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    Application of Half-Sandwich Metal-Phosphinite Compounds to Biological Activities: Determine the energies of the HOMO and LUMO levels
    (Wiley-V C H Verlag Gmbh, 2023) Meric, Nermin; Rafikova, Khadichakhan; Zazybin, Alexey; Guzel, Remziye; Kayan, Cezmi; Karakas, Duygu Elma; Dundar, Abdurrahman
    Mononuclear transition metal complexes 1-(furan-2-yl)ethyldiphenyl[dichloro(eta(6)-p-cymene)ruthenium(II)]phosphinite, (2), 1-(furan-2-yl)ethyldiphenyl[dichloro(eta(6)-benzene) ruthenium(II)] phosphinite (3), 1-(furan-2-yl)ethyldipheny[chloro(eta(4)-1,5-cyclooctadiene)rhodium(I)]phosphinite (4), 1-(furan-2-yl)ethyldiphenyl[dichloro (eta(5)pentamethylcyclopentadienyl)iridium (III)] phosphinite (5) were synthesized and characterized by microanalysis, infrared, MS, and NMR spectroscopy. The biological activities of the complexes were also tested. Compounds 2 and 5 were the best complexes at DPPH radical scavenging and reducing power activity at 73.27 % and 0.41 at 200 mu g/mL, respectively. The highest antimicrobial activity exhibited by complex 3 as 14 mm inhibition zone against S. aureus. All of the complexes have cleaved the DNA from the double-strand and exhibited three bands on gel electrophoresis. Moreover, cyclic voltammetry studies of the phosphinite complexes were carried out to determine the energies of the HOMO and LUMO levels as well as to estimate their electrochemical and some electronic properties.
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    Öğe
    Half-sandwich ruthenium(II) and iridium(III) complexes of imidazole based phosphinite ligands: antioxidant and antibacterial activities as well as electrochemical properties
    (Wiley-V C H Verlag Gmbh, 2024) Isik, Ugur; Rafikova, Khadichakhan; Meric, Nermin; Guzel, Remziye; Kerimkulova, Aygul; Akimbek, Arailym; Okumus, Veysi
    Ruthenium(II) and iridium(III) complexes of phosphinites including imidazole moiety were synthesized and characterized by microanalysis, IR, MS, and NMR spectroscopies. Antibacterial activity against Gram-positive and Gram-negative bacterial strains was assessed in all complexes. The highest radical scavenging (72.2 %) was obtained for [3-(3-chloro-2-({[dichloro(eta 6-benzene)ruthenium]diphenylphosphanyl}oxy)propyl)-1-butyl-1H-imidazol-3-ium chloride], 4 at 200 mu g/mL concentration, while [3-(3-chloro-2-({[dichloro(eta 5-pentamethylcyclopentadienyl)-iridium]diphenylphosphanyl}oxy)pro-pyl)-1-butyl-1H-imidazol-3-ium chloride], 6 demonstrated the highest antibacterial activity as 13 mm inhibition zone against E. hirea. Furthermore, optical and electrochemical featured of metal complexes containing imidazole phosphinite were investigated utilizing UV-vis absorption and cyclic voltammetry techniques. Consequently, all complexes can be proposed as metal-based charge convertible phosphinite complexes which may be employed as new generation and synergistic Dye-Sensitized Solar Cell (DSSC) materials. Ruthenium(II) and iridium(III) complexes of phosphinites including imidazole moiety are synthesized and characterized by microanalysis, IR, MS, and NMR spectroscopies. Their antibacterial activity against Gram-positive and Gram-negative bacterial strains is assessed. Furthermore, optical and electrochemical features of the metal complexes are investigated utilizing UV-vis absorption and cyclic voltammetry techniques. image
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    Öğe
    Removal and Preconcentration of Pb(II), Cr(III), Cr(VI) from the Aqueous Solution and Speciation of Cr(III)-Cr(VI) by Using Functionalized Amberlite XAD-16 Resin with Dithioethylenediamine
    (Asian Journal Of Chemistry, 2010) Dolak, Ibrahim; Tegin, Ibrahim; Guzel, Remziye; Ziyadanogullari, Recep
    Amberlit XAD-16 was functionalized using dithioethylenediamine as a ligand and characterized by elemental analysis and FTIR spectroscopy. The effects of contact time, pH, electrolyte and the concentration of eluent on separation and preconcentration of Pb(II), Cr(III) and Cr(VI) were studied. In addition, the batch capacity for each ion was determined under the optimum conditions. The preconcentration yields of Pb(II), Cr(III) and Cr(VI) were found to be 96.60 +/- 3.02, 102.20 +/- 3.00 and 100.64 +/- 2.24 %, respectively, with 500 times preconcentration factor under the optimum conditions. The speciation of Cr(III)-Cr(VI) was studied, it was determined that Cr(III) separated in 93.24 +/- 2.21 % yield from the solution containing Cr(III)-Cr(VI) by using Amberlit XAD-16-dithioethylenediamine and Cr(VI) remained in the solution at pH 4, while Cr(VI) separated in 101.43 +/- 3.09 % yield from the solution containing Cr(III)-Cr(VI) and Cr(III) remained in the solution. at pH 7.50 by using Amberlit XAD-16-dithioethylenediamine-Pb(II).
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    Öğe
    Removal and Preconcentration of Pb(II), V(V), Cr(VI) from the Aqueous Solution and Selective Separation of V(V)-Cr(VI) by Using Functionalized Amberlite XAD-16 Resin with Dithioethylenediamine
    (Asian Journal Of Chemistry, 2010) Dolak, Ibrahim; Tegin, Ibrahim; Guzel, Remziye; Ziyadanogullari, Recep
    Amberlit XAD-16 was functionalized using dithioethylenediamine as a ligand. and characterized by elemental analysis and FTIR spectroscopy. The effects of contact time, pH, electrolyte and the concentration of eluents on separation and preconcentration of Pb(II), Cr(VI) and V(V) were studied. In addition, the batch capacity for each ion was determined under the optimum conditions. The preconcentration yields of Pb(II), Cr(VI) and V(V) were found to be 96.60 +/- 3.02, 100.64 +/- 2.24 and 98.20 +/- 3.00 %, respectively, with 500 times preconcentration factor under the optimum conditions. The selective separation of Cr(VI)-V(V) was studied in terms of pH. It was determined that V(V) separated in 98.24 +/- 1.21 % yield from the solution containing Cr(VI)-V(V) and Cr(VI) remained in the solution at pH 2.5, while Cr(VI) separated in 101.43 +/- 3.09 % yield from the solution containing Cr(VI)-V(V) and V(V) remained in the solution at pH 8.5 by using Amberlit XAD-16-dithioethylenediamine -Pb(II).
  • Küçük Resim
    Öğe
    Removal of Cadmium and Lead from Aqueous Solution by Calcite
    (Pol. J. Environ. Stud., 2007) Yavuz, Omer; Guzel, Remziye; Aydın, Fırat; Tegin, İbrahim; Ziyadanoğulları, Recep
    The removal of toxic cadmium(II ) and lead(II ) from aqueous solutions was investigated using calcite, which is inexpensive and widespread over the globe, as the effective inorganic adsorbent. The experimental data of the removal equilibrium were correlated by either the Langmuir or Freundlich equations. Results indicate that the Langmuir model gave a better fit to the experimental data than the Freundlich equation. Maximum adsorption capacities were determined as 18.52 mg/g Cd and 19.92 mg/g Pb for natural calcite at 25°C, respectively.
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    Transition metals of arene derivatives with functionalized ionic liquid: DFT investigation, biological applications and electrochemical behavior of complexes
    (Elsevier Science Sa, 2022) Rafikova, Khadichakhan; Meric, Nermin; Guzel, Remziye; Arslan, Nevin; Binbay, Nil Ertekin; Kayan, Cezmi; Okumus, Veysi
    Mononuclear transition metal complexes based on ionic liquid have been prepared and characterized in detail. The biological properties of the three complexes were evaluated using radical scavenging activity, reducing power, antibacterial effect, DNA binding and cleavage activity. Among the complexes, [3-[(2R)-2-({[dichloro(eta(6)-benzene)ruthenium]diphenylphosphanyl}oxy)-2-phenylethyl]-1-methyl-1H-imidazol-3-ium chloride] (4), demonstrated the highest radical scavenging (64.7 %) and reducing power activity (0.467) at 200 mu g/ml concentration. The highest zone of inhibition was obtained from [3-[(2R)-2-({[dichloro(eta(6)-p-cymene)ruthenium]diphenyl phosphanyl}oxy)-2-phenylethyl]-1-methyl-1H-imidazol-3-ium chloride] (3), against Bacillus cereus as 14 mm. Furthermore, all complexes were determined to have DNA binding and cleavage activities. Furthermore, theoretical DFT computations have also been carried out for the cationic complexes, to obtain minimum energy configuration of molecules. The effects of the chemical structures of three cationic complexes were also examined in relation to the variable property of electron-donating ligands for ruthenium-based complexes and iridium complex and their potential energy levels in ground and excited states HOMO and LUMO were determined.