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Novel phthalocyanines containing resorcinol azo dyes; synthesis, determination of pKa values, antioxidant, antibacterial and anticancer activity

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Date

2015

Author

Kantar, Cihan
Akal, Hayriye
Kaya, Bülent
İslamoğlu, Fatih
Türk, Mustafa
Şaşmaz, Selami

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Kantar, C., Akal, H., Kaya, B., Islamoglu, F., Turk, M., Sasmaz, S. (2015). Novel phthalocyanines containing resorcinol azo dyes; synthesis, determination of pKa values, antioxidant, antibacterial and anticancer activity. Journal of Organometallic Chemistry, 783, 28-39. https://doi.org/10.1016/j.jorganchem.2014.12.042

Abstract

There are many studies about effects on health of compounds having azo groups in literature. However, anticancer, antimicrobial and antioxidant properties of phthalocyanines containing azo dyes are unknown. Therefore, the new metallophthalocyanines (M: Mn, Co, Zn) substituted with resorcinol azo dyes were synthesized and anticancer, antimicrobial and antioxidant properties investigated. All phthalocyanines were synthesized by the microwave assisted method. the structures were characterized by elemental analysis, H-1 NMR, C-13 NMR, UV/vis, IR and Mass spectroscopy techniques. the antioxidant capacities were analyzed through radical scavenging of DPPH and chelating ability to ferrous cation. the highest DPPH activity was obtained from compounds (1c and 2c) and the best ferrous ion chelating activity was determined from compound 2. the antibiotic activities were evaluated by disc diffusion method. Compound 2 exhibited antibacterial activity against studied bacteria, but the other compounds had no significant antibacterial effect. Cytotoxicity, apoptotic and necrotic effects were examined on cancer cells MCF-7 and healthy fibroblast cells. Compounds 1, 1a and 2a seem to be proper for the future cancer therapy researches. pKa values were determined by potentiometrically according to the half-neutralization method in N,N-dimethyl formamide. the effect of pH on the electronic absorption spectra of compounds (1, 2, 1c and 2c) was reported. the newly synthesized compounds show positive solvatochromism behavior. (C) 2015 Elsevier B.V. All rights reserved.

Source

Journal of Organometallic Chemistry

Volume

783

URI

https://doi.org/10.1016/j.jorganchem.2014.12.042
https://hdl.handle.net/11436/2844

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  • FEF, Kimya Bölümü Koleksiyonu [474]
  • Scopus İndeksli Yayınlar Koleksiyonu [5931]
  • WoS İndeksli Yayınlar Koleksiyonu [5260]



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