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Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

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Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
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Atomic fluorescence spectroscopy (AFS) is an analytical technique that involves the electronic transitions of atoms in a flame, furnace, or plasma being excited by electromagnetic (EM) radiation. When these atoms absorb energy, they become excited and subsequently release energy as they return to their original state. This emitted light, or "fluorescence," is observed at a right angle to the incident beam. Both absorption and emission processes transpire at distinct wavelengths, which...
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Amines to Sulfonamides: The Hinsberg Test01:23

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The Hinsberg test is a method to identify primary, secondary and tertiary amines, named after its pioneer, Oscar Hinsberg. Here, amines are treated with benzenesulfonyl chloride, also known as the Hinsberg reagent, in the presence of an excess of aqueous base, followed by acidification. Based on the nature of the amines, different changes are observed.
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing...
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Gas Chromatography: Types of Detectors-II01:19

Gas Chromatography: Types of Detectors-II

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In gas chromatography, different detectors are employed to meet specific analytical needs. These detectors are often categorized based on their detection mechanisms and the types of compounds they are best suited to analyze. Thermal Conductivity Detectors (TCD), Flame Ionization Detectors (FID), and Electron Capture Detectors (ECD) represent common categories, each with unique operating principles and applications. However, beyond these, several other detectors are designed for more specialized...
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Labeling DNA Probes03:31

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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
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Updated: Sep 24, 2025

A Sensitive Visual Method for the Detection of Hydrogen Sulfide Producing Bacteria
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Hydrogen sulfide sensing using an aurone-based fluorescent probe.

Arjun Kafle1, Shrijana Bhattarai1, Justin M Miller1,2

  • 1Molecular Bioscience Program, Middle Tennessee State University Murfreesboro TN 37132 USA justin.miller@mtsu.edu scott.handy@mtsu.edu.

RSC Advances
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Summary
This summary is machine-generated.

Researchers developed a new, low-molecular-weight fluorescent probe for sensitive hydrogen sulfide detection. This aurone-based probe offers a fast and selective method for sensing hydrogen sulfide in biological and environmental samples.

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Area of Science:

  • Analytical Chemistry
  • Biochemistry
  • Environmental Science

Background:

  • Hydrogen sulfide (H₂S) detection is crucial for environmental monitoring and biological studies.
  • Existing sensitive fluorescent probes for H₂S often use large, complex scaffolds that are difficult to synthesize and modify.
  • There is a need for simpler, more adaptable fluorescent probes for H₂S sensing.

Purpose of the Study:

  • To design and synthesize a novel, low-molecular-weight, turn-on fluorescent probe for hydrogen sulfide detection.
  • To overcome limitations of existing probes, such as synthetic complexity, solubility, and performance in biological media.
  • To develop a sensitive, selective, and rapid method for H₂S sensing.

Main Methods:

  • Rational design and synthesis of a new aurone-based fluorescent probe, (Z)-2-(4'-azidobenzylidene)-5-fluorobenzofuran-3(2H)-one (6g).
  • Modular synthesis approach to address issues with solubility, excitation overlap, and reaction rates.
  • Utilized cationic surfactant cetyltrimethylammonium bromide (CTAB) to enhance reaction speed and fluorescence in biological media.

Main Results:

  • Successfully synthesized a low-molecular-weight aurone fluorophore probe (6g).
  • The probe demonstrated efficient and sensitive detection of hydrogen sulfide with high fluorescence enhancement.
  • Achieved a fast response time (10-30 min), good sensitivity (1 μm detection limit), and high selectivity for H₂S.
  • CTAB addition improved reaction kinetics and fluorescence intensity in biologically relevant conditions.

Conclusions:

  • The developed aurone-based fluorescent probe offers a significant advancement for hydrogen sulfide detection.
  • Its low molecular weight, modular synthesis, and improved performance in biological media make it highly applicable.
  • This probe provides a sensitive, selective, and rapid tool for both environmental and biological H₂S sensing applications.