ArticleJournal of fluorescence2016
Effect of π-Extended Substituents on Photophysical Properties of BODIPY Dyes in Solutions.
Article in Journal of fluorescence, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed.
- Solvatochromic Sensitivity of BODIPY Probes: A New Tool for Selecting Fluorophores and Polarity Mapping.International journal of molecular sciences · 2023Article
- Semi-Empirical Calculation of Bodipy Aggregate Spectroscopic Properties through Direct Sampling of Configurational Ensembles.International journal of molecular sciences · 2022Article
- Article
- A Xanthene Dye-based Sensor for Viscosity and Cell Imaging.Journal of fluorescence · 2021Article
- Effects of Concentration on Aggregation of BODIPY-Based Fluorescent Dyes Solution.Journal of fluorescence · 2020Article
- Synthesis and Spectral Characteristics of BODIPY Dyes with Two or Three Dipyrrin Domains.Journal of fluorescence · 2019Article
- Spectral Properties and Possibilities of meso-Substituted BODIPY Usage in Sol-Gel Process and Materials.Journal of fluorescence · 2018Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Four boron-dipyrrine (BODIPY) based dyes with π-extended substituents in 8-position of dipyrrin ligand have been synthesized and characterized. Photophysical properties of the obtained compounds have been investigated in different individual solvents. Deposits of solvent polarity and viscosity were evaluated. BODIPY with 8-biphenyl substituent was found to be the fluorescent molecular rotor in contrast to more extended substituents. The complex nature of solvent-solute interactions leads to the poor applicability of standard multiparameter approaches to BODIPY solvatochromic properties. Fluorescence intensity was found to increase in case of solvent polarity growth, it is not typical for BODIPY. Taking that into account the BODIPY with π-extended substituents could be used for fluorescence viscosity measurements, and as the fluorescent media polarity indicators in analytical chemistry and biochemistry.
Indexed as
Identifiers
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Registered trials
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