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Turnover Number and Catalytic Efficiency01:19

Turnover Number and Catalytic Efficiency

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The turnover number of an enzyme is the maximum number of substrate molecules it can transform per unit time. Turnover numbers for most enzymes range from 1 to 1000 molecules per second. Catalase has the known highest turnover number, capable of converting up to 2.8×106 molecules of hydrogen peroxide into water and oxygen per second. Lysozyme has the lowest known turnover number of half a molecule per second.
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Catalytically Perfect Enzymes01:07

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The theory of catalytically perfect enzymes was first proposed by W.J. Albery and J. R. Knowles in 1976. These enzymes catalyze biochemical reactions at high-speed. Their catalytic efficiency values range from 108-109 M-1s-1. These enzymes are also called 'diffusion-controlled' as the only rate-limiting step in the catalysis is that of the substrate diffusion into the active site. Examples include triose phosphate isomerase, fumarase, and superoxide dismutase.
 
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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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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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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.
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Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

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Introduction
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Updated: Feb 7, 2026

Aqueous Droplets Used as Enzymatic Microreactors and Their Electromagnetic Actuation
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Aqueous Droplets Used as Enzymatic Microreactors and Their Electromagnetic Actuation

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Cucurbit[7]uril-based high-performance catalytic microreactors.

Xiaohe Ren1, Ziyi Yu, Yuchao Wu

  • 1Melville Laboratory for Polymer Synthesis, Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK. oas23@cam.ac.uk.

Nanoscale
|July 28, 2018
PubMed
Summary
This summary is machine-generated.

Researchers developed novel catalytic microreactors using supramolecular chemistry. Metallic nanoparticles immobilized on microchannels offer high catalytic activity without complex separation, enabling efficient, reusable reactions.

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Area of Science:

  • Supramolecular Chemistry
  • Materials Science
  • Chemical Engineering

Background:

  • Microfluidic devices are increasingly used for catalytic reactions.
  • Immobilizing metallic nanoparticles (NPs) on microchannel walls is crucial for efficient catalysis but remains challenging.
  • Current methods often require complex catalyst separation and recycling.

Purpose of the Study:

  • To develop a facile method for immobilizing metallic NPs onto microchannels for catalytic applications.
  • To create multifunctional, high-performance in situ catalytic platforms using supramolecular complexation.
  • To enhance catalytic efficiency by leveraging the high surface area to volume ratio of microreactors.

Main Methods:

  • Utilized cucurbit[7]uril (CB[7]) and methyl viologen for supramolecular complexation.
  • Immobilized metallic NPs onto microchannel walls via the CB[7] complex.
  • Fabricated catalytic microreactors based on this supramolecular approach.

Main Results:

  • Demonstrated a facile preparation of CB[7]-based catalytic microreactors.
  • Achieved remarkable catalytic activity due to high surface area to volume ratio.
  • Eliminated the need for post-reaction separation and catalyst recycling.
  • Showcased the versatility of CB[7] in complexing various metallic NPs.

Conclusions:

  • CB[7]-based catalytic microreactors offer a highly efficient and reusable platform for catalysis.
  • Supramolecular complexation provides a simple yet effective method for NP immobilization in microchannels.
  • This approach significantly simplifies catalytic processes, moving beyond conventional heterogeneous reactions.