Derivative Voltammetry

In addition to chromatography based on adsorption, ion pair chromatography (IP-HPLC) and capillary electrophoresis (CE) or capillary zone electrophoresis (CZE) are new methods that became popular and are sufficiently accurate for these types of investigations. Other methods involving electrochemical responses include differential pulse polarography, adsorptive and derived voltammetry, and more recently, electrochemical sensors. 

Ni, Y. and Bai, 1., Simnltaneons determination of Amaranth and Snnset Yellow by ratio derivative voltammetry, Talanta, 44, 105, 1997. 

This last value coincides with that deduced previously for Double Derivative Voltammetry [43] as indicated. 

Composite films of CNTs with other materials, such as conducting polymers or ceramics, are very fascinating materials for the development of electrochemical sensors. Yang and co-workers fabricated an electrode via electropolymerization of acid chrome blue K at an MWNT-functionalized glassy carbon electrode for simultaneous determination of dihydrox-ybenzene isomers in real water samples through applying the first-order linear sweep derivative voltammetry. Polypyrrole (PPy) or polyaniline (PANI) was electrochemically deposited on SWNT networks by Ferrer-Anglada and co-workers ° in 2006, which has been used as solid-state pH sensors. 

Ding YP, Liu WL, Wu QS et al (2005) Direct simultaneous determination of dihydrox-ybenzene isomers at C-nanotube-modified electrodes by derivative voltammetry. J Electroanal Chem 575 275-280... 

More recent research provides reversible oxidation-reduction potential data (17). These allow the derivation of better stmcture-activity relationships in both photographic sensitization and other systems where electron-transfer sensitizers are important (see Dyes, sensitizing). Data for an extensive series of cyanine dyes are pubflshed, as obtained by second harmonic a-c voltammetry (17). A recent "quantitative stmcture-activity relationship" (QSAR) (34) shows that Brooker deviations for the heterocycHc nuclei (discussed above) can provide estimates of the oxidation potentials within 0.05 V. An oxidation potential plus a dye s absorption energy provide reduction potential estimates. Different regression equations were used for dyes with one-, three-, five-methine carbons in the chromophore. Also noted in Ref. 34 are previous correlations relating Brooker deviations for many heterocycHc nuclei to the piC (for protonation/decolorization) for carbocyanine dyes the piC is thus inversely related to oxidation potential values. 

Julid investigated the behavior of terfuran 22 and bis(thienyl)furan 23 by cyclic voltammetry as well as the EPR spectra of the radical cations derived from these two compounds. Condensation of the diketone 20 with sulfuric acid furnished furan 22 in 18% yield, while reaction of diketone 21 with hydrochloric acid produced 23 in 84% yield.In a related report, Luo prepared oligomeric bis(thienyl)furans via similar methodology. ... 

Figure 6. Voltammetry at microeleclrode of different zinc derivates in PEO the CsCI adduct corresponds to P(EO)9(ZnCI2 CsCl. For the triflate derivative, the current is magnified by a factor of 10. Reprinted from D. Baril, C. Michot. M. Armand, Solid State Ionics 1997, 94, 35, Copyright 1997, with kind permission of Elsevier Science—NL, Sara Burgerhartstraat 25, 1055 KV Amsterdam, The Netherlands.

CP = current-potential curves CV = cyclic voltammetry EXI VA = derivative cyclic voltabsorptometry IP = impedance method. See also list of symbols. 

The redox properties of a series of heterometal clusters were assessed by electrochemical and FPR measurements. The redox potentials of derivatives formed in D. gigas Fdll were measured by direct square wave voltammetry promoted by Mg(II) at a vitreous carbon electrode, and the following values were determined 495, 420,... 

Not only the absorption behaviour, but also all the physical properties of derivatives (32) are related to the nature of the 2,5-substitution pattern. For example, a blue-green emission is observed for di(2-pyridyl)phosphole (32b) whereas the emission of di(2-thienyl)phosphole (32a) is red-shifted (AAj,nj= 35 nm) [36]. Likewise, cyclic voltammetry (CV) revealed that derivative (32a), featuring electron-rich thienyl substituents, is more easily oxidised than compound (32b), which possesses electron-deficient pyridyl substituents [36]. 

Voltammetry Ratio derivative Direct measurement using hanging mercury Soft drinks o D 0) o (/)... 

In conclusion, synthetic dyes can be determined in solid foods and in nonalcoholic beverages and from their concentrated formulas by spectrometric methods or by several separation techniques such as TEC, HPLC, HPLC coupled with diode array or UV-Vis spectrometry, MECK, MEECK, voltammetry, and CE. ° Many analytical approaches have been used for simultaneous determinations of synthetic food additives thin layer chromatography, " " derivative spectrophotometry, adsorptive voltammetry, differential pulse polarography, and flow-through sensors for the specific determination of Sunset Yellow and its Sudan 1 subsidiary in food, " but they are generally suitable only for analyzing few-component mixtures. 

Under optimum conditions LPS voltammetry is an order of magnitude more sensitive than polarography (i.e., the detection limit is about 10 M). As in classical polarography, somewhat higher sensitivity and selectivity can be attained when using a differential version (i.e., when recording, as a function of potential, not the current but its derivative with respect to potential). 

LCEC is a special case of hydrodynamic chronoamperometry (measuring current as a function of time at a fixed electrode potential in a flowing or stirred solution). In order to fully understand the operation of electrochemical detectors, it is necessary to also appreciate hydrodynamic voltammetry. Hydrodynamic voltammetry, from which amperometry is derived, is a steady-state technique in which the electrode potential is scanned while the solution is stirred and the current is plotted as a function of the potential. Idealized hydrodynamic voltammograms (HDVs) for the case of electrolyte solution (mobile phase) alone and with an oxidizable species added are shown in Fig. 9. The HDV of a compound begins at a potential where the compound is not electroactive and therefore no faradaic current occurs, goes through a region... 

Figure 1.6 The variation of log Jqkr with Vciah expected based on (1.5), with the coverage hy surface oxygen derived from voltammetry [Urihe et al., 1992].

In this chapter, the voltammetric study of local anesthetics (procaine and related compounds) [14—16], antihistamines (doxylamine and related compounds) [17,22], and uncouplers (2,4-dinitrophenol and related compounds) [18] at nitrobenzene (NB]Uwater (W) and 1,2-dichloroethane (DCE)-water (W) interfaces is discussed. Potential step voltammetry (chronoamperometry) or normal pulse voltammetry (NPV) and potential sweep voltammetry or cyclic voltammetry (CV) have been employed. Theoretical equations of the half-wave potential vs. pH diagram are derived and applied to interpret the midpoint potential or half-wave potential vs. pH plots to evaluate physicochemical properties, including the partition coefficients and dissociation constants of the drugs. Voltammetric study of the kinetics of protonation of base (procaine) in aqueous solution is also discussed. Finally, application to structure-activity relationship and mode of action study will be discussed briefly. 

In deriving theoretical equations of the current-potential (or time) curves of ion-transfer voltammetry of a dibase we shall make the following assumptions ... 

Polythiophene films can be electrochemically cycled from the neutral to the conducting state with coulombic efficiencies in excess of 95% [443], with little evidence of decomposition of the material up to + 1.4 V vs. SCE in acetonitrile [37, 54, 56, 396,400] (the 3-methyl derivative being particularly stable [396]), but unlike polypyrrole, polythiophene can be both p- and n-doped, although the n-doped material has a lower maximum conductivity [444], Cyclic voltammetry shows two sets of peaks corresponding to the p- and n-doping reactions, with E° values at approximately + 1.1 V and — 1.4 V respectively (vs. an Ag+/Ag reference electrode)... 

Benzo[r]bcnzo[3,4]cinnolino[l,2- ]cinnoline 61 and a series of 5,6-dihydrobenzo[c]cinnoline derivatives, including compounds 62, were studied by cyclic voltammetry. The unusual shape of the voltammograms of the investigated compounds can be explained by an EiE-DISP mechanism with a slow disproportionation reaction <1996JA5020>. 

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