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Cyclic voltammetry selective binding

Similar structures 37 and 38, bearing ureido functions on the lower rim of calix[4]diquinone or monoquinone moieties, were used for anion recognition with the aid of electrochemistry (cyclic voltammetry) [47,48]. Some of these compounds were found [49] to bind selectively HSOj or H2POj anions. [Pg.81]

Binding constants in solution are usually determined from potentiometric titrations or plots of cyclic voltammetry peak potentials vs. CyD concentration after assessing the guest/host ratio in the complex [3, 4]. Potentiometric measurements are more frequently used, and ion-selective electrodes are employed, for the direct measurement of the guest activity in the solution. Measurements of pH allow the evaluation of concentrations of several reaction components. [Pg.304]

CD2CI2, acetone-Je and CD3CN [121], which revealed that the incorporation of one or more electron-rich TTF subunits improved the binding ability and changed the binding selectivity. The complexation for halides was also monitored by cyclic voltammetry in 1,2-dichloroethane, which revealed electrochemical response to CF and Br ions. [Pg.167]


See other pages where Cyclic voltammetry selective binding is mentioned: [Pg.69]    [Pg.2]    [Pg.311]    [Pg.295]    [Pg.112]    [Pg.203]    [Pg.218]    [Pg.265]    [Pg.691]    [Pg.178]    [Pg.261]    [Pg.140]    [Pg.304]    [Pg.305]    [Pg.250]    [Pg.505]    [Pg.751]    [Pg.691]    [Pg.64]    [Pg.69]    [Pg.72]    [Pg.25]    [Pg.307]    [Pg.1871]    [Pg.380]    [Pg.10]    [Pg.441]    [Pg.5692]    [Pg.400]   
See also in sourсe #XX -- [ Pg.6 , Pg.551 ]




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Binding selection

Binding selectivity

Cyclic selective

Cyclic voltammetry

Voltammetry selectivity

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