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^1h Nmr, Infrared And Mass Spectrometry Of Di- And Tri-Organotin Derivatives Of 1-Nitroso-2-Naphthol, Saqib Ali, Muhammad Mazhar, Moazzam Hussain Bhatti, Sohail Mahmood, Abida Kalsoom
^1h Nmr, Infrared And Mass Spectrometry Of Di- And Tri-Organotin Derivatives Of 1-Nitroso-2-Naphthol, Saqib Ali, Muhammad Mazhar, Moazzam Hussain Bhatti, Sohail Mahmood, Abida Kalsoom
Turkish Journal of Chemistry
The di- and tri-organotin derivatives R\2SnL\2 and R\3SnL where R = CH\3, n--C\4H\9, C\6H\5, C\6H_{11} and C\6H\5CH\2 and L = 1-nitroso-2-naphthoxy were synthesized. These derivatives were characterized by elemental analysis, infrared, ^1H NMR and mass spectrometry.
Synthesis Characterization And Miscibility Of Polyvinyl Butyrals Of Varying Vinyl Alcohol Contents, Z. M. Zhou, D. J. David, W. J. Macknight, F. E. Karasz
Synthesis Characterization And Miscibility Of Polyvinyl Butyrals Of Varying Vinyl Alcohol Contents, Z. M. Zhou, D. J. David, W. J. Macknight, F. E. Karasz
Turkish Journal of Chemistry
Polyvinyl butyrals (PVB) of systematically varying vinyl alcohol content have been synthesized and characterized using wet chemistry, IR, DSC, and TGA. The miscibility of PVB-PVB blends was studied by DSC as a function of vinyl alcohol content and vinyl alcohol content differences between the respective blend components. These data were use to construct an isothermal miscibility map of PVB and to calculate the intramolecular interaction parameter \chi_{VA,VB}. The \chi_{VA,VB} was a function of the absolute level of the vinyl alcohol (VA) and vinyl butyral (VB) contents of the polymers. In addition, the thermal stability of polyvinyl butyral was found to …
Dielectric Studies Of Various Olefin/So2 Copolmers, B. Baysal, Candan Erbi̇l, Paul L. Morganelli, W. H. Stockmayer
Dielectric Studies Of Various Olefin/So2 Copolmers, B. Baysal, Candan Erbi̇l, Paul L. Morganelli, W. H. Stockmayer
Turkish Journal of Chemistry
Dielectric constant and loss have been measured at low and high frequencies for several poly(1-olefin sulfones) as well as for the polysulfones of allybenzene and allyl cyclopentane. The low-frequency dispersion in allylbenzene due to helical sequences is weaker in benzene than in dioxane, and in both solvents is much lower than for the 1-olefin polymers. Solvent effects on the high frequency process are also reported, but yield no simple uniform picture.
Some Remarks On Solid State Polymerization, George Adler
Some Remarks On Solid State Polymerization, George Adler
Turkish Journal of Chemistry
No abstract provided.
Network Characterization Of Energetic Poly(Glycidyl-Azide), Mehmet S. Eroğlu, Olgun Güven
Network Characterization Of Energetic Poly(Glycidyl-Azide), Mehmet S. Eroğlu, Olgun Güven
Turkish Journal of Chemistry
Energetic poly(glycidyl azide) (PGA) elastomers with different crosslink densities were prepared by varying the NCO/OH reactive-groups ratio from 0.8 to 1.0. In the preparation of the elastomers, PGA chains were end-liked with a mixture of hexamethylene diisocyanate (HMDI) and trimethylol propane (TMP) at a fixed TMP/PGA mole ratio. The number average molar mass between junction points of the network chains \overline{{\rm M}}_c was calculated using data obtained from swelling and uniaxial tensile tests and the results were compared. For the mechanical characterization of the networks, Mooney-Rivlin plots were prepared and the values of the constants 2C_1 and 2C_2 of PGA …
Synthesis Of The New Cation Exchange Resins Having Poly (Styrene-Caprolactone) Units, S. Savaşkan Yilmaz, Hulisi Özbayrak, Baki Hazer
Synthesis Of The New Cation Exchange Resins Having Poly (Styrene-Caprolactone) Units, S. Savaşkan Yilmaz, Hulisi Özbayrak, Baki Hazer
Turkish Journal of Chemistry
The crosslinked polystyrene-polycaprolactone , PS-PCL-, block copolymers were prepared by the copolymerization of styrene and poly(caprolacton dimethylmethacrylate) (PCL-DM). The molecular weights of polycaprolactone, PCL, PCL-DM were 1250 and 2000. The swelling in H_2O or CHCl_3 of the sulfonated and unsulfonated block copolymers were determined under comparable conditions and investigated. The capacities of the obtained ion exchange resins were 1.31 and 1.10 meq/g.
Thermal Stabilities Of Hydroxyalkyl Terminated Polydimethylsiloxane Oligomers, İskender Yi̇lgor, Emel Yi̇lgor
Thermal Stabilities Of Hydroxyalkyl Terminated Polydimethylsiloxane Oligomers, İskender Yi̇lgor, Emel Yi̇lgor
Turkish Journal of Chemistry
The thermal stabilities of \alpha,\omega-hydroxypropyl, \alpha,\omega-hydroxybutyl \alpha,\omega-2-hydroxypentyl and \alpha,\omega-hydroxyhexyl terminated polydimethylsiloxane oligomers were investigated. Hydroxypropyl and hydroxybutyl terminated polydimethylsiloxane oligomers showed degradation upon heating through the loss of functional end groups, as determined by FTIR spectroscopy and gel permeation chromatography. \alpha,\omega-Hydroxyhexyl and \alpha,\omega-2-hydroxypentyl terminated polydimethylsiloxane oligomers were stable under similar conditions. The instability of the end groups is due to the backbiting of the terminal silicon in the PDMS by the primary hydroxyl oxygen, leading to the formation of 5-and 6-membered stable, heterocylic compounds. Loss of end groups also resulted in a dramatic increase in the molecular weights of the …
New Synthetic Approach For The Synthesis Of Liquid Crystalline Block And Graft Copolymers, Yeşim Hepuzer, İ. Ersin Serhatli, Yusuf Yağci
New Synthetic Approach For The Synthesis Of Liquid Crystalline Block And Graft Copolymers, Yeşim Hepuzer, İ. Ersin Serhatli, Yusuf Yağci
Turkish Journal of Chemistry
Liquid crystalline block and graft copolymers were synthesized according to the macroinitiator and macroinimer concept. For this purpose, side chain block copolymers (polytetrahydrofuran-b-polymethylmethacrylate) having liquid crystalline 4,4'- cyanobiphenyl blocks were prepared and characterized. Unlike the liquid-crystalline homopolymer with mesogenic units in the side chain, all block and graft copolymers showed a smectic A mesophase. The transition temperatures are hardly affected by the composition and molecular weight of the blolck copolymers.
Electrical Conductivity Of Sodium Doped Poly(4-Vinylpyridine), Murat Özyalçin, Zuhal Küçükyavuz, Aref Jarvaherian, Savaş Küçükyavuz
Electrical Conductivity Of Sodium Doped Poly(4-Vinylpyridine), Murat Özyalçin, Zuhal Küçükyavuz, Aref Jarvaherian, Savaş Küçükyavuz
Turkish Journal of Chemistry
Poly(4-Vinylpyridine) was synthesized by free radicalic polymerization. Solution doping process with metallic sodium was carried out. A conductivity value around 10^{-6} S/cm was obtained. Relative change in the coductivity with dopant concentration, temperature dependence of conductivity, conductivity behavior in atmospheric conditions for the samples were analyzed. SEM and EDX techniques were also used for the characterization of the polymer.
Crystal Structure Effect In Radiation-Induced Solid-State Polymerization Of Acrylamide, Ali Usanmaz
Crystal Structure Effect In Radiation-Induced Solid-State Polymerization Of Acrylamide, Ali Usanmaz
Turkish Journal of Chemistry
Crystal structure of arcylamide at -150^{\circ}C was studied to understand the role of the crystal structure on the reaction mechanism of radiation-induced polymerization in the solid-state. Acrylamide crystallizes in the monoclinic unit cell with the unit cell parameters as ; a=828.0(2) pm, b=578.0(4) pm, c=974.9(2) pm, \beta=119.62(4)^0, space group =P 2_1/c, Z=4 molecules/unit cell, d_x = 1.165 g/cm^3. From the results of the structural data a polymerization mechanism in the solid-state is suggested. The radiation damage in single crystal of acrylamide was also investigated in detail. The result showed the formation of the amorphous polymer, that phase separated from the …
Electrical Conductivities Of Poly (Alkyl Vinyl Ketones) Reacted With Dopant Solutions, Jun Hui Ma, J. David Tauber, Ülkü S. Ramelow
Electrical Conductivities Of Poly (Alkyl Vinyl Ketones) Reacted With Dopant Solutions, Jun Hui Ma, J. David Tauber, Ülkü S. Ramelow
Turkish Journal of Chemistry
Poly ethyl vinyl ketone (PEVK) and poly methyl vinyl ketone (PMVK) were prepared using photochemical processes. The irradiation of monomers with UV light provides a new method, different from the methods previously used for the polymerization of these monomers. FTIR and UV spectroscopies were used for the structure and reaction mechanism of the polymers. NMR was used to calculate the conversion percentage of MVK and EVK polymers. The conductivity change at various temperatures was traced during reactions of PMVK and PEVK with various dopant concentrations and the activation energy of these reactions were calculated by adding dopants and by adjusting …
A Two-Dimensional Monte Carlo Polymerization Of 5-Membered Rings, Okan Esentürk, H. Önder Pamuk, E. Yurtsever
A Two-Dimensional Monte Carlo Polymerization Of 5-Membered Rings, Okan Esentürk, H. Önder Pamuk, E. Yurtsever
Turkish Journal of Chemistry
A modification of the kinetic growth model in two dimensions for the polymerization of 5-membered rings is presented. The preliminary results reveal the validity of the modified model.
Phase Transition Of Hydrolyzed Polyacrylamide Gels In Aqueous Solutions Of Poly(Ethylene Glycol), Nilhan Kayaman, Oğuz Okay, B. M. Baysal
Phase Transition Of Hydrolyzed Polyacrylamide Gels In Aqueous Solutions Of Poly(Ethylene Glycol), Nilhan Kayaman, Oğuz Okay, B. M. Baysal
Turkish Journal of Chemistry
Hydrolyzed polyacrylamide gels immersed in aqueous solutions of poly(ethylene glycol) (PEG) of molecular weight 300 exhibit a discontinuous volume change upon continuous increase of the PEG concentration in the external solution. As the duration of hydrolysis increases, that is, as the proportion of the ionic groups on the network chains increases, the critical concentration of PEG required for a discontinuous volume change rises and, also, the magnitude of the volume collapse becomes larger. Experimental results indicate that the gel collapse in PEG solution is due to the osmotic deswelling of the ionic gel rather than due to a complex formation …
A Quantum-Chemical Investigation On 5,5'-Bi(1h-1.2,4-Triazole)), A. A. İki̇zler, R. Abbasoğlu, N. Saltek, M. Şeri̇fova
A Quantum-Chemical Investigation On 5,5'-Bi(1h-1.2,4-Triazole)), A. A. İki̇zler, R. Abbasoğlu, N. Saltek, M. Şeri̇fova
Turkish Journal of Chemistry
The conformational analysis of flexible 5,5'-bi(1H-1,2,4-triazole) molecule containing various reaction centers has been performed by the semiempirical methods MNDO,AM1 and PM3, and the internal rotation barrier calculated. The most stable conformation of the molecule has been determined to be the planar trans conformation. According to the three methods, 5,5'-bi(1H-1,2,4-triazole) molecule (C) has been found to be relatively more stable than its tautomer 3,3'-bi(1H-1,2,4-triazole)(B) and to be less stable than its other tautomer 3,3'-bi(4H-1,2,4-triazole)(A). Moreover, the electronic properties of 5,5'-bi(1H-1,2,4-triazole) molecule and the effect of conformational changing on electronic and geometric properties have also been investigated. To determine the protonation sites …
High Rates Of Fluorescence Quenching Between Perylene Dodecyldiimide And Certain \Pi-Electron Donors, S. İçli̇, H. İci̇l, İ. Gürol
High Rates Of Fluorescence Quenching Between Perylene Dodecyldiimide And Certain \Pi-Electron Donors, S. İçli̇, H. İci̇l, İ. Gürol
Turkish Journal of Chemistry
Perylene bis-n-dodecyl diimide is found to quench fluorescenc emissions of naphthalene, phenanthrene and dihydrocarbazolocarbazole molecules at rates of 4.4\times10^{11}, 2.8\times10^{12} and 2.5\times10^4 M^{-1} sec^{-1}, in respective order of aromaticity. These unusulally high rates of fluorecence quenchings are attributed to Perrin model static quenching and presence of electron transfer through singlet excited state of perylene diimide. Calculated free energy of electron transfer, \Delta G_{ET}=-120.5 kJ/mol, between perylene diimide and dihydrocarbazolocarbazole is taken as evidence for observation of high fluorescence quenching rate for carbazolocarbazole molecule. Keywords: Fluorescence quenching, Photoenergy transfer, Perylene diimide and Carbazolocarbazole
Possible Roles Of Transition Metals In Cloudwater Relative To The Solar Short-Wave Radiation Absorption Anomaly, Xudong Huang, S. Sinan Keski̇n, Francis Pink, İlhan Ölmez
Possible Roles Of Transition Metals In Cloudwater Relative To The Solar Short-Wave Radiation Absorption Anomaly, Xudong Huang, S. Sinan Keski̇n, Francis Pink, İlhan Ölmez
Turkish Journal of Chemistry
Measurements of the absorption of solar short-wave radiation by clouds exceed those predicted by theoretical calculations. In order to understand the roles of minor and trace species in this absorption anomaly, cloudwater samples were collected from individual precipitating clouds and analyzed for trace metals and anionic species. Two generalized approaches were used to assess the direct impact of the absorption of solar short-wave radiation by transition metals and/or their anionic complexes. Additionally, it was suggested that iron and manganese may act as catalyts in the formation of sulfate aerosols which efficiently scatter solar radiation.
Constituents Of Salvia Verticillata, Ufuk Sönmez, Gülaçtı Topçu, Ayhan Ulubelen
Constituents Of Salvia Verticillata, Ufuk Sönmez, Gülaçtı Topçu, Ayhan Ulubelen
Turkish Journal of Chemistry
Three new and fourteen known compounds were isolated from the roots of {\it Salvia verticillata L.} Spectral methods were used for the structure determination besides TLC comparisons with authentic samples for the known compounds.
The Reliability Of Jung-Biggs-Moorhead Method For Cholesterol Determination In The Presence Of Ergosterol, Lemi Türker, Şahinde Demi̇rci̇, Marjan Akdağ
The Reliability Of Jung-Biggs-Moorhead Method For Cholesterol Determination In The Presence Of Ergosterol, Lemi Türker, Şahinde Demi̇rci̇, Marjan Akdağ
Turkish Journal of Chemistry
In the present study, the reliability of Jung-Biggs-Moorhead method for cholesterol determination has been tested in the presence of another steroid, ergosterol. It was observed that presence of ergosterol interferes with the absorbance measurement of cholesterol. When both steroids are present in the sample maximum absorption wavelength are not shifted by the mutual interaction but absorbance values are changed considerably. Therefore this method may be used only for qualitative bu not quantitative analysis for cholesterol in the presence of ergosterol.
Immobilization Of Glucose Oxidase And Urease In Hydrogel Matrices, İhsan Gürel, M.Yakup Arica, Vasıf Hasirci
Immobilization Of Glucose Oxidase And Urease In Hydrogel Matrices, İhsan Gürel, M.Yakup Arica, Vasıf Hasirci
Turkish Journal of Chemistry
Immobilization of glucose oxidase and urease in hydrogels of 2-hydroxyethyl methacrylae, and N-vinyl pyrrolidone (NVP) was achieved by irradiation (using UV kand \gamma- rays). The effect of radiation on entrapment efficiencies, retention of activities and swelling rates was obtained. To optimize the system, duration of exposure, reaction temperature, co-monomer concentrations, initiator and cross linker compositions were varied. The repeated reusability of the generated products was also tested. It was found that\gamma-irradiation at very low temperatures did not have a detrimental effect on the enzyme activity. Incorporation of more hydrophilic monomer (NVP), influenced matrix morphology and entrapment efficiencies and retained enzyme …
Photoelectron Spectroscopy: A Tool In Sorption Studies, Şefik Süzer, Hasan N. Erten
Photoelectron Spectroscopy: A Tool In Sorption Studies, Şefik Süzer, Hasan N. Erten
Turkish Journal of Chemistry
Photoelectron spectroscopy using AlK\alpha (h\nu=1486.3 eV) has been applied to study the sorption of Cs^+, Sr^{2+}, Ba^{2+}, Zn^{2+} and Co^{2+} on magnesite kaolinite, smectite and chlorite. From the observed intensities of photoelectron peaks it was determined that in magnesite the sorption affinity of the above ions follow the order: Ba^{2+}>Co^{2+}\congSr^{2+}\congZn^{2+}>Cs^+. The order for the sorption of Ba^{2+} and Cs^+ are also determined as chlorite>magnesite>smectite>kaolinite and smectite>chlorite\congkaolinite>magnesite, respectively.
A Topological Approach To The Stabilities Of Isomeric Hückel And Mobius Type Cyclacenes, Lemi Türker
A Topological Approach To The Stabilities Of Isomeric Hückel And Mobius Type Cyclacenes, Lemi Türker
Turkish Journal of Chemistry
Within the constraints of Hückel molecular orbital theory, Hückel and Mobius type cyclacenes were investigated in terms of their angle of total \pi-electron energy, O_{\pi}, and cos O_{\pi} to find out how structural changes affect the stabilities. It has been theoretically deduced that as the number of benzenoid rings (R) increases the isomeric Hückel and Mbius type cyclacenes should have comparable stabilities, although for low values of R odd-Hückel type and even-Mobius type are predicted to be more stable.
Hydrolysis And Condensation Reactions Of Methacrylate-Modified Aluminum Alkoxides, Ertuğrul Arpaç, Efraim Avşar
Hydrolysis And Condensation Reactions Of Methacrylate-Modified Aluminum Alkoxides, Ertuğrul Arpaç, Efraim Avşar
Turkish Journal of Chemistry
The hydrolysis of aluminum tri-sec-butoxide and compounds obtained by substituting the larger functional groups for the present alkly groups in Al(O-sec-Bu)_3, and the reaction of these products with a polymerizable organic ligand, i.e. methacrylic acid, were studied together with the hydrolysis reactions of the final products. A good method of preparing high-tech materials and new composites uses organo-substituted silicon esters and/or alkoxides of various elements in a polycondensation process. Introducing a suitable organic network into the inorganic backbone gives desirable properties in new coating materials. The preparation of such materials is possible via the hydrolysis of metal alkoxides. Usually, different …
Potentiometric And Spectroscopic Determinaton Of Acid Dissociation Constants Of Some Phenols And Salicylic Acids, Rahmiye Aydin, Ulviye Özer, Naciye Türkel
Potentiometric And Spectroscopic Determinaton Of Acid Dissociation Constants Of Some Phenols And Salicylic Acids, Rahmiye Aydin, Ulviye Özer, Naciye Türkel
Turkish Journal of Chemistry
The dissociation constant of the catechol derivatives 4-nitrocatechol (NCAT), 2,3-dihydroxybenzoic acid (2,3-DHBA), 3,4-dihydroxybenzoic acid (3,4-DBHA), 3,4-dihydroxyhenylacetic acid (3,4-DPHA) and 3,4-dihydroxycinnamic acid (3,4-DHCA) were identified in 0.1M NaClO_4 ionic medium, at t=25^{\circ}C, by potentiometry. In addition, the first and second dissociation constants of the salicylic acid derivatives 5-nitrosalicylic acid (5-NSA), 4-hydroxysalicylic acid (4-HSA) 5-nitrosalicylic acid (5-HSA) were also determined by potentiometry. Furthermore, the second acid dissociation constants of these ligands were evaluated in I=0.1M NaClO_4 ionic medium, at a temperature of 25^{\circ}C by computer analysis of spectroscopic data.
The Investigation Of Aluminum Sulfate-Potassium Chloride Solid Phase Reaction, İ. Ayhan Şengi̇l
The Investigation Of Aluminum Sulfate-Potassium Chloride Solid Phase Reaction, İ. Ayhan Şengi̇l
Turkish Journal of Chemistry
It was found that aluminum sulfate reacts with potassium chloride to produce K_{2}SO_{4}, Al_{2}O_{3}, and Cl_{2} in the solid phase at 700 ^{\circ}C. This reaction was investigated with thermal analysis under air and nitrogen atmosphere. By changing temperature and time parameters, the actual yield of conversion in question was examined analytically and the optimum temperature and time were found for the reaction. The rate expression of the solid phase reaction was also investigated and the rate equation was obtained.
Analysis Of Retention In Supercritical Fluid Chromatography And Its Relation To Solubility, Z. Şermin Gönenç, Uğur Akman, Aydın K. Sunol
Analysis Of Retention In Supercritical Fluid Chromatography And Its Relation To Solubility, Z. Şermin Gönenç, Uğur Akman, Aydın K. Sunol
Turkish Journal of Chemistry
The effects of temperature, pressure and supercritical fluid density on the solubility-retention relationship of solutes in supercritical fluid chromatography are investigated. New retention data for naphthalene, phenanthrene, benzoic acid and 2-methoxy-naphthalene is obtained as a function of pressure at different temperatures. The bulk of the data is taken near the critical region of the mobile gas where the anomalities are expected. This data is used to compare two approaches for thermodynamic modeling of pressure dependence of solute retention. In these approaches, mobile-phase partial molar volumes of the solutes are determined either from bulk solubility data or from infinite-dilution fugacity coefficients. …
Quantum-Chemical Investigations On The Functionalized 1h-Pyrimidines, İsmail Yildirim, Makbule Tezcan, Yahya Güzel, Emin Saripinar, Yunus Akçamur
Quantum-Chemical Investigations On The Functionalized 1h-Pyrimidines, İsmail Yildirim, Makbule Tezcan, Yahya Güzel, Emin Saripinar, Yunus Akçamur
Turkish Journal of Chemistry
Conformational analysis and quantum-chemical calculations were carried out by means of the methods MMP2 and SCF MO LCAO in the CNDO/2 and MNDO approximation for the series of compounds being functionalized 1H- pyrimidines. The analysis of the electron density distribution depending on the substituents' nature was done on the basis of the data obtained.
Investigation Of Acid Sites On V_{2}O_{5}/Tio_{2}(A) Catalysts By Ftir With Adsorption Of Pyridine, Ahmet Akbaş, Holger Mi̇tzel, Dieter Höni̇ce
Investigation Of Acid Sites On V_{2}O_{5}/Tio_{2}(A) Catalysts By Ftir With Adsorption Of Pyridine, Ahmet Akbaş, Holger Mi̇tzel, Dieter Höni̇ce
Turkish Journal of Chemistry
The V_{2}O_{5}/TiO_{2}(A) catalysts were prepared by the grafting and their Br\"{o}nsted and Lewis acid sites were investigated with pyridine adsorption by using FTIR Spectroscopy. The results obtained showed that monolayer or less coverage of the surface of the support, TiO_{2}(A), took place up to V_{2}O_{5} content of 11.88 \%. When V_{2}O_{5} amount was higher then 11.88 \%, the support was covered as multilayer. Pyridine adsorption studies showed that the number of the Lewis acid sites of the V_{2}O_{5}/TiO_{2}(A) catalysts decreased with increasing of V_{2} O_{5} amount. The number of the Br\"{o}nsted acid sites increased with increasing V_{2}O_{5} content, reached a …
Poly (D,L-Lactic Acid) Homopolymers: Synthesis And Characterization, Xu Kaitian, Ahmet Kozluca, Emir B. Denkbaş, Erhan Pi̇şki̇n
Poly (D,L-Lactic Acid) Homopolymers: Synthesis And Characterization, Xu Kaitian, Ahmet Kozluca, Emir B. Denkbaş, Erhan Pi̇şki̇n
Turkish Journal of Chemistry
In this study, poly(D,L-lactic acid or D,L-lactide) (PDLLA) homopolymers were synthesized with different molecular weights. Low molecular weight PDLLAs (MW_n: 500-2300) were synthesized by direct polycondensation of DL-lactic acid without using any catalyst, while high molecular weight PDLLAs ( MW_n: 8x10^3-150x10^3) were produced by ring-opening polymerization of DL-lactide with stannous chloride as catalyst (initiator). Average molecular weights of PDLLAs were determined by end-group analysis, by viscosimetric measurements and by HPLC. PDLLA homopolymers were characterized by FTIR, NMR and DSC. In the production of PDLLAs by direct polymerization, molecular weights of the PDLLAs increased with the increase in the polymerization time …
Catalysis Of Autoxidation Of 2,6-Di-Tert-Butylphenol In Water By Metallophthalocyanine Tetrasulfonates Bound To Polyelectrolyte Supports, Yasemin Tura Kopkalli, Hayrettin Türk
Catalysis Of Autoxidation Of 2,6-Di-Tert-Butylphenol In Water By Metallophthalocyanine Tetrasulfonates Bound To Polyelectrolyte Supports, Yasemin Tura Kopkalli, Hayrettin Türk
Turkish Journal of Chemistry
2,6-and 2,10-Ionenes and soluble poly(vinylbenzyl)trimethylammonium chloride polyelectrolytes were synthesized and used as catalyst supports for cobalt-, iron- and copper-phthalocyanine tetrasulfonates on the autoxidation of 2,6-di-{\it tert}-butylphenol in water by molecular oxygen. Polyelectrolyte supported cobalt-phthalocyanine tetrasulfonate showed the highest activity in comparison with the supported analogous of iron- and copper-phthalocyanine tetrasulfonates. The supported metallophthalocyanine tetrasulfonates had better catalytic activities than the unsupported analogous for the reaction. The reaction yielded 3,3',5,5'-tetra-tert-butyl- 4,4'-diphenoquinone as the only oxidation product of 2,6-di-tert-butylphenol. The extent of the reaction was affected by time, temperature, pH, the types and concentrations of supports and metallophthalocyanine tetrasulfonates.
A Kinetic Study Of Homogeneous Bulk Polymerization Of Ethyl Methacrylate Initiated By Benzoyl Peroxide And An N, N^{\Prime} -Dimethylaniline Redox Pair, Serap Şenel, Belma Işik-Yürüksoy, Olgun Güven
A Kinetic Study Of Homogeneous Bulk Polymerization Of Ethyl Methacrylate Initiated By Benzoyl Peroxide And An N, N^{\Prime} -Dimethylaniline Redox Pair, Serap Şenel, Belma Işik-Yürüksoy, Olgun Güven
Turkish Journal of Chemistry
The homogenous bulk polymerization of ethyl methacrylate (EMA) was studied using benzoyl peroxide (BPO) and an N,N^{\prime}-dimethylaniline (DMA) redox pair with the dilatometric method. The half-order dependence of the polymerization rate upon both the BPO and DMA concentrations was obtained. The overall activation energy of the polymerization was found to be between 32.3-55.3 kJ/mole for different initial molar ratios of the redox pair. A retaring effect was observed at lower polymerization temperatures for low concentrations of BPO. The formation of reddish colored polymers at higher DMA concentrations was explained by the adsorption of adduct formed between DMA radicals.