Copyright (c) 2025 Kingsley Michieka

This work is licensed under a Creative Commons Attribution 4.0 International License.
Cationic Iron Half-Sandwich Complexes of Aminopyridines: Synthesis and Characterisation
Corresponding Author(s) : Kingsley Michieka
Asian Journal of Chemistry,
Vol. 38 No. 1 (2026): Vol 38 Issue 1, 2026
Abstract
The reaction of [(η5-C5H5)Fe(CO)2]+, with the aminopyridine ligands lead to formation of cationic organometallic complexes of the general formula [(η5-C5H5)Fe(CO)2L]+ (where L = 2-Apy, 3-Apy, 4-Apy and Apy = aminopyridine). These ligands have the ability to coordinate to a metal center in monodentate fashion via the pyridine ring or amine nitrogen atoms, can form chelate complexes with one metal center or bridge two metal ions. Spectroscopic data (FTIR, 1H and 13C NMR and elemental analysis) collected for the five metal complexes is consistent with monodenate coordination mode through the pyridyl nitrogen in complexes 2, 3 and 4 atoms and amine nitrogen in complexes 1 and 4.
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J.L. Templeton, J. Am. Chem. Soc., 101, 4906 (1979); https://doi.org/10.1021/ja00511a020 DOI: https://doi.org/10.1021/ja00511a020
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