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Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide02:44

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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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Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

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Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
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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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Radical Oxidation of Allylic and Benzylic Alcohols01:21

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Activated manganese(IV) oxide can selectively oxidize allylic and benzylic alcohols via a radical intermediate mechanism. Primary allylic alcohols are oxidized to aldehydes, while secondary allylic alcohols yield ketones. The redox reaction of potassium permanganate with an Mn(II) salt such as manganese sulfate (under either alkaline or acidic conditions), followed by thorough drying, yields the oxidizing agent: activated MnO2. While MnO2 is insoluble in the solvents used for the reaction, the...
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Reduction of Alkenes: Catalytic Hydrogenation02:13

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Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
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Oxidative Cleavage of Alkenes: Ozonolysis01:46

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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.
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Electronic Structure Modulation of AlN4 Single-Atom Catalyst for Oxygen Reduction Reaction.

Shahan Atif1, Omeshwari Yadorao Bisen1, Soumen Midya1

  • 1Materials Research Center, Indian Institute of Science, Bangalore, 560012, India.

Small (Weinheim an Der Bergstrasse, Germany)
|July 25, 2025
PubMed
Summary
This summary is machine-generated.

Researchers developed advanced aluminium single-atom catalysts (Al-N4-C) for efficient oxygen reduction reactions (ORR). These catalysts show high activity and durability, comparable to platinum, offering a promising alternative for energy applications.

Keywords:
aluminium phthalocyaninedensity functional theorydicyandiamideoxygen reduction reactionsingle atom catalystszinc‐air battery

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Catalysis

Background:

  • Mechanistic understanding of oxygen reduction reaction (ORR) in p-block metal single-atom catalysts (SACs) is limited.
  • Aluminium (Al) typically shows poor ORR activity due to strong oxygen intermediate binding.

Purpose of the Study:

  • To investigate the high intrinsic activity of AlN4 active sites in carbon nanostructures for ORR.
  • To uncover the origins of catalytic activity in Al-based SACs through electronic structure analysis.

Main Methods:

  • Comprehensive analysis of surface and bulk electronic structures.
  • Theoretical calculations including Density Functional Theory (DFT) and Bader charge analysis.
  • Fabrication and testing of Al-N4-C as cathode material in zinc-air batteries.

Main Results:

  • Atomically dispersed AlN4 sites exhibit superior ORR activity, selectivity, and durability compared to macrocyclic aluminium phthalocyanine and Pt/C.
  • Al-N4-C demonstrated stable performance over 36 hours in zinc-air batteries.
  • Charge delocalization and local coordination environment are key factors for enhanced 4e- transfer ORR activity.

Conclusions:

  • Tailoring the electronic structure and coordination environment of Al atoms optimizes the p-band center for enhanced ORR catalysis.
  • Al-based SACs offer a viable alternative to precious metal catalysts for energy conversion applications.
  • Findings provide insights for engineering main-group metal catalysts by tuning the p-band center.