All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Electron Transfer Triggers Fast Dimer/Monomer Switching of Pyridinium and Quinolinium Cations

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F12%3A00377424" target="_blank" >RIV/61388963:_____/12:00377424 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388955:_____/12:00377424 RIV/60461373:22340/12:43894063

  • Result on the web

    <a href="http://dx.doi.org/10.1021/jp211122n" target="_blank" >http://dx.doi.org/10.1021/jp211122n</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/jp211122n" target="_blank" >10.1021/jp211122n</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Electron Transfer Triggers Fast Dimer/Monomer Switching of Pyridinium and Quinolinium Cations

  • Original language description

    N-Heteroaromatic cations with quaternary pyridine-type nitrogen atoms have a rich application potential due to their bioactivity, fluorescence, and redox properties. Reactivity of radicals formed by reduction of such compounds is of key importance. We report the electron transfer mechanism of four novel compounds containing pyridinium, quinolinium, and benzothiazolium moiety. The reduction of pyridinium and quinolinium derivatives by one electron yields radicals that very rapidly form a-dimers. Dimers can be converted to parent cations by oxidation, which proceeds at considerably higher potentials. Hence the dimerization can be reversibly switched by application of the appropriate electrode potential. In contrast, in benzothiazolium derivative the electron transfer yields a stable radical in which the follow-up dimerization reaction is completely blocked. Analysis of experimental data as well as theoretical models led to the identification of dimerization sites in reduced pyridinium an

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CF - Physical chemistry and theoretical chemistry

  • OECD FORD branch

Result continuities

  • Project

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

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2012

  • 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 Physical Chemistry C

  • ISSN

    1932-7447

  • e-ISSN

  • Volume of the periodical

    116

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    3779-3786

  • UT code for WoS article

    000299985300071

  • EID of the result in the Scopus database