Mainz
Hierarchische Selbstorganisation von Helicaten mit substituierten 8-Hydroxychinolinliganden
Abstract
dc:descriptionAim of this work was the synthesis of complexes with different divalent metals, starting from alkyl 8-hydroxyquinoline-7-carboxylate and 1-alkyl-3-(8-hydroxyquinolin-7-yl)urea and investigations of the monomer-dimer-equilibrium. Hydrophilic and hydrophobic ligands had been done and used successfully for hierarchical self-assembly of dinuclear, triple-stranded, helicate-type complexes, which has been studied intensivly (Build-up and disaggregation, formation of dynamic combinatorial libraries and magnetochemical properties).These results could be revealed:1. Esterification could be done in good yield to build up ligands with different properties.2. Complexation with different divalent transition metals (Zn2+, Ni2+, Co2+ and Mn2+) was successful and lead to dinuclear triple stranded helicate type complexes. The equilibrium was always shifted to the dimer.3. Assembly of a DCC by mixing of two different ligands followed by time depending ESI-MS-investigation succeed.4. Synthesis and complexation of 5-chloro-8-hydroxyquinoline-7-carbaldehyde and 1-(8-hydroxyquinolin-7-yl)ethanone had been done and lead us to the dimeric species [Li3(L)6M2]+[OAc]-.5. Neutral complexes were realised by use of 1-alkyl-3-(8-hydroxyquinolin-7-yl)urea ligands and divalent transition metals. X-ray crystallographic investigations document that the M-M-M distances are less than 3 Å. Antiferromagnetic behaviour can be found for Co(II) and Ni(II) complexes and ferromagnetic behaviour for Mn(II) by magnetochemical investigations.
Degree
thesis:*- Grantor dc:publisher
- Mainz
- Year dc:date
- 2009
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
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- Fiege, Marcel
- Contributors dc:contributor
-
- Albrecht, Markus
Subjects
dc:subject × 12Rights
dc:rights- Statement dc:rights
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- info:eu-repo/semantics/openAccess
- Language dc:language
- ger