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Excitation/detection energy controlled anisotropy dynamics in asymmetrically cyano substituted tri-podal molecules

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F20%3A39916360" target="_blank" >RIV/00216275:25310/20:39916360 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://doi.org/10.1039/D0CP01726D" target="_blank" >https://doi.org/10.1039/D0CP01726D</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d0cp01726d" target="_blank" >10.1039/d0cp01726d</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Excitation/detection energy controlled anisotropy dynamics in asymmetrically cyano substituted tri-podal molecules

  • Popis výsledku v původním jazyce

    In the present work, the photophysical properties of two series of asymmetrical tri-podal molecules are studied, in order to determine the dependence of energy localization/delocalization phenomena on excitation and detection wavelength, by means of steady state, femtosecond time-resolved fluorescence and anisotropy spectroscopy. The molecules bear triphenylamine as an electron donating core and an acetylenic or olefinic pi-conjugated bridge. At the periphery, they are substituted by no, one, two or three -CN groups used as electron acceptors. Thus, the compounds with only one or two -CN groups are asymmetrically substituted. As a comparison, the photophysics of their dipolar and quadrupolar analogues is also presented. The steady state absorption spectra of the asymmetrical tri-podal compounds exhibit a broadening and a low energy shoulder due to the splitting of the excited states. The fluorescence spectra are more red-shifted in the tri-podal molecules with a single -CN group, providing the first evidence of its mostly dipolar nature. Time-resolved anisotropy measurements by using different excitation and detection wavelengths provide clear evidence that the asymmetrical tri-podal molecules with one or two -CN groups behave like octupolar molecules upon high-energy excitation (the initial anisotropy is found 0.1-0.15), while upon low-energy excitation they reveal a behavior expected for linear dipolar or V-shaped quadrupolar molecules (the initial anisotropy is very close to 0.4 and 0.17, respectively). The symmetrical tri-podal compounds with no or three cyano groups, exhibit an anisotropy depolarization time of 2.5 ps attributed to energy hopping. The amplitude of this energy hopping component is wavelength dependent and increases as the excitation is shifted towards the long wavelength edge.

  • Název v anglickém jazyce

    Excitation/detection energy controlled anisotropy dynamics in asymmetrically cyano substituted tri-podal molecules

  • Popis výsledku anglicky

    In the present work, the photophysical properties of two series of asymmetrical tri-podal molecules are studied, in order to determine the dependence of energy localization/delocalization phenomena on excitation and detection wavelength, by means of steady state, femtosecond time-resolved fluorescence and anisotropy spectroscopy. The molecules bear triphenylamine as an electron donating core and an acetylenic or olefinic pi-conjugated bridge. At the periphery, they are substituted by no, one, two or three -CN groups used as electron acceptors. Thus, the compounds with only one or two -CN groups are asymmetrically substituted. As a comparison, the photophysics of their dipolar and quadrupolar analogues is also presented. The steady state absorption spectra of the asymmetrical tri-podal compounds exhibit a broadening and a low energy shoulder due to the splitting of the excited states. The fluorescence spectra are more red-shifted in the tri-podal molecules with a single -CN group, providing the first evidence of its mostly dipolar nature. Time-resolved anisotropy measurements by using different excitation and detection wavelengths provide clear evidence that the asymmetrical tri-podal molecules with one or two -CN groups behave like octupolar molecules upon high-energy excitation (the initial anisotropy is found 0.1-0.15), while upon low-energy excitation they reveal a behavior expected for linear dipolar or V-shaped quadrupolar molecules (the initial anisotropy is very close to 0.4 and 0.17, respectively). The symmetrical tri-podal compounds with no or three cyano groups, exhibit an anisotropy depolarization time of 2.5 ps attributed to energy hopping. The amplitude of this energy hopping component is wavelength dependent and increases as the excitation is shifted towards the long wavelength edge.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10401 - Organic chemistry

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2020

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    Physical Chemistry Chemical Physics

  • ISSN

    1463-9076

  • e-ISSN

  • Svazek periodika

    22

  • Číslo periodika v rámci svazku

    29

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    10

  • Strana od-do

    16681-16690

  • Kód UT WoS článku

    000556485900017

  • EID výsledku v databázi Scopus

    2-s2.0-85088881717