Synthesis, Photophysical and Electrochemical Properties of Novel Carbazole-Triazine Based High Triplet Energy, Solution-Processable Materials

dc.contributor.author Öner, Saliha
dc.contributor.author Aydemir, Murat
dc.contributor.author Yeşil, Fatih
dc.contributor.author Şahin, Çiğdem
dc.contributor.author Varlıklı, Canan
dc.coverage.doi 10.1016/j.dyepig.2018.06.014
dc.date.accessioned 2020-02-04T07:42:05Z
dc.date.available 2020-02-04T07:42:05Z
dc.date.issued 2018
dc.description.abstract A series of molecules; tBuCz1SiTrz, tBuCz2SiTrz and tBuCz3SiTrz, which contain carbazole unit as hole-transporting group (donor-D) and triazine unit as electron transporting group (acceptor-A) were synthesized and characterized as high-triplet energy (>2.9 eV), solution-processable bipolar emitting materials. The conjugation between the D-A groups was interrupted by using bulky tetraphenylsilane groups as spacer aiming to obtain large bandgap and high-triplet energy. The photophysical behaviors of the molecules were investigated by UV-Vis absorption, photoluminescence, phosphorescence, photoluminescence quantum yield and lifetime measurements. Solvent polarity effects were investigated on the intramolecular charge transfer (ICT) behaviour and large solvatochromic effect was observed with the increasing solvent polarity. Electrochemical properties were determined by cyclic voltammetry. All molecules showed oxidation bands arise from the carbazole groups. Reduction bands were originated from the triazine groups and the intramolecular charge transfer between D-A groups. Photophysical, electrochemical and computational characterizations addressed that tBuCz2SiTrz has the weakest ICT character, highest photoluminescence quantum yield (PLQY) and charge balance. en_US
dc.description.sponsorship TUBITAK (113Z253) and IYTE Biological Mass Spectrometry and Proteomic Laboratory en_US
dc.identifier.citation Öner, S., Aydemir, M., Yeşil, F., Şahin, Ç., and Varlıklı, C. (2018). Synthesis, photophysical and electrochemical properties of novel carbazole-triazine based high triplet energy, solution-processable materials. Dyes and Pigments, 159, 92-99. doi:10.1016/j.dyepig.2018.06.014 en_US
dc.identifier.doi 10.1016/j.dyepig.2018.06.014 en_US
dc.identifier.doi 10.1016/j.dyepig.2018.06.014
dc.identifier.issn 0143-7208
dc.identifier.scopus 2-s2.0-85048436287
dc.identifier.uri https://doi.org/10.1016/j.dyepig.2018.06.014
dc.identifier.uri https://hdl.handle.net/11147/7653
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.relation.ispartof Dyes and Pigments en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Bipolar materials en_US
dc.subject Carbazole en_US
dc.subject Charge transfer en_US
dc.subject Triazine en_US
dc.subject Cyclic voltammetry en_US
dc.title Synthesis, Photophysical and Electrochemical Properties of Novel Carbazole-Triazine Based High Triplet Energy, Solution-Processable Materials en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id 0000-0002-1081-0803
gdc.author.institutional Varlıklı, Canan
gdc.bip.impulseclass C4
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Photonics en_US
gdc.description.endpage 99 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 92 en_US
gdc.description.volume 159 en_US
gdc.description.wosquality Q1
gdc.identifier.openalex W2806379258
gdc.identifier.wos WOS:000442333700011
gdc.index.type WoS
gdc.index.type Scopus
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.downloads 2
gdc.oaire.impulse 5.0
gdc.oaire.influence 2.8147824E-9
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gdc.oaire.keywords Cyclic voltammetry
gdc.oaire.keywords Energy
gdc.oaire.keywords Polarity
gdc.oaire.keywords Carbazole
gdc.oaire.keywords Photoluminescence quantum yields
gdc.oaire.keywords Bands
gdc.oaire.keywords Molecules
gdc.oaire.keywords Intra-molecular charge transfer
gdc.oaire.keywords 540
gdc.oaire.keywords Intramolecular charge transfers
gdc.oaire.keywords Photophysical behavior
gdc.oaire.keywords Polycyclic aromatic hydrocarbons
gdc.oaire.keywords Charge transfer
gdc.oaire.keywords Triazine
gdc.oaire.keywords Electrochemical properties
gdc.oaire.keywords Synthesis (chemical)
gdc.oaire.keywords Bipolar materials
gdc.oaire.keywords Solvents
gdc.oaire.keywords Charge Transfer
gdc.oaire.keywords Solvent polarity effect
gdc.oaire.keywords Photoluminescence
gdc.oaire.keywords Quantum yield
gdc.oaire.keywords Materials
gdc.oaire.popularity 5.1404045E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
gdc.oaire.views 4
gdc.openalex.collaboration National
gdc.openalex.fwci 0.61376185
gdc.openalex.normalizedpercentile 0.71
gdc.opencitations.count 7
gdc.plumx.crossrefcites 7
gdc.plumx.mendeley 16
gdc.plumx.scopuscites 7
gdc.relation.tubitak info:eu-repo/grantAgreement/TUBITAK/KBAG/113Z253
gdc.scopus.citedcount 7
gdc.wos.citedcount 7
relation.isAuthorOfPublication.latestForDiscovery cd9c11a2-82e1-4d82-b7f4-f96eec6a9e0f
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