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Straightforward Synthesis and Properties of Highly Fluorescent [5]- and [7]-Helical Dispiroindeno[2,1-c]fluorenes
- 1.0511987 - ÚFCH JH 2020 RIV DE eng J - Článek v odborném periodiku
Kaiser, R. P. - Nečas, D. - Cadart, T. - Gyepes, R. - Císařová, I. - Mosinger, J. - Pospíšil, Lubomír - Kotora, M.
Straightforward Synthesis and Properties of Highly Fluorescent [5]- and [7]-Helical Dispiroindeno[2,1-c]fluorenes.
Angewandte Chemie - International Edition. Roč. 58, č. 48 (2019), s. 17169-17174. ISSN 1433-7851. E-ISSN 1521-3773
Grant CEP: GA ČR(CZ) GA18-04682S
Institucionální podpora: RVO:61388955
Klíčová slova: nonlinear-optical properties * field-effect transistors * host materials * dihydroindenofluorene derivatives * organic semiconductors * spiro compounds * solar-cells * efficient * spirobifluorene * dye
Obor OECD: Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)
Impakt faktor: 12.959, rok: 2019
Způsob publikování: Omezený přístup
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.
Trvalý link: http://hdl.handle.net/11104/0302216
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