1 Ocak 1992 Dergi makalesi Açık Erişim

MUSLUOGLU, E; GUREK, A; AHSEN, V; GUL, A; BEKAROGLU, O

Dublin Core

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  <dc:creator>MUSLUOGLU, E</dc:creator>
  <dc:creator>GUREK, A</dc:creator>
  <dc:creator>AHSEN, V</dc:creator>
  <dc:creator>GUL, A</dc:creator>
  <dc:creator>BEKAROGLU, O</dc:creator>
  <dc:date>1992-01-01</dc:date>
  <dc:description>Unsymmetrical phthalocanines (5 - 7) with a single macrocyclic substituent are synthesized by the reaction of the boron complex of phthalonitrile (1) with the iminoisoindoline derivatives 2 - 4 of macrocyclic compounds, i.e. 15-crown-5, mono-aza-15-crown-5, and tetraazacyclotetradecane. The mono-macrocycle-substituted phthalocyanines are less soluble than the tetra-substituted one.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/103899</dc:identifier>
  <dc:identifier>oai:zenodo.org:103899</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>CHEMISCHE BERICHTE-RECUEIL 125(10) 2337-2339</dc:source>
  <dc:title>UNSYMMETRICAL PHTHALOCYANINES WITH A SINGLE MACROCYCLIC SUBSTITUENT</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
</oai_dc:dc>