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Related Concept Videos

Oxidative Cleavage of Alkenes: Ozonolysis01:46

Oxidative Cleavage of Alkenes: Ozonolysis

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In ozonolysis, ozone is used to cleave a carbon–carbon double bond to form aldehydes and ketones, or carboxylic acids, depending on the work-up.
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
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Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

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Alkenes can be dihydroxylated using potassium permanganate.  The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
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Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids02:04

Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids

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Diols are compounds with two hydroxyl groups. In addition to syn dihydroxylation, diols can also be synthesized through the process of anti dihydroxylation. The process involves treating an alkene with a peroxycarboxylic acid to form an epoxide. Epoxides are highly strained three-membered rings with oxygen and two carbons occupying the corners of an equilateral triangle. This step is followed by ring-opening of the epoxide in the presence of an aqueous acid to give a trans diol.
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Oxidation of Alcohols02:37

Oxidation of Alcohols

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In this lesson, the oxidation of alcohols is discussed in depth. The various reagents used for oxidation of primary and secondary alcohols are detailed, and their mechanism of action is provided.
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Acid-Catalyzed Ring-Opening of Epoxides02:24

Acid-Catalyzed Ring-Opening of Epoxides

7.4K
Epoxides that are three-membered ring systems are more reactive than other cyclic and acyclic ethers. The high reactivity of epoxides originates from the strain present in the ring. This ring strain acts as a driving force for epoxides to undergo ring-opening reactions either with halogen acids or weak nucleophiles in the presence of mild acid. The acid catalyst converts the epoxide oxygen, a poor leaving group, into an oxonium ion, a better leaving group, making the reaction feasible. The...
7.4K
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide02:44

Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

10.4K
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
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Protocol of Electrochemical Test and Characterization of Aprotic Li-O2 Battery
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Spin-Polarization Strategy for Enhanced Acidic Oxygen Evolution Activity.

Ling Li1, Jing Zhou2, Xiao Wang3

  • 1College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Jiangsu, 215123, China.

Advanced Materials (Deerfield Beach, Fla.)
|July 12, 2023
PubMed
Summary
This summary is machine-generated.

This study introduces a novel spin-polarization strategy using manganese-doped ruthenium dioxide (RuO2) to boost the acidic oxygen evolution reaction (OER) for industrial applications.

Keywords:
RuO2acidicmagnetic fieldoxygen evolution reactionspin

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Catalysis

Background:

  • Spin-polarization is a promising approach for enhancing the oxygen evolution reaction (OER) due to spin-dependent behaviors of intermediates and products.
  • Few ferromagnetic catalysts have been practically reported for acidic OER, limiting industrial applications.

Purpose of the Study:

  • To develop a spin-polarization-mediated strategy to create ferromagnetism in antiferromagnetic RuO2.
  • To enhance the acidic OER activity of RuO2 through dilute manganese (Mn2+) doping.

Main Methods:

  • Dilute Mn2+ doping of RuO2 to induce ferromagnetism.
  • Element-selective X-ray magnetic circular dichroism (XMCD) to probe magnetic coupling.
  • First-principles calculations to interpret magnetic interactions.
  • Electrochemical measurements to evaluate OER activity and stability.

Main Results:

  • Ferromagnetic coupling between Mn and Ru ions was confirmed, consistent with the Goodenough-Kanamori rule.
  • Mn-doped RuO2 (Mn-RuO2) exhibited enhanced OER activity, with a low overpotential of 143 mV at 10 mA cm-2.
  • Magnetic field significantly enhanced OER activity and stability, showing negligible decay over 480 hours.
  • Intrinsic turnover frequency improved to 5.5 s-1 at 1.45 VRHE.

Conclusions:

  • The developed spin-engineering strategy effectively enhances acidic OER activity and stability in RuO2.
  • This work presents a new avenue for designing efficient electrocatalysts by leveraging spin properties.