Coordination compounds consist of a central metal atom or ion and coordinated ligands. This thesis focuses on the coordination compounds of zinc(II), using [Zn(quin)$_2$(H$_2$O)] as a starting compound, in which quin− denotes the ligand quinaldinate. It binds to the zinc(II) ion in a N,O-bidentate chelating manner. Quinaldinate was chosen because of its strong chelating interaction with the metal ion, which limits the number of possible reaction products. The reactions were carried out with the following amino alcohols: 2-amino-1-propanol (2a1pOH), 2-amino-2-methyl-1-propanol (2a2m1pOH), 2-amino-1-butanol (2a1bOH), 1-amino-2-propanol (1a2pOH), 1-amino-2-methyl-2-propanol (1a2m2pOH), 1-amino-2-butanol (1a2bOH). The goal was to substitute coordinated water with an amino alcohol. Amino alcohols are organic compounds with two functional groups, amino and hydroxyl, both of which can act as Lewis bases and thus bind to a metal ion.
The reactions were carried out under different conditions: in an autoclave at 105 °C, at room temperature and under reflux conditions. In the first two cases, acetonitrile was used as a solvent, and nitromethane was used in reflux reactions. The reactions were carried out using different amounts of amino alcohol and different reaction times.
The results varied considerably among the individual amino alcohols. In reactions with 2a1pOH and 2a1bOH, one amino alcohol coordinated to the zinc(II) ion, and in reactions with 1a2m2pOH and 1a2bOH, two were bound in a trans configuration. In reactions with 1a2bOH, in addition to the trans product, the cis product was also isolated. Reactions with 1a2pOH yielded three different products: a coordination compound with one amino alcohol, a coordination compound with two, and an ionic compound [Zn(1a2pOH)$_3$]quin$_2$. In one case, the reaction with 2a1pOH also led to the formation of a coordination polymer. With 2a2m1pOH, no product was isolated.
The obtained products were characterized by various methods. Infrared (IR) spectroscopy and nuclear magnetic resonance (NMR) spectroscopy were used. The crystals that formed during the synthesis were analyzed by single-crystal X-ray diffraction, which provided detailed information about the structures of the compounds.
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