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Rhodium-Catalyzed Enantioselective Synthesis of Highly Fluorescent and CPL-Active Dispiroindeno[2,1-c]fluorenes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F21%3A00542907" target="_blank" >RIV/61388955:_____/21:00542907 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388963:_____/21:00542907 RIV/00216208:11310/21:10438715 RIV/60461373:22310/21:43921916

  • Result on the web

    <a href="http://hdl.handle.net/11104/0321723" target="_blank" >http://hdl.handle.net/11104/0321723</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/chem.202100759" target="_blank" >10.1002/chem.202100759</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Rhodium-Catalyzed Enantioselective Synthesis of Highly Fluorescent and CPL-Active Dispiroindeno[2,1-c]fluorenes

  • Original language description

    The enantioselective synthesis of chiral [7]-helical dispirodihydro[2,1-c]indenofluorenes (DSF-IFs) was achieved for the first time in good yields with high er values (er up to 99 : 1). The crucial step of the whole reaction sequence was the enantioselective intramolecular [2+2+2] cycloaddition of tethered triynediols to indenofluorenediols, which was catalyzed by a Rh/SEGPHOS (R) complex. Further transformations led to the corresponding DSF-IFs. The prepared helically chiral DSF-IFs combine circularly polarized luminescence (CPL) activity (g(lum)=similar to 10(-3)) with exceptionally high fluorescence quantum yields (up to phi(lum)=0.97).

  • 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

    10403 - Physical chemistry

Result continuities

  • Project

    <a href="/en/project/GA18-17823S" target="_blank" >GA18-17823S: Syntheses of Fluorenes, Indenofluorenes and Derivatives Thereof Based on Catalytic Reactions</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Chemistry - A European Journal

  • ISSN

    0947-6539

  • e-ISSN

    1521-3765

  • Volume of the periodical

    27

  • Issue of the periodical within the volume

    44

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    6

  • Pages from-to

    11279-11284

  • UT code for WoS article

    000652755300001

  • EID of the result in the Scopus database

    2-s2.0-85106210663