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Related Concept Videos

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride01:26

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride

1.9K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
1.9K
Halogenation of Alkenes02:46

Halogenation of Alkenes

16.5K
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
16.5K
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene01:13

Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene

6.5K
Bromination and chlorination of aromatic rings by electrophilic aromatic substitution reactions are easily achieved, but fluorination and iodination are difficult to achieve. Fluorine is so reactive that its reaction with benzene is difficult to control, resulting in poor yields of monofluoroaromatic products. To address this, Selectfluor reagent is used as a fluorine source in which a fluorine atom is bonded to a positively charged nitrogen.
6.5K
Alkyl Halides02:45

Alkyl Halides

17.5K
Structural Properties
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
17.5K
Nucleophilic Aromatic Substitution: Elimination–Addition01:11

Nucleophilic Aromatic Substitution: Elimination–Addition

4.2K
Simple aryl halides do not react with nucleophiles. However, nucleophilic aromatic substitutions can be forced under certain conditions, such as high temperatures or strong bases. The mechanism of substitution under such conditions involves the highly unstable and reactive benzyne intermediate. Benzyne contains equivalent carbon centers at both ends of the triple bond, each of which is equally susceptible to nucleophilic attack. This 50–50 distribution of products is...
4.2K
Reactions at the Benzylic Position: Halogenation01:11

Reactions at the Benzylic Position: Halogenation

2.8K
Benzylic halogenation takes place under conditions that favor radical reactions such as heat, light, or a free radical initiator like peroxide.
2.8K

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Related Experiment Video

Updated: Sep 22, 2025

Solution-Processed "Silver-Bismuth-Iodine" Ternary Thin Films for Lead-Free Photovoltaic Absorbers
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Solution-Processed "Silver-Bismuth-Iodine" Ternary Thin Films for Lead-Free Photovoltaic Absorbers

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Indirect Substitution Constructing Halogen-Vacancy BiOCl1-I Solid Solution with a Suitable Surface Structure for

Jintao Wang1, Hao Mei2, Dai Jin2

  • 1Key Laboratory of Jiangxi Province for Environment and Energy Catalysis, the College of Chemistry, Nanchang University, 999# Xuefu Road, Nanchang 330031, China.

Inorganic Chemistry
|May 23, 2022
PubMed
Summary

This study introduces a novel method to create halogen vacancies in bismuth oxyhalide solid solutions, enhancing their efficiency for environmental remediation. These engineered photocatalysts show improved performance in degrading heavy metals and organic pollutants.

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A Facile Synthetic Method to Obtain Bismuth Oxyiodide Microspheres Highly Functional for the Photocatalytic Processes of Water Depuration
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A Facile Synthetic Method to Obtain Bismuth Oxyiodide Microspheres Highly Functional for the Photocatalytic Processes of Water Depuration

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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

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Last Updated: Sep 22, 2025

Solution-Processed "Silver-Bismuth-Iodine" Ternary Thin Films for Lead-Free Photovoltaic Absorbers
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Solution-Processed "Silver-Bismuth-Iodine" Ternary Thin Films for Lead-Free Photovoltaic Absorbers

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A Facile Synthetic Method to Obtain Bismuth Oxyiodide Microspheres Highly Functional for the Photocatalytic Processes of Water Depuration
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A Facile Synthetic Method to Obtain Bismuth Oxyiodide Microspheres Highly Functional for the Photocatalytic Processes of Water Depuration

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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
06:44

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

69.2K

Area of Science:

  • Materials Science
  • Environmental Science
  • Chemistry

Background:

  • Photocatalysis shows promise for environmental remediation but struggles with persistent pollutants.
  • Bismuth oxyhalides (BiOX) are effective photocatalysts, but their performance needs optimization.
  • Synthesizing BiOCl$_{1-x}$I$_x$ solid solutions with controlled structures is key for advanced applications.

Purpose of the Study:

  • To develop a strategy for synthesizing BiOCl$_{1-x}$I$_x$ solid solutions with in situ introduced halogen vacancies.
  • To investigate the effect of halogen vacancies on the band structure and surface properties of BiOCl$_{1-x}$I$_x$.
  • To evaluate the enhanced photocatalytic performance for environmental remediation.

Main Methods:

  • Synthesis of BiOCl$_{1-x}$I$_x$ solid solutions with controlled halogen vacancies using glycerol.
  • Characterization of the material's band structure and surface active sites.
  • Testing photocatalytic activity for Cr(VI) reduction and phenol oxidation.

Main Results:

  • Successfully introduced halogen vacancies into BiOCl$_{1-x}$I$_x$ via chemical bonding with glycerol.
  • Widened the band gap and formed active sites centered at halogen vacancies.
  • Achieved enhanced photocatalytic performance in reducing Cr(VI) and oxidizing phenol.

Conclusions:

  • Controlling halogen vacancy formation is a viable strategy for designing efficient photocatalysts.
  • The developed halogen-vacancy BiOCl$_{1-x}$I$_x$ shows significant potential for environmental remediation.
  • This approach offers new insights into optimizing photocatalyst design for pollutant degradation.