Synthesis and photophysical properties of tripod BODIPY dyes bearing mono-phenolic derivatives
A series of new tripod boron dipyrromethene (BODIPY) dyes bearing mono-phenolic derivatives were synthesized and characterized. An optimized reaction condition for the synthesis of the bis-substituted intermediates was obtained. An unanticipated phenol-dependent effect on the yields was found and a...
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Veröffentlicht in: | Tetrahedron 2015-02, Vol.71 (8), p.1304-1310 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A series of new tripod boron dipyrromethene (BODIPY) dyes bearing mono-phenolic derivatives were synthesized and characterized. An optimized reaction condition for the synthesis of the bis-substituted intermediates was obtained. An unanticipated phenol-dependent effect on the yields was found and a hypothetic mechanism was proposed to elucidate the reactivity of the tripod dipyrromethene species during the complexation step. The new dyes showed typical photophysical properties of the BODIPY fluorophore.
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ISSN: | 0040-4020 1464-5416 |
DOI: | 10.1016/j.tet.2014.12.072 |