<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Kilbas B</dc:creator>
  <dc:creator>Mirtschin S</dc:creator>
  <dc:creator>Riis-Johannessen T</dc:creator>
  <dc:creator>Scopelliti R</dc:creator>
  <dc:creator>Severin K</dc:creator>
  <dc:date>2012</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Ruthenium complexes with bridging dicarboxylate ligands were combined with 1,2-di-4-pyridylethylene (dpe), 2,4,6-tri-4-pyridyltriazine (4-tpt), or 2,4,6-tri-3-pyridyltriazine (3-tpt) to give a tetranuclear rectangle or hexanuclear coordination cages. The cages display a trigonal-prismatic geometry, as evidenced by single-crystal X-ray crystallography. The 4-tpt-based cages are able to encapsulate polyaromatic molecules such as pyrene, triphenylene, or coronene, whereas the 3-tpt-based cages were found to be incompetent hosts for these guests.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/27991</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/ic300330p</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/22571390</dc:relation>
  <dc:source>Inorganic chemistry. - 2012</dc:source>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Dicarboxylate-bridged ruthenium complexes as building blocks for molecular nanostructures.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>