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Fused dual boron core based BODIPY dyes: synthesis and optical character.
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Apr2016, Vol. 57 Issue 14, p1605-1609. 5p. - Publication Year :
- 2016
-
Abstract
- Here we report that two boron dipyrromethene derivatives ( BNB-1 and BNB-2 ), bearing double boron atomic centers, have been synthesized and characterized. The additional boron atom was introduced into the skeleton of typical BODIPY dyes through the reaction of BF 3 ·Et 2 O and the two ligands, phenol and Schiff’s base. The maximum emission wavelength of both dyes moved to 584–603 nm with the larger Stokes’ shift (Δ λ ≈ 40 nm). Moreover, less solvent polarity dependence of the Stokes’ shift (40 ± 6 nm) was found in different organic solvents. Furthermore, fluorescent lifetime and CV methods were also performed to explore the photophysical and electrochemical behaviors of both dyes. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 57
- Issue :
- 14
- Database :
- Academic Search Index
- Journal :
- Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 113726848
- Full Text :
- https://doi.org/10.1016/j.tetlet.2016.02.109