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Catalysis

Catalysis

The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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...

[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.

Diels–Alder Reaction: Characteristics of Dienes

Diels–Alder Reaction: Characteristics of Dienes

The Diels–Alder reaction brings together a diene and a dienophile to form a six-membered ring. Both components have unique characteristics that influence the rate of the reaction.
Characteristics of the diene
Conformation
The simplest example of a diene is 1,3-butadiene, an acyclic conjugated π system. At room temperature, the molecule exists as a mixture of s-cis and s-trans conformers by virtue of rotation around the carbon–carbon single bond. Although the s-trans isomer is...

Diels–Alder Reaction: Characteristics of Dienophiles

Diels–Alder Reaction: Characteristics of Dienophiles

In a Diels–Alder reaction, the diene is usually an electron-rich system and acts as a nucleophile, whereas the dienophile is electron-deficient and functions as an electrophile. Much like the diene, the nature of the dienophile significantly impacts the outcome of the reaction.
Characteristics of Dienophiles
Generally, the best dienophiles are alkenes containing electron-withdrawing substituents such as carbonyl, nitrile, and nitro groups. The feasibility of a Diels–Alder reaction depends...

Ziegler–Natta Chain-Growth Polymerization: Overview

Ziegler–Natta Chain-Growth Polymerization: Overview

Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...

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Updated: Sep 30, 2025

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs

Published on: January 17, 2020

Heterogeneous Dendrimer-Based Catalysts.

Eduard Karakhanov¹, Anton Maximov², Anna Zolotukhina²

¹Department of Petroleum Chemistry and Organic Catalysis, Moscow State University, 119991 Moscow, Russia.

|March 10, 2022

Summary

This review covers advances in dendritic catalysis, focusing on heterogeneous dendrimer-based catalysts. These catalysts offer easy separation and high efficiency for various chemical reactions.

Keywords:

cross-coupling dendrimers heterogeneous catalysis hydrogenation nanocatalysis supramolecular chemistry

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

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HKUST-1 as a Heterogeneous Catalyst for the Synthesis of Vanillin

HKUST-1 as a Heterogeneous Catalyst for the Synthesis of Vanillin

Published on: July 23, 2016

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Last Updated: Sep 30, 2025

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs

Published on: January 17, 2020

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

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

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HKUST-1 as a Heterogeneous Catalyst for the Synthesis of Vanillin

HKUST-1 as a Heterogeneous Catalyst for the Synthesis of Vanillin

Published on: July 23, 2016

Area of Science:

Catalysis
Materials Science
Organic Chemistry

Background:

Dendrimer-based catalysts offer unique properties for chemical synthesis.
Heterogeneous catalysts are desirable for ease of separation and recyclability.

Purpose of the Study:

To review advances in heterogeneous dendrimer-based catalysts over the past two decades.
To highlight synthesis approaches and applications in key chemical transformations.

Main Methods:

Review of literature on dendrimer synthesis and immobilization techniques.
Analysis of applications in hydrogenation, oxidation, and cross-coupling reactions.
Consideration of magnetically separable dendritic catalysts.

Main Results:

Three primary methods for synthesizing immobilized heterogeneous dendrimer-based catalysts are discussed: impregnation/adsorption, covalent grafting, and cross-linking.
These catalysts can be easily separated and stored, similar to traditional heterogeneous catalysts.
They maintain high efficiency comparable to homogeneous dendritic catalysts.

Conclusions:

Heterogeneous dendrimer-based catalysts represent a significant advancement in catalysis.
The described synthesis strategies enable the development of efficient and recyclable catalytic systems.
Future research can further explore their application in diverse chemical processes.