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Yıl 2023, Cilt: 25, 59 - 66, 01.12.2023
https://doi.org/10.55549/epstem.1403010

Öz

Kaynakça

  • Agarwal, N., Nayak, P. K., Ali, F., Patankar, M. P., Narasimhan, K. L., & Periasamy, N. (2011). Tuning of HOMO levels of carbazole derivatives: New molecules for blue OLED. Synthetic Metals, 161(5-6), 466-473.
  • Al-Ibrahim, M., Roth, H. K., Schroedner, M., Konkin, A., Zhokhavets, U., Gobsch, G., & Sensfuss, S. (2005). The influence of the optoelectronic properties of poly (3-alkylthiophenes) on the device parameters in flexible polymer solar cells. Organic Electronics, 6(2), 65-77.
  • Ambrose, J. F., & Nelson, R. F. (1968). Anodic oxidation pathways of carbazoles: I. carbazole and N‐substituted derivatives. Journal of the Electrochemical Society, 115(11), 1159.

Synthesis and Some Electrochemical Properties of Carbazole Derivative Monomers for Optoelectronic Device Design

Yıl 2023, Cilt: 25, 59 - 66, 01.12.2023
https://doi.org/10.55549/epstem.1403010

Öz

Low-cost instruments are used to achieve high sensitivity, accuracy and precision with electrochemical techniques, making them the most suitable analytical methods used to investigate the electrochemical properties of a new molecule. Among these techniques, cyclic voltammetry, which is widely employed, allows for the determination of electronic characteristics such as molecular energy levels and orbital structure, redox properties, sensor capabilities, surface activity, and more. The carbazole molecule can undergo derivatization from various positions, allowing for alterations in its electrical and optical properties. These compounds serve as heterocyclic building blocks that can be utilized as materials for organic sensitizers and semiconductors in optoelectronic devices. Due to the presence of a hydrogen atom in the nitrogen-hydrogen (N-H) bond within the carbazole structure, which can be replaced with different functional groups, carbazole is highly suitable for nitrogen-based derivatization studies. In this study, two different carbazole monomers (IIa and IIIa), which could be potential optoelectronic, were synthesized using the Ullman and Suzuki-Miyaura reaction and characterized using 1H NMR, 13C NMR, UV-Vis, and Flouresence spectroscopy techniques. The cyclic voltammetry experiments were performed using three different working electrodes (Au, Gc, Pt disk electrodes) for each compound. Since the optimum oxidation of the compounds was obtained from the voltammograms on the gold disk electrode, this electrode was used in the calculation of energy levels. HOMO and Eg values of the compounds were deduced from cyclic voltammetry experiments and the optical absorption bands, respectively.

Kaynakça

  • Agarwal, N., Nayak, P. K., Ali, F., Patankar, M. P., Narasimhan, K. L., & Periasamy, N. (2011). Tuning of HOMO levels of carbazole derivatives: New molecules for blue OLED. Synthetic Metals, 161(5-6), 466-473.
  • Al-Ibrahim, M., Roth, H. K., Schroedner, M., Konkin, A., Zhokhavets, U., Gobsch, G., & Sensfuss, S. (2005). The influence of the optoelectronic properties of poly (3-alkylthiophenes) on the device parameters in flexible polymer solar cells. Organic Electronics, 6(2), 65-77.
  • Ambrose, J. F., & Nelson, R. F. (1968). Anodic oxidation pathways of carbazoles: I. carbazole and N‐substituted derivatives. Journal of the Electrochemical Society, 115(11), 1159.
Toplam 3 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Çevresel ve Sürdürülebilir Süreçler
Bölüm Makaleler
Yazarlar

Merve Yandimoglu

Kamuran Gorgun

Evrim Hur

Erken Görünüm Tarihi 11 Aralık 2023
Yayımlanma Tarihi 1 Aralık 2023
Yayımlandığı Sayı Yıl 2023Cilt: 25

Kaynak Göster

APA Yandimoglu, M., Gorgun, K., & Hur, E. (2023). Synthesis and Some Electrochemical Properties of Carbazole Derivative Monomers for Optoelectronic Device Design. The Eurasia Proceedings of Science Technology Engineering and Mathematics, 25, 59-66. https://doi.org/10.55549/epstem.1403010