Related Experiment Video
Updated: Oct 14, 2025

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Cyclometallated complexes as catalysts for C-H activation and functionalization.
Janis Mikelis Zakis1,2, Tomas Smejkal1, Joanna Wencel-Delord2
1Process Chemistry Research, Syngenta Crop Protection AG, Schaffhauserstrasse 101, Stein AG 4332, Switzerland. tomas.smejkal@syngenta.com.
Researchers are developing advanced catalysts for C-H activation, focusing on tridentate pincer ligands and metallacyclic intermediates for enhanced reactivity and selectivity in Ruthenium- and Iridium-based systems.
Area of Science:
- Catalysis and Organometallic Chemistry
- Focuses on the development of novel catalysts for C-H activation reactions.
Background:
- Significant interest in C-H activation catalysts over the last two decades.
- Tridentate pincer ligands form stable C-M bonds, showing promising results.
- Mechanistic studies reveal the catalytic role of metallacyclic intermediates.
Purpose of the Study:
- Discuss recent breakthroughs in C-H activation catalysis.
- Highlight the rational design of advanced catalysts based on experimental observations.
- Emphasize the role of metallacyclic intermediates in Ru- and Ir-based systems.
Main Methods:
- Review of experimental observations and mechanistic studies.
- Focus on Ru- and Ir-based catalytic systems.
- Analysis of catalysts employing tridentate pincer ligands.
Main Results:
- Development of advanced C-H activation catalysts.
- Improved reactivity and selectivity achieved.
- Demonstration of the catalytic role of metallacyclic intermediates.
Conclusions:
- Metallacyclic intermediates play a key role in advanced C-H activation catalysis.
- Rational catalyst design has led to significant breakthroughs.
- Ruthenium and Iridium systems show particular promise.
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...
Properties of Organometallic Compounds
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
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.
Cycloaddition Reactions: MO Requirements for Thermal Activation
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction

