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Electron Storage System Based on a Two-Way Inversion of Redox Potentials

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F20%3A00523365" target="_blank" >RIV/61388955:_____/20:00523365 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388963:_____/20:00523628

  • Result on the web

    <a href="http://hdl.handle.net/11104/0307724" target="_blank" >http://hdl.handle.net/11104/0307724</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/jacs.9b12762" target="_blank" >10.1021/jacs.9b12762</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Electron Storage System Based on a Two-Way Inversion of Redox Potentials

  • Original language description

    Molecular-level multielectron handling toward electrical storage is a worthwhile approach to solar energy harvesting. Here, a strategy which uses chemical bonds as electron reservoirs is introduced to demonstrate the new concept of “structronics” (a neologism derived from “structure” and “electronics”). Through this concept, we establish, synthesize, and thoroughly study two multicomponent “super-electrophores”: 1,8-dipyridyliumnaphthalene, 2, and its N,N-bridged cyclophane-like analogue, 3. Within both of them, a covalent bond can be formed and subsequently broken electrochemically. These superelectrophores are based on two electrophoric (pyridinium) units that are, on purpose, spatially arranged by a naphthalene scaffold. A key characteristic of 2 and 3 is that they possess a LUMO that develops through space as the result of the interaction between the closely positioned electrophoric units. In the context of electron storage, this “super-LUMO” serves as an empty reservoir, which can be filled by a two-electron reduction, giving rise to an elongated C–C bond or “super-HOMO”. Because of its weakened nature, this bond can undergo an electrochemically driven cleavage at a significantly more anodic—yet accessible—potential, thereby restoring the availability of the electron pair (reservoir emptying). In the representative case study of 2, an inversion of potential in both of the two-electron processes of bond formation and bond-cleavage is demonstrated. Overall, the structronic function is characterized by an electrochemical hysteresis and a chemical reversibility. This structronic superelectrophore can be viewed as the three-dimensional counterpart of benchmark methyl viologen (MV).nn

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of the American Chemical Society

  • ISSN

    0002-7863

  • e-ISSN

  • Volume of the periodical

    142

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    15

  • Pages from-to

    5162-5176

  • UT code for WoS article

    000526392600029

  • EID of the result in the Scopus database

    2-s2.0-85081695049