Journals / Turkish Journal of Analytical Chemistry / 2020 / Cilt: 2 - Sayı: 1

The new tetra substituted metallophthalocyanines bearing four Schiff bases on periphery: Synthesis, spectroscopic properties and investigation of the effect of various central metals on aggregation properties

Pages
29–36
Publication Date
2020-06-23
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Aggregation properties of the obtained metallophthalocyanines were researched in polar and apolar solvents.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:In the present study, new Schiff base compound (Z)-4-((quinolin-2-ylmethyleneamino)methyl)phenol (3), its phthalonitrile derivative (Z)-4-(4-((quinolin-2-ylmethyleneamino)methyl)phenoxy)phthalonitrile (4) were synthesized in the first step.
📊
Key Findings & Data:Then, zinc(II) (Pc‒5), cobalt(II) (Pc‒6) and copper(II) (Pc‒7) phthalocyanines containing Schiff base group with quinolin moiety on peripheral positions were synthesized.
💡
Conclusion & Impact:Aggregation properties of the obtained metallophthalocyanines were researched in polar and apolar solvents.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Aggregation · Metallophthalocyanine · Phthalocyanine

Abstract

In the present study, new Schiff base compound (Z)-4-((quinolin-2-ylmethyleneamino)methyl)phenol (3), its phthalonitrile derivative (Z)-4-(4-((quinolin-2-ylmethyleneamino)methyl)phenoxy)phthalonitrile (4) were synthesized in the first step. Then, zinc(II) (Pc‒5), cobalt(II) (Pc‒6) and copper(II) (Pc‒7) phthalocyanines containing Schiff base group with quinolin moiety on peripheral positions were synthesized. All new compounds were characterized by general spectroscopic techniques. Aggregation properties of the obtained metallophthalocyanines were researched in polar and apolar solvents.

🔖

Cite This Article

YALAZAN, H., KAMİLOĞLU, A. A., KANTEKİN, H., OCAK, Ü. (2020). The new tetra substituted metallophthalocyanines bearing four Schiff bases on periphery: Synthesis, spectroscopic properties and investigation of the effect of various central metals on aggregation properties. Turkish Journal of Analytical Chemistry, Cilt: 2 - Sayı: 1, 29–36. https://ajindex.com/articles/808293

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (17)

  1. C.C. Leznoff, A.B.P. Lever. 1989. Phthalocyanines: Properties and Applications, VCH Publishers, New York,, vol. 1
  2. K. Kadish, K.M. Smith, R. (Eds.) Guilard, The Porphyrin Handbook, Academic Press, Boston, 2003, vol. 15–20
  3. N.B. McKeown, Phthalocyanine Materials Synthesis, Structure and Function, Cambridge University Press, 1998
  4. B. Ertem, H. Yalazan, Ö. Güngör, G. Sarkı, M. Durmuş, E.T. Saka, H. Kantekin, J. Luminescence, 204, 2018, 464‒471
  5. H. Kantekin, E.T. Saka, B. Ertem, M.N. Mısır, H. Yalazan, G. Sarkı, J. Coord. Chem., 71:1, 2018, 164‒182
  6. K. Kameyama, M. Morisue, A. Satake, Y. Kobuke, Angewandte Chemie International Edition, 44, 2005, 4763–4766
  7. J.L. Sesler, J. Jayawickramarajah, A. Gouloumis, G.D. Patnos, T. Torres, D.M. Guldi, Tetrahedron, 62, 2006, 2123–2131
  8. X. Huang, F.Q. Zhao, Z.Y. Li, L. Huang, Y.W. Tang, F. Zhang, C.H. Tung, Chemistry Letters, 36, 2007, 108–115
  9. X. Huang, F.Q. Zhao, Z.Y. Li, Y.W. Tang, F. Zhang, C.H. Tung, Langmuir, 23, 2007, 5167–5172
  10. M. Morisue, Y. Kobuke, Chemistry – A European Journal, 14, 2008, 4993–5000
  11. H. Manfred, Alkaloids: Nature's Curse or Blessing?,Weinheim, Wiley-VCH, 2002
  12. C.Y. Poon, P. Chiu, A synthesis of the tetracyclic carboskeleton of isaindigotidione. Tetrahedron Lett., 45, 2004, 2985-8
  13. S. Ökten, O. Çakmak, Ş. Tekin, The structure activity relationship (SAR) study of 6,8-disubstituted quinoline derivatives as anti cancer agents, Turk J Clin Lab., 8(4), 2017, 152‒159
  14. I. Jacquemond-Collet, F. Benoit-Vical, A. Valentin, E. Stanislas, M. Mallié, I. Fourasté Antiplasmodial and cytotoxic activity of galipinine and other tetrahydroquinolines from Galipea officinalis, Planta Med., 68(1), 2002, 68‒69
  15. KC. Fang, YL. Chen, J. Sheu, T.C. Wang, C.C. Tzeng, Synthesis, antibacterial, and cytotoxic evaluation of certain 7-substituted norfloxacin derivatives, J Med Chem., 43, 20, 2000, 3809‒3812
  16. P. Palit, P. Paira, A. Hazra, S. Banerjee, A.D. Gupta, S.G. Dastidar, N.B. Mondal, Phase transfer catalyzed synthesis of bisquinolines: Antileishmanial activity in experimental visceral leishmaniasis and in vitro antibacterial evaluation, Eur J Med Chem., 44, 2009, 845−853
  17. B. Podeszwa, H. Niedbala, J. Polanski, R. Musiol, D.Tabak, J.Finster, K. Serafin, M. Milczarek, J. Wietrzyk, S. Boryczka, W. Mol, J. Jampilek, J. Dohnal, D.S. Kalinowski, Dolezal, D.R. Richardson, Investigating the antiproliferative activity of quinoline-5,8-diones and styrylquinol