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ALTINÖLÇEK GÜLTEKİN, NURAY

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ALTINÖLÇEK GÜLTEKİN

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    Carbazole-based D-π-A molecules: Determining the photophysical properties and comparing ICT effects of π-spacer and acceptor groups
    (Elsevier, 2021-04-11) Altınölçek, Nuray; Battal, Ahmet; Vardallı, Cemre Nur; Tavaslı, Mustafa; Yu, Holly A.; Peveler, William J.; Skabara, Peter J.; ALTINÖLÇEK GÜLTEKİN, NURAY; Vardalli, Cemre Nur; TAVASLI, MUSTAFA; Bursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.; 0000-0002-9466-1111; JCN-8292-2023 ; EDG-8300-2022 ; AAB-1630-2020
    4-(9'-Hexylcarbazol-3'-yl)benzaldehyde (Cz-Ph-CHO: 4 ) and 4-(9'-hexylcarbazol-3'- yl)benzylidenemalononitrile (Cz-Ph-CN: 5 ) were synthesised with the structure of D-pi-A,where carbazole, phenylene and formyl/dicyanovinyl groups act as electron donor (D), pi-spacer (pi) and electron acceptor (A) units, respectively. The thermal, electrochemical, optical and intramolecular charge transfer (ICT) properties of compounds 4 and 5 were investigated. Compounds 4 and 5 , in particular their ICT behaviour, were also compared with the closely related structure, 2-(9'-hexylcarbazol-3'-yl)-5-pyridinecarbaldehyde (Cz-Py-CHO: 7 ). For the purpose of tuning chemical structure to obtain targeted properties, electrochemical data and absorption and emission measurements suggest that the dicyanovinyl unit in compound 5 is a better acceptor than formyl in compound 4, and that pyridine in compound 7 is a better pi-spacer than benzene in compound 4 , in exerting ICT characteristics such as fluorosolvatochromism and Stokes shifts.
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    A red-orange carbazole-based iridium(III) complex: Synthesis, thermal, optical and electrochemical properties and OLED application
    (Elsevier Science, 2021-07-21) Altınölçek, Nuray; Battal, Ahmet; Tavaslı, Mustafa; Cameron, Joseph; Peveler, William J.; Yu, Holly A.; Skabara, Peter J.; Fairbairn, Nicola J.; Hedley, Gordon J.; ALTINÖLÇEK GÜLTEKİN, NURAY; TAVASLI, MUSTAFA; Bursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.; 0000-0002-9466-1111; JCN-8292-2023; AAB-1630-2020
    A novel heteroleptic iridium(III) acetylacetonate (acac) complex, (L-5-CHO)(2)Ir(acac) (3b), was synthesised from 2-(9'-hexylcarbazole-3'-yl)-5-formylpyridine (L-5-CHO) (1b). The complex 3b was determined to be thermally and electrochemically stable. The photoluminescence properties of the compound were studied, with a dichloromethane solution of 3b giving structureless emission at 662 nm, showing that the formyl group red-shifted the emission by 151 nm compared to the parent complex. Complex 3b was also shown to possess a moderate photoluminescence quantum yield (67%) and a short emission lifetime (tau = 280 ns). Organic light-emitting diodes (OLEDs) were fabricated with a solution-processed emissive layer (EML) consisting of poly(N-vinylcarbazole) (PVK), 2-(4-tert-butylphenyl)-5-(4-biphenylyl)-1,3,4-oxadiazole (PBD) and iridium complex (3b). The OLEDs containing complex 3b showed red-orange electroluminescence (EL) at 624 nm. The influence of the host materials was studied and the best performance was achieved with both PVK and PBD in the emissive layer, with the resulting OLEDs exhibiting a current efficiency of 0.84 cd/A, a power efficiency of 0.20 lm/W, and an external quantum efficiency (EQE) of 0.66% at a brightness of 2548 cd/m(2).