Related Experiment Video
Updated: May 24, 2026

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
Published on: August 23, 2018
Making expensive dirhodium(II) catalysts cheaper: Rh(II) recycling methods
Nuno R Candeias1, Carlos A M Afonso, Pedro M P Gois
1Research Institute for Medicines and Pharmaceutical Sciences (iMed.UL), Faculty of Pharmacy, University of Lisbon, Av. Prof. Gama Pinto, 1649-003 Lisbon, Portugal. nunocandeias@ff.ul.pt
Expensive dirhodium(II) catalysts are vital in organic synthesis. This review details methods for recovering and reusing these valuable metal complexes, promoting sustainable chemistry in catalysis.
Area of Science:
- Catalysis
- Organic Synthesis
- Sustainable Chemistry
Background:
- Dirhodium(II) complexes are essential catalysts in organic synthesis, facilitating numerous transformations and the creation of diverse compounds, including drug intermediates.
- The high cost of dirhodium complexes necessitates the development of efficient recovery and reuse strategies for economic and environmental viability.
Purpose of the Study:
- To provide a comprehensive overview of existing methods for recovering and reusing dirhodium(II) metal complexes in catalytic applications.
- To highlight strategies that support more sustainable chemical practices by enabling catalyst reutilisation.
Main Methods:
- Review of literature on homogeneous catalysis methods for dirhodium(II) complex recovery.
- Analysis of heterogenisation techniques designed to immobilize dirhodium(II) catalysts for easier separation and reuse.
- Compilation of different approaches for the recycling of dirhodium(II) catalysts.
Main Results:
- Multiple viable methods exist for the recovery and reuse of dirhodium(II) catalysts.
- Both homogeneous and heterogenised approaches offer pathways to catalyst reutilisation.
- The development of these methods contributes to greener synthetic processes.
Conclusions:
- Effective strategies for dirhodium(II) catalyst recovery and reuse are available, supporting sustainable catalysis.
- The implementation of these methods can significantly reduce waste and cost in synthetic organic chemistry.
- Further research into catalyst recycling will continue to advance green chemistry principles.
More Related Videos
10:52Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
11:44Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
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...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
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.
Catalysis
Catalysis
Heterogeneous Catalysis
Reduction of Alkenes: 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 surface of...