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Related Concept Videos

Heterogeneous Catalysis01:22

Heterogeneous Catalysis

Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...
Catalysis02:50

Catalysis

The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
Catalysis01:27

Catalysis

Catalysis influences the rate of chemical reactions by providing an alternative reaction pathway with lower activation energy. A catalyst speeds up a reaction, but it is not consumed during the process. The fundamental principle of catalysis is the ability of a catalyst to alter the reaction mechanism, often introducing a more efficient pathway than the uncatalyzed process.In a catalyzed reaction, the catalyst participates directly in the reaction mechanism. It interacts with reactants to form...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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...
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

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.
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids02:04

Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids

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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Updated: Jun 19, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
10:57

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

Published on: April 10, 2018

Product protection, the key to developing high performance methane selective oxidation catalysts.

Mårten Ahlquist1, Robert J Nielsen, Roy A Periana

  • 1Materials and Process Simulation Center (MC 139-74), California Institute of Technology, Pasadena, California 91125, USA.

Journal of the American Chemical Society
|November 7, 2009
PubMed
Summary

Directly converting methane to methanol is challenging due to high C-H bond energy. A novel catalytic approach protects methanol as methyl bisulfate, enabling efficient conversion and suggesting potential for even higher performance.

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Area of Science:

  • Chemical catalysis
  • Organic synthesis

Background:

  • Direct methane to methanol conversion is thermodynamically challenging due to the high C-H bond dissociation energy of methane (105 kcal mol⁻¹).
  • Existing methods often lack selectivity or require harsh conditions.

Purpose of the Study:

  • To investigate a selective direct conversion of methane to methanol.
  • To understand the mechanism behind the success of the Catalytica catalyst.

Main Methods:

  • Utilized the Catalytica catalyst for methane conversion.
  • Analyzed the reaction pathway involving methanol protection as methyl bisulfate.

Main Results:

  • The Catalytica catalyst achieves selective methane to methanol conversion.
  • Methanol is protected as methyl bisulfate, reducing its reactivity towards the catalyst.
  • This protection mechanism is key to the catalyst's success.

Conclusions:

  • The protection of methanol as methyl bisulfate is a viable strategy for direct methane to methanol conversion.
  • This approach offers a pathway to overcome the inherent challenges of methane activation.
  • The identified mechanism suggests that higher performance limits are achievable beyond the current Catalytica system.