Sürdürülebilir Kalkınma Amaçları
Yazarlar
- Canpolat, Erdal(5)
- Şahal, Hakan(5)
- Kaya, İsmet(2)
- Solmaz, Adnan(2)
- Tekin, Suat(2)
- Öz, Samet(2)
- Özkan, Mustafa(2)
- İdil, Önder(2)
- Abuawad, Mohammed Majed Shible(1)
- Adiguzel, Ragip(1)
- Aktağ, Işıl Gürsul(1)
- Aras, Abdülmelik(1)
- Bayır, Erdal(1)
- Evren, Enes(1)
- Gökmen, Vural(1)
- Kaya, Mehmet(1)
- Keskin, Tuba(1)
- Onkol, Tijen(1)
- Torğut, Gülben(1)
- Türkan, Fikret(1)
- Yağmur, Hatice Karaer(1)
- Yildiko, Ümit(1)
Yayınlar
- MakaleAçık Erişim2026Scopus SJRQ1Comparative Study of Enzymatic and Oxidative Polymerization of a Benzothiazole-Based Schiff Base and Its Antibacterial Properties
Kaya, İsmet; Solmaz, Adnan; Abuawad, Mohammed Majed Shible
In this study, the Schiff base 1-(((6-nitrobenzo[d]thiazol-2-yl) imino)methyl)naphthalen-2-ol (NBTIMN) was synthesized and subsequently polymerized by two different methods. Oxidative polymerization in the presence of organic (o-(NBTIMN)-O) and aqueous alkaline media (o-(NBTIMN)-A) was one of the techniques. The other was enzyme-catalyzed oxidative polymerization (o-(NBTIMN)-E), which was conducted at room temperature with hydrogen peroxide and the enzyme horse radish peroxidase (HRP). The structures of the obtained oligomers were characterized using FT-IR, 1H-13C-NMR, UV–Vis, CV, and GPC analyses, and their electrochemical and optical band gaps were determined as 2.68, 2.66, and 2.49 eV, and 3.08, 2.90, and 3.07 eV for o-(NBTIMN)-O, o-(NBTIMN)-A, and o-(NBTIMN)-E, respectively. Thermal analyses demonstrated that the o-(NBTIMN)-O and o-(NBTIMN)-A derivatives exhibited enhanced thermal stability, characterized by higher decomposition temperatures and LOI values. SEM analyses revealed distinct differences in surface morphologies depending on the polymerization conditions. Antibacterial assays showed that o-(NBTIMN)-O exhibited the strongest broad-spectrum inhibition, whereas NBTIMN displayed pronounced activity against S. aureus. In contrast, o-(NBTIMN)-A and o-(NBTIMN)-E were found to be inactive. These results highlight the critical influence of polymerization conditions on both the physicochemical characteristics and the biological activities of the synthesized structures. Importantly, the comparative design of enzymatic and chemical polymerization demonstrates the potential for environmentally friendly synthesis strategies. The distinct electrochemical and thermal properties suggest applicability in electronics and sensor-related fields, while the pronounced antibacterial activity of o-(NBTIMN)-O holds promise for biomedical and antimicrobial applications.
- MakaleAçık Erişim2025Scopus SJRQ2Synthesis and characterization of oligomers contain phenylhydrazyne unit via oxidative polycondensation: Adsorption studies, kinetic modeling and validation methods
Bayır, Erdal; Solmaz, Adnan; Kaya, İsmet; Yağmur, Hatice Karaer
In this study, 4-((2-phenylhydrazono)methyl)benzene-1,2-diol (4-PHBD) Schiff base was obtained from the condensation reaction between 3,4-dihydroxybenzaldehyde (3,4-DHBA) and phenylhydrazine (PH). The obtained Schiff base (4-PHBD) was polymerized using H2O2, NaOCl, and O2 oxidants in an aqueous basic medium (10 % KOH) and 4-PHBD was converted to o-(4-PHBD)-P (by H2O2 oxidant), o-(4-PHBD)-H (by NaOCl oxidant) and o-(4-PHBD)-O (by O2 oxidant). The structures of Schiff base and oligomers were characterized with FT-IR, NMR, SEM, TGA, UV-Vis, CV and GPC measurements. The Cyclic Voltammetry and UV-Vis measurements were used to ascertain the compounds' optical (Eg) and electrochemical (Eg’) band gaps, respectively. The Eg values of o-(4-PHBD)-P, o-(4-PHBD)-O and o-(4-PHBD)-H were found be 2.99, 2.63 and 3.26 eV, respectively. o-(4-PHBD)-O was used as an adsorbent in the removal of methylene green (MG) from an aqueous solution. The obtained data were applied to pseudo-first order and pseudo-second order kinetic models. It was determined that the adsorption process obeyed the pseudo first order kinetic model. The kinetic model was validated with R2, RMSE, SSE, SD, Δqe (%), MSE and ARE validation methods. The activation energy (Ea) was calculated as 7.31 kJ mol−1 using the Arrhenius equation. It was determined that the adsorption of MG on o-(4-PHBD)-O was physical adsorption.
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İncele - MakaleAçık Erişim2024Scopus SJRQ2New sulfa drug derivatives and their zinc(II) complexes: synthesis, spectroscopic properties and in vitro cytotoxic activities
Şahal, Hakan; Öz, Samet; Keskin, Tuba; Tekin, Suat; Canpolat, Erdal; Kaya, Mehmet
Synthesis of four sulfa drug derivatives (L1–L4) and Zn(II) complexes derived from sulfonamide group antibiotic substances was carried out using the hydrothermal technique (HT) and their structures of the obtained compounds were explained using elemental analysis (EA), FT-IR and NMR (1H- and 13C-). Cytotoxic activities of four novel sulfa drug based-Schiff base compounds and their Zn(II) complexes were determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay using MCF-7 (human breast cancer), Caco-2 (human colorectal adenocarcinoma), A2780 (human ovarian cancer) and LNCaP (human prostate adenocarcinoma) cell lines. LogIC50 values of all obtained compounds were computed with the Graphpad Prism 6 program after 24 h of treatment for MCF-7, Caco-2, A2780 and LNCaP cells. Comet assay experiments were performed using LogIC50 concentrations of all compounds to determine DNA damage. Based on the data obtained, all compounds significantly decreased MCF-7, Caco-2, A2780 and LNCaP cell viability compared to the control groups (p < 0.05).
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İncele - MakaleAçık Erişim2023Scopus SJRQ2Synthesis, structural characterizations and in vitro cytotoxic activities of new sulfonamide-based Schiff base derivatives
Şahal, Hakan; Öz, Samet; Tekin, Suat; Canpolat, Erdal
Synthesis of five different new compounds (1-5) were carried out. Their structures were characterized by spectroscopic methods such as Fourier transform infrared, Proton nuclear magnetic resonance, Carbon-13 nuclear magnetic resonance and Elemental analysis. Cytotoxic activities of five new sulfonamide based-Schiff base compounds were determined by MTT assay using A-2780 (human ovarian cancer) and MCF-7 (breast cancer) cell lines. LogIC50 values of the sulfonamide derivates compounds were calculated by Graphpad Prism 12 programme after a 24-hour treatment for A2780 and MCF-7 cells. Comet assay experiments were performed to determine DNA damage using LogIC50 concentrations of all compounds in A2780 and MCF-7 cells. All compounds significantly reduced A2780 and MCF-7 cell viability compared to control groups (p < 0.05). In addition, all compounds caused DNA damage in A2780 and MCF-7 cells (p < 0.05). These results show that the synthesized compounds exhibit cytotoxic effects against cancer cells and that the cause of cell death is due to DNA damage. Communicated by Ramaswamy H. Sarma.
AtıfScopus5WoS5OpenAlex5İncele - MakaleAçık Erişim2023Scopus SJRQ3Synthesis, Characterization, Antimicrobial and Time Killing Activities of New SulfaDerived Schiff Bases Coordinated with Cu(II)
İdil, Önder; Şahal, Hakan; Canpolat, Erdal; Özkan, Mustafa
Synthesis of three Schiff bases of 5-bromo-3-nitro salicylaldehyde containing different sulfonamide group antibiotic compounds and their Cu(II) complexes was carried out. Structures of all compounds were characterized with spectroscopic methods, including Fourier transform infrared, proton nuclear magnetic resonance, and elemental analysis. The in vitro antimicrobial activity of ligands and complexes against Gramnegative and Gram-positive bacteria and the yeast Candida albicans was evaluated. It was determined that the ligand and complexes showed outstanding antimicrobial activity against almost all of the microorganisms tested. It has been observed that the newly synthesized complexes have more antimicrobial effects than the corresponding ligands. It has been determined that the newly synthesized complexes have more antimicrobial effects than the others (E. coli, L. monocytogenes, and C. albicans), especially on Staphylococcus aureus and Pseudomonas aeruginosa.
AtıfScopus4WoS3OpenAlex2İncele - MakaleYalnız künye2023Scopus SJRQ1Acrylamide formation in apple juice concentrates during storage
Aktağ, Işıl Gürsul; Gökmen, Vural
This study investigated the acrylamide formation in model systems, laboratory-scale produced apple juice concentrates obtained from different stages of process, and commercial apple juice concentrates at different Brix levels during the storage. Changes in the concentrations of reducing sugars, asparagine, 5-hydroxymethylfurfural, 3-deoxyglucosone, and acrylamide were monitored. In addition, Schiff bases of 3-deoxyglucosone and 5-hydroxymethylfurfural with asparagine were confirmed using high-resolution mass spectrometry in order to understand the contribution of intermediates to acrylamide formation. The results revealed that acrylamide formed in both acidic-aqueous model systems and laboratory-scale apple juice concentrates during production. The concentrations of 3-deoxyglucosone, 5-hydroxymethylfurfural, and acrylamide increased significantly (p < 0.05) with the increase in Brix levels whereas asparagine levels decreased in commercial apple juice concentrates during storage. The concentration of acrylamide reached at the maximum level of 0.30 ± 0.02 µmol/kg dry matter in 70°Bx of the concentrates. The findings showed that long-term storage of apple juice concentrates at high Brix levels contributes the acrylamide formation even in unsuitable systems such as acidic and high moisture medium. The confirmation of Schiff base of 3-deoxyglucosone and 5-hydroxymethylfurfural with asparagine demonstrated that the acrylamide formation was attributed to the accumulation of intermediates leading to the conversion of asparagine to acrylamide.
AtıfScopus9WoS8OpenAlex9İncele - MakaleAçık Erişim2023Scopus SJRQ4Cu(II) Complexes of New Sulfa Drug Schiff Base Ligands: Synthesis, Structural Characterization, Antimicrobial Activities, and Time-Killing Kinetics
Şahal, Hakan; İdil, Önder; Canpolat, Erdal; Özkan, Mustafa
Abstract: Synthesis of three different new sulfonamide compounds (L1–L3) and their Cu(II) complexes were carried out. Their structures were characterized by spectroscopic methods such as Fourier transform infrared, Proton nuclear magnetic resonance and elemental analysis. Cu(II) complexes were screened for Gram-positive, Gram-negative bacteria and against yeast using the microdilution method. In particular, CuL2 was found to have significant antimicrobial effects on Gram (–), Gram (+) and eukaryotic yeast. The results showed that CuL2 exhibited better antimicrobial activity than other complexes. Depending on the antimicrobial activity results, time killing experiments of CuL2, the most effective complex, were performed.
AtıfScopus3WoS2OpenAlex2İncele - MakaleAçık Erişim2022Scopus SJRQ2Optimization of Electrical Conductivity of SA-graphene Nanocomposites Using Response Surface Methodology
Şahal, Hakan; Torğut, Gülben; Canpolat, Erdal
Synthesis and characterization of 4-{(E)-[(5-bromo-2-hydroxyphenyl)methylidene]amino}-N-carbamimidoylbenzene-1-sulfonamide(SA) and its composites with graphene(SA-GF) were performed. Compound SA and SA-GF were characterized by FTIR and 1H NMR. The GF dispersion in the composites was analyzed by means of scanning electron microscopy(SEM) for morphology. Thermal properties of SA and nanocomposites were investigated using differential thermal analysis(DTA) and thermogravimetric analysis(TGA). The optimum electrical conductivity of the new sulfonamide-based Schiff base was determined to be 1.78×10−5 S/cm at a frequency of 9923 Hz, an applied voltage of −19 V, a mass fraction of 9.38% for graphene loading using a central composite design in the response surface methodology. The significance of the selected parameters(frequency, voltage and GF amount) in the model was determined by the analysis of variance(ANOVA). The results showed that frequency and graphene loading represent important model terms and have considerable effects on the conductivity of SA.
AtıfScopus3WoS3OpenAlex2İncele - MakaleYalnız künye2021Scopus SJRQ2Synthesis and in silico studies of Novel Ru(II) complexes of Schiff base derivatives of 3-[(4-amino-5-thioxo-1,2,4-triazole-3-yl)methyl]-2(3H)-benzoxazolone compounds as potent Glutathione S-transferase and Cholinesterases Inhibitor
Adiguzel, Ragip; Türkan, Fikret; Yildiko, Ümit; Aras, Abdülmelik; Evren, Enes; Onkol, Tijen
Novel Ru(II) complexes of Shiff base derivatives of 3-[(4-amino-5-thioxo-1,2,4-triazole-3-yl)methyl]-2(3H)-benzoxazolone were synthesized. The ligands (1a-e) were confirmed by IR, 1H NMR, and 13C NMR spectra (only 1b and 1c). Structures of the synthesized Ru(II) complexes (2a-e) were illuminated by elemental analysis, IR, 1H NMR, 13C NMR, and mass spectra. As the biological studies, the inhibitory potency of the ligands and the novel synthesized complexes were evaluated against the glutathione S-transferase (GST), acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes in vitro conditions. Ki values in the range of 26.87-47.63 µM for AChE, 23.51-42.81 µM for BChE, and 33.14-51.73 µM for GST, respectively. The free binding energy of most active inhibitors against AChE, BChE, and GST enzymes were detected as -10.183 kcal/mol, -9.111 kcal/mol, and -6.097 kcal/mol, respectively. All compounds docked were observed to bind in the active site of the enzymes with similar binding orientation and binding interactions with the surrounding amino acids.
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