Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

3.6K
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...
3.6K
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation

8.3K
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.
8.3K
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration02:40

Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration

9.4K
Introduction
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.       
9.4K
Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

12.9K
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...
12.9K
Hydrolysis of Chlorobenzene to Phenol: Dow Process01:10

Hydrolysis of Chlorobenzene to Phenol: Dow Process

3.4K
Simple aryl halides do not react with nucleophiles under normal conditions. However, the reaction can proceed under drastic conditions involving high temperatures and high pressure to give the substituted products. For example, chlorobenzene is converted to phenol using aqueous sodium hydroxide at 350 °C under high pressure by the Dow process. The reaction follows an elimination-addition mechanism involving a benzyne intermediate. Here, the chloride ion is...
3.4K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

2.0K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
2.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Synthesis of polymethylene-linked bis(cyclobutane-fused chromanones) mediated by gold photocatalysis.

Organic & biomolecular chemistry·2026
Same author

Guanidine-based azines from N-heterocyclic carbene (NHC)-derived selenoureas and diazo compounds: synthesis, structural diversification, and biological evaluation.

Organic & biomolecular chemistry·2026
Same author

A Well-Defined Cu─NHC (NHC═N─Heterocyclic Carbene) Complex for Energy-Transfer Photocatalysis.

Chemistry (Weinheim an der Bergstrasse, Germany)·2026
Same author

Mechanochemically assembled organometallic complexes: a mechanistic study.

Chemical science·2026
Same author

Gold(I)-indomethacin anticancer candidates with anti-breast cancer stem cell properties.

Dalton transactions (Cambridge, England : 2003)·2026
Same author

Challenges in data-driven catalysis modelling: case study on palladium-NHC catalyzed Suzuki-Miyaura reactions.

Chemical science·2026

Related Experiment Video

Updated: Oct 27, 2025

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
09:37

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry

Published on: October 18, 2019

9.8K

Platinum-Catalyzed Alkene Hydrosilylation: Solvent-Free Process Development from Batch to a Membrane-Integrated

Tahani A C A Bayrakdar1, Benon P Maliszewski1, Fady Nahra1,2

  • 1Department of Chemistry, Ghent University, Krijgslaan 281, S-3, 9000, Ghent, Belgium.

Chemsuschem
|July 22, 2021
PubMed
Summary
This summary is machine-generated.

This study integrates membrane separation with platinum-catalyzed hydrosilylation for efficient olefin conversion. A novel platinum catalyst was successfully recovered in high yield after a single-step reaction and separation process.

Keywords:
continuous processeshomogeneous catalysishydrosilylationorganic solvent nanofiltrationplatinum

More Related Videos

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
12:08

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes

Published on: June 24, 2022

3.7K
Hydrogen Production and Utilization in a Membrane Reactor
10:00

Hydrogen Production and Utilization in a Membrane Reactor

Published on: March 10, 2023

2.7K

Related Experiment Videos

Last Updated: Oct 27, 2025

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
09:37

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry

Published on: October 18, 2019

9.8K
Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
12:08

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes

Published on: June 24, 2022

3.7K
Hydrogen Production and Utilization in a Membrane Reactor
10:00

Hydrogen Production and Utilization in a Membrane Reactor

Published on: March 10, 2023

2.7K

Area of Science:

  • Catalysis
  • Separation Science
  • Materials Chemistry

Background:

  • Platinum-catalyzed hydrosilylation is crucial for olefin functionalization.
  • Efficient catalyst recovery and separation are key challenges in homogeneous catalysis.
  • Membrane technology offers potential for integrated reaction and separation processes.

Purpose of the Study:

  • To investigate the integration of membrane separation with platinum-catalyzed hydrosilylation.
  • To optimize a platinum catalyst and membrane for efficient, solvent-free olefin conversion.
  • To demonstrate a single-step reaction and catalyst separation process.

Main Methods:

  • Optimization of platinum catalysts, including [Pt(IPr*)(dms)Cl2] and [Pt(SIPr)(dms)Cl2], in batch hydrosilylation reactions.
  • Screening of membranes to identify suitable filtration conditions for catalyst separation.
  • Continuous flow hydrosilylation of 1-octene using the optimized catalyst and membrane separation.

Main Results:

  • [Pt(IPr*)(dms)Cl2] exhibited superior catalytic activity compared to [Pt(SIPr)(dms)Cl2].
  • Efficient separation of the platinum catalyst was achieved using the Borsig oNF-2 membrane under solvent-free conditions.
  • The intact catalyst was recovered in 80% yield after the integrated process.

Conclusions:

  • The integration of membrane separation with platinum-catalyzed hydrosilylation is a viable and efficient process.
  • This approach enables a single-step reaction and catalyst separation, enhancing process sustainability.
  • High catalyst recovery rates were achieved, facilitating catalyst reuse and reducing waste.