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- Keyword
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- 1 (5)
- 3 (4)
- 2 (3)
- Biodiesel (3)
- 4 (2)
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- 4-Thiadiazole (2)
- Anti-Helicobacter pylori activity. (2)
- Antibacterial activity. (2)
- Dithienylpyrrole (2)
- Fuel cell (2)
- Heterogeneous catalyst (2)
- Iridoid glycosides (2)
- Metal complexes (2)
- Nitrofuran (2)
- Phenol (2)
- 1'-dinaphthalene (BINOL) (1)
- 1-(4-Dimethyl aminophenyl)-2-(5H-phenanthridine-6-ylidene)-ethanone (1)
- 1-b]furan; Benzofuran; Ketoxime. (1)
- 10-perylenetetracarboxylic diimide (1)
- 2'-binaphthylene phosphorochloridite (BINOL-PCl) (1)
- 2'-dihydroxy-1 (1)
- 2-a]pyrrolidin- 2-one (1)
- 2-cyclic diketones (1)
- 2-methyl-1-indanone (1)
- 2\alpha (1)
- 2\beta (1)
- 3-component reaction. (1)
- 3-methly-1-indanone (1)
- 3-thiazoles (1)
- 3\alpha (1)
Articles 1 - 30 of 82
Full-Text Articles in Physical Sciences and Mathematics
Development Of Alumina Supported Alkaline Catalysts Used For Biodiesel Production, Oğuzhan İlgen, Ayşe Ni̇lgün Akin
Development Of Alumina Supported Alkaline Catalysts Used For Biodiesel Production, Oğuzhan İlgen, Ayşe Ni̇lgün Akin
Turkish Journal of Chemistry
The transesterification of canola oil with methanol was studied in a heterogeneous system, using \gamma-Al_2O_3 supported alkaline catalysts. All the catalysts were prepared by incipient-wetness impregnation of an aqueous solution of alkaline compounds on \gamma-Al_2O_3 support. The effects of alkaline compound, methanol/canola oil molar ratio, reaction temperature, catalyst amount, and reaction time in biodiesel production were investigated. The catalyst with KOH loaded on \gamma-Al_2O_3 gave the highest basicity and the best catalytic activity for this reaction. The highest FAME yield obtained was 89.40%.
Investigation Of Biodiesel Production From Canola Oil Using Amberlyst-26 As A Catalyst, Oğuzhan İlgen, Ayşe Ni̇lgün Akin, Nezahat Boz
Investigation Of Biodiesel Production From Canola Oil Using Amberlyst-26 As A Catalyst, Oğuzhan İlgen, Ayşe Ni̇lgün Akin, Nezahat Boz
Turkish Journal of Chemistry
The transesterification of canola oil to fatty acid methyl esters was studied using Amberlyst-26 as a solid catalyst. The influence of reaction conditions, such as the reaction time, methanol to oil molar ratio, amount of catalyst, effect of co-solvent, and alcohol and oil types, were determined. When the reaction was carried out at 45 °C with a canola oil to methanol molar ratio of 6:1, a reaction time of 1.5 h, and 3 wt.% of catalyst, oil conversion was about 67%. Methanol was much more reactive than ethanol and isopropyl alcohol (IPA) in the transesterification reaction. The conversion of canola …
A Mild Method For The Cleavage Of Ketals Using Ibx, Abdul Rauf Raza
A Mild Method For The Cleavage Of Ketals Using Ibx, Abdul Rauf Raza
Turkish Journal of Chemistry
Investigation on the total synthesis of batrachotoxin 1 revealed that the cyclic ketals could be cleaved to ketone with IBX in DMSO at 70-81 °C under very mild conditions. A variety of functional groups showed no interference under these conditions except vinyl bromides, which, in fact, inhibits the single electron transfer to IBX.
Voltammetric Determination Of Ascorbic Acid And Dopamine Simultaneously At A Single Crystal Au(111) Electrode, Zekerya Dursun, Levent Peli̇t, Isao Taniguchi
Voltammetric Determination Of Ascorbic Acid And Dopamine Simultaneously At A Single Crystal Au(111) Electrode, Zekerya Dursun, Levent Peli̇t, Isao Taniguchi
Turkish Journal of Chemistry
A single-crystal Au(111) electrode was used for the simultaneous determination of dopamine (DA) and ascorbic acid (AA) in a phosphate buffer solution at pH 6.9. The single-crystal Au(111) electrode displayed excellent electrocatalytic activity for DA and AA oxidation in comparison to a Au disk electrode. Although the anodic peaks of both reagents overlapped on the Au disk electrode, the anodic peak potentials of DA and AA in their mixture were well separated since the peak potential of AA was shifted to more negative values by cyclic and differential pulse voltammetry. The oxidation peak current increased linearly with the concentration of …
The Role Of The Entropy Factor On The Adsorption Of An Optical Brightener On Pulp, Greta Radeva, Eva Valcheva, Stefka Veleva
The Role Of The Entropy Factor On The Adsorption Of An Optical Brightener On Pulp, Greta Radeva, Eva Valcheva, Stefka Veleva
Turkish Journal of Chemistry
The present paper reports results of the thermodynamic study of adsorption of 2 optical brighteners (Tinopal UP and Leucophor AP) on pulp. The entropy non-homogeneity of the pulp surface was confirmed and the coefficients of entropy non-homogeneity were determined. The entropy effect on the variation of Gibbs free energy of the process studied was followed.
Synthesis And In Vitro Anti-Helicobacter Pylori Activity Of 2-(Substituted Benzylthio)-5-(5-Nitro-2- Furyl)-1, 3, 4-Thiadiazole Derivatives, Negar Mohammadhosseini, Ali Asadipor, Bahram Letafat, Mohsen Vosooghi, Farideh Siavoshi, Abbas Shafiee, Alireza Foroumadi
Synthesis And In Vitro Anti-Helicobacter Pylori Activity Of 2-(Substituted Benzylthio)-5-(5-Nitro-2- Furyl)-1, 3, 4-Thiadiazole Derivatives, Negar Mohammadhosseini, Ali Asadipor, Bahram Letafat, Mohsen Vosooghi, Farideh Siavoshi, Abbas Shafiee, Alireza Foroumadi
Turkish Journal of Chemistry
Starting from (5-nitrofuran-2-yl)methylene diacetate, a new series of 2-[(substituted benzyl)thio]-5-(5-nitro-2-furyl)-1,3,4-thiadiazoles (6a-n) were synthesized and the structures of the compounds were determined using spectroscopic methods including mass spectrometry, ^1H-nuclear magnetic resonance, infrared spectroscopy, and elemental analysis. The in vitro anti-Helicobacter pylori activity of the synthesized compounds was evaluated by the disk diffusion method against the clinical isolates of Helicobacter pylori. The results indicated that most of the synthesized compounds exhibited significant inhibitory activity against H. pylori with respect to standard drug metronidazole. Compound 6l, containing the 2-chloro-6-fluorobenzylthio moiety, was the most potent compound tested.
Comparison Of Photochromic Properties And Thermal Stabilities Of Fulgide, Fulgimide, And Benzimidazole[1,2-A]Pyrrolidine-2-One Derivatives, Mahmut Köse, Ersi̇n Orhan
Comparison Of Photochromic Properties And Thermal Stabilities Of Fulgide, Fulgimide, And Benzimidazole[1,2-A]Pyrrolidine-2-One Derivatives, Mahmut Köse, Ersi̇n Orhan
Turkish Journal of Chemistry
New thermally stable photochromic fulgimides and benzimidazole[1,2-a]pyrrolidin-2-one derivatives of furylfulgide and thienylfulgide were prepared and their photochromic properties were investigated. Thermal stabilities of some of the new isomers in an alcoholic solution and in PMMA (poly(methyl methacrylate)) polymer films, and pyrolytic behaviors in inert atmosphere with TGA were compared. The colored form of fulgimide and that of benzimidazole[1,2-a]pyrrolidin- 2-one derivatives showed large bathochromic shifts for visible absorption maximum compared with the colored form of corresponding fulgides. The imides and benzimidazole[1,2-a]pyrrolidin-2-one derivatives of fulgide displayed better thermal stability than corresponding fulgides.
Dynamic ^1h-Nmr Demonstration Of Anomeric Effect And Structure: Conformational And Configurational Analysis Of N-2-(1,4-Dioxane)-N'-(P-Methylbenzenesulfonyl)- O-(P-Methylphenoxy) İsourea, Ali Reza Modarresi-Alam, Hossein A. Dabbagh
Dynamic ^1h-Nmr Demonstration Of Anomeric Effect And Structure: Conformational And Configurational Analysis Of N-2-(1,4-Dioxane)-N'-(P-Methylbenzenesulfonyl)- O-(P-Methylphenoxy) İsourea, Ali Reza Modarresi-Alam, Hossein A. Dabbagh
Turkish Journal of Chemistry
The conformational and configurational behavior and the structure of N-2-(1,4-dioxane)-N'-(p-methylbenzenesulfonyl)-O- (p-methylphenoxy) isourea (1) were studied using dynamic NMR. The endo-anomeric effect, hydrogen bonding, temperature, and polarity of solvent control the population of dioxane ring conformers or anomers but not the configuration interconversion of the imine of the imidoyl moiety. Dynamic ^1H-NMR, \Delta H°, \Delta S°, \Delta G°, and \Delta G^{\ddag} analysis of 1 demonstrates that the dioxane ring adopts the chair conformation, that the imidoyl amino group prefers axial conformation, and that the tosyl and tolyl groups about the C=N bond retain the E configuration.
Secondary Metabolites From Nepeta Heliotropifolia, Zühal Güvenalp, Hi̇lal Özbek, Ayşe Kuruüzüm-Uz, Cavi̇t Kazaz, L. Ömür Demi̇rezer
Secondary Metabolites From Nepeta Heliotropifolia, Zühal Güvenalp, Hi̇lal Özbek, Ayşe Kuruüzüm-Uz, Cavi̇t Kazaz, L. Ömür Demi̇rezer
Turkish Journal of Chemistry
Two iridoid glycosides, ixoroside (1) and nepetanudoside B (2); 1 phenylpropanoid glycoside, coniferine (3); 2 flavone glycosides, apigenin 7-O-glucuronide (4) and apigenin 7-O-glucopyranoside (5); 2 triterpenes, oleanolic acid (6) and ursolic acid (7); and 1 sterol, \beta-sitosterol (8), were isolated from the aerial parts of Nepeta heliotropifolia Lam. (Lamiaceae). Their structures were identified by means of spectroscopic methods (1D- and 2D-NMR, UV, and EIMS).
An Efficient One Pot Synthesis Of 1,4-Dihydropyridines Using Alumina Sulfuric Acid (Asa) Catalyst, Mustafa Arslan, Cüneyt Faydali, Mustafa Zengi̇n, Mustafa Küçüki̇slamoğlu, Hülya Demi̇rhan
An Efficient One Pot Synthesis Of 1,4-Dihydropyridines Using Alumina Sulfuric Acid (Asa) Catalyst, Mustafa Arslan, Cüneyt Faydali, Mustafa Zengi̇n, Mustafa Küçüki̇slamoğlu, Hülya Demi̇rhan
Turkish Journal of Chemistry
An efficient synthetic method for 1,4-dihydropyridines has been developed using 3 or 4 component condensation reactions of aldehydes, 1,3-dicarbonyl compounds, and ammonium acetate in the presence of alumina sulfuric acid catalyst in minimum methanol at reflux temperature. This procedure offers several advantages including high yields, an environmentally friendly procedure, short reaction times, and a simple work-up procedure.
4h-Pyran-4-One Derivatives:; Leading Molecule For Preparation Of Compounds With Antimycobacterial Potential, Demet Us, Ece Gürdal, Barkin Berk, Si̇nem Öktem, Tanil Kocagöz, Berrak Çağlayan, Işil Aksan Kurnaz, Di̇lek Demi̇r Erol
4h-Pyran-4-One Derivatives:; Leading Molecule For Preparation Of Compounds With Antimycobacterial Potential, Demet Us, Ece Gürdal, Barkin Berk, Si̇nem Öktem, Tanil Kocagöz, Berrak Çağlayan, Işil Aksan Kurnaz, Di̇lek Demi̇r Erol
Turkish Journal of Chemistry
A series of 3-hydroxy-6-methyl-2-((4-substitutedpiperazin-1- yl)methyl)-4H-pyran-4-one structured compounds were synthesized by reacting 5-hydroxy-2-methyl-4H-pyran-4-one with suitable piperazine derivatives using Mannich reaction conditions. Antibacterial activities of the compounds for E. coli, S. paratyphi, S. flexneri, E. gergoviae, and M. smegmatis were assessed in vitro by using broth dilution for determination of the minimum inhibitory concentration (MIC). In addition, their inhibitory effects over DNA gyrase enzyme were evaluated using a DNA gyrase supercoiling assay. Among the synthesized compounds; compound 7 showed a 4 \mu g/mL MIC value for M. smegmatis, whereas the other compounds demonstrated moderate to high activity. Those tested in the supercoiling …
Synthesis And Leishmanicidal Evaluation Of Novel 4-Substituted-2,2-Dimethyl-7-(Prop-2-Ynyloxy)Chromenes, Babak H. Alizadeh, Alireza Foroumadi, Susan K. Ardestani, Fatemeh Poorrajab, Abass Shafiee
Synthesis And Leishmanicidal Evaluation Of Novel 4-Substituted-2,2-Dimethyl-7-(Prop-2-Ynyloxy)Chromenes, Babak H. Alizadeh, Alireza Foroumadi, Susan K. Ardestani, Fatemeh Poorrajab, Abass Shafiee
Turkish Journal of Chemistry
Substituted 4-chromenes were synthesized via the Grignard coupling reaction of various substituted phenyl- and benzylmagnesium chlorides with 2,2-dimethyl-7-(prop-2-ynyloxy)chroman-4-one (1) in relatively good yield (60%-85%). The benzylic-substituted derivatives were a mixture of 2 exo and endo regioisomers, and the exo compounds were a mixture of E and Z isomers. Structural analysis of the exo and endo isomers, as well as E and Z of exo isomers were based on H-NMR, ^{13}C-NMR, and NOESY experiments. The synthetic compounds were examined for in vitro activity against Leishmania major and compound 9 (a, b) was the most active, with inhibitory activity of 36%.
Study Of The Polymerization Of Methyl Methacrylate Initiated By Thioxanthone Derivatives: A Magnetic Field Effect, Sevnur Keski̇n, Meral Aydin, Igor Khudyakov, Nergi̇z Arsu
Study Of The Polymerization Of Methyl Methacrylate Initiated By Thioxanthone Derivatives: A Magnetic Field Effect, Sevnur Keski̇n, Meral Aydin, Igor Khudyakov, Nergi̇z Arsu
Turkish Journal of Chemistry
Free radical photopolymerization of methyl methacrylate (MMA) initiated by 2-mercaptothioxanthone (TX-SH), thioxanthone-thioacetic acid (TXSCH_2COOH), and thioxanthone-carboxymethoxy acetic acid (TXOCH_2COOH) as so called one-component initiators was performed with and without an external magnetic field (MF). These initiators contain light-absorbing and electron/hydrogen-donating fragments in one molecule and do not require an additional hydrogen donor, and initiate the polymerization of MMA in the air. Polymerization experiments were performed in solutions with 3 different optical densities at \lambda 365 nm, where the photoinitiator absorbs. It was observed that application of MF leads to both larger conversion and higher molecular weight of the prepared PMMA, …
Water-Gas Shift Reaction Over Bimetallic Pt-Ni/Al_2o_3 Catalysts, Burcu Selen Çağlayan, Ahmet Erhan Aksoylu
Water-Gas Shift Reaction Over Bimetallic Pt-Ni/Al_2o_3 Catalysts, Burcu Selen Çağlayan, Ahmet Erhan Aksoylu
Turkish Journal of Chemistry
The water-gas shift (WGS) activity of bimetallic Pt-Ni/Al_2O_3 catalysts was investigated in the temperature range 200-450 °C using an idealized feed composition consisting of 3% CO and 6%-10% H_2O. The effects of the Ni content, space velocity, and H_2O/CO ratio on the catalytic performance of the catalysts were studied. An increase in the Ni content and H_2O/CO ratio shifted the carbon monoxide conversion--temperature curve toward lower reaction temperatures. No detectable methane formation was observed in the catalytic reaction tests. The results indicate that Pt-Ni/Al_2O_3 catalysts are highly selective and active for water-gas shift reactions under idealized conditions.
Spectroscopic And Structural Study Of Ni(Ii) Dipicolinate Complex With 2-Amino-4-Methylpyrimidine, İclal Bulut, İbrahi̇m Uçar, Canan Kazak
Spectroscopic And Structural Study Of Ni(Ii) Dipicolinate Complex With 2-Amino-4-Methylpyrimidine, İclal Bulut, İbrahi̇m Uçar, Canan Kazak
Turkish Journal of Chemistry
Nickel(II) dipicolinate complex containing 2-amino-4- methylpyrimidine (2A-4Mpy), [Ni(2A-4Mpy)(dpc) (H_2O)_2] . 2H_2O was synthesized in solid state and its structural and spectroscopic properties were determined by XRD, IR, and UV-Vis techniques. The crystal data revealed that the Ni complex is in triclinic crystal systems with space group P-1 and Z = 2. The Ni(II) ion is bonded to dipicolinate ligand through pyridine N atom together with one O atom of each carboxylate group, 2 aqua ligands, and the N atom of 2-amino-4-methylpyrimidine, forming distorted octahedral geometry. IR and UV-Vis spectra of the complexes all agree with the observed crystal structure.
Synthesis And Antimicrobial Activity Of Dinaphtho[2,1-B]Furan-2-Yl-Methanone And Their Oxime Derivatives, Cumhur Kirilmiş, Murat Koca, Süleyman Servi̇, Seher Gür
Synthesis And Antimicrobial Activity Of Dinaphtho[2,1-B]Furan-2-Yl-Methanone And Their Oxime Derivatives, Cumhur Kirilmiş, Murat Koca, Süleyman Servi̇, Seher Gür
Turkish Journal of Chemistry
The reaction of 2-hydroxy-1-naphthaldehyde with 1,3-dichloroacetone and potassium carbonate was used to prepare dinaphtho[2,1-b]furan-2-yl-methanone (1) as starting reagents. In order to obtain dinaphtho[2,1-b]furan-2-yl-methanole (2), compound 1 was reduced with NaBH_4. N-oxime derivative of this compound (3) was synthesized by the reaction of the compound 1 with hydroxylamine. Alkyl and acyl substituted N-oxime ethers (4-11) were obtained by the reaction compound 3 with various halogen containing compounds. Compound 12 was obtained by reflux of the compound 11 with hydrazine monohydrate in ethanol. Compound 13 was synthesized by the reaction of the compound 11 with NaOH. The synthesized compounds were tested for …
Synthesis, Characterization, And Optical Properties Of Novel 2,5-Bis[4-(2-(-Arylvinyl)Phenyl]-1,3,4-Oxadiazoles, Dao-Hang He, Yong-Chuang Zhu, Zhuo-Ru Yang, Ai-Xi Hu, Gao Cao
Synthesis, Characterization, And Optical Properties Of Novel 2,5-Bis[4-(2-(-Arylvinyl)Phenyl]-1,3,4-Oxadiazoles, Dao-Hang He, Yong-Chuang Zhu, Zhuo-Ru Yang, Ai-Xi Hu, Gao Cao
Turkish Journal of Chemistry
Six novel 2,5-bis[4-(2-arylvinyl)phenyl]-1,3,4-oxadiazoles were synthesized by introducing 1,3,4-oxadiazole moiety into the stilbene skeleton. The synthesis route included the cyclization of p-toluic acid and hydrazine hydrate catalyzed by polyphosphoric acid (PPA), bromination of 1,3-dibromo-5,5-dimethylhydantoin (DBDMH), esterification, and the Wittig-Horner reaction. All the title compounds were characterized by ^1H-NMR, MS, and elemental analysis. UV-Vis absorption and fluorescence emission spectra in THF solution were investigated; the compounds may have potential for use in organic optical materials.
2,2'-Binaphthylene Phosphorochloridite (Binol-Pcl) As A Bulky And Efficient Reagent For The Conversion Of Primary And Secondary Alcohols Into Iodides, And Tertiary Alcohols Stereo- And/Or Regioselectively Into Olefin(S), Nader Noroozi-Pesyan, Jabbar Kalaphy, Hossein Khani-Meinagh
2,2'-Binaphthylene Phosphorochloridite (Binol-Pcl) As A Bulky And Efficient Reagent For The Conversion Of Primary And Secondary Alcohols Into Iodides, And Tertiary Alcohols Stereo- And/Or Regioselectively Into Olefin(S), Nader Noroozi-Pesyan, Jabbar Kalaphy, Hossein Khani-Meinagh
Turkish Journal of Chemistry
Primary and secondary alcohols were transformed in high yield to corresponding iodides by 4-chloro-3,5-dioxaphosphacyclohepta [2,1-\alpha; 3,4-\alpha'] dinaphthalene (BINOL-PCl) at room temperature. The tertiary alcohols formed corresponding alkenes by stereo- and/or regioselective elimination reactions. (E)-1,2-Diphenyl-1-propene and 2,3-diphenyl-1-propene were stereoselectively obtained from 1,2-diphenyl-2-propanol, as representative. No (Z)-1,2-diphenyl-1-propene was observed. 2-Methyl-1-phenylcyclopentene and 3-methyl-2-phenylcyclopentene were regioselectively obtained from 2-methyl-1-phenylcyclopentanol. ^{13}C chemical shifts for the \alpha-methylene carbon of some alkyl iodides empirically calculated through a very simple additive relationship lead to similar or even better values than the reported values. All primary alkyl iodides showed the iodine heavy atom effect on the \alpha-methylene carbon chemical …
Oxorhenium(V)-Mediated Syntheses And Structures Of Oxypyridinium-Ammonium Zwitterions, Abubak'r Abrahams, Thomas Gerber, Eric Hosten, Peter Mayer
Oxorhenium(V)-Mediated Syntheses And Structures Of Oxypyridinium-Ammonium Zwitterions, Abubak'r Abrahams, Thomas Gerber, Eric Hosten, Peter Mayer
Turkish Journal of Chemistry
Treatment of N,N-bis(2-hydroxybenzyl)-2-(2-aminoethyl) dimethylamine (H_2had) with trans-[ReO_2(py)_4]I in acetone affords the iodide salts of the oxypyridinium-ammonium zwitterions N^1-(2-hydroxybenzyl)-N^2,N^2-dimethyl-N^1-((2-oxypyridinium)-1- methyl)ethane-1,2-diamine [Hhpd]^+ and N^2,N^2-dimethyl-N^1- bis((2-oxypyridinium)-1- methyl)ethane-1,2-diamine [dod]^+. The products were characterized by X-ray structure analysis, and NMR and IR spectroscopy.
Spectroscopic Studies And Hartree-Fock Ab Initio Calculations Of A Substituted Amide Of Pyrazine-2-Carboxylic Acid - C_{16}H_{18}Cln_3o, Chacko Yohannan Panicker, Hema Tresa Vanghese, Thaha Thansani
Spectroscopic Studies And Hartree-Fock Ab Initio Calculations Of A Substituted Amide Of Pyrazine-2-Carboxylic Acid - C_{16}H_{18}Cln_3o, Chacko Yohannan Panicker, Hema Tresa Vanghese, Thaha Thansani
Turkish Journal of Chemistry
A substituted amide of pyrazine-2-carboxylic acid was prepared and the IR spectrum was recorded and analysed. The compound prepared was identified by NMR and mass spectra. The vibrational frequencies of the title compound were computed using the Hartree-Fock level of theory using the 6-31G* basis set and compared with the experimental data. The red shift of the NH stretching frequency indicates weakening of the NH bond. The splitting of the NH stretching bond is due to Davidov coupling between neighbouring units. The first hyperpolarizability, infrared intensities, and Raman activities are reported. Methyl substitution affects all the carbon-nitrogen and carbon-carbon bond …
Electrochemical And Optical Properties Of An Azo Dye Based Conducting Copolymer, Ati̇lla Ci̇haner, Fati̇h Algi
Electrochemical And Optical Properties Of An Azo Dye Based Conducting Copolymer, Ati̇lla Ci̇haner, Fati̇h Algi
Turkish Journal of Chemistry
The electrochemical and optical properties of a novel conducting copolymer called poly(2,5'-dimethyl-[4-(2,5-di-thiophen- 2-yl-pyrrol-1-yl)-phenyl]azobenzene-co-(3,4-ethylenedioxythiophene)) (poly(1-co-EDOT)) are reported. Electrochemically synthesized poly(1-co-EDOT) based on the azo dye has a well-defined and reversible redox couple (0.37 V vs. Ag/AgCl) with good cycle stability. The copolymer film exhibits high conductivity (13 S/cm) as well as electrochromic behavior (magenta when neutralized and transmissive sky blue when oxidized). Furthermore, electro-optically active copolymer film has a low band gap of 1.79 eV with a \pi-\pi* transition at 555 nm.
Three-Component Process For The Synthesis Of Some Pyrrole Derivatives Under Microwave Irradiation, Farhad Hatamjafari, Nasser Montazeri
Three-Component Process For The Synthesis Of Some Pyrrole Derivatives Under Microwave Irradiation, Farhad Hatamjafari, Nasser Montazeri
Turkish Journal of Chemistry
We report a short and efficient 3-component reaction for synthesis of a series of [1,2-b]pyrrole derivatives from ninhydrin, alkyl propiolates, and simple primary amines under solvent free and microwave irradiation. This method provides a new route to produce pyrrole derivatives in good to excellent yields.
6-Ketomethyl Phenanthridine As A New Carrier In The Construction Of A Highly Selective Fe(Iii) Ion-Selective Membrane Electrode, R. Maleki, Reza Hosseinzadeh, Hossein Mehrabi, Ali Hassanzadeh, Khalil Farhadi
6-Ketomethyl Phenanthridine As A New Carrier In The Construction Of A Highly Selective Fe(Iii) Ion-Selective Membrane Electrode, R. Maleki, Reza Hosseinzadeh, Hossein Mehrabi, Ali Hassanzadeh, Khalil Farhadi
Turkish Journal of Chemistry
A new Fe^{3+} ion-selective membrane electrode based on 6-ketomethyl phenanthridine (6-KMPT) and 1-(4-dimethyl aminophenyl)-2-(5H-phenanthridine-6-ylidene)-ethanone, which were incorporated in a plasticized polyvinyl chloride (PVC) membrane, is described. The optimized membrane demonstrated a linear dynamic range of 5.2 \times 10^{-6}-1.0 \times 10^{-2} M, with a near Nernstian slope of 19.5 \pm 1.5 mV per decade and a detection limit of 1.2 \times 10^{-6} M. The electrode showed high selectivity for Fe^{3+} ions in comparison to other metal ions. The effect of membrane composition on the potential response of the electrode was studied. The best performance was observed for the membrane comprised of …
On The Structure Sensitivity Of Co Oxidation On Alumina Supported Pd--Pt Bimetallic Catalysts, Sarp Kaya, Ebru Erunal, Riad Shaltaf, Şi̇nasi̇ Elli̇altioğlu, Deni̇z Üner
On The Structure Sensitivity Of Co Oxidation On Alumina Supported Pd--Pt Bimetallic Catalysts, Sarp Kaya, Ebru Erunal, Riad Shaltaf, Şi̇nasi̇ Elli̇altioğlu, Deni̇z Üner
Turkish Journal of Chemistry
CO oxidation reaction was studied over monometallic and bimetallic palladium--platinum catalysts at 25:75, 50:50, and 75:25 Pd:Pt atomic fractions co-impregnated over a \gamma -Al_2O_3 support. The size of the metal particles, measured by modified hydrogen chemisorption, increased as the Pd fractions in the catalyst increased. The surface compositions and site metal distributions of the catalysts determined from Monte Carlo simulations indicated that Pd atoms segregated to the surface: at low Pd levels, Pd occupied preferentially 6 and 7 coordinated defect-like sites. As the Pd fraction increased, first 8 coordinated (100) and then 9 coordinated (111) planes were populated. At low …
A Facile Method For The Preparation Of Poly(4-Vinylpyridine) Nanoparticles And Their Characterization, Nurettin Sahiner
A Facile Method For The Preparation Of Poly(4-Vinylpyridine) Nanoparticles And Their Characterization, Nurettin Sahiner
Turkish Journal of Chemistry
Submicron size particles were synthesized from 4-vinylpyridine (4-VP) using an oil-in-water emulsion system. Divinyl benzene (DVB) and ethylene glycol dimethacrylate (EGDMA) were utilized as crosslinkers for the synthesis of p(4-VP) hydrogel nanoparticles in sodium dodecyl sulfate (SDS) surfactant systems. Characterization of the particles was made by transmission electron microscopy (TEM) and dynamic light scattering (DLS) methods. To render a positive charge, p(4-VP) particles were reacted with 1-bromo butane (1-BB).
A Convenient Synthesis Of 2-Azido And 2-Thiocyanato-2,3-Unsaturated Cyclic Ketones, Mesut Boz, Ömer Zai̇m, Hi̇lal Esen
A Convenient Synthesis Of 2-Azido And 2-Thiocyanato-2,3-Unsaturated Cyclic Ketones, Mesut Boz, Ömer Zai̇m, Hi̇lal Esen
Turkish Journal of Chemistry
2-Azido and 2-thiocyanato-2,3-unsaturated ketones were synthesized by utilizing functionalization of 5- or 6-membered cycloalkane-1,2-diones, namely diosphenols, with dimethylthiocarbomoyl chloride, which activates the system towards reaction with nucleophiles in acidic conditions. Replacement of the enolic oxygen of the diosphenols with azide and thiocyanate may be achieved by treating their dimethylthiocarbamates with sodium azide or potassium thiocyanate in boiling acetonitrile/acetic acid.
Mild And Efficient Iodination Of Aromatic Compounds With Trichloroisocyanuric Acid/I_2/Wet Sio_2 System, Batool Akhlaghinia, Marzieh Rahmani
Mild And Efficient Iodination Of Aromatic Compounds With Trichloroisocyanuric Acid/I_2/Wet Sio_2 System, Batool Akhlaghinia, Marzieh Rahmani
Turkish Journal of Chemistry
Iodoarenes can be obtained using trichloroisocyanuric acid/I_2/wet SiO_2 system at room temperature with high yield in CH_2Cl_2.
Bromination Of Tetrachlorobenzobarrelene: Polyhalogenated Benzobicyclics, Mehmet Emi̇n Şengül, Demet Demi̇rci̇ Gülteki̇n, Selçuk Eşsi̇z, Ari̇f Daştan
Bromination Of Tetrachlorobenzobarrelene: Polyhalogenated Benzobicyclics, Mehmet Emi̇n Şengül, Demet Demi̇rci̇ Gülteki̇n, Selçuk Eşsi̇z, Ari̇f Daştan
Turkish Journal of Chemistry
The low and high temperature bromination reaction of tetrachlorobenzobarrelene was studied and the possible role of a neighboring group in rearrangements was investigated. New polyhalogenated benzobicyclic compounds were synthesized. All compounds were characterized properly using NMR spectroscopy.
Synthesis And Characterization Of Tetraoxime Ligand, Bis-[(2e,3e,2´E)-3,3´-(1,2-Phenylene-Dinitrilo)Dibutan-2-One Dioxime] And Its Dinuclear And Tetranuclear Copper(Ii)/Nickel(Ii) Complexes, Nevi̇n Karaböcek, Pinar Ekmekçi̇oğlu, Asligül Küçükdumlu, Serdar Karaböcek
Synthesis And Characterization Of Tetraoxime Ligand, Bis-[(2e,3e,2´E)-3,3´-(1,2-Phenylene-Dinitrilo)Dibutan-2-One Dioxime] And Its Dinuclear And Tetranuclear Copper(Ii)/Nickel(Ii) Complexes, Nevi̇n Karaböcek, Pinar Ekmekçi̇oğlu, Asligül Küçükdumlu, Serdar Karaböcek
Turkish Journal of Chemistry
A new tetraoxime, (H_4L), was prepared in EtOH by reacting biphenyl-3,3´,4,4´-tetramine with butane-2,3-dione oxime. The tetraoxime ligand was characterized by elemental analyses, H-NMR and ^{13}C-NMR, IR, and mass spectral studies. Dinuclear copper(II), nickel(II) and tetranuclear copper(II) complexes of tetraoxime ligand were prepared and characterized by elemental analyses, magnetic moments, IR, and mass spectral studies. In the dinuclear metal complexes, metal:ligand ratio was found as 2:1. Elemental analyses and stoichiometric and spectroscopic data of the metal complexes indicated that the metal ions were coordinated to the nitrogen atoms of oxime groups (C=N). In addition, total energy and heat formation for ligand …
Synthesis And Antimicrobial And Antitumor Activity Of Some New [1,2,4] Triazole-5-One Derivatives, Yasemi̇n Ünver, Esra Düğdü, Kemal Sancak, Mustafa Er, Sengül Alpay Karaoğlu
Synthesis And Antimicrobial And Antitumor Activity Of Some New [1,2,4] Triazole-5-One Derivatives, Yasemi̇n Ünver, Esra Düğdü, Kemal Sancak, Mustafa Er, Sengül Alpay Karaoğlu
Turkish Journal of Chemistry
4-[Arylidene-amino]-3-thiophen-2-ylmethyl-4,5-dihydro[1,2,4]triazole-5-one compounds (3a-g) with Schiff base character were obtained from the reaction of 4-amino-3-thiophen-2-ylmethyl-4,5-dihydro-1H-[1,2,4]triazole-5-one (2) with various aldehydes. 1-(2-Oxo-2-phenyl-ethyl)-4-[arylidene-amino]-3-thiophen-2-ylmethyl-4,5- dihydro-1H-[1,2,4]triazole-5-ones (4a-g) were synthesized from the reaction of corresponding compounds 3a-g with bromoacetophenone. 1-(2-Hydroxy-2-phenyl-ethyl)- 3-thiophen-2-ylmethyl-4-[aryl-amino]4,5-dihydro-1H-[1,2,4]triazole-5-ones (5a-g) and 1-(2-hydroxy-2-phenyl-ethyl)-3-thiophen-2-ylmethyl-4-[arylidene-amino] 4,5-dihydro-1H-[1,2,4]triazole-5-ones (6b,d,e) were obtained from the selective reduction of 1-(2-oxo-2-phenyl-ethyl)-4-[arylidene-amino]-3-thiophen-2ylmethyl- 4,5-dihydro-1H-[1,2,4] triazole-5-ones (4) with NaBH_4. They were characterized by IR, H-NMR,^{13}C-NMR, and elemental analyses. Compounds 2, 3a, 3c, 3g, 4f, 5b, and 5g showed good antifungal activity against yeast-like fungi. Compounds selected by the National Cancer Institute (NCI, USA) were investigated for antitumor activity.