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Nuran Asmafiliz Zeynel Kılıç Aslı Öztürk Yasemin Süzen Tuncer Hökelek Leyla Açık 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):1723-1742
Abstract The condensation reactions of hexachlorocyclotriphosphazene (N3P3Cl6) with mono (1 and 2) and bisferrocenyldiamines (3–5 and 7) resulted in the formation of tetrachloro mono- (8 and 9) and bisferrocenylspirocyclotriphosphazenes (10–13). In addition the tetramorpholino mono- (8a and 9a) and bisferrocenylphosphazenes (10a–12a) were obtained from the reactions of the corresponding tetrachlorophosphazenes (8–12) with excess morpholine. The structures of all the phosphazenes were determined using FTIR, MS, 1H, 13C, and 31P NMR and 2-dimensional NMR techniques. The structures of 9a and 13 were determined by single crystal X-ray diffraction techniques. Cyclic voltammetric investigations of compounds 8a, 9a, and 11a revealed that ferrocene redox centers undergo reversible oxidation. These ferrocenylphosphazenes appear to be quite robust electrochemically. Interactions between the compounds 8a, 9a, 11a, and 12a and pBR322 plasmid DNA were investigated by agarose gel electrophoresis. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfer, and Silicon and the Related Elements for the following free supplemental files: Additional text and figures.] 相似文献
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Vida Krikstolaityte Yasemin Oztekin Jurgis Kuliesius Almira Ramanaviciene Zafer Yazicigil Mustafa Ersoz Aytug Okumus Asta Kausaite‐Minkstimiene Zeynel Kilic Ali Osman Solak Asta Makaraviciute Arunas Ramanavicius 《Electroanalysis》2013,25(12):2677-2683
A single compartment biofuel cell (BFC) based on an anode and a cathode powered by the same fuel glucose is reported. Glucose oxidase (GOx) from Aspergillus niger was applied as a glucose consuming biocatalyst for both anode and cathode of the BFC. The 5‐amino‐1,10‐phenanthroline modified graphite rod electrode (GRE) with cross‐linked GOx was used as the bioanode, and the GRE with co‐immobilised horseradish peroxidase and GOx was exploited as the biocathode of the BFC. The open‐circuit voltage of the designed BFC exceeded 450 mV and a maximal power density of 3.5 µW/cm2 was registered at a cell voltage of 300 mV. 相似文献
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Güven Kuzey Nur Cemaloğlu Reşit Yakut Mehtap Asmafiliz Nuran Kılıç Zeynel Aydın Betül Açık Leyla Hökelek Tuncer 《Research on Chemical Intermediates》2021,47(10):3933-3962
Research on Chemical Intermediates - The N3P3 ring of hexachlorocyclotriphosphazene, N3P3Cl6 (1) (HCCP; trimer), was used significantly as a scaffold for the syntheses of... 相似文献
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Zeliha Hayvali Mustafa Hayvali Zeynel Kiliç Tuncer Hökelek Edwin Weber 《Journal of inclusion phenomena and macrocyclic chemistry》2003,45(3-4):285-294
Condensation reactions between 4'-formyl-5'-hydroxybenzo-15-crown-5and 2-aminopyridine, 2-amino-6-methylpyridine, 2-amino-4-methylpyridine or2-(aminomethyl)furan yielded the new laterally functionalized crown ethers1–4. The crown compounds 1–3 form crystalline 1:1 (Na+:ligand) complexes 1a–3a with sodium perchlorate. Ligands and complexes have been characterized by elemental analyses, IR, UV-Vis, 1H-, 13C-NMR and mass spectra. The tautomeric equilibria (phenol-imine, O...H–N and keto-amine, O...H–N forms) have been systematically studied by using UV-Vis absorption spectra. The spectra of the ligands 1–4 and complexes 1a–3a were recorded in polar, non-polar, acidic, and basic media. In solutions of polar solvents, tautomeric interconversion of the Schiff base into the keto-amine form has been observed. A crystal structure [monoclinic, space group P21/c,a = 14.292(2), b = 9.449(6), c = 16.059(2) Å, = 114.20(1)°,V = 1978.4(13) Å3, Z = 4 and Dx = 1.314 g cm-3] shows that compound 4 is in the form of phenol-imine in solid state. There is a strong intramolecular [O–H...N 1.78(6), O...N 2.581(7), O–H 0.89(6) Å and N...H–O 148.4(5)°] hydrogen bond between the phenolic oxygen and imine nitrogen atoms. The C=N imine bond reveals a trans planar (1E) configuration. The molecules stack in columns parallel to the a/c plane of the unit cell. 相似文献
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Ergin Yalçin Marija Matković Marijana Jukić Ljubica Glavaš Obrovac Ivo Piantanida Zeynel Seferoğlu 《Tetrahedron》2018,74(5):535-543
A series of structurally similar 1-substitued heteroaryl fluorene derivatives were prepared in a simple single step reaction, oxidized to fluorenones and then both, fluorenes and fluorenones, were methylated to enhance the solubility and increase the affinity to DNA/RNA. Interactions of both, fluorene and fluorenone analogues with various ds-DNA, ds-RNA revealed strong ds-DNA/RNA binding, and various thermal stabilization effects. Most intriguingly, some fluorene derivatives showed opposite fluorescence change (increase for ds-RNA and decrease for ds-DNA), which was not previously reported for any fluorene analogue. CD experiments along with other methods support ds-DNA minor groove binding and major groove ds-RNA binding. All compounds showed negligible interaction with G-quadruplex DNA. Very low cell cytotoxicity of studied compounds combined with very efficient cellular uptake makes these fluorescent dyes safe for laboratory applications. Moreover, especially compounds which show opposite fluorescence response to ds-DNA and ds-RNA, are promising lead compounds for further studies aimed toward ds-RNA-specific fluorescence markers. 相似文献
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Tuncer Hökelek Necla Gündüz Zeliha Hayvali Zeynel Kiliç 《Journal of chemical crystallography》1995,25(12):831-836
The Schiff base ligand (1), [C15H17NO] crystallizes in the monoclinic space group P21/c witha=10.054(3),b=10.313(3), c=13.173(4)Å, =107.42(4)°,V=1303.2(7)Å3,Z=4,Dx=1.159 g cm–3, and (MoK)=0.674 cm–1. The C2-O[1.23(1)Å] and C3–C4 [1.33(2)Å] bond lengths are short, due to its quinoidal structure. In the Schiff base nickel complex (2), [Ni(C16H18NO)2] the asymmetric unit is comprised of two half-complexes. It crystallizes in the triclinic space group
witha=5.124(3),b=16.227(3),c=16.886(4)Å, =95.47(8), =96.00(1), =90.71(4)°,V=1389.6(9) Å3,Z=2,Dx=1.289 g cm–3, and (MoK) =12.1 cm–1. The coordination of the Ni(II) ions are square planar with bond angles between 87.9(1) and 92.1(1)°. The Ni–O and Ni–N distances are 1.819(2), 1.922(2) and 1.823(2), 1.914(3)Å in these two complexes. 相似文献