Analytical chemistry
Ghobad Mansouri; Mohammd Bagher Gholivand; Zarrin Eshaghi
Abstract
A single-use electrochemical sensor using ionic liquid mediated hollow fiber-graphite working electrode was fabricated for the first time. The screening tool was developed by coupling this electrode with differential pulse voltammetry (DPV) for in-situ pre-concentration and determination of Zn(II) and ...
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A single-use electrochemical sensor using ionic liquid mediated hollow fiber-graphite working electrode was fabricated for the first time. The screening tool was developed by coupling this electrode with differential pulse voltammetry (DPV) for in-situ pre-concentration and determination of Zn(II) and Cu(II). In our plot, porous polypropylene hollow fiber membrane was divided into pieces of 2 cm, then fiber's lumen and pores were satiated with homogeneous mixture of reduced graphene oxide (rGO) and three types used ionic liquids:(1-ethyl-3-methylimidazolium tetrafuoroborate), (1-butyl-3-methylimidazoliumhexafluorophosphate) and (1-butyl-2,3-dimethylimidazolium hexafluorophosphate) individually. Thereafter, a pencil graphite rod was placed inside the fiber. Fabricated sensors were used for single-step simultaneous purification and determination of Zn(II) and Cu(II) ions from water samples. The response surface method (RSM) was used as the basis of the design and analysis of the experiments. Parameters that were mostly important in the separation part of the study, such as: molar mass of ionic liquids, amount of nanoparticle and sonication time have been investigated. Analysis of variance (ANOVA) and RSM contour plots were presented for effect of all factors (input parameters) on the maximum current of differential pulse voltammetry (DPV) peaks (output responses). The results disclosed that the metal removal was impressed by the molar mass of ionic liquids, amount of nanoparticle and sonication time respectively. The efficiency specifications of this procedure were evaluated by calculating precision and response linearity. Under the optimal experimental conditions linear concentration ranges of 0.9–550µgL-1 and 0.7–500 µgL-1 were obtained for Zn(II) and Cu(II) ions respectively. The reported limit of detection for Zn(II) and Cu(II) were 0.27 and 0.21µgL-1 with relative standard deviations (RSD) 3.2%, and 4.4%, respectively. In addition, this sensor was successfully applied to real water samples.
Organic chemistry
Abdolkarim Zare; Manije Dianat; Nahid Varavi; Mina Aali-Hosaini; Hanafieh Deisi
Abstract
Nano-silica-bonded 3-n-propyl-1-sulfonic acid imidazolium chloride (nano-SB-[PSIM]Cl) was applied as a highly efficient, general and heterogeneous catalyst for one pot multi-component reaction of 2-naphthol, arylaldehydes, and thioacetamide leading to 1-thioamidolakyl-2-naphthols. All reactions proceeded ...
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Nano-silica-bonded 3-n-propyl-1-sulfonic acid imidazolium chloride (nano-SB-[PSIM]Cl) was applied as a highly efficient, general and heterogeneous catalyst for one pot multi-component reaction of 2-naphthol, arylaldehydes, and thioacetamide leading to 1-thioamidolakyl-2-naphthols. All reactions proceeded with excellent yields in short times under solvent-free conditions. Our protocol was superior than most of the reported methods for the preparation of 1-thioamidolakyl-2-naphthols in terms of some factors included relatively short reaction times, moderate to high yields, and absence of organic solvents.
Organic chemistry
Ashraf Sadat Shahvelayati; Leila Hajiaghababaei; Akram Panahi Sarmad
Volume 5, Issue 3, pp. 237-363, Serial No. 16 , July 2017, , Pages 262-267
Abstract
In this research, an efficient synthesis toward 2-(2-((4-Methoxybenzoyl)imino)-4-(4-methoxyphenyl)thiazol-3(2H)-yl)-2-phenylacetic acid via a three-component tandem reaction using aroylisothiocyanate, phenyl glycine, and 4-methoxyphenacyl bromide in an ionic liquid (IL) has been described. 1-Methyl-3-pentylimidazolium ...
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In this research, an efficient synthesis toward 2-(2-((4-Methoxybenzoyl)imino)-4-(4-methoxyphenyl)thiazol-3(2H)-yl)-2-phenylacetic acid via a three-component tandem reaction using aroylisothiocyanate, phenyl glycine, and 4-methoxyphenacyl bromide in an ionic liquid (IL) has been described. 1-Methyl-3-pentylimidazolium bromide (IL) has been employed as a recyclable green solvent. The work-up procedure was fairly simple and the product did not require further purification. The influence of various reaction parameters such as solvent, temperature, and time was examined and among the various solvents such as ethanol, acetonitrile, n-hexane, water, and ionic liquid for synthesis of the final product, the best result was obtained in 1-methyl-3-pentylimidazolium bromide at 50oC for 1 hours.
Organic chemistry
Seyed Sajad Sajadikhah
Volume 5, Issue 2, pp. 121-236, Serial No. 15 , April 2017, , Pages 121-128
Abstract
An extremely facile and efficient procedure which has been developed for the synthesis of dihydropyrrol-2-ones. One-pot four-component reaction of amines, dialkyl acetylenedicarboxylates and formaldehyde in the presence of N,N,N,N-tetramethylguanidinium acetate [TMG][Ac] in methanol at ambient temperature ...
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An extremely facile and efficient procedure which has been developed for the synthesis of dihydropyrrol-2-ones. One-pot four-component reaction of amines, dialkyl acetylenedicarboxylates and formaldehyde in the presence of N,N,N,N-tetramethylguanidinium acetate [TMG][Ac] in methanol at ambient temperature provides substituted dihydropyrrol-2-ones in good to high yields. The important aspects of this multi-component heteroannulation are simple operations under mild conditions, readily available starting material and catalyst. Furthermore, All products were obtained through a simple filtration and washed with ethanol and no need for column chromatography. It is found that the catalyst is recyclable and can be used up to four times without significant loss of its activity.
Organic chemistry
Saeid Azimi; Marziyeh Hariri
Volume 4, Issue 1, pp. 1-132, Serial No. 10 , January 2016, , Pages 13-20
Abstract
In this work, the ionic liquid triethylamine-bonded sulfonic acid {[Et3N–SO3H]Cl}, N,N-diethyl-N-sulfoethanammonium chloride was used as a green acidic homogeneous catalyst to synthesis of 3,4-dihydropyrimidin-2(1H)-ones and 3,4-dihydropyrimidin-2(1H)-thiones as two categories of heterocycles, ...
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In this work, the ionic liquid triethylamine-bonded sulfonic acid {[Et3N–SO3H]Cl}, N,N-diethyl-N-sulfoethanammonium chloride was used as a green acidic homogeneous catalyst to synthesis of 3,4-dihydropyrimidin-2(1H)-ones and 3,4-dihydropyrimidin-2(1H)-thiones as two categories of heterocycles, from aldehyde, dicarbonyl compound and urea or thiourea throughout the one-pot three components cyclocondensation reactions. The dihidropyrimidineones and dihydropyrimidinethiones derivatives that synthesized in this method are two important categories of heterocyclic compounds with biologic and pharmacologic activity. The ionic liquid that used in these reactions act as Bronsted acid and green homogeneous catalyst and has N-S bond in its cationic fragment and easily synthesised. The advantages of our method are solvent-free conditions, green process and high isolated yield of products.
Organic chemistry
Seyyedeh Cobra Azimi; Kurosh Rad-Moghadam
Volume 3, Issue 4, pp. 283-387, Serial No. 9 , October 2015, , Pages 356-366
Abstract
A homogeneous ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate doped with LiCl ([BMIm]BF4-LiCl) was found as catalyst solvents for the synthesis of dicoumarols by the condensation of 4-hydroxycoumarin and aldehyde at 80 ˚C. In this field, several types of aromatic aldehyde, containing electron-withdrawing ...
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A homogeneous ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate doped with LiCl ([BMIm]BF4-LiCl) was found as catalyst solvents for the synthesis of dicoumarols by the condensation of 4-hydroxycoumarin and aldehyde at 80 ˚C. In this field, several types of aromatic aldehyde, containing electron-withdrawing groups as well as electron-donating groups, were rapidly changed to the corresponding derivatives in good to excellent yields. Application of this new homogeneous catalyst system offered the advantages of short reaction times, solvent-free conditions, high yields, and easy work-up procedure compared to the conventional methods of the syntheses. The ionic liquid can be recovered for the subsequent reactions and reused without any loss of efficiency.
Organic chemistry
Esmayeel Abbaspour-Gilandeh; Seyyedeh Cobra Azimi
Volume 3, Issue 3, pp. 180-282,Serial No. 8 , July 2015, , Pages 218-231
Abstract
Abstract-A novel and efficient method has been developed for the synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives by the convenient ultrasound-mediated condensation of 4-hydroxyquinolin-2-one with Meldrum’s acid and aldehydes in the presence of a catalytic amount of [HMIm]HSO4 as a green, ...
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Abstract-A novel and efficient method has been developed for the synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives by the convenient ultrasound-mediated condensation of 4-hydroxyquinolin-2-one with Meldrum’s acid and aldehydes in the presence of a catalytic amount of [HMIm]HSO4 as a green, efficient and reusable acidic ionic liquid medium. The stability of the ionic liquid during the reaction was high and, used for several times to recycled form. Placing the reaction mixture under ultrasound condition causes that we have lower energy consumption and achieve to the desired product in the optimal time. The method is simple, starts from readily accessible commercial starting materials, and provides biologically interesting products in good yields and short reaction times.