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Updated: Jul 20, 2025

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
A new binuclear Ni(II) complex, an effective A3-coupling catalyst in solvent-free condition
Ayda Sheykhi1, Ali Akbar Khandar1, Jan Janczak2
1Department of Inorganic Chemistry, Faculty of Chemistry, University of Tabriz, P.O. Box 5166616471, Tabriz, Iran.
A novel binuclear nickel(II) complex efficiently catalyzes the synthesis of propargylamines from aldehydes, amines, and acetylenes. This reusable catalyst system operates under solvent-free conditions, offering a green chemistry approach.
Area of Science:
- Inorganic Chemistry
- Organic Synthesis
- Catalysis
Background:
- Binuclear metal complexes offer unique catalytic properties.
- Propargylamines are valuable synthetic intermediates.
- Solvent-free reactions are desirable for green chemistry.
Purpose of the Study:
- To synthesize and characterize a novel binuclear nickel(II) complex.
- To investigate the catalytic activity of the complex in organic synthesis.
- To explore the reusability of the catalytic system.
Main Methods:
- Synthesis of [Ni2(en)4(ox)](ClO4)2 (1) from nickel(II) chloride, ethylenediamine, ammonium oxalate, and sodium perchlorate.
- X-ray crystallography and infra-red spectroscopy for structural determination.
- One-pot reaction of aldehydes, amines, and acetylenes under solvent-free conditions.
Main Results:
- Successful isolation and structural elucidation of the binuclear nickel(II) complex.
- Efficient one-pot synthesis of propargylamines with good yields.
- Demonstration of catalyst reusability over five reaction cycles.
Conclusions:
- The newly synthesized binuclear nickel(II) complex is an effective catalyst for propargylamine synthesis.
- The catalytic system is efficient, operates under solvent-free conditions, and is reusable.
- This work presents a sustainable approach to propargylamine synthesis.
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