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  <ref-type name="Thesis">32</ref-type>
  <contributors>
    <authors>
      <author>Sturm, Lisa</author>
      <author>Oppel, Iris Marga</author>
      <author>Albrecht, Markus</author>
    </authors>
    <subsidiary-authors>
      <author>151520</author>
      <author>150000</author>
    </subsidiary-authors>
  </contributors>
  <titles>
    <title>Einfluss von Pseudohalogeniden und Carboxylaten auf die Komplexierung zweiwertiger Metallionen durch Tris(2-pyridinylen-N-oxid)triaminoguanidin</title>
  </titles>
  <periodical/>
  <publisher>RWTH Aachen University</publisher>
  <pub-location>Aachen</pub-location>
  <language>German</language>
  <pages>1 Online-Ressource : Illustrationen</pages>
  <number/>
  <volume/>
  <abstract>C3-symmetric triaminoguanidine based ligands are established as triangular building blocks in supramolecular compounds like polymers or discrete monomers, dimers, and polyhedra. The reaction of tris(2-pyridinylene-N-oxide)triaminoguanidine with zinc(II) carboxylates in presence of (pseudo)halides results in protein-sized metallocycles consisting of twelve ligands linked by octahedrally coordinated zinc(II) centers. Besides crystals of the metallocycles, the crystallization of carboxylate-bridged coordination di/polymers is observed in the same reaction vessel. To address this issue, the influence of the solvent, the chain length of the carboxylate, the co-ligands and their stoichiometry is investigated, while other factors are kept as constant as possible. In this way, a sensitive dependence of the binding motif on the stoichiometric pseudohalide-carboxylate ratio was revealed. Small or no amounts of pseudohalide combined with sufficient equivalents of carboxylate lead to the formation of carboxylate-bridged di/polymers. Increasing the pseudohalide stoichiometry results in the crystallization of mixed compounds and finally of metallocycles. By adjusting the co-ligand stoichiometry, crystallization of a desired compound can be predicted and selectively induced. Applying this principle to the chemically related cadmium(II) yields in a series of carboxylate-bridged di/polymers, whereas the addition of thiocyanate gives a cadmium(II)-bridged structure, which can be considered as metallocycle fragment. Cadmium(II) prefers coordination numbers of six and higher due to its ionic radius, which inhibits the formation of a metallocycle. Cobalt(II) ions instead built up polymers and metallocycles showing the same co-ligand dependence as zinc(II). Magnetic measurements revealed predominantly antiferromagnetic behavior of these compounds due to short Co(II)-Co(II) distances. In heterometallic metallocycles, zinc(II) ions may isolate the cobalt(II) centers, which could probably result in very large discrete molecules with interesting magnetic properties.</abstract>
  <notes>
    <note>Veröffentlicht auf dem Publikationsserver der RWTH Aachen University ; </note>
    <note>Dissertation, RWTH Aachen University, 2022 ; </note>
  </notes>
  <label>2, ; PUB:(DE-HGF)11, ; </label>
  <keywords/>
  <accession-num/>
  <work-type>Dissertation / PhD Thesis</work-type>
  <volume>Dissertation</volume>
  <publisher>RWTH Aachen University</publisher>
  <dates>
    <pub-dates>
      <year>2022</year>
    </pub-dates>
    <year>2022</year>
  </dates>
  <accession-num>RWTH-2022-09881</accession-num>
  <year>2022</year>
  <urls>
    <related-urls>
      <url>https://publications.rwth-aachen.de/record/854946</url>
    </related-urls>
  </urls>
</record>

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