Dergiler / Turkish Journal of Analytical Chemistry / 2023 / Cilt: 5 Sayı: 1

Electroanalytical characterization of chloroquinoline substituted redox-active phthalocyanines

Sayfa
25–31
Yayın Tarihi
2023-06-30
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

All in all, this study's results inevitably create a useful way to use them in possible future studies, which will particularly attempt to use the compound investigated in potential areas of use.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:In the first part of this study, the synthesis and characterization of organosoluble 5-chloroquinolin-8-yloxy substituted iron(II) (2) and oxo-titanium (IV) phthalocyanines (3) are reported for the first time.
📊
Temel Bulgular & Veri:These compounds have been characterized by elemental analysis, Fourier transform infrared, electronic spectroscopy, and mass spectra.
💡
Sonuç & Katkı:All in all, this study's results inevitably create a useful way to use them in possible future studies, which will particularly attempt to use the compound investigated in potential areas of use.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Iron · Titanium · Electrochemistry

Abstract

In the first part of this study, the synthesis and characterization of organosoluble 5-chloroquinolin-8-yloxy substituted iron(II) (2) and oxo-titanium (IV) phthalocyanines (3) are reported for the first time. These compounds have been characterized by elemental analysis, Fourier transform infrared, electronic spectroscopy, and mass spectra. Electrochemical behaviors of metal-free and cobalt phthalocyanines and further new types of iron and oxo-titanium phthalocyanines were investigated using electroanalytical methods, such as cyclic (CV) and square wave voltammetry (SWV). According to the electrochemical results, phthalocyanines by and large showed one-electron metal- and/or ligand-based reversible or quasi-reversible reduction and oxidation processes. All in all, this study's results inevitably create a useful way to use them in possible future studies, which will particularly attempt to use the compound investigated in potential areas of use.

🔖

Bu Makaleye Atıf Yap

NAS, A., DİLBER, G., BIYIKLIOĞLU, Z. (2023). Electroanalytical characterization of chloroquinoline substituted redox-active phthalocyanines. Turkish Journal of Analytical Chemistry, Cilt: 5 Sayı: 1, 25–31. https://ajindex.com/articles/946933

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (9)

  1. A. Suzuki, H. Okumura, Y. Yamasaki, T. Oku, Fabrication and characterization of perovskite type solar cells using phthalocyanine complexes, Appl Surf Sci, 488, 2019, 586-596 (https://doi.org/10.1016/j.apsusc.2019.05.305)
  2. J. Xu, W. Yang, R. Chen, The photovoltaic performance of highly asymmetric phthalocyanine-sensitized brookite-based solar cells, Optik, 200, 2020, 163413. (https://doi.org/10.1016/j.ijleo.2019.163413)
  3. B. Yıldız, E. Güzel, D. Akyüz, B.S. Arslan, A. Koca, M.K. Şener, Unsymmetrically pyrazole-3-carboxylic acid substituted phthalocyanine-based photoanodes for use in water splitting photoelectrochemical and dye-sensitized solar cells, Sol Energy, 191, 2019, 654-662. (https://doi.org/10.1016/j.solener.2019.09.043)
  4. S. Kong, X. Wang, L. Bai, Y. Song, F. Meng, Multi-arm ionic liquid crystals formed by pyridine-mesophase and copper phthalocyanine, J Mol Liq, 288, 2019, 111012. (https://doi.org/10.1016/j.molliq.2019.111012) J.A. Jiménez-Tejada, A. Romero, J. González, N.B. Chaure, A.N. Cammidge, I. Chambrier, A.K. Ray, M.J. Deen, Evolutionary Computation for Parameter Extraction of Organic Thin-Film Transistors Using Newly Synthesized Liquid Crystalline Nickel Phthalocyanine, Micromachines, 10, 2019, 683. ( https://doi.org/10.3390/mi10100683)
  5. E.M. Bauer, T. De Caro, P. Tagliatesta, M. Carbone, Unraveling The Real pigment composition of tattoo inks: the case of bi-components phthalocyanine based greens, Dyes Pigments, 167, 2019, 225-235. ( http://dx.doi.org/10.1016/j.dyepig.2019.04.018)
  6. Y. Zhao, J. W. Ying, Q. Sun, M. R. Ke, B. Y. Zheng, J. D. Huang, A novel silicon(IV) phthalocyanine-oligopeptide conjugate as a highly efficient photosensitizer for photodynamic antimicrobial therapy, Dyes Pigments, 172, 2020, 107834. (https://doi.org/10.1016/j.dyepig.2019.107834)
  7. Q. Li, Z. Sun, Q. Liang, M. Zhou, D. Sun, Novel tetrasubstituted zinc phthalocyanine-attapulgite composites for efficient catalytic oxidation of styrene with tert-butyl hydroperoxide as oxidant, Solid State Sci, 97, 2019, 106010. (https://doi.org/10.1016/j.solidstatesciences.2019.106010)
  8. R. Bahluli, S. Keshipour, Microcrystalline cellulose modified with Fe(II)- and Ni(II)-phthalocyanines: Syntheses, characterizations, and catalytic applications, Polyhedron, 169, 2019, 176-182. ( https://doi.org/10.1016/j.poly.2019.05.010)
  9. H.S. Majumdar, A. Bandyopadhyay, A.J. Pal, Data-storage devices based on layer-by-layer self-assembled films of a phthalocyanine derivative, Org Electron, 4, 2003, 39. (http