Journals / Turkish Journal of Chemistry / 2000 / Cilt: 24 - Sayı: 2

High fluorescence emissions of some natural benzofurane derivatives isolated from Styrax officinalis

Pages
199–207
Publication Date
2022-11-05
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

It is concluded that the first excited singlet state of egonol molecule is a more efficient electron acceptor.

📌 3 Key Takeaways

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Objective & Hypothesis:The fluorescent properties of several natural benzofuran derivatives, egonols, isolated from {\it Styrax officinalis}, were determined.
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Key Findings & Data:The studied egonol derivatives were found to be effective UV organic luminophores, with quantum yields of near to unity, \( jf \) = 0.92.
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Conclusion & Impact:It is concluded that the first excited singlet state of egonol molecule is a more efficient electron acceptor.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Fluorescence emission · Styrax officinalis · egonol

Abstract

The fluorescent properties of several natural benzofuran derivatives, egonols, isolated from {\it Styrax officinalis}, were determined. The studied egonol derivatives were found to be effective UV organic luminophores, with quantum yields of near to unity, \( jf \) = 0.92. The fluorescence quenching experiments with electron donor molecules of aniline, N,N-dimethylaniline and carbazolocarbazole, presented very high efficiency of quenching at above diffusion quenching rates of 4.5\times10\( 10 \), 2.1\times10\( \times \) and 5.6\times10\( 12 \) s\( -1 \)mol\( -1 \), respectively. A strong electron acceptor molecule, tetranitrofluorenone, presented quenching rate of 2.6\times10\( 11 \) s\( -1 \)mol\( -1 \). It is concluded that the first excited singlet state of egonol molecule is a more efficient electron acceptor.

Özet

The fluorescent properties of several natural benzofuran derivatives, egonols, isolated from {\it Styrax officinalis}, were determined. The studied egonol derivatives were found to be effective UV organic luminophores, with quantum yields of near to unity, \( jf \) = 0.92. The fluorescence quenching experiments with electron donor molecules of aniline, N,N-dimethylaniline and carbazolocarbazole, presented very high efficiency of quenching at above diffusion quenching rates of 4.5\times10\( 10 \), 2.1\times10\( \times \) and 5.6\times10\( 12 \) s\( -1 \)mol\( -1 \), respectively. A strong electron acceptor molecule, tetranitrofluorenone, presented quenching rate of 2.6\times10\( 11 \) s\( -1 \)mol\( -1 \). It is concluded that the first excited singlet state of egonol molecule is a more efficient electron acceptor.

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Cite This Article

İÇLİ, S., ALP, S., DİNDAR, B., ANIL, H., ÇALIŞKAN, A. Ö., YAYLA, Y., DOROSHENKO, A. O. (2022). High fluorescence emissions of some natural benzofurane derivatives isolated from Styrax officinalis. Turkish Journal of Chemistry, Cilt: 24 - Sayı: 2, 199–207. https://ajindex.com/articles/602434

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