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Full-Text Articles in Chemistry
Synthesis And Reactions Of Di(Thiophen-2-Yl)Alkane Diones: Cyclocondensation, Teki̇n Artunç, Abdullah Menzek
Synthesis And Reactions Of Di(Thiophen-2-Yl)Alkane Diones: Cyclocondensation, Teki̇n Artunç, Abdullah Menzek
Turkish Journal of Chemistry
Known 1,6-di(thiophen-2-yl)hexane-1,6-dione (2) and novel 1,7-di(thiophen-2-yl)heptane-1,7-dione (4) were obtained from the reactions of thiophene with the corresponding diacyl chlorides. Furthermore, compounds with furan and pyrrole units in place of thiophene units in compound 2 were obtained in the same way. Bromination of 2 and 4 gave bromides regioselectively. The reaction of each of the compounds 2 and 4 in HOAc medium yielded cyclocondensation products. In total, four known and eleven novel compounds were synthesized.
Unsymmetrical Zinc Phthalocyanines Containing Thiophene And Amine Groups As Donor For Bulk Heterojunction Solar Cells, Gülnur Keser Karaoğlan, Öznur Dülger Kutlu, Ahmet Altindal
Unsymmetrical Zinc Phthalocyanines Containing Thiophene And Amine Groups As Donor For Bulk Heterojunction Solar Cells, Gülnur Keser Karaoğlan, Öznur Dülger Kutlu, Ahmet Altindal
Turkish Journal of Chemistry
Photovoltaic technology is an alternative resource for renewable and sustainable energy and low costs organic photovoltaic devices such as bulk-heterojunction (BHJ) solar cells, which are selective candidates for the effective conversion of solar energy into electricity. Asymmetric phthalocyanines containing electron acceptor and donor groups create high photovoltaic conversion efficiency in dye sensitized solar cells. In this study, a new unsymmetrical zinc phthalocyanine was designed and synthesized including thiophene and amine groups at peripherally positions for BHJ solar cell. The structure of the targeted compound (4) was characterized comprehensively by FT-IR, UV-Vis, 1H-NMR, and MALDI-TOF MS spectroscopies. The potential of this …
An Anthracene Based Fluorescent Probe For The Selective And Sensitive Detection Of Chromium (Iii) Ions In An Aqueous Medium And Its Practical Application, Erman Karakuş
Turkish Journal of Chemistry
An anthracene based fluorescent probe, integrated with thiophene moiety, exhibited selective and sensitive detection of chromium (III) ions over other metal ions. Its synthesis was achieved by simple mixing of two commercially available compounds, 2-aminoanthracene, and 2-thiophenecarboxaldehyde, in onestep without the needed complex purification process. The probe molecule (ANT-Th) offered exceptional features such as "turn-on" fluorescence response, low detection limit (0.4 μM), and fast response time (< 1 min) via C$=$N bond hydrolysis. Also, a simple test paper system was developed for the rapid detection of chromium (III) ions with the naked eye.
Synthesis And Characterization Of New Thiophene--Benzimidazole-Based Electrochromes, Emi̇ne Gül Cansu Ergün
Synthesis And Characterization Of New Thiophene--Benzimidazole-Based Electrochromes, Emi̇ne Gül Cansu Ergün
Turkish Journal of Chemistry
In the present study, two new donor--acceptor--donor-type molecules were synthesized and the electro-optical properties of the resulting monomers and their corresponding polymers were investigated. Thiophene was selected as the donor unit and cycloheptyl- and cyclooctyl- substituted benzimidazoles were used as the acceptor units. The synthesized monomers and their electrochemically obtained polymers were characterized using cyclic voltammetry and UV-Vis spectrometry. The optical band gap values of the polymers were 1.62 eV and the polymer films changed color to gray upon oxidation, while they were brick red in their neutral states. Moreover, changing the ring size on the acceptor group from seven …
Cyanoacetamide Derivatives As Synthons In Heterocyclic Synthesis, Ahmed Ali Fadda, Samir Bondock, Ramy Rabie, Hassan Ali Etman
Cyanoacetamide Derivatives As Synthons In Heterocyclic Synthesis, Ahmed Ali Fadda, Samir Bondock, Ramy Rabie, Hassan Ali Etman
Turkish Journal of Chemistry
This review presents a systematic and comprehensive survey of the methods of preparation and the chemical reactivity of cyanoacetamide derivatives. These compounds are important intermediates for the synthesis of a variety of otherwise difficult to obtain synthetically useful and novel heterocyclic systems.
Acid-Base Equilibria Of Some N-Substituted Thiophene-2-Carboxamidoximes In Non-Aqueous Media, Nedi̇me Dürüst, Yaşar Dürüst, İlknur Meri̇ç
Acid-Base Equilibria Of Some N-Substituted Thiophene-2-Carboxamidoximes In Non-Aqueous Media, Nedi̇me Dürüst, Yaşar Dürüst, İlknur Meri̇ç
Turkish Journal of Chemistry
The protonation constants of the amino nitrogens of some N-substituted thiophene-2-carboxamidoximes have been determined in acetic acid by means of potentiometric titration with perchloric acid. pK_{a} values of the title compounds were interpreted on the basis of structural effects due to the substituents and the main skeleton.