Related Experiment Video
Updated: Oct 20, 2025

A Simple and Efficient Protocol for the Catalytic Insertion Polymerization of Functional Norbornenes
Published on: February 27, 2017
Tris-NHC-propagated self-supported polymer-based Pd catalysts for heterogeneous C-H functionalization
Tanmoy Mandal1, Tapas Kumar Dutta2, Sunit Mohanty3
1Organometallics & Smart Materials Laboratory, Department of Chemistry, Indian Institute of Science Education and Research (IISER) Bhopal, Bhopal 462 066, India. joyanta@iiserb.ac.in.
New single-site catalysts based on coordination and organic polymers enable efficient C-H functionalization reactions. These highly active, recyclable catalysts offer promising advancements for heterogeneous catalysis.
Area of Science:
- Materials Science
- Catalysis
- Organic Chemistry
Background:
- Developing efficient heterogeneous catalysts for C-H functionalization is crucial in organic synthesis.
- Single-site catalysts offer high activity and selectivity but often suffer from poor stability and recyclability.
Purpose of the Study:
- To develop novel single-site heterogenized palladium-N-heterocyclic carbene (Pd-NHC) catalysts.
- To investigate their efficiency in oxidative arene and heteroarene C-H functionalization reactions.
Main Methods:
- Synthesized three-dimensionally propagated imidazolium-containing mesoporous coordination polymer and organic polymer-based platforms.
- Immobilized single-site Pd-NHC catalysts onto these platforms.
- Evaluated catalyst performance in directed arene halogenation and nondirected arene/heteroarene arylation reactions.
Main Results:
- The developed Pd-NHC catalysts exhibited high catalytic activity in both directed and nondirected C-H functionalization reactions.
- Excellent heterogeneity and recyclability were demonstrated for the catalyst systems.
- The catalysts were effective for both arene and heteroarene substrates.
Conclusions:
- The novel polymer-supported single-site Pd-NHC catalysts represent a significant advancement in heterogeneous C-H functionalization.
- These systems offer a promising solution for efficient, recyclable, and selective C-H activation catalysis.
- The developed platforms provide a robust foundation for future catalyst design in this field.
More Related Videos
12:19Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
Published on: November 29, 2018
19:58Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Related Concept Videos
Cationic Chain-Growth Polymerization: Mechanism
Ziegler–Natta Chain-Growth Polymerization: Overview
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...
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
Catalysis
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.