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851.
Formation of the complex of ethyl viologen in its cationic (Ev+?) and neutral (Ev°) forms with β-cyclodextrin (β-CD) was investigated by means of voltammetric technique in buffer solution of pH 7.00. The number of βCD (n or m) per viologen species (Ev+?) or (Ev°), bonding equilibrium constants as well as bonding rate constants was calculated. The calculated values of $K_{\text{eq}}^{(1)}$ and $K_{\text{eq}}^{ ( 2)}$ (pertaining to the bonding of Ev+? and Ev° with βCD) are 13.6 M–n and 2.1 × 103 M?m , respectively, whereas the calculated values of n and m are 0.54 and 1.25, respectively. The bimolecular rate constant for the Ev°?βCD inclusion complex formation is 3.03 × 103 M?1s?1. These results are supported by the simulation of the experimental cyclic voltammograms. This study also highlights the significance of the proposed electrochemical method as compared to earlier studies on viologen-Cyclodextrin systems. 相似文献
852.
M. Rafiq S. Ali S. Shahzadi M. Shahid S. K. Sharma K. Qanungo 《Journal of the Iranian Chemical Society》2014,11(1):169-178
Organotin complexes have been synthesized by refluxing 2-mercapto-5-methyl benzimidazole with R2SnCl2/R3SnCl (R = Me, n-Bu, Ph) in 1:1 molar ratio in the first step. In the second step, synthesized organotin(IV) complexes were treated with CS2 and R2SnCl2/R3SnCl/PdCl2 to yield homo- and heterobimetallic complexes. The composition of the synthesized complexes, the bonding behavior of the donor groups, and structural assignments were studied by elemental analysis and different spectral techniques, including IR and multinuclear NMR (1H, 13C). The IR data shows bidentate nature of the ligand which is also confirmed by semiempirical study, while NMR data confirms the four-coordinated geometry in solution. The free ligand and its respective homo- and heterobimetallic complexes were screened in vitro against a number of microorganisms to assess their biocidal properties. The biological activity data show that complexes exhibits significant antibacterial and antifungal activities as compared to ligand with few exceptions. 相似文献
853.
Mohammad Mahdi Ahari-Mostafavi Ali Sharifi Mojtaba Mirzaei Massoud Amanlou 《Journal of the Iranian Chemical Society》2014,11(4):1113-1119
The objective was to obtain new scaffold of compounds possessing anti-urease activity. For this new and simple method for the synthesis of β-aryl-β-mercapto ketone derivatives based on Michael addition of thiophenol to chalcones in an ionic liquid as a solvent was improved. The products were obtained in good to moderate yields with high purity and characterized by spectral and elemental analyses. The activities of synthesized compounds were investigated as new inhibitors of jack bean urease. Among 22 synthesized compounds, all of them have shown inhibitory effect in micromolar range, and the most potent one has IC50 = 6 μM compared to hydroxyurea IC50 = 100 μM as a reference inhibitor. A docking study was performed using Autodock 4.2 in parallel to in vitro experiments to illustrate the corresponded binding affinities as well as binding site, and involved residues in interaction. These computational results complimented the experimental inhibition activity and enabled us to report a potent urease inhibitors based on β-aryl-β-mercapto ketone scaffold. 相似文献
854.
Nader Noroozi Pesyan Mohammad Jalilzadeh Nasim Yalabi Torkaman Ertan Şahin 《Journal of the Iranian Chemical Society》2014,11(1):35-45
Reaction of symmetrical and unsymmetrical (thio)barbituric acids with aldehydes in the presence of triethylamine afforded a new form of bis-(thio)barbiturate containing charge-separated inter- and eight-membered intramolecular H-bonds. The reaction products were obtained as bis-(thio)barbiturates containing eight-membered intramolecular H-bond in the presence of l-(+)-tartaric acid (TA). The intramolecular H-bond strength (kcal/mol) and corresponding pKa value for 4ab′ were estimated to be 37 kcal/mol and ?1.3, respectively. 相似文献
855.
Preparation of antibody-coated gold nanoparticles (GNPs) specific to aflatoxins B1, B2, G1 and G2 and its use in developing aflatoxins diagnostic method were presented in this paper. The formation of gold-labeled antibodies was accomplished at optimal condition. Due to severe overlapping between the emission profiles for the aflatoxins, they cannot be determined by direct inspection of data. The strategy used in this study, constituted by artificial neural network (ANN), was easy to implement and to originate reliable results. ANN can be successfully applied to spectrofluorimetric spectra matrices to simultaneous determination of total aflatoxins. Quantitative results obtained using ANN method for aflatoxins in pistachio nuts samples were compared to those obtained using the HPLC method. Obtained results using these two methods did not show significant differences. 相似文献
856.
Hadi Baharifar Ali Reza Fakhari Hakimeh Ziyadi Mohammad Ali Oghabian Amir Amani Reza Faridi-Majidi 《Journal of the Iranian Chemical Society》2014,11(1):279-284
In this work, electrophoresis was successfully used to separate three different polymer-coated magnetic iron oxide nanoparticles with similar sizes (nominally 50 nm) using high-pH borate buffer system. The coating polymers were dextran, polyethylene glycol, or carboxymethyl dextran. The results showed that the migration time of carboxymethyl dextran coated nanoparticles is the longest due to relatively more negative surface charges. Investigation of the effects of buffer concentration, pH, electric field strength and the capillary temperature, on electrophoretic properties of samples was also carried out. The results showed that pH, electric field strength and the capillary temperature had indirect relations with both of the migration time and the separation resolution of three different polymer-coated nanoparticles while the buffer concentration had a direct relation. 相似文献
857.
Firouzeh Nemati Mehrnoosh Golmohammadi Afkham Ali Elhampour 《Green Chemistry Letters and Reviews》2014,7(1):79-84
Sulfonic acid-functionalized silica-coated nano-Fe3O4particles (Fe3O4@SiO2–SO3H) serve as a novel heterogeneous catalyst for the synthesis of acylals by direct condensation of aldehydes with acetic anhydride under solvent-free conditions at room temperature in short reaction times and excellent yields. The catalyst could be easily separated from the final product using an external magnet and reused several times without consequential loss of reactivity. 相似文献
858.
859.
Mohammad Vatankhah‐Varnoosfaderani Amin GhavamiNejad Saud Hashmi Florian J. Stadler 《Macromolecular rapid communications》2015,36(5):447-452
Copolymers of N‐isopropylacrylamide (NIPAM) and dopamine methacrylate can establish a reversible, self‐healing 3D network in aprotic solvents based on hydrogen bonding. The reactivity and hydrogen bonding formation of catechol groups in copolymer chains are studied by UV–vis and 1H NMR spectroscopy, while reversibility from sol to gel and inverse as well as self‐healing properties are tested rheologically. The produced reversible organogel can self‐encapsulate physically interacting or chemically bonded solutes such as drugs due to thermosensitivity of the used copolymer. This system offers dual‐targeted and controlled drug delivery and release—by slowing down release kinetics by supramolecular bonding of the drug and by reducing diffusion rates due to modulus increase.
860.
Zia‐ur‐ Rehman Muhammad Moazzam Naseer Afzal Shah Saqib Ali Auke Meetsma 《Heteroatom Chemistry》2015,26(2):123-133
A fascinating ligand, 4‐formylpiperazinium 4‐formylpiperazine‐1‐carbodithioate (L‐salt) has been reacted with two electronically and sterically different trimethyltin(IV) chloride and triphenyltin(IV) chloride. The complexes 1 and 2 were characterized by elemental analysis, spectroscopic techniques, and X‐ray single crystal analysis. The latter technique confirmed the polymeric and monomeric nature of 1 and 2 , respectively. Both 1 and 2 showed intriguing molecular packing properties in the solid state. However, the packing of 1 is more interesting and unique where one‐dimensional polymer chains self assemble in two‐over‐two saltire‐shaped fashion to provide an overall multilayered structure. The different behavior of L toward two different tin(IV) compounds can be attributed to different electronic and steric environments around metal center. 相似文献