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Catalysis02:50

Catalysis

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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.
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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: Syn Dihydroxylation with Osmium Tetraoxide02:44

Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

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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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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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Phase I Oxidative Reactions: Overview01:19

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Phase I biotransformation, or functionalization, is a crucial chemical process that converts drugs and other xenobiotics into more water-soluble forms, facilitating expulsion from the body. It involves oxidative, reductive, and hydrolytic reactions that add or unveil polar functional groups on lipophilic substrates. Key players in phase I reactions are the mixed-function oxidases. Situated in liver cell microsomes, these enzymes predominantly carry out drug metabolism. They require molecular...
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Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

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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.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
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Single-Site vs. Cluster Catalysis in High Temperature Oxidations.

Pedro Serna1, Aida Rodríguez-Fernández2, Sara Yacob1

  • 1ExxonMobil Research and Engineering Co., Corporate Strategic Research, Annandale, NJ, 08801, USA.

Angewandte Chemie (International Ed. in English)
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Single platinum atoms and small platinum clusters exhibit distinct behaviors in high-temperature oxidations. Cluster size significantly impacts oxygen activation and stability, influencing catalytic performance in alkane and CO oxidation reactions.

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Area of Science:

  • Materials Science
  • Catalysis
  • Surface Chemistry

Background:

  • Understanding the role of platinum (Pt) atom and cluster size is crucial for designing efficient oxidation catalysts.
  • High-temperature oxidation processes involve complex surface reactions including oxygen dissociation and C-H bond activation.

Purpose of the Study:

  • To investigate the distinct behaviors of single Pt atoms and small Pt clusters during high-temperature oxidations.
  • To elucidate the structure-performance relationships in Pt-catalyzed oxidation reactions.

Main Methods:

  • Experimental investigation of single Pt atoms and small Pt clusters under high-temperature oxidation conditions.
  • Analysis of gas/metal/support interactions influencing catalytic activity.

Main Results:

  • Single Pt atoms and large Pt clusters (>1 nm) are ineffective for O2 activation at moderate temperatures (200°C).
  • Smaller Pt clusters (<1 nm) catalytically activate O2 but are prone to oxidative fragmentation.
  • Stable single Pt atoms are key for high-temperature alkane oxidation, with C-H cleavage being rate-determining.
  • CO combustion catalysis is predominantly driven by Pt clusters, not single atoms.

Conclusions:

  • The catalytic performance in oxidation reactions is highly sensitive to the atomic structure and size of platinum species.
  • Distinct mechanisms govern O2 activation, alkane oxidation, and CO combustion, with varying Pt nuclearity requirements.