Taguchi-Optimized Green Synthesis of a Novel Nickel-bis-thiazoline Complex: A Bifunctional Platform for Sustainable Ullmann-type N-Arylation and Antibacterial Applications

A novel bis-thiazoline ligand and its nickel(II) complex were synthesized via an environmentally benign and mild protocol.Synthesis parameters were systematically optimized using the Taguchi Design of Experiments (DoE), achieving high yields (> 98%) and ensuring a scalable, reproducible green process. The novel Ni(II) complex was shown to be an efficient catalyst for the Ullmann-type C-N coupling, which was further utilized to synthesize mefenamic acid and its derivatives. Biological studies showed that the complex significantly enhanced the antibacterial efficacy compared to the free ligand, demonstrating its bifunctional potential in sustainable catalysis and medicinal chemistry.

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Journal
SynOpen
Published
2026-10-16
DOI
https://doi.org/10.1055/a-2983-4079
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Taguchi-Optimized Green Synthesis of a Novel Nickel-bis-thiazoline Complex: A Bifunctional Platform for Sustainable Ullmann-type N-Arylation and Antibacterial Applications

Kamel Landolsi, Abderrahmen Merghni, Jamil Kraı̈em, Thierry Ollevier et al.
SynOpen
Catalytic Cross-Coupling Reactions
article

Taguchi-Optimized Green Synthesis of a Novel Nickel-bis-thiazoline Complex: A Bifunctional Platform for Sustainable Ullmann-type N-Arylation and Antibacterial Applications

Kamel Landolsi, Abderrahmen Merghni, Jamil Kraı̈em, Thierry Ollevier, Hanen Slimi, Fraj Echouchene, Naceur Hamdi, Amina Zemam, Yosra B Abdallah
article en

Abstract

A novel bis-thiazoline ligand and its nickel(II) complex were synthesized via an environmentally benign and mild protocol.Synthesis parameters were systematically optimized using the Taguchi Design of Experiments (DoE), achieving high yields (> 98%) and ensuring a scalable, reproducible green process. The novel Ni(II) complex was shown to be an efficient catalyst for the Ullmann-type C-N coupling, which was further utilized to synthesize mefenamic acid and its derivatives. Biological studies showed that the complex significantly enhanced the antibacterial efficacy compared to the free ligand, demonstrating its bifunctional potential in sustainable catalysis and medicinal chemistry.

SynOpen
University of Monastir (TN), Higher Institute of Management (RU), Université Laval (CA), Tunis El Manar University (TN)
Université Laval, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 25%
Catalytic Cross-Coupling Reactions
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