ArticleJournal of fluorescence2014
Fluorescent coumarin derivatives with viscosity sensitive emission--synthesis, photophysical properties and computational studies.
Article in Journal of fluorescence, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 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.
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Who cites it
8 citing papers in PubMed, 16 citations in OpenAlex.
- A Xanthene Dye-based Sensor for Viscosity and Cell Imaging.Journal of fluorescence · 2021Article
- The Role of Zinc(II) Ion in Fluorescence Tuning of Tridentate Pincers: A Review.Molecules (Basel, Switzerland) · 2020Review
- Cyclodextrin-Promoted Fluorescence Detection of Aromatic Toxicants and Toxicant Metabolites in Commercial Milk Products.Food analytical methods · 2018Article
- Coumarin-Rhodamine Hybrids-Novel Probes for the Optical Measurement of Viscosity and Polarity.Journal of fluorescence · 2017Article
- Coumarin-Pyrazole Hybrid with Red Shifted ESIPT Emission and AIE Characteristics - a Comprehensive Study.Journal of fluorescence · 2017Article
- Coumarin Push-Pull NLOphores with Red Emission: Solvatochromic and Theoretical Approach.Journal of fluorescence · 2016Article
- AIE Based Coumarin Chromophore - Evaluation and Correlation Between Solvatochromism and Solvent Polarity Parameters.Journal of fluorescence · 2016Article
- Phenalenone fluorophores-synthesis, photophysical properties and DFT study.Journal of fluorescence · 2014Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
New derivatives of (benzo[d]azolyl)-benzo[f]chromenone were synthesized from the intermediate 3-(1,3-benzazol-2-yl)naphthalen-2-ol, obtained from 3-hydroxynaphthalene-2-carboxylic acid and 2-amino phenol in the presence of PCl3 in chlorobenzene at 130-135 °C. The compounds were characterized by FT-IR, (1) H NMR, mass spectroscopy and elemental analysis. The synthesized compounds are fluorescent which absorb in the range of 296 to 332 nm while emit in the range of 368 to 404 nm. The experimental absorption and emission wavelengths for the compounds 5 and 6 are in good agreement with those predicted using the Time-Dependent Density Functional Theory (TD-DFT) [B3LYP/6-31G(d)]. The largest wavelength difference between the experimental and computed absorption maxima was 29 nm (tetrahedrofuran) for compound 5 while for emission it was 61 nm (dichloromethane) for compound 7. The emission intensities of all the compounds decrease continuously as the viscosity of the microenvironment increases. The compounds are thermally stable up to a temperature range of 300 to 350 °C.
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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.