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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 31 (1998), S. 57-70 
    ISSN: 1573-1111
    Keywords: cyclodextrins ; atrazine ; inclusion complex ; electrochemistry ; preceding reaction ; stability constants ; kinetic currents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reduction of atrazine in acidic aqueous media on mercury electrodes proceeds only after the protonation reaction. In fact, the efficiency of the reduction process is very low at pHs greater than 4. However, the addition of cyclodextrins (CDs) to neutral aqueous solutions of atrazine yields a kinetically controlled polarographic reduction wave, whose limiting current depends on the size of the CD cavity, and increases with the concentration of the CD itself. In particular, the size of the increase follows the order β-CD 〈 γ-CD 〈 α-CD for the same CD concentration. The half-wave potential shifts toward more negative values when the concentration of CDs increases. These findings lead to the conclusion that atrazine and CDs form an inclusion complex, whose stability constant we have estimated, and also that atrazine undergoes protonation facilitated by complexation with CDs. The stability constants of 1:1 complexes evaluated from polarographic data in 0.1M-KCl and at neutral pH for α-CD, β-CD and γ-CD are 4900, 1970 and 19000, respectively. The formation of the inclusion complex was indirectly confirmed by UV-Vis measurements in the presence of methylred and phenolphthalein, which both compete with atrazine in the formation of the corresponding inclusion compounds with CDs.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 9 (1986), S. 168-171 
    ISSN: 0935-6304
    Keywords: Supercritical fluids ; Infrared spectrometry ; Solvent elimination ; Microscopy ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The feasibility of supercritical fluid chromatography/Fourier transform-infrared (SFC/FT-IR) microspectrometry is presented. In this approach to SFC/FT-IR, the chromatographic eluates are aspirated from the restrictor directly onto the surface of a moving window which then passes into the beam focus of an infrared microscope. Because the mobile phase is gaseous at ambient conditions, elimination of the mobile phase is easily accomplished. Detection limits in all interfaces between a chromatograph and an FT-IR spectrometer in which the mobile phase is eliminated are determined in large part by the area over which the sample is deposited. We have shown that SFC eluates can be condensed at ambient temperature into spots of 100 to 200μm in diameter. The microscope interface therefore serves to increase the sensitivity of the SFC/FT-IR measurements of these spots and detection limits in the low nanogram range are possible. Preliminary results obtained before any real attempts were made to optimize the deposition process indicate that identifiable spectra can be obtained in real time at the 50 ng level for chromatographic separations performed with a 100μm i.d. wall coated open tubular column. Reproducible reconstructed chromatograms are obtained as each deposited eluate travels through the beam focus of the microscope. The concentration profile of deposited peaks was determined by IR measurements performed at 50 μm increments over the width of the peak to ascertain the deposition size. The results described in this paper, while not yet optimized, indicate the great potential of SFC/FT-IR microspectrometry.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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