ArticleChemistry of materials : a publication of the American Chemical Society2009
Bright, Red Single-Molecule Emitters: Synthesis and Properties of Environmentally Sensitive Dicyanomethylenedihydrofuran (DCDHF) Fluorophores with Bisaromatic Conjugation.
Article in Chemistry of materials : a publication of the American Chemical Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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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.
- Molecular Deformation Is a Key Factor in Screening Aggregation Inhibitor for Intrinsically Disordered Protein Tau.ACS central science · 2024Article
- Photophysics of Fluorescent Contact Sensors Based on the Dicyanodihydrofuran Motif.Chemphyschem : a European journal of chemical physics and physical chemistry · 2021Article
- Tunable Non-linear Refraction Properties and Ultrafast Excited State Dynamics of Dicyanomethylene Dihydrofuran Derivative.Frontiers in chemistry · 2020Article
- Hot exciton transition for organic light-emitting diodes: tailoring excited-state properties and electroluminescence performances of donor-spacer-acceptor molecules.RSC advances · 2018Article
- Fluorescence microscopy visualization of contacts between objects.Angewandte Chemie (International ed. in English) · 2015Article
- Fluorescent flippers for mechanosensitive membrane probes.Journal of the American Chemical Society · 2015Article
- Azido push-pull fluorogens photoactivate to produce bright fluorescent labels.The journal of physical chemistry. B · 2010Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
A group of new fluorescent dye materials for single-molecule imaging applications comprised of an amine donor, a π-system comprised of phenyl and thiophene rings and a 2-dicyanomethylene-3-cyano-2,5-dihydrofuran acceptor group have been synthesized. Relative to comparable single-ring compounds these doubly aromatic conjugated fluorophores have red-shifted absorption and emission usually accompanied by significantly increased quantum yields. Solvatochromism studies indicate that the photophysical properties of these dyes are sensitive to the solvent polarity and environmental rigidity. Photophysical studies demonstrate that these DCDHF dye materials are strong single-molecule emitters and the total number of detected photons per molecule is among the highest thus far for this family of fluorophores.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.