1 Ocak 2007 Dergi makalesi Açık Erişim

Sarac, A. Sezal; Sarioglan, Serife Ozkara; Dziomba, Thorsten; Sezer, Esma

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/97091</identifier>
  <creators>
    <creator>
      <creatorName>Sarac, A. Sezal</creatorName>
      <givenName>A. Sezal</givenName>
      <familyName>Sarac</familyName>
    </creator>
    <creator>
      <creatorName>Sarioglan, Serife Ozkara</creatorName>
      <givenName>Serife Ozkara</givenName>
      <familyName>Sarioglan</familyName>
    </creator>
    <creator>
      <creatorName>Dziomba, Thorsten</creatorName>
      <givenName>Thorsten</givenName>
      <familyName>Dziomba</familyName>
    </creator>
    <creator>
      <creatorName>Sezer, Esma</creatorName>
      <givenName>Esma</givenName>
      <familyName>Sezer</familyName>
    </creator>
  </creators>
  <titles>
    <title>Synthesis And Electrocoating Of Indole-Thiophene Comonomer On Carbon Fiber Microelectrode, And Surface Topography By Afm</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2007</publicationYear>
  <dates>
    <date dateType="Issued">2007-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/97091</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.eurpolymj.2007.05.040</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>
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  <descriptions>
    <description descriptionType="Abstract">5,2-thiophenylindole(5,2 In-Th) comonomer is synthesized by means of palladium catalyzed Stille cross-coupling reaction with an aim of obtaining extensively conjugated, low oxidation potential comonomer relative to its corresponding monomer. The comonomer is characterized by UV-Visible, FTIR, and NMR spectroscopic techniques, and the resulting conjugated copolymer exhibited the properties of both polyindole and polythiophene (having low oxidation potential and high conductivity).</description>
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