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Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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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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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.
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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Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

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Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
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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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Nitriles to Amines: LiAlH4 Reduction00:55

Nitriles to Amines: LiAlH4 Reduction

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Nitriles are reduced to amines in the presence of strong reducing agents like lithium aluminum hydride through a typical nucleophilic acyl substitution. The reaction requires two equivalents of the reducing agent. The reducing agent acts as a source of hydride ions.
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Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation01:28

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Unlike the easy catalytic hydrogenation of an alkene double bond, hydrogenation of a benzene double bond under similar reaction conditions does not take place easily. For example, in the reduction of stilbene, the benzene ring remains unaffected while the alkene bond gets reduced. Hydrogenation of an alkene double bond is exothermic and a favorable process. In contrast, to hydrogenate the first unsaturated bond of benzene, an energy input is needed; that is, the process is endothermic. This is...
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Updated: May 16, 2025

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
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l-Arginine-Functionalized Pd-Ni Catalyst Enhances Direct H2O2 Synthesis in Microreactors.

Xuan Chen1, Zheng Chen1, Lang Wu1

  • 1School of Chemistry and Chemical Engineering, Guizhou Key Laboratory for Green Chemical and Clean Energy Technology, Guizhou University, Guiyang, Guizhou 550025, China.

Langmuir : the ACS Journal of Surfaces and Colloids
|May 14, 2025
PubMed
Summary

This study developed a novel l-arginine functionalized palladium-nickel catalyst for efficient direct hydrogen peroxide (H2O2) synthesis. The catalyst achieved high yields and stability, offering a promising route for H2O2 production.

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Area of Science:

  • Catalysis
  • Materials Science
  • Chemical Engineering

Background:

  • Direct synthesis of hydrogen peroxide (H2O2) is crucial for various industrial applications.
  • Developing stable and highly active catalysts for H2O2 production remains a significant challenge.
  • Palladium-based catalysts are known for their activity but often require specific conditions or modifications.

Purpose of the Study:

  • To develop a novel l-arginine (LA)-functionalized Pd-Ni catalyst for direct H2O2 synthesis.
  • To investigate the catalytic activity, stability, and underlying mechanism of the functionalized catalyst.
  • To propose a systematic strategy for designing efficient Pd-based catalysts for H2O2 production.

Main Methods:

  • Synthesis of an l-arginine (LA)-functionalized Pd-Ni catalyst.
  • Direct synthesis of H2O2 using a self-designed microreactor at ambient conditions.
  • Catalytic activity evaluation, characterization (e.g., electronic structure), and simulation studies.

Main Results:

  • Achieved a high H2O2 yield of 574.31 g kg_cat⁻¹ h⁻¹ with a concentration of 4.05 wt % per hour.
  • The LA-functionalized Pd-Ni catalyst demonstrated high stability over five cycles with online activation.
  • Ni doping and LA-functionalization were shown to synergistically modulate the electronic structure of Pd, enhancing catalytic performance.

Conclusions:

  • The LA-functionalized Pd-Ni catalyst offers an efficient and stable pathway for direct H2O2 synthesis.
  • Modulation of the electronic structure of Pd by Ni doping and LA-functionalization is key to improved performance.
  • This study presents a viable strategy for designing advanced Pd-based catalysts for direct H2O2 production.