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Carbonyl mediated fluorescence in aceno[n]helicenones and fluoreno[n]helicenes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F24%3A00586800" target="_blank" >RIV/61388963:_____/24:00586800 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1039/D4SC00892H" target="_blank" >https://doi.org/10.1039/D4SC00892H</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d4sc00892h" target="_blank" >10.1039/d4sc00892h</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Carbonyl mediated fluorescence in aceno[n]helicenones and fluoreno[n]helicenes

  • Original language description

    Helicenes are very attractive chiral non-planar polycyclic aromatic hydrocarbons possessing strong chiroptical properties. However, most of the helicenes absorb light mainly in the ultraviolet region, with only a small segment in the blue part of the visible spectrum. Furthermore, carbo[n]helicenes exhibit only weak luminescence that limits their utilization. Herein, we demonstrate that peripheral decoration of the helicene backbone with an aryl-carbonyl group shifts the absorption to the visible region and simultaneously improves their fluorescence quantum yields. We thus show that the carbonyl group, commonly considered as detrimental to emission, has the capability of improving optical and photophysical properties. Two different families, aceno[n]helicenones and fluoreno[n]helicenes, are presented with comprehensive spectrochemical characterization. TD-DFT calculations were implemented to clarify their electronic profiles. We show that increasing the helical length in aceno[n]helicenes increases absorption onset, g(abs) and g(lum). Extension of the peripheral aromatic part in fluoreno[n]helicenes leads to a blue shift in both absorption and emission.

  • 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

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GA20-23566S" target="_blank" >GA20-23566S: The synthesis and properties of polycyclic inherently chiral aromatics</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Chemical Science

  • ISSN

    2041-6520

  • e-ISSN

    2041-6539

  • Volume of the periodical

    15

  • Issue of the periodical within the volume

    25

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    9

  • Pages from-to

    9842-9850

  • UT code for WoS article

    001234393800001

  • EID of the result in the Scopus database

    2-s2.0-85194384925