Comparative Review of O,O′-, N,O-, and N,N′-Bidentate Ligands: Structural and Electronic Properties of β-Diketones, Enaminones, and β-Diketiminates

'-bidentate ligands. Overall, the comparison demonstrates that donor atom substitution within a conserved conjugated scaffold provides a systematic approach to tuning acidity, coordination behaviour, and redox properties, offering a coherent framework for understanding structure-property relationships in 1,3-dicarbonyl-derived chelating ligands.

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Publication Details

Journal
Molecules
Published
2026-04-07
DOI
https://doi.org/10.3390/molecules31071223
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
Field-Weighted Citation Impact
0.00

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article

Comparative Review of O,O′-, N,O-, and N,N′-Bidentate Ligands: Structural and Electronic Properties of β-Diketones, Enaminones, and β-Diketiminates

Jeanet Conradie
Molecules
Synthesis and Characterization of Pyrroles
article

Comparative Review of O,O′-, N,O-, and N,N′-Bidentate Ligands: Structural and Electronic Properties of β-Diketones, Enaminones, and β-Diketiminates

Jeanet Conradie
article en

Abstract

'-bidentate ligands. Overall, the comparison demonstrates that donor atom substitution within a conserved conjugated scaffold provides a systematic approach to tuning acidity, coordination behaviour, and redox properties, offering a coherent framework for understanding structure-property relationships in 1,3-dicarbonyl-derived chelating ligands.

MoleculesVol. 31(7)
University of the Free State (ZA)
National Research Foundation, Universiteit van die Vrystaat
Openalex Percentile: Top 32%
Synthesis and Characterization of Pyrroles
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