Výsledky vyhledávání - "Ayşe Aktaş Kamiloğlu"

In Vitro Leishmanicidal Activity of Different Chalcone, Phthalonitrile and Their Peripheral Tetra Zinc Phthalocyanine Derivatives

Autor: Ayşe AKTAŞ KAMİLOĞLU, Şahin DİREKEL, Gonca ÇELİK

Publikováno v: Erzincan Üniversitesi Fen Bilimleri Enstitüsü Dergisi. 15:802-818

In this study, in vitro leishmanicidal activity of different chalcone compounds (5-8), phthalonitrile derivatives (5a-8a), and zinc phthalocyanine (5b-8b) complexes bearing chalcone compound in peripheral positions were investigated. Phthalonitrile d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::86ef81677be3da863c2dcf17f44f5670
https://doi.org/10.18185/erzifbed.1150203

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Fluorocarbon Substituted Peripherally and Non-Peripherally Tetra Phthalocyanine Compounds: Synthesis, Characterization and Aggregation Properties

Autor: Ayşe Aktaş Kamiloğlu

Publikováno v: Erzincan Üniversitesi Fen Bilimleri Enstitüsü Dergisi. 13:1158-1176

This work presents a series of novel peripherally and non-peripherally tetra substituted phthalocyanine derivatives containing 4-[(4,4,5,5,5-pentafluoropentyl)oxy groups. Firstly, phthalonitrile derivatives (2 and 3) were synthesized. These phthaloni

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::583118875a4bc6dd8c26e89dd536d44d
https://doi.org/10.18185/erzifbed.750043

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Antioxidant activity of phthalonitrile derivatives bearing different chalcone groups

Autor: Ayşe AKTAŞ KAMİLOĞLU, Zehra CAN, Gonca ÇELİK

Publikováno v: Volume: 2, Issue: 2 69-74
Turkish Journal of Analytical Chemistry

This work presents the synthesis of four phthalonitrile compunds (3a-d) bearing chalcone moiety which have biological activities. Phthalonitrile compounds are considerable pioneer in synthesis of novel photoactive phthalocyanine derivatives. The spec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a66e1a7c87e0c849daca72495d3bba69
https://doi.org/10.51435/turkjac.806398

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Synthesis and electrochemical properties of new metal-free and metallophthalocyanines bearing 2,6-dimethylquinoline-4-yl derivatives

Autor: Ayşe Aktaş Kamiloğlu, İrfan Acar, Zekeriya Bıyıklıoğlu

Publikováno v: Polyhedron. 137:10-16

4-[(2,6-Dimethylquinoline-4-yl)oxy] peripherally substituted metal free (4), cobalt(II) (5), copper(II) (6) and manganese(III) (7) phthalocyanines were synthesized by using phthalonitrile derivative (3). The synthesized compounds were characterized b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bc9bc0acda7caa9920a45e1ef0933848
https://doi.org/10.1016/j.poly.2017.07.024

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Novel peripherally tetra substituted metal-free, cobalt(II), copper(II) and manganese(III) phthalocyanines bearing polyethoxy chain attached by 2,6-diphenylphenol groups: synthesis, characterization and their electrochemical studies

Autor: Ayşe Aktaş Kamiloğlu, Zekeriya Bıyıklıoğlu, İrfan Acar

Publikováno v: Journal of Inclusion Phenomena and Macrocyclic Chemistry. 88:219-228

Metal free (6), cobalt(II) (7), copper(II) (8) and manganese(III) (9) phthalocyanines, which are tetra substituted at the peripheral positions with 2-[2-(1,1':3',1''-terphenyl-2'-yloxy)ethoxy]ethoxy groups, were synthesized and characterized by IR, H

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d756377d71bf1b0960a099db353ebd2e
https://doi.org/10.1007/s10847-017-0721-9

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Peripherally tetra-{2-(2,3,5,6-tetrafluorophenoxy)ethoxy} substituted cobalt(II), iron(II) metallophthalocyanines: Synthesis and their electrochemical, catalytic activity studies

Autor: Zekeriya Bıyıklıoğlu, Ayşe Aktaş Kamiloğlu, Ece Tuğba Saka, İrfan Acar

Publikováno v: Journal of Organometallic Chemistry. 828:59-67

In this study, new electron-withdrawing peripherally tetra {2-[2,3,5,6-tetrafluorophenoxy]ethoxy} groups substituted CoII Pc and FeII Pc have been synthesized for the first time and their structures have been characterized by using IR, 1H NMR, mass a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b3838a48480cd2f36f0142886f25509d
https://doi.org/10.1016/j.jorganchem.2016.11.022

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