Related Experiment Video
Updated: Apr 18, 2026

Generation of Zerovalent Metal Core Nanoparticles Using n-2-aminoethyl-3-aminosilanetriol
Published on: February 11, 2016
Stable carboxylic acid derivatized alkoxy silanes
A Feinle1, S Flaig, M Puchberger
1Materials Chemistry, Paris Lodron University Salzburg, Hellbrunner Str. 34, A-5020 Salzburg, Austria. nicola.huesing@sbg.ac.at.
This study presents a simple one-pot reaction to create novel organofunctional silanes. These silanes contain both carboxy and alkoxy groups, synthesized efficiently using platinum(IV) dioxide catalysis.
Area of Science:
- Organometallic Chemistry
- Materials Science
Background:
- Hydrosilylation reactions are crucial for synthesizing organosilicon compounds.
- Developing efficient methods for creating multifunctional silanes is an ongoing challenge.
Purpose of the Study:
- To develop a convenient and straightforward one-pot method for synthesizing organofunctional silanes.
- To combine carboxy and alkoxy functionalities within a single molecule.
Main Methods:
- One-pot hydrosilylation reaction of unsaturated carboxylic acids with trialkoxysilanes.
- Catalysis using platinum(IV) dioxide.
Main Results:
- Achieved excellent yields of organofunctional silanes.
- Successfully combined carboxy and alkoxy groups in the synthesized molecules.
Conclusions:
- The developed method offers an efficient route to valuable organofunctional silanes.
- This approach simplifies the synthesis of molecules with dual functionalities.
Related Concept Videos
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Alkynes to Carboxylic Acids: Oxidative Cleavage
Preparation of Carboxylic Acids: Hydrolysis of Nitriles
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
α-Halogenation of Carboxylic Acid Derivatives: Overview
Preparation of Aldehydes and Ketones from Nitriles and Carboxylic Acids
Reducing carboxylic acid derivatives like acyl chlorides (RCOCl), esters (RCO2R′), and nitriles (RCN) using milder aluminum hydride agents like lithium tri-tert-butoxyaluminum hydride [LiAlH(O-t-Bu)3] and diisobutylaluminum hydride [DIBAL-H]...

