1 Ocak 1992 Dergi makalesi Açık Erişim

GUMUS, G; OZTURK, ZZ; AHSEN, V; GUL, A; BEKAROGLU, O

Dublin Core

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  <dc:creator>GUMUS, G</dc:creator>
  <dc:creator>OZTURK, ZZ</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>New phthalocyanines (M = Cu, Zn, Ni, Co or 2H) substituted with four 17-membered trioxadiaza macrocycles have been prepared. Detosylation of aza groups with concentrated sulfuric acid simultaneously leads to sulfonated groups on the aromatic rings of the macrocyclic substituents. While the N-tosylated derivatives are soluble in organic solvents, the detosylated ones are extremely soluble in water. The electrical conductivities of the phthalocyanines measured as gold sandwiches are about 10(-12) S m-1 in vacuo and show some increase in the presence of dry air.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/103243</dc:identifier>
  <dc:identifier>oai:zenodo.org:103243</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS 16 2485-2489</dc:source>
  <dc:title>SYNTHESIS, CHARACTERIZATION AND ELECTRICAL-PROPERTIES OF PHTHALOCYANINES SUBSTITUTED WITH 17-MEMBERED TRIOXADIAZA MACROCYCLES</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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