Related Experiment Video
Updated: Jun 28, 2026

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron
Published on: August 12, 2019
Metal complexation with 2-hydroxy-6-methylpyridine-3-carboxylic acid
Veena Kushwaha1, R P Singh, M Katyal
1Department of Chemistry, University of Delhi Delhi-7, India.
This study investigated metal complexation using 2-hydroxy-6-methylpyridine-3-carboxylic acid, a ligand useful for detecting iron (III). The research determined the stability order of bivalent transition metal complexes, finding copper to be the most stable.
Area of Science:
- Coordination Chemistry
- Analytical Chemistry
Background:
- 2-hydroxy-6-methylpyridine-3-carboxylic acid is a versatile ligand.
- This compound has potential applications in analytical chemistry, particularly for metal ion detection.
Purpose of the Study:
- To investigate the complexation behavior of 2-hydroxy-6-methylpyridine-3-carboxylic acid with various metal ions.
- To determine the stability constants of the resulting metal complexes.
- To evaluate the ligand's utility in the detection and determination of iron (III).
Main Methods:
- Synthesis and characterization of metal complexes.
- Spectrophotometric and potentiometric titration methods for stability constant determination.
- Comparative analysis of complex stability across different bivalent transition metals.
Main Results:
- The ligand forms stable complexes with bivalent transition metals.
- The order of stability constants was determined as Cu > Zn > Fe > Ni > Co > Mn.
- The ligand demonstrated effectiveness in the detection and determination of iron (III).
Conclusions:
- 2-hydroxy-6-methylpyridine-3-carboxylic acid is a suitable ligand for studying transition metal complexation.
- The stability order provides insights into the coordination preferences of these metals with the ligand.
- The ligand's application in iron (III) analysis is confirmed.
More Related Videos
Related Concept Videos
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...
Complexometric Titration: Ligands
Complexation Equilibria: The Chelate Effect
Amides to Carboxylic Acids: Hydrolysis
Acid-catalyzed hydrolysis:
Hydrolysis of amides under acidic conditions yields carboxylic acids. Since the reaction occurs slowly, hydrolysis requires the conditions of heat.
The mechanism begins with the protonation of the carbonyl oxygen by the acid catalyst. The protonation makes the amide carbonyl carbon more...
EDTA: Chemistry and Properties
EDTA: Auxiliary Complexing Reagents

