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Tetrabutylammonium perchlorate, as supporting electrolyte

A combination of HPLC and amperometric detection was proposed for determination of tributylstannyl oxide in antifouling paint. The detector is of the static hanging Hg drop type in a flow cell, the solvent is CH2CI2/THF, containing tetrabutylammonium perchlorate as supporting electrolyte. The oxidation mechanism depicted in reactions 4... [Pg.377]

Conducting polymers are usually synthesized from the appropriate monomers by either chemical or electrochemical oxidative polymerization. Electrochemical polymerization is preferred for better penetration inside the nanopores. Polypyrrole (PPy) is one of the most important and extensively studied conducting polymers (Moreno et al. 1999 Vrkoslav et al. 2006 Lewis et al. 1997 Akundy and Iroh 2001). The deposition of PPy into PSi templates could be achieved by the electrochemical oxidation of pyrrole monomers at constant current or potential in the acetonitrile solution containing tetrabutylammonium perchlorate as supporting electrolyte. Typical potential (E-t) and current transients (i-t) recorded during the deposition of PPy into mesoporous silicon templates are shown in Fig. 3. The mechanism of polymer infiltration into the pores is of major importance in order to obtain the desired structures and control the final morphology. [Pg.457]

The one-electron reduction of a 1 mM solution of benzoquinone (BQ) in acetonitrile containing 0.5 M tetrabutylammonium perchlorate as supporting electrolyte,... [Pg.170]

I. 4-methoxyacetophenone (30 //moles) was added as an internal standard. The reaction was stopped after 2 hours by partitioning the mixture between methylene chloride and saturated sodium bicarbonate solution. The aqueous layer was twice extracted with methylene chloride and the extracts combined. The products were analyzed by GC after acetylation with excess 1 1 acetic anhydride/pyridine for 24 hours at room temperature. The oxidations of anisyl alcohol, in the presence of veratryl alcohol or 1,4-dimethoxybenzene, were performed as indicated in Table III and IV in 6 ml of phosphate buffer (pH 3.0). Other conditions were the same as for the oxidation of veratryl alcohol described above. TDCSPPFeCl remaining after the reaction was estimated from its Soret band absorption before and after the reaction. For the decolorization of Poly B-411 (IV) by TDCSPPFeCl and mCPBA, 25 //moles of mCPBA were added to 25 ml 0.05% Poly B-411 containing 0.01 //moles TDCSPPFeCl, 25 //moles of manganese sulfate and 1.5 mmoles of lactic acid buffered at pH 4.5. The decolorization of Poly B-411 was followed by the decrease in absorption at 596 nm. For the electrochemical decolorization of Poly B-411 in the presence of veratryl alcohol, a two-compartment cell was used. A glassy carbon plate was used as the anode, a platinum plate as the auxiliary electrode, and a silver wire as the reference electrode. The potential was controlled at 0.900 V. Poly B-411 (50 ml, 0.005%) in pH 3 buffer was added to the anode compartment and pH 3 buffer was added to the cathode compartment to the same level. The decolorization of Poly B-411 was followed by the change in absorbance at 596 nm and the simultaneous oxidation of veratryl alcohol was followed at 310 nm. The same electrochemical apparatus was used for the decolorization of Poly B-411 adsorbed onto filter paper. Tetrabutylammonium perchlorate (TBAP) was used as supporting electrolyte when methylene chloride was the solvent. [Pg.520]

Tetrahexylammonium perchlorate and tetrabutylammonium tetrafluoroborate have been used as supporting electrolyte in benzene and chlorobenzene, respectively. The latter was suggested [418] to be an excellent solvent for the study of reversible oxidations and reductions of aromatic compounds. The TLV for chlorobenzene is 75 ppm. [Pg.270]

Figure 4. Cyclic voltammograms of selected compounds. The types of molecule tested are shown in insets. For measurements an electroanalytical Cypress System Model CS-1090 was used. A platinum 1 mm disk electrode was used as the working electrode and an Ag-AgCl electrode served as the reference electrode. The supporting electrolyte was 0.5 m tetrabutylammonium perchlorate in dry acetonitrile. Figure 4. Cyclic voltammograms of selected compounds. The types of molecule tested are shown in insets. For measurements an electroanalytical Cypress System Model CS-1090 was used. A platinum 1 mm disk electrode was used as the working electrode and an Ag-AgCl electrode served as the reference electrode. The supporting electrolyte was 0.5 m tetrabutylammonium perchlorate in dry acetonitrile.
Experiments have been carried out in HF-contained acetonitrile (MeCN), dimethyl-formamide (DMF), and dimethylsulfoxide (DMSO) with tetrabutylammonium perchlorate (TBAP) as the supporting electrolyte [76-80]. The oxidation current for p-type (in the dark, p = 100 — 0.2 cm) and -type Si (under illumination) increases linearly because of the comhined solution and semiconductor resistance. Neither a critical current peak (icrit) nor an electropolishing region is observed. There was no H2 evolution when water-free HF was used. [Pg.193]

Here, we consider electropolymerized 3,4-ethylenedioxythiophene (EDT), prepared with different supporting electrolytes (see [135]) polystyrenesulfonic add (PSS), p-toluenesulfonic acid (Tos), and tetrabutylammonium perchlorate (BU4NCIO4). The anion produced from the dissociation of toluene-sulfonic acid is also called tosylate (< -SO i). Additionally, we address chemically prepared PEDOT-PSS, in a water emulsion, sodium free (<0.5 ppm), provided by Agfa Gevaert N.V. None of these blends contains PSS -Na" ", as was the case for Baytron P discussed above. The conductivity values a obtained for the polymers are summarized in Table 21.1. PEDOT/Tos is the most conductive (450 S cm ). The polyanion-based materials give lower conductivities 80 S cm for electropolymerized PEDOT-PSS and 0.03 S cm for chemically polymerized PEDOT-PSS. [Pg.931]

Other methods of polystannane synthesis include electrochemical methods [22], Thus, [ Bu2Sn]n 10,900 MJM = 2.6) and [ Oet2Sn]n (M = 5900 MJMn = 1.7) were prepared by the eleetroehemieal polymerization of dibutyldichlorostannane and dioctyldiehlorostannane, respectively, by using a platinum cathode and a silver anode. Tetrabutylammonium perchlorate is used as the supporting electrolyte and dimethoxy ethane is used as the solvent. [Pg.302]

DiMarco et al. [195] oxidatively polymerized yV-vinyl-thionaphthene-indole in methylene chloride at 1.2 V (versus SCE). Tetrabutylammonium perchlorate was added as the supporting electrolyte the monomer was used in concentrations greater than 5 x 10" M. Elemental analysis and mass spectroscopy results indicate that the polymer consists of four or more monomer units and that the benzene rings... [Pg.782]

Supporting electrolyte 0.1 M tetrabutylammonium perchlorate (TBAP), or same as that used in electrochemical cell. [Pg.94]

A supporting electrolyte that produces negligible alkaline error, such as salts of magnesium, calcium, barium, or organic cations, should be used. Lithium chloride or sodium perchlorate are recommended for alcoholic media. Some common solvents in which tetrabutylammonium iodide (BU4NI) and tetraethylammonium perchlorate (Et4NC104) are soluble are listed in Chapter 3. [Pg.113]


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See also in sourсe #XX -- [ Pg.275 ]




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Electrolyte supported

Electrolytes perchlorate

Supporting electrolyte

Tetrabutylammonium

Tetrabutylammonium perchlorate

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