Open Access. Powered by Scholars. Published by Universities.®
Physical Sciences and Mathematics Commons™
Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 14 of 14
Full-Text Articles in Physical Sciences and Mathematics
Kinetics Of Silver(I)-Catalyzed Oxidation Of Allyl Alcohol By Peroxodiphosphate Inacetate Buffers, Priyamvada Sharma, Riya Sailani, Deepmala Pareek, Chandra Lata Khandelwal
Kinetics Of Silver(I)-Catalyzed Oxidation Of Allyl Alcohol By Peroxodiphosphate Inacetate Buffers, Priyamvada Sharma, Riya Sailani, Deepmala Pareek, Chandra Lata Khandelwal
Turkish Journal of Chemistry
The kinetics and mechanism of silver(I)-catalyzed oxidation of allyl alcohol with peroxodiphosphate in acetate buffers have been studied. The rate is independent of allyl alcohol concentration. The effect of other reaction parameters such as hydrogen and acetate ions has also been studied. The rate law accounting for all experimental observations corresponds to the proposed mechanism. The energy and entropy of activation have also been evaluated by employing Eyring plots.
Singlet Oxygen Generation From Poly[4-Diacetoxyiodo]Styrene And Hydrogen Peroxide, Mustafa Çatir
Singlet Oxygen Generation From Poly[4-Diacetoxyiodo]Styrene And Hydrogen Peroxide, Mustafa Çatir
Turkish Journal of Chemistry
Treatment of hydrogen peroxide with a polymer-supported hypervalent iodine compound, poly[4-diacetoxyiodo] styrene (PDAIS), generates singlet molecular oxygen ($^{1}$O$_{2})$. Singlet oxygen generation was proved by trapping with typical organic compounds such as conjugated dienes, aromatic dienes, and electron-rich alkene. When compared to monomer analogue, the use of PDAIS in peroxidation of substrates gave slightly better yields (45%-96%). Regeneration and reuse of PDAIS showed similar activity. The mechanism underlying generation of singlet oxygen and reaction scope was examined.
Oxidation Of Hydrocarbons With Tetra-N-Butylammonium Peroxy Monosulfate Catalyzed By \Beta-Tetrabromo-Meso-Tetrakis(4-Methoxyphenyl)- And \Beta-Tetrabromo-Meso-Tetraphenylporphyrinatomanganese(Iii), Saeed Rayati, Saeed Zakavi, Hossein Valinejad
Oxidation Of Hydrocarbons With Tetra-N-Butylammonium Peroxy Monosulfate Catalyzed By \Beta-Tetrabromo-Meso-Tetrakis(4-Methoxyphenyl)- And \Beta-Tetrabromo-Meso-Tetraphenylporphyrinatomanganese(Iii), Saeed Rayati, Saeed Zakavi, Hossein Valinejad
Turkish Journal of Chemistry
\beta-Tetrabromo-meso-tetrakis(4-methoxyphenyl)porphyrin, H_2T(4-OCH_3P)PBr_4, was synthesized and characterized by UV-Vis and ^1H NMR spectroscopy. Oxidation of alkanes and olefins with tetra-n-butylammonium peroxymonosulfate (n-Bu_4NHSO_5) was studied in the presence of MnT(4-OCH_3P)PBr_4(OAc) and MnTPPPBr_4(OAc) (TPP = meso-tetraphenylporphyrin). While significance differences were observed between the catalytic activities of the title complexes in the oxidation of alkanes, the 2 manganese porphyrins showed comparable activities in oxidation of most of the olefins used. However, the latter showed greater catalytic performance in the oxidation of the hydrocarbons. Moreover, the oxidative degradation of the former (60 %) was greater than that of the latter (45 %) in the oxidation …
N-Bridged Dimers Of Tetrapyrroles Complexed By Transition Metals: Syntheses, Characterization Methods, And Uses As Oxidation Catalysts, Ümi̇t İşci̇, Fabienne Dumoulin, Alexander B. Soroki̇n, Vefa Ahsen
N-Bridged Dimers Of Tetrapyrroles Complexed By Transition Metals: Syntheses, Characterization Methods, And Uses As Oxidation Catalysts, Ümi̇t İşci̇, Fabienne Dumoulin, Alexander B. Soroki̇n, Vefa Ahsen
Turkish Journal of Chemistry
N-bridged dimers of tetrapyrroles complexed by transition metals have been known for nearly four decades, and gained renewed attention when their powerful oxidation properties were recently evidenced. This article is a state of the art review of the reported complexes and of their synthetic methods. Beyond classical chemistry characterization tools, specific methods appropriate to their structure are used and are presented in detail. Finally, their uses and importance of oxidation catalysts are reviewed.
Selective Oxidation Of Sulfides And Hydrocarbons With H_2o_2 Over Manganese Catalyst Supported On Nanoparticles, Massomeh Ghorbanloo, Roghayeh Tarasi, Jun Tao, Hidenori Yahiro
Selective Oxidation Of Sulfides And Hydrocarbons With H_2o_2 Over Manganese Catalyst Supported On Nanoparticles, Massomeh Ghorbanloo, Roghayeh Tarasi, Jun Tao, Hidenori Yahiro
Turkish Journal of Chemistry
A new magnetically separable catalyst consisting of binuclear Mn(II) complex [Mn_2(HL)_2(H_2O)_4], HL = 2-[(2-hydroxy-benzylidene)-amino]-3-(4-hydroxyphenyl)-propionic acid, supported on (3-chloropropyl)-trimethoxysilane (CPTMS) functionalized silica-coated magnetic nanoparticles (MNPs) was prepared. The synthesized catalyst was characterized by several physico-chemical and spectroscopic methods. This immobilized complex was found to be an efficient heterogeneous catalyst for the oxidation of different sulfides and hydrocarbons using hydrogen peroxide (H_2O_2) as an oxidant. The catalyst is readily recovered by simple magnetic decantation and can be recycled several times with no considerable loss of catalytic activity.
Synthesis, Structural Characterization, And Benzyl Alcohol Oxidation Activity Of Mononuclear Manganese(Ii) Complex With 2,2'-Bipyridine: [Mn(Bipy)_2(Clo_4)_2], İbrahi̇m Kani̇, Mehmet Kurtça
Synthesis, Structural Characterization, And Benzyl Alcohol Oxidation Activity Of Mononuclear Manganese(Ii) Complex With 2,2'-Bipyridine: [Mn(Bipy)_2(Clo_4)_2], İbrahi̇m Kani̇, Mehmet Kurtça
Turkish Journal of Chemistry
A manganese(II) complex of 2,2'-bipyridine (bipy) was synthesized and characterized by X-ray diffraction, IR, and UV-vis spectroscopy. The activity of the complex was tested for oxidation of benzyl alcohols using t-BuOOH as an oxidant in organic solvents and in an organic/water biphasic system (hexane/H_2O, toluene/H_2O). The effect of solvent, temperature, oxidant, and some additives (KBr, N(C_4H_9)Br, and N-bromosuccinimide) on the oxidation of benzyl alcohol is reported. The results show that benzyl alcohol was selectively converted to benzaldehyde in 71.9% yield within 4 h in acetonitrile. Control experiments performed without catalyst and the corresponding metal salt as catalyst produced no benzaldehyde …
Kinetics Of Co Oxidation Over Pt-Ceo_X Supported On Air-Oxidized Activated Carbon, Berri̇n Gülyüz, Şeyma Özkara Aydinoğlu, Ahmet Erhan Aksoylu, Zeynep İlsen Önsan
Kinetics Of Co Oxidation Over Pt-Ceo_X Supported On Air-Oxidized Activated Carbon, Berri̇n Gülyüz, Şeyma Özkara Aydinoğlu, Ahmet Erhan Aksoylu, Zeynep İlsen Önsan
Turkish Journal of Chemistry
Kinetics of low-temperature CO oxidation was studied under atmospheric pressure at 383 K in the initial rates region over 1wt%Pt-1wt%CeO_x supported on air-oxidized activated carbon (AC2). Feed concentrations of 1-5 mol% CO and 1-2.5 mol% O_2 with balance He were used for CO oxidation in the absence of hydrogen. A simple power-function rate expression was obtained with reaction orders of -0.24 in CO and 0.98 in O_2, and a plausible LHHW expression compatible with mechanisms reported in the literature was proposed. Feed concentrations of 5 mol% CO and 2.5 mol% O_2 were used for investigating the effect of the presence …
The Synthesis Of 2-(Chloromethyl)-6-Hydroxy-2h-Pyran-3 (6h)-One Via Achmatowicz Rearrangement, Zuhal Gerçek
The Synthesis Of 2-(Chloromethyl)-6-Hydroxy-2h-Pyran-3 (6h)-One Via Achmatowicz Rearrangement, Zuhal Gerçek
Turkish Journal of Chemistry
Achmatowicz rearrangement was carried out with 2-chloro-1-(furan-2-yl) ethanol, which was synthesized starting from 1-(furan-2-yl) ethanone. It was shown that the oxidation of 2-chloro-1-(furan-2-yl) ethanol with m-CPBA produced 2-(chloromethyl)-6-hydroxy-2H-pyran-3 (6H)-one in good yield (70%).
Low Temperature Co Oxidation Kinetics Over Activated Carbon Supported Pt-Sno_X Catalysts, Fatma Soyal Baltacioğlu, Berri̇n Gülyüz, Ahmet Erhan Aksoylu, Zeynep İlsen Önsan
Low Temperature Co Oxidation Kinetics Over Activated Carbon Supported Pt-Sno_X Catalysts, Fatma Soyal Baltacioğlu, Berri̇n Gülyüz, Ahmet Erhan Aksoylu, Zeynep İlsen Önsan
Turkish Journal of Chemistry
The kinetics of low temperature CO oxidation were studied over sequentially impregnated 1wt%Pt-0.25wt%SnO_x supported on HNO_3-oxidized activated carbon (AC3) using a wide range of CO (1-10 mol%) and O_2 (1-4 mol%) concentrations. Intrinsic kinetic data were obtained in the initial rates region at 383 K in the absence and presence of 5-45 mol% H_2 in the feed. A power-function rate expression with positive dependence on CO (0.96) and negative dependence on oxygen (--0.31) was obtained for the low temperature oxidation of CO. The effect of H_2 on CO oxidation rates was also investigated under similar conditions.
Fast Oxidation Of Lactams To Cyclic Imides Using Microwave Irradiation, Avat Arman Taherpour, Hamid Reza Mansuri
Fast Oxidation Of Lactams To Cyclic Imides Using Microwave Irradiation, Avat Arman Taherpour, Hamid Reza Mansuri
Turkish Journal of Chemistry
Since polar reactants can adsorb microwave irradiation, chemists can utilize the microwave oven for some organic reactions. In this paper, we report a rapid conversion of lactams to cyclic imides using peracetic acid (CH_3-CO_3H) and manganic chloride (MnCl_2) in ethyl acetate (CH_3-COOEt) as a solvent and under microwave irradiation (90 W, 5 min) in good yields.
Kinetics Of Oxidation Of Pyridylmethylsulphinylbenzimidazole By Cerium(Iv) In An Aqueous Perchloric Acid Medium, Dinesh C. Bilehal, Ravi̇raj M. Kulkarni, Sharanappa T. Nandibewoor
Kinetics Of Oxidation Of Pyridylmethylsulphinylbenzimidazole By Cerium(Iv) In An Aqueous Perchloric Acid Medium, Dinesh C. Bilehal, Ravi̇raj M. Kulkarni, Sharanappa T. Nandibewoor
Turkish Journal of Chemistry
The kinetics of oxidation of pyridylmethylsulphinylbenzimidazole [PMSB] by Ce(IV) in an aqueous perchloric acid medium at a constant ionic strength of 1.50 mol dm^{-3} were studied spectrophotometrically. The reaction showed first order kinetics with respect to Ce(IV) concentration and an apparent less than unit order dependence in [PMSB] and a zero order in [H^+]. The initial addition of products has no significant effect on the rate of the reaction. A possible mechanism is proposed here. The reaction constants involved in the mechanism have been computed. There is good agreement between the observed and calculated rate constants under different experimental conditions. …
Application Of Ibx Method For The Synthesis Of Ketones From Carboxylic Acids, H. R. Ferhat Karabulut, Mesut Kaçan, Hasan Özyildirim
Application Of Ibx Method For The Synthesis Of Ketones From Carboxylic Acids, H. R. Ferhat Karabulut, Mesut Kaçan, Hasan Özyildirim
Turkish Journal of Chemistry
Methoxy phenyl propionic acid and some derivatives are converted to ketones using a new method. All classical methods to obtain ketones from carboxylic acids via acid halide consistently gave very low yields and regularly generated intermolecular cyclisation products or polymeric materials. However, high ketones yields are obtained by using the new IBX method.
Kinetics And Mechanism Of Oxidation Of L-Isoleucine And L-Ornithine Hydrochloride By Sodium N-Bromobenzenesulphonamide In Perchloric Acid Medium, Hemmige S. Yathirajan, Chapuradoddi R. Raju, Kikkeri N. Mohana, Sheena Shashikanth, Padmarajaiah Nagaraja
Kinetics And Mechanism Of Oxidation Of L-Isoleucine And L-Ornithine Hydrochloride By Sodium N-Bromobenzenesulphonamide In Perchloric Acid Medium, Hemmige S. Yathirajan, Chapuradoddi R. Raju, Kikkeri N. Mohana, Sheena Shashikanth, Padmarajaiah Nagaraja
Turkish Journal of Chemistry
Kinetic studies of the oxidation of L-isoleucine (ISL) and L-ornithine hydrochloride (ORH) by sodium N-bromobenzenesulphonamide (bromamine-B or BAB) were studied in aqueous perchloric acid medium. The rate shows first-order dependence on both [BAB]_0 and [amino acid]_0 and inverse first-order dependence on [H^+] for ISL and first-order dependence on [H^+] for ORH. The rate of reaction decreased with decreases in the dielectric constant of the medium. The addition of benzenesulphonamide (BSA), which is one of the reaction products, had no significant effect on the reaction rate. The rate remained unchanged with the variation in the ionic strength of the medium for …
Oxidation Of Ethylenediaminetetraacetic Acid By N-Bromosuccinimide In Aqueous Alkaline Medium -- A Kinetic Study, S. K. Mavalangi, M. R. Kembhavi, S. T. Nandibewoor
Oxidation Of Ethylenediaminetetraacetic Acid By N-Bromosuccinimide In Aqueous Alkaline Medium -- A Kinetic Study, S. K. Mavalangi, M. R. Kembhavi, S. T. Nandibewoor
Turkish Journal of Chemistry
The kinetics of oxidation of ethylenediaminetetraacetic acid (EDTA) by N-bromosuccinimide (NBS) in aqueous alkaline media was investigated at 25°C. Analysis of the results showed the reaction is first -- order with respect to [NBS] and apparently less than unit order each with respect to [EDTA] and [alkali]. The influence of the reaction products, ionic strength, temperature effect and dielectric constant of the medium on the rate of reaction was studied. The proposed mechanism is consistent with the observed kinetics. The reaction constants involved in the mechanism were derived. There is a good agreement between the observed and calculated rate constants …