Synthesis and photophysical properties of borondipyrromethene dyes bearing aryl substituents at the boron center.
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Summary
Several borondipyrromethene (Bodipy) dyes bearing an aryl nucleus linked directly to the boron center have been prepared under mild conditions, with strong fluorescence observed from the Bodipy fluorophore present in each of the new dyes, with the radiative rate constant being independent of the nature of the aryal substituent.
- Type
- article
- Published
- 2006-07-07
- Cited by
- 160
- References
- 3
- OpenAlex
- https://openalex.org/W1992354154
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:33993127
Keywords
Chemistry, BODIPY, Aryl, Substituent, Photochemistry
References
Cited by
- Luminescent Di- and Trinuclear Boron Complexes Based on Aromatic Iminopyrrolyl Spacer Ligands: Synthesis, Characterization, and Application in OLEDs.
- Scope and Limitations of the Liebeskind-Srogl Cross-Coupling Reactions Involving the Biellmann BODIPY.
- Synthesis of 4,4′-functionalized BODIPYs from dipyrrins
- Novel pyrromethene dyes with N-ethyl carbazole at the meso position: a comprehensive photophysical, lasing, photostability and TD-DFT study.
- Postfunctionalization of the BODIPY Core: Synthesis and Spectroscopy
- Synthesis and photo-property of 2-cyano boron-dipyrromethene and the application for detecting fluoride ion
- Synthesis and Transformations of 5-Chloro-2,2′-Dipyrrins and Their Boron Complexes, 8-Chloro-BODIPYs
- Some observations relating to the stability of the BODIPY fluorophore under acidic and basic conditions
- Synthesis and optical properties of 2-(benzo[b]thiophene-3-yl)pyrroles and a new BODIPY fluorophore (BODIPY = 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene).
- Convenient one-pot procedure for synthesizing 4,4′-dimethoxy-boradiaza-s-indacene dyes and their application to cell labeling
- Synthesis and reactivity of 4,4-Dialkoxy-BODIPYs: an experimental and computational study.
- Facile functionalization of a fully fluorescent perfluorophenyl BODIPY: photostable thiol and amine conjugates.
- Activation and deprotection of F-BODIPYs using boron trihalides.
- Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives.
- Functionalization of the 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) core.
- A sensitive fluorescent chemosensor for anions based on a styryl–boradiazaindacene framework
- A facile and high-yield formation of dipyrrin-boronic acid dyads and triads: a light-harvesting system in the visible region based on the efficient energy transfer.
- Chemical and electrochemical dimerization of BODIPY compounds: electrogenerated chemiluminescent detection of dimer formation.
- Borenium cations derived from BODIPY dyes.
- Highly near‐infrared emissive boron di(iso)indomethene‐based polymer: Drastic change from deep‐red to near‐infrared emission via quantitative polymer reaction
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