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Total 25 records

    Investigation of the interfacial electron transfer kinetics in ferrocene-terminated oligophenyleneimine self-assembled monolayers

    , Article Langmuir ; Volume 36, Issue 42 , 2020 , Pages 12572-12579 Taherinia, D ; Sharif University of Technology
    American Chemical Society  2020
    Abstract
    In this article, the synthesis, characterization, and cyclic voltammetry (CV) measurements are reported for ferrocene-terminated oligophenyleneimine (OPI_Fc) and ferrocene-terminated conjugation-broken oligophenyleneimine (CB-OPI_Fc) self-assembled monolayers (SAMs) in two different electrolytes, namely, 1-ethyl-3-methylimidazolium-bis (trifluoromethyl-sulfonyl) imide (EMITFSI) ionic liquid and tetrabutylammonium hexafluorophosphate (Bu4NPF6) in acetonitrile (0.1 M solution). The SAMs were synthesized on Au surfaces by the sequential imine condensation reactions. CV was used to investigate the kinetics of electron transfer (ET) to the ferrocene, and it was observed that the standard ET rate... 

    Miniaturized salting-out liquid-liquid extraction in a coupled-syringe system combined with HPLC-UV for extraction and determination of sulfanilamide

    , Article Talanta ; Vol. 121 , April , 2014 , pp. 199-204 ; ISSN: 00399140 Sereshti, H ; Khosraviani, M ; Sadegh Amini-Fazl, M ; Sharif University of Technology
    Abstract
    In salting-out liquid-liquid extraction (SALLE) technique, water-miscible organic solvents are used for extraction of polar analytes from saline solutions. In this study, for the first time, a coupled 1-mL syringes system was utilized to perform a miniaturized SALLE method. Sulfanilamide antibiotic was extracted and determined via the developed method followed by high performance liquid chromatography-ultraviolet detection (HPLC-UV). The extraction process was carried out by rapid shooting of acetonitrile as extraction solvent (syringe B) into saline aqueous sample solution (syringe A), and then the shooting was repeated several times at a rate of 1 cycle s-1. Thereby, an extremely large... 

    Synthesis of functionalized benzothiadiazine 1,1-dioxide derivatives via intramolecular C–H activation reactions of trichloroacetamidine and benzenesulfonyl chloride

    , Article Tetrahedron Letters ; Volume 59, Issue 21 , 23 May , 2018 , Pages 2054-2056 ; 00404039 (ISSN) Nematpour, M ; Rezaee, E ; Jahani, M ; Tabatabai, S. A ; Sharif University of Technology
    Elsevier Ltd  2018
    Abstract
    The synthesis of functionalized benzothiadiazine 1,1-dioxide derivatives was achieved through a novel three-component intramolecular C–H activation reaction of trichloroacetonitrile, benzenesulfonyl chloride, and various primary amines. This reaction was performed in the presence of catalytic copper(I) and L-proline as the ligand in tetrahydrofuran at room temperature. © 2018 Elsevier Ltd  

    An unbreakable on-line approach towards sol-gel capillary microextraction

    , Article Journal of Chromatography A ; Volume 1218, Issue 26 , 2011 , Pages 3952-3957 ; 00219673 (ISSN) Bagheri, H ; Piri-Moghadam, H ; Es'haghi, A ; Sharif University of Technology
    2011
    Abstract
    In this work a novel unbreakable sol-gel-based in-tube device for on-line solid phase microextraction (SPME) was developed. The inner surface of a copper tube, intended to be used as a high performance liquid chromatography (HPLC) loop, was electrodeposited by metallic Cu followed by the self assembled monolayers (SAM) of 3-(mercaptopropyl) trimethoxysilane (3MPTMOS). Then, poly (ethyleneglycol) (PEG) was chemically bonded to the -OH sites of the SAM already covering the inner surface of the copper loop using sol-gel technology. The homogeneity and the porous surface structure of the SAM and sol-gel coatings were examined using the scanning electron microscopy (SEM) and adsorption/desorption... 

    How does the axial ligand of cytochrome p450 biomimetics influence the regioselectivity of aliphatic versus aromatic hydroxylation?

    , Article Chemistry - A European Journal ; Volume 15, Issue 22 , 2009 , Pages 5577-5587 ; 09476539 (ISSN) De Visser, S. P ; Tahsini, L ; Nam, W ; Sharif University of Technology
    2009
    Abstract
    The catalytic activity of highvalent iron-oxo active species of heme enzymes is known to be dependent on the nature of the axial ligand trans to the iron-oxo group. In a similar fashion, experimental studies on iron-oxo porphyrin biomimetic systems have shown a significant axial ligand effect on ethylbenzene hydroxylation, with an axial acetonitrile ligand leading to phenyl hydroxylation products and an axial chloride anion giving predominantly benzyl hydroxylation products. To elucidate the fundamental factors that distinguish this regioselectivity reversal in iron-oxo porphyrin catalysis, we have performed a series of density functional theory calculations on the hydroxylation of...