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71.
A unique combination of a supported cobalt complex and the first example of supported NHPI in acetic acid gives a surprisingly stable heterogeneous catalytic system for the selective aerobic oxidation of methylaromatics to benzaldehydes at atmospheric pressure. 相似文献
72.
A simple, precise, sensitive and accurate method was developed for rapid determination of trace quantities of periodate. The method is based on the accelerating effect of periodate on the reaction of bromate and hydrochloric acid in the presence of hydrazine. The decolorization of methyl orange with the reaction products was used to monitor the reaction spectrophotometrically at 525 nm. Periodate could be determined in the concentration ranges of 0.02–1.5 g/mL. The relative standard deviation for ten replicate determinations of 0.3 g/mL of periodate was 1.12%. The method was applied to the determination of periodate in water samples and indirect determination of ethylene glycol in gasoline and glycerol in vegetable oil via Malaprade reaction with satisfactory results. 相似文献
73.
In this investigation, a facile sonochemical route has been developed for the preparation of silver vanadium oxide (SVO) micro/nanorods by using silver salicylate and ammonium metavanadate as silver and vanadate precursor, respectively. Here, silver salicylate, [Ag(HSal)], is introduced as a new silver precursor to fabricate AgVO3 nanorods. The effect of numerous solvents and surfactants on the morphology and sonochemical formation mechanism of AgVO3 nanorods was studied. AgVO3 nanorods were characterized by SEM and TEM images, XRD patterns, FT-IR, XPS, and EDS spectroscopy. SEM, TEM, and XRD results showed that AgO nanoparticles were formed onto AgVO3 nanorods in the presence of ethanol, cyclohexanol, dimethylsulfoxide (DMSO), and acetone. By using polyethylene glycol (PEG-6000) and N,N-dimethylformamide (DMF) as organic additives, the thickness of AgVO3 nanorods decreased. 相似文献
74.
Khodayar Gholivand Nilufar Dorosti Fatemeh Ghaziany Manouchehr Mirshahi Sina Sarikhani 《Heteroatom Chemistry》2012,23(1):74-83
A new series of N‐phosphinylureas 5b, 6a–7c was synthesized and characterized by 1H, 13C, 31P NMR, IR, and elemental analysis. The three‐dimensional structure of 5b has been determined by X‐ray crystallography. The crystal structure revealed the existence of four independent molecules. All structures form two chains with different arrangements and connect to each other via hydrogen bonds to produce two‐dimensional polymeric chains. The cytotoxicity of cyclophosphamide (a standard antitumor compound) and its nine analogues with formula R1C6H4 NHC(O)NHP(O)XCH2C(R2)2 CH2Y(X = Y = NH, R2 = CH3, R1 = H ( 5a ), CH3 ( 5b ), NO2 ( 5c ), X = O, Y = NH, R2 = H, R1 = H ( 6a , CH3 ( 6b ), NO2 ( 6c ), and X = Y = O, R2 = CH3, R1 = H ( 7a ), CH3 ( 7b ), NO2 ( 7c )) as well as phenyl urea were evaluated in vitro against three human tumor cell lines K562, MDA‐MB‐231, and HepG2. The results showed that most of the compounds have significant activity against the selected cell lines. Also, HepG2 cells were more sensitive to all the tested compounds than other cell lines. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 23:74–83, 2012; View this article online at wileyonlinelibrary.com . DOI 10.1002/hc.20754 相似文献
75.
A straightforward and modular preparative approach to 1,3,5-triaroylbenzene-based functionalized cyclophane ring systems has been developed. The key cyclophane-forming macrocyclization reaction was accomplished during the course of a regioselective cross-benzannulation between bis(aryl ethynyl) ketone and enaminone reactants. Macrocyclic products with ring sizes ranging from 18- to 22-membered were successfully constructed. The composition of the tether connecting the two aryl ethynyl ketone fragments can be easily varied; consequently, this method is suitable for construction of a diverse range of structurally distinct cyclophane products. To illustrate this feature, cyclophanes possessing xylyl, alkyl, di(ethylene triamine), and di(ethylene oxy) bridging units were synthesized in isolated yields of 11-46%. Three new cyclophanes (calixarene-like macrocyles 8 and 9, as well as crownophane 18) were structurally characterized by X-ray diffractometry. 相似文献
76.
Zeenat Zara Deepti Mishra Saurabh Kumar Pandey Eva Csefalvay Fatemeh Fadaei Babak Minofar David eha 《Molecules (Basel, Switzerland)》2022,27(1)
The effect of aqueous solutions of selected ionic liquids solutions on Ideonella sakaiensis PETase with bis(2-hydroxyethyl) terephthalate (BHET) substrate were studied by means of molecular dynamics simulations in order to identify the possible effect of ionic liquids on the structure and dynamics of enzymatic Polyethylene terephthalate (PET) hydrolysis. The use of specific ionic liquids can potentially enhance the enzymatic hydrolyses of PET where these ionic liquids are known to partially dissolve PET. The aqueous solution of cholinium phosphate were found to have the smallest effect of the structure of PETase, and its interaction with (BHET) as substrate was comparable to that with the pure water. Thus, the cholinium phosphate was identified as possible candidate as ionic liquid co-solvent to study the enzymatic hydrolyses of PET. 相似文献
77.
78.
Susan Sadeghi Fatemeh Fathi 《Journal of inclusion phenomena and macrocyclic chemistry》2010,67(1-2):91-98
A new PVC membrane coated graphite electrode for cesium ion based on 4′,4″(5′)di–tert-butyl di-benzo-18-crown-6 (DTBDB18C6) as ionophore was prepared. The electrode shows a near Nernstian response of 57.0 ± 1.8 mV decade?1 over a wide activity range of 6.0 × 10?6–1.0 × 10?1 mol L?1 with a limit of detection 4.0 × 10?6 mol L?1. The proposed electrode is suitable for use in aqueous solution in the pH range of 3.0–9.5. It has a fast response time of 10 s and can be used for at least 1 month without any considerable divergence in potential. The selectivity coefficients for Cs+ ion with respect to ammonium, alkali, alkaline earth and some selected transition metal ions were determined and showed a superior selectivity over Li+, Na+ and alkaline earth metal ions. The new electrode was applied for determination of Cs+ in spiked tap water. The electrode was also used as indicator electrode in potentiometric titration of Cs+ with sodium tetraphenyl borate. 相似文献
79.
M. R. Ganjali Tahereh Poursaberi Fatemeh Basiripour Masoud Salavati-Niassari Mohammad Yousefi Mojtaba Shamsipur 《Analytical and bioanalytical chemistry》2001,370(8):1091-1095
A PVC membrane electrode based on a cadmium–salen (N,N′-bis-salicylidene-1,2ethylenediamine) complex as an anion carrier is described. The electrode has an anti-Hofmeister selectivity
sequence with a preference for thiocyanate at pH 1.5–11.0. It has a linear response to thiocyanate from 1.0 × 10–6 to 1.0 × 10–1 mol L–1 with a slope of 59.1 ± 0.2 mV per decade, and a detection limit of 7 × 10–7 mol L–1. This electrode has high selectivity for thiocyanate relative to many common organic and inorganic anions. The proposed sensor
has a fast response time of approximately 15 s. It was applied to the determination of thiocyanate in a milk sample.
Received: 1 December 2000 / Revised: 19 April 2001 / Accepted: 30 April 2001 相似文献
80.
Afsaneh Safavi Norouz Maleki Fatemeh Honarasa Fariba Tajabadi Fatemeh Sedaghatpour 《Electroanalysis》2007,19(5):582-586
A new type of potentiometric sensor based on a recently constructed carbon ionic liquid electrode (CILE) is described. Two kinds of ionic liquids, i.e., N‐octylpyridinium hexafluorophosphate (OPFP) and 1‐butyl‐3‐methylimidazoluim hexafluorophosphate (BMFP) were tested as binder for construction of the carbon composite electrode. The characteristics of these electrodes as potentiometric sensors were evaluated and compared with those of the traditional carbon paste electrode (CPE). The results indicate that potentiometric sensors constructed with ionic liquid show an increase in performance in terms of Nernstian slope, selectivity, response time, and response stability compared to CPE. 相似文献