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Full-Text Articles in Physical Sciences and Mathematics
New Pyrimidine-N-Ss-D-Glucosides: Synthesis, Biological Evaluation, And Molecular Docking Investigations, Nuran Kahri̇man, Kivanç Peker, Vi̇ldan Serdaroğlu, Ali̇ Aydin, Burçi̇n Türkmenoğlu, Asu Usta, Nuretti̇n Yayli
New Pyrimidine-N-Ss-D-Glucosides: Synthesis, Biological Evaluation, And Molecular Docking Investigations, Nuran Kahri̇man, Kivanç Peker, Vi̇ldan Serdaroğlu, Ali̇ Aydin, Burçi̇n Türkmenoğlu, Asu Usta, Nuretti̇n Yayli
Turkish Journal of Chemistry
In this study, syntheses of new pyrimidine-coupled N-ß-glucosides and tetra-O-acetyl derivatives were carried out. All glycoconjugates were investigated in comparison with known chemotherapeutic agents in terms of their antimicrobial and anticancer functions and DNA/protein binding affinities. Spectral data showed that all glycoside derivatives were obtained by diastereoselectivity as ß-anomers. Both tested groups exhibited strong antiproliferative activity (2.29?66.84 ?g/mL), but some of them had sufficiently ideal % cytotoxicity values (10.01%?16.78%). And also all synthetic compounds exhibited remarkable antibacterial activity against human pathogenic bacteria. Binding of these compounds to CT-DNA resulted in significant changes in spectral properties, consistent with groove binding. Molecular …
Imidazole Derivative Improves Antioxidant Status And Causes Differential Alteration Of Redox-Status In Drosophila Melanogaster, Elizabeth Temidayo Oluwayemi, Oluwakemi Josephine Awakan, Abiodun Omokehinde Eseola, Winfried Plass, Oluyomi Stephen Adeyemi
Imidazole Derivative Improves Antioxidant Status And Causes Differential Alteration Of Redox-Status In Drosophila Melanogaster, Elizabeth Temidayo Oluwayemi, Oluwakemi Josephine Awakan, Abiodun Omokehinde Eseola, Winfried Plass, Oluyomi Stephen Adeyemi
Karbala International Journal of Modern Science
This study investigated the toxicity of a new imidazole compound, 1-(1,4,5-triphenyl-1H-imidazol-2-yl)-naphthalen-2-ol, through the evaluation of selected oxidative stress markers and antioxidants. Both male and female D. melanogaster (3–5 days old) were fed a diet containing the imidazole derivative (20, 50, and 100 mg IMZ/kg diet) for five days. After cessation of imidazole treatment, half the population of the imidazole-exposed flies was homogenized for biochemical assays, while the other half of the flies was allowed to have a normal diet for an additional five days to see if any induced effect would be resolved. Imidazole derivatives did not significantly …
Analysis Of The Electronic Effects And Reactivity Of Benzhydrols In The Formation Of Benzhydryl Ethers, Katherine Quesada, Daniel Chabeda, Jaeger Johnson, Alex Shore
Analysis Of The Electronic Effects And Reactivity Of Benzhydrols In The Formation Of Benzhydryl Ethers, Katherine Quesada, Daniel Chabeda, Jaeger Johnson, Alex Shore
The Yale Undergraduate Research Journal
Benzhydryl ethers were synthesized through the use of microwave irradiation in a proto-ionic liquid solvent. The resulting products were separated from the reaction mixture by vacuum filtration with a silica gel plug. The products were analyzed using GCMS and 1 H NMR techniques to identify and quantify products. Analysis of the resultant data indicated the syntheses of the desired benzhydryl products were successful for 4,4-dimethoxybenzhydrol (conversion: 83% (1-propyl ether), 11% (2-propyl ether), 11% (menthyl ether)) and 4,4-dimethylbenzhydrol (conversion to desired product: 100% (1-propyl ether), 100% (2-propyl ether), 26% (menthyl ether)). However, the syntheses were unsuccessful for reactant 4,4-difluorobenzhydrol and benzhydrol. …
Synthesis, Characterization, Crystal Structures, And Antibacterial Activity Of Some New 1-(3,4,5-Trimethoxybenzoyl)-3-Aryl Thioureasreas, Aamer Saeed, Rasheed Ahmad Khera, Naeem Abbas, Muhammad Latif, Imran Sajid, Ulrich Flörke
Synthesis, Characterization, Crystal Structures, And Antibacterial Activity Of Some New 1-(3,4,5-Trimethoxybenzoyl)-3-Aryl Thioureasreas, Aamer Saeed, Rasheed Ahmad Khera, Naeem Abbas, Muhammad Latif, Imran Sajid, Ulrich Flörke
Turkish Journal of Chemistry
Synthesis of some novel 1-(3,4,5-trimethoxy)benzoyl-3- arylthiourea derivatives (1a-o) was accomplished in 2 steps. The synthetic route involves the reaction of 1-(3,4,5-trimethoxy)benzoyl chloride with potassium thiocyanate in 1:1 molar ratio in acetone to afford the corresponding isothiocyante followed by treatment with suitably substituted anilines. The structures of the products were established by elemental analyses, IR, ^1H- and ^{13}C-NMR, and mass spectroscopy and for 1b and 1m from single crystal X-ray diffraction data. All of the synthesized compounds (1a-o) were screened for antibacterial activity against gram positive and gram negative bacterial strains and were found to exhibit low activity towards the tested …
A Systematic Study On The Absorption And Fluorescence Properties Of 2,4,6-Triaryl And Tripyridylpyridines, Esra Findik, Mustafa Arik, Mustafa Ceylan
A Systematic Study On The Absorption And Fluorescence Properties Of 2,4,6-Triaryl And Tripyridylpyridines, Esra Findik, Mustafa Arik, Mustafa Ceylan
Turkish Journal of Chemistry
Eight different 2,4,6-triaryl, and tripyridylpridines compounds were synthesized and their fluorescent properties were studied by using steady-state and time-resolved fluorescence and UV-Vis absorption spectroscopy techniques in 6 different solvents. Especially, 2,4,6-triarylpyridines showed strong fluorescence properties with high fluorescence quantum yields but small Stokes shifts.
A Highly Soluble Asymmetric Perylene-Bis (Dicarboximide)-Acceptor System Incorporating A Methylene Bridged Methoxybenzene-Donor: Solvent Dependence Of Charge Transfer Interactions, Rene M. Williams
Turkish Journal of Chemistry
The synthesis and photophysical properties of an asymmetrically substituted perylene-bis(dicarboximide), (PDI), system (1) containing a methylene bridged 4-methoxy-benzene donor and a solubilizing branched C_{13} alkyl chain are described. As compared to most PDIs, the fluorescence of 1 is strongly quenched in polar (but not in non-polar) solvents due to a photo-induced electron transfer process. Transient absorption spectroscopy and time resolved emission in e.g. acetonitrile indicates that upon excitation the radical anion of the PDI is formed with a rate of ca. 3.5 \times 10^9s^{-1}, and the charge transfer state has a lifetime of ca. 3 ns. A Frontier Molecular Orbital …
Electrochemical Reductive Behaviors Of 3,4,5,6-Tetrachloro-2-Trichloromethylpyridine At Ag Electrode, Chun-An Ma, Yi-Jiao Hu, Ying-Hua Xu
Electrochemical Reductive Behaviors Of 3,4,5,6-Tetrachloro-2-Trichloromethylpyridine At Ag Electrode, Chun-An Ma, Yi-Jiao Hu, Ying-Hua Xu
Journal of Electrochemistry
The electrochemical reductive behavior of 3,4,5,6-tetrachloro-2-trichloropyridine(heptachloropyridine) on silver electrode in the mixture of acetonitrile and water solutions containing TBAP was investigated by cyclic voltammetry.The influences of scan rate,concentration and temperature on the electrochemical behavior were discussed.It was shown that the reduction of heptachloropyridine on the silver electrode was a diffusion-controlled irreversible process.The diffusion coefficient of heptachloropyridine in the acetonitrile solution was 3.0×10-5 cm2/s.The mechanism of the dechloration of 3,4,5,6-tetrachloro-2-trichloropyridine was also discussed.
Oxidative Cyclisation Of 3-Oxopropanenitriles Mediated Manganese(Iii) Acetate With 2-Thienyl Substituted Alkenes, Mehmet Yilmaz, Neşe Uzunali̇oğlu, Mehtap Yakut, A. Tarik Pekel
Oxidative Cyclisation Of 3-Oxopropanenitriles Mediated Manganese(Iii) Acetate With 2-Thienyl Substituted Alkenes, Mehmet Yilmaz, Neşe Uzunali̇oğlu, Mehtap Yakut, A. Tarik Pekel
Turkish Journal of Chemistry
The oxidative cyclisation of 3-oxopropanenitriles 1a-g with alkenes 2a-c containing 2-thienyl group by manganese(III) acetate was studied. Treatment of 3-oxopropanenitriles 1a-d with 2-[(E)-2-phenylvinyl] thiophene 2a gave 4-phenyl-5-(2-thienyl)-4,5-dihydrofuran-3-carbonitriles 3a-d in moderate yields (52%-60%). 5-(2-thienyl) substituted 4,5-dihydrofuran-3-carbonitriles 3e-i were obtained by the oxidative cyclisation of these 3-oxopropanenitriles with 2-[(E)-1-methyl-2- phenylvinyl]thiophene 2b in good yields (54%-68%). In addition, the reactions of 2-(1-phenylvinyl)thiophene 2c with various 3-oxopropanenitriles produced 4,5-dihydrofurans 3j-n containing heterocycle in 77%-91% yields.
Preparation, Characterization, And Potentiometric Titrations Of Some New Di-[3-(3-Alkyl/Aryl-4,5-Dihydro-1h-1,2,4-Triazol-5-One-4-Yl)-Azomethinphenyl] Isophthalate/Terephthalate Derivatives, Haydar Yüksek, Özlem Gürsoy Kol
Preparation, Characterization, And Potentiometric Titrations Of Some New Di-[3-(3-Alkyl/Aryl-4,5-Dihydro-1h-1,2,4-Triazol-5-One-4-Yl)-Azomethinphenyl] Isophthalate/Terephthalate Derivatives, Haydar Yüksek, Özlem Gürsoy Kol
Turkish Journal of Chemistry
3-Alkyl(Aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2) reacted with di-(3-formylphenyl) isophthalate (3) and di-(3-formylphenyl) terephthalate (6) to afford the corresponding 6 novel di-[3-(3-alkyl/aryl-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)- azomethinphenyl] isophthalates (4) and 6 novel di-[3-(3-alkyl/aryl-4,5- dihydro-1H-1,2,4-triazol-5-one-4-yl)-azomethinphenyl] terephthalates (7), respectively. The acetylation reactions of compounds 4 and 7 were investigated, and 5 and 8 type compounds were obtained, respectively. The new compounds synthesized were characterized by using IR, ^1H-NMR, ^{13}C-NMR, and UV spectral data together with elemental analysis. In addition, to investigate the effects of solvents and molecular structure upon acidity, compounds 4 and 7 were titrated potentiometrically with tetrabutylammonium hydroxide in 5 non-aqueous solvents (isopropyl alcohol, tert-butyl alcohol, N,N-dimethylformamide, acetone, …
A New And Convenient Method Of Generating Alkyl Isocyanates From Alcohols, Thiols, And Trimethylsilyl Ethers Using A 2,4,6-Trichloro[1,3,5] Triazine/N-Bu_4nocn, Batool Akhlaghinia, Sima Samiei
A New And Convenient Method Of Generating Alkyl Isocyanates From Alcohols, Thiols, And Trimethylsilyl Ethers Using A 2,4,6-Trichloro[1,3,5] Triazine/N-Bu_4nocn, Batool Akhlaghinia, Sima Samiei
Turkish Journal of Chemistry
Alkyl isocyanates are prepared in good to excellent yields by treatment of alcohols, thiols, and trimethylsilyl ethers with 2,4,6-trichloro[1,3,5] triazine/n-Bu_4NOCN in acetonitrile. This method is highly selective for conversion of 1° alcohols to alkyl isocyanates in the presence of 2° and 3° alcohols, thiols, and trimethylsilyl ethers.
New Aromatic Polyamide With Azo And Phosphine Oxide Groups In The Main Chain, Khalil Faghihi, Mohsen Hagibeygi
New Aromatic Polyamide With Azo And Phosphine Oxide Groups In The Main Chain, Khalil Faghihi, Mohsen Hagibeygi
Turkish Journal of Chemistry
A new flame-retardant polyamide containing phosphine oxide and azobenzene moieties in the main chain was synthesized by the solution polycondensation reaction of 4,4`-azodibenzoic acid with bis(3-aminophenyl) phenyl phosphine oxide using thionyl chloride, N-methyl-2-pyrrolidone and pyridine. This new polymer was obtained in high yield (96%) and showed high inherent viscosity (0.55 dL/g) and was characterized by elemental analysis, FT-IR spectroscopy, thermal gravimetric analysis (TGA and DTG) and solubility test. Furthermore, another polyamide was prepared by solution polycondensation reaction of 4,4`-azodibenzoic acid with 1,4-phenylene diamine and its flame-retardant behavior was compared by the use of the LOI with the previous one.
Efficient Method For Tetrahydropyranylation Of Phenols And Alcohols Using 2,4,6-Trichloro[1,3,5]Triazine, Batool Akhlaghinia, Elham Roohi
Efficient Method For Tetrahydropyranylation Of Phenols And Alcohols Using 2,4,6-Trichloro[1,3,5]Triazine, Batool Akhlaghinia, Elham Roohi
Turkish Journal of Chemistry
Alcohols and phenols were tetrahydropyranylated in the presence of 2,4,6-trichloro[1,3,5]triazine in good to excellent yields in acetonitrile.
Synthesis Of Nitrogen-Containing Heterocycles From The Reaction Of Amidrazones With \Alpha-Haloesters, Hany M. Dalloul, Peter H. Boyle
Synthesis Of Nitrogen-Containing Heterocycles From The Reaction Of Amidrazones With \Alpha-Haloesters, Hany M. Dalloul, Peter H. Boyle
Turkish Journal of Chemistry
The reaction of amidrazones 1 with \alpha-haloesters 2 formed 1,3,5-substituted 4,5-dihydro-1,2,4-triazin-6-ones (4a-z) rather than 1,2,4-triazin-5-one derivatives (5a-z). The microanalysis and spectral data of the synthesized compounds are in full agreement with their molecular structure.
Manganese(Iii) Acetate Mediated Free Radical Cyclization Of 1,3-Dicarbonyl Compounds With Sterically Hindered Olefins, Mehmet Yilmaz, Emre Bi̇çer, A. Tarik Pekel
Manganese(Iii) Acetate Mediated Free Radical Cyclization Of 1,3-Dicarbonyl Compounds With Sterically Hindered Olefins, Mehmet Yilmaz, Emre Bi̇çer, A. Tarik Pekel
Turkish Journal of Chemistry
The manganese(III) acetate mediated radical cyclization of dimedone 1a, 2,4-pentanedione 1b, ethyl acetoacetate 1c, 1,3-cyclohexanedione 1d and 5-phenyl-1,3-cyclohexanedione 1e with 1,1-diphenyl-1-butene 2a afforded 4,5-dihydrofurans (3c, 3e) and tetrahydrobenzofurans (3a, 3g, 3h) in good yields (55% - 77%). Additionally, the reactions of trifluoromethyl-group containing 1,3-dicarbonyls, 4,4,4-trifluoro-1-phenylbutane-1,3-dione 1f and 4,4,4-trifluoro-1-thien-2ylbutane-1,3-dione 1g with 2a 3-trifluoroacetyl-4,5-dihydrofurans gave in 74% and 78% yields, respectively. Treatment of 1a, 1b and 1c with 1,2-diphenyl-1-pentene 2a resulted in the formation of tetrahydrobenzofuran 3b and 4,5-dihydrofurans 3d and 3f in lower yields.
Synthesis Of 2-[2-(3,4,5-Trimethoxybenzoyloxy)Ethyl]Pyrrolidine Hydrochloride Controlled By Gc-Ms, ^1h And ^{13}C Nmr Analyses, Alicja Wodnicka, Malgorzata Dzieciol
Synthesis Of 2-[2-(3,4,5-Trimethoxybenzoyloxy)Ethyl]Pyrrolidine Hydrochloride Controlled By Gc-Ms, ^1h And ^{13}C Nmr Analyses, Alicja Wodnicka, Malgorzata Dzieciol
Turkish Journal of Chemistry
The synthesis of 2-[2-(3,4,5-trimethoxybenzoyloxy)ethyl]pyrrolidine hydrochloride was performed using 2-(2-hydroxyethyl)pyrrolidine as a starting material. Before the O-acylation reaction with 3,4,5-trimethoxybenzoyl chloride, the amino group was protected using benzyl chlorocarbonate. The removal of the blocking group was carried out in modified conditions, avoiding the alcoholysis of the ester bond. The final product was separated from its structural isomer by precipitation as its hydrochloride salt. Some steps of the synthesis were controlled by GC-MS. The identification of the respective compounds was performed by mass spectra analyses and confirmed by ^1H NMR, ^{13}C NMR, IR and elemental analyses.
A Convenient Synthesis Of 3,6-Disubstituted-1,4-Dihydro-[1,2,4,5]Tetrazines And Preparation Of New Acetic Acid Derivatives Containing 5-Oxo-4-Phenylamino- 4,5-Dihydro-[1,2,4]Triazole, Ahmet Demi̇rbaş
Turkish Journal of Chemistry
A series of compounds 8a-e, was synthesized by condensation of compounds 7a-e with ethyl bromoacetate. The treatment of compounds 8a-e with hydrazine hydrate afforded the corresponding hydrazide derivatives (9a-e). Subsequently, compounds 9a-e were converted to alkylidene hydrazides (10a-e). Moreover, upon heating in the presence of carboxylic acids, compounds 9a-e unexpectedly gave 1,4-dihydro-[1,2,4,5]tetrazine derivatives (11a-e).
Direct Dyes Derived From 4,4'-Diaminobenzanilide Synthesis, Characterization And Toxicity Evaluation Of A Disazo Symmetric Direct Dye, Georgeta Maria Simu, Sergiu Adrian Chicu, Nicole Morin, Walter Schmidt, Eugen Şişu
Direct Dyes Derived From 4,4'-Diaminobenzanilide Synthesis, Characterization And Toxicity Evaluation Of A Disazo Symmetric Direct Dye, Georgeta Maria Simu, Sergiu Adrian Chicu, Nicole Morin, Walter Schmidt, Eugen Şişu
Turkish Journal of Chemistry
The synthesis of a new symmetric disazo direct dye containing the non--carcinogenic 4,4'-diaminobenzanilide as the middle component and salicylic acid as the coupling component is presented. The synthesized dye is an analog of the benzidine based dye C. I. Direct Yellow 1 (C. I. 22,250) and was analyzed by thin layer chromatography (TLC), electronic spectra (VIS) and mass spectroscopy (FAB-MS). The coloristic and fastness properties of the synthesized dye were determined and compared with those of C. I. Direct Yellow 1. The toxicities of the dye and of its precursors were evaluated by biological tests, using the process of metamorphosis …
The Electrochemical Behaviors Of Superoxide Dismutase At Promoter Modified Gold Electrode, Xiaqin Wu, Xiaoyun Meng, Zhesu Wang, Zongrang Zhang
The Electrochemical Behaviors Of Superoxide Dismutase At Promoter Modified Gold Electrode, Xiaqin Wu, Xiaoyun Meng, Zhesu Wang, Zongrang Zhang
Journal of Electrochemistry
The electron_transfer process of superoxide dismutase was investigated by cyclic voltammetry at the 4,4'_dithiodipyridine,L_cysteine,histidine and arginine modified gold wire electrodes repectively.The quasi_reversible behavior was observed at L_cysteine modified gold electrode.An irreversible electrochemical behavior has been observed at hisdinine modified gold wire electrode.
Study On The Electron Transfer Process Of Cytochrome C With Different Charge Transfer Promoters, Guoxin Tang
Study On The Electron Transfer Process Of Cytochrome C With Different Charge Transfer Promoters, Guoxin Tang
Journal of Electrochemistry
The diffusion coefficient D. standard rate constant and transfer coefficient afor electron transfer process of cytochrome C at OTTLE in the presence of 4,4'-Dithiedipyridine(PySSPy),Adenine and L-Cysteine were determined by the chronoadsorptometric technique with Au-OTTLE. A computer fitting method was used to calculated these kinetic parameters.The mechanismsof PysSPy,Adenine and L-Cysteine were used as the promoters,and were also discussed.