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New Triazaborine Chromophores: Their Synthesis via Oxazaborines and Electrochemical and DFT Study of Their Fundamental Properties

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F14%3A39897769" target="_blank" >RIV/00216275:25310/14:39897769 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388955:_____/14:00437636

  • Result on the web

    <a href="http://dx.doi.org/10.1021/om500219g" target="_blank" >http://dx.doi.org/10.1021/om500219g</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/om500219g" target="_blank" >10.1021/om500219g</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    New Triazaborine Chromophores: Their Synthesis via Oxazaborines and Electrochemical and DFT Study of Their Fundamental Properties

  • Original language description

    Eight new and stable triazaborine chromophores featuring various substituents as donor and acceptor moieties were prepared and investigated. Interpretation of the measured electrochemical data (CV, RDV, and dc-polarography), and UV/Vis spectra as well asthe quantum chemical calculations was presented. In the homologous series the first reduction proceeds as a one-electron reversible process localized at the -N=C-C=N- part of the central heterocycle being in conjugation with the attached carbonyl. The first oxidation of triazaborines proceeds as a two-electron irreversible process, most probably of the ECE type, localized at the negatively charged boron atom and surrounding unsaturated structures including the substituted phenyl ring. For better understanding of the relationship between the structure and redox properties, the LFER approach was applied for the first oxidation as well as reduction potential using the Hammett' sigma (para) substituent constants. The energies of the longes

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/EE2.3.30.0021" target="_blank" >EE2.3.30.0021: Strenthening of Research and Development Teams at the University of Pardubice</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Organometallics

  • ISSN

    0276-7333

  • e-ISSN

  • Volume of the periodical

    33

  • Issue of the periodical within the volume

    18

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    4931-4939

  • UT code for WoS article

    000342180800040

  • EID of the result in the Scopus database