1 Ocak 1997 Dergi makalesi Açık Erişim

Dabak, S; Bekaroglu, O

DataCite XML

<?xml version='1.0' encoding='utf-8'?>
<resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd">
  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/102459</identifier>
  <creators>
    <creator>
      <creatorName>Dabak, S</creatorName>
      <givenName>S</givenName>
      <familyName>Dabak</familyName>
    </creator>
    <creator>
      <creatorName>Bekaroglu, O</creatorName>
      <givenName>O</givenName>
      <familyName>Bekaroglu</familyName>
    </creator>
  </creators>
  <titles>
    <title>Synthesis Of Phthalocyanines Crosswise-Substituted With Two Alkylsulfanyl And Two Amino Groups</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>1997</publicationYear>
  <dates>
    <date dateType="Issued">1997-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/102459</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsVersionOf">10.81043/aperta.102458</relatedIdentifier>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.81043/aperta.102459</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">Crosswise-substituted phthalocyanines (4, 4a-c) with two nitro and two dodecylsulfanyl groups are synthesized by a 2:2 condensation of 1,3-dihydro-1,3-diimino-6-(n-dodecylsulfanyl)isoiminoindolenine (2) with 6-nitro-1,3,3-trichloroisoindolenine (3) in the presence of sodium methoxide, hydroquinone and triethylamine. Nitro substituents are reduced to amines by sodium sulfide and condensation of the amine groups with ferrocenylaldehyde results in a new pc with two ferrocenylimino substituents, The novel compounds are characterized by UV/vis, mass and H-1-NMR spectroscopy.</description>
  </descriptions>
</resource>