1 Ocak 2016 Dergi makalesi Açık Erişim

Turkoglu, G.; Cinar, M. E.; Buyruk, A.; Tekin, E.; Mucur, S. P.; Kaya, K.; Ozturk, T.

Dublin Core

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  <dc:creator>Turkoglu, G.</dc:creator>
  <dc:creator>Cinar, M. E.</dc:creator>
  <dc:creator>Buyruk, A.</dc:creator>
  <dc:creator>Tekin, E.</dc:creator>
  <dc:creator>Mucur, S. P.</dc:creator>
  <dc:creator>Kaya, K.</dc:creator>
  <dc:creator>Ozturk, T.</dc:creator>
  <dc:date>2016-01-01</dc:date>
  <dc:description>Two novel D-A (donor-acceptor) and one D-A-D small molecules containing mesitylborane as an acceptor and triphenylamine as a donor, linked through a thieno[3,2-b]thiophene p-conjugated spacer, are synthesized and characterized. Their photo- and electrochemical properties were investigated by experimental and computational studies. The emission quantum efficiencies were determined to be between 46% and 68% in THF. Their solid-state quantum yields were recorded up to 42%. The fabricated electroluminescent devices as emitting materials showed sky-blue to yellowish green emissions. Their devices exhibit high performance with a turn-on voltage, maximal brightness, and highest luminescence efficiency of up to 4.0 V, 1200 cd m(-2) and 1.13 cd A(-1), respectively. These results pave new avenues for the future molecules possessing D and A units connected via fused thiophenes.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/90283</dc:identifier>
  <dc:identifier>oai:zenodo.org:90283</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 MATERIALS CHEMISTRY C 4(25) 6045-6053</dc:source>
  <dc:title>Novel organoboron compounds derived from thieno[3,2-b]thiophene and triphenylamine units for OLED devices</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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