Straightforward Synthesis and Properties of Highly Fluorescent [5]- and [7]-Helical Dispiroindeno[2,1-c]fluorenes
Status PubMed-not-MEDLINE Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
18-17823S
Grantová Agentura České Republiky - International
18-04682S
Grantová Agentura České Republiky - International
CZ.02.1.01/0.0/0.0/15_003/0000417
European Regional Development Fund - International
430516
Grantová Agentura, Univerzita Karlova - International
RVO 61388955
Ústav Organické Chemie a Biochemie, Akademie Věd České Republiky - International
PubMed
31539185
DOI
10.1002/anie.201908348
Knihovny.cz E-zdroje
- Klíčová slova
- alkynes, catalysis, cyclotrimerization, helical compounds, indenofluorene,
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
This work presents a general approach for synthesis of substituted [5]-helical dispiroindeno[2,1-c]fluorenes based on Rh-catalyzed intramolecular cyclotrimerization of triynes. This approach was further extended for the first synthesis of configurationally stable [7]-helical dispiroindeno[2,1-c]fluorenes. A series of variously substituted derivatives was prepared and their photophysical and electrochemical properties were evaluated. Their fluorescence emission maxima were in the region of 351-428 nm and quantum yields up to 88 % are the highest measured among the full-carbon helical compounds.
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