society of Chemistry (RSC)
                1359-7345
                1364-548X
                2016
                2016
                : 52
                : 58
                : 8957-8971
                Article
                10.1039/C6CC00805D
                5bc37d8d-0e52-437b-952b-4c67062deb34
                © 2016
                History

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