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Preparation using

Figure C2.17.2. Transmission electron micrograph of a gold nanoneedle. Inverse micelle environments allow for a great deal of control not only over particle size, but also particle shape. In this example, gold nanocrystals were prepared using a photolytic method in surfactant-rich solutions the surfactant interacts strongly with areas of low curvature, thus continued growth can occur only at the sharjD tips of nanocrystals, leading to the fonnation of high-aspect-ratio nanostmctures [52]. Figure C2.17.2. Transmission electron micrograph of a gold nanoneedle. Inverse micelle environments allow for a great deal of control not only over particle size, but also particle shape. In this example, gold nanocrystals were prepared using a photolytic method in surfactant-rich solutions the surfactant interacts strongly with areas of low curvature, thus continued growth can occur only at the sharjD tips of nanocrystals, leading to the fonnation of high-aspect-ratio nanostmctures [52].
For large scale preparations use a tliree-necked flask equipped with two reflux condensers and an oil-sealed stirrer. [Pg.715]

Indol-2-ylcopper reagents can also be prepared from 2-lithioindoles and they have some potential for the preparation of 2-substituted indoles. 1-Methyl-indol-2-ylcopper can be prepared by reaction of 2-lithio-l-methylindole with CuBr[10]. It reacts with aryl iodides to give 2-aryl-1-methylindoles. Mixed cyanocuprate reagents can be prepared using CuCN[ll], The cyan-ocuprate from 1-methylindole reacts with allyl bromide to give 2-allyl-l-methylindole. [Pg.97]

Enantioselective synthesis of tryptophans has been accomplished via alkylation of 2,5-diethoxy-3,6-dihydropiperazines by the method developed by Schbllkopf[18]. For example, I> - -)-6-methoxytryptophan ethyl ester was prepared using l-(phcnylsulfonyl)-3-(bromomethyl)-6-methoxyindolefor alkyl-ationfl 9],... [Pg.132]

Carbocyanines with three methine groups can be prepared using Pvo equivalents of selenazolium quaternary salt and one equivalent of ethyl orthoformate in pyridine solution (53). [Pg.257]

A calibration curve prepared using several external standards. [Pg.109]

This reaction occurs quickly and is of known stoichiometry. A titrant of SCN is easily prepared using KSCN. To indicate the titration s end point we add a small amount of Fe + to the solution containing the analyte. The formation of the red-colored Fe(SCN) + complex signals the end point. This is an example of a direct titration since the titrant reacts with the analyte. [Pg.275]

Since all samples and standards are prepared using the same volume of ammonium acetate buffer, the contribution of this source of iron is accounted for by the calibration curve s reagent blank. [Pg.399]

Sensitivity Sensitivity in flame atomic emission is strongly influenced by the temperature of the excitation source and the composition of the sample matrix. Normally, sensitivity is optimized by aspirating a standard solution and adjusting the flame s composition and the height from which emission is monitored until the emission intensity is maximized. Chemical interferences, when present, decrease the sensitivity of the analysis. With plasma emission, sensitivity is less influenced by the sample matrix. In some cases, for example, a plasma calibration curve prepared using standards in a matrix of distilled water can be used for samples with more complex matrices. [Pg.440]

When prepared using a saturated solution of KCl, the Ag/AgCl electrode has a potential of +0.197 V at 25 °C. Another common Ag/AgCl electrode uses a solution of 3.5 M KCl and has a potential of +0.205 at 25 °C. The Ag/AgCl electrode prepared with saturated KCl, of course, is more temperature-sensitive than one prepared with an unsaturated solution of KCl. [Pg.473]

This experiment describes the preparation and evaluation of two liquid-membrane Na+ ion-selective electrodes, using either the sodium salt of monensin or a hemisodium ionophore as ion exchangers incorporated into a PVG matrix. Electrodes prepared using monensin performed poorly, but those prepared using hemisodium showed a linear response over a range of 0.1 M to 3 X 10 M Na+ with slopes close to the theoretical value. [Pg.534]

Students determine the concentrations of caffeine, acetaminophen, acetylsalicylic acid, and salicylic acid in several analgesic preparations using both CZE (70 mM borate buffer solution, UV detection at 210 nm) and HPLC (C18 column with 3% v/v acetic acid mixed with methanol as a mobile phase, UV detection at 254 nm). [Pg.614]

In the eadiest known paintings, the primitive cave paintings, paint was appHed directly onto the cave wall, with tittle or no preparation. As early as the Old Kingdom in ancient Egypt, however, wall surfaces were specially prepared using a coating of plaster. In time, the refinement and complexity of the preparation layers increased until in the Renaissance several layers of different composition and fineness were superimposed. Other preparations used, especially in the Far East, consisted of a clay layer. [Pg.419]

PVF has low solubdity in all solvents below about 100°C (61). Polymers with greater solubdity have been prepared using 0.1% 2-propanol polymerization modifier and were characterized in /V, /V- dim ethyl form am i de solution containing 0.1 AlLiBr. ranged from 76,000 to 234,000... [Pg.380]

Telomers. Bromotrifluoroethylene telomers have been prepared using chain-transfer agents such as CF SSCF (31), C2p I (32), CBr (32), or CBr F (33). For example, when the olefin is slowly added to tribromofluoromethane under light from sunlamps, a Hquid is obtained which, after saturation... [Pg.397]

Bisa2iridine compounds and A/-(2-chloroethyl)carbodiimides have also been prepared using isocyanide dichlorides and ethyleneimine (178,179). The iodide-cataly2ed rearrangement of the formerly mentioned compounds provides a method for preparing the tetrahydroimida2oimida2ole system ... [Pg.7]


See other pages where Preparation using is mentioned: [Pg.23]    [Pg.362]    [Pg.433]    [Pg.1990]    [Pg.2669]    [Pg.2782]    [Pg.235]    [Pg.824]    [Pg.238]    [Pg.62]    [Pg.573]    [Pg.127]    [Pg.170]    [Pg.342]    [Pg.396]    [Pg.443]    [Pg.443]    [Pg.582]    [Pg.655]    [Pg.660]    [Pg.707]    [Pg.713]    [Pg.775]    [Pg.61]    [Pg.232]    [Pg.241]    [Pg.14]    [Pg.21]    [Pg.118]    [Pg.169]    [Pg.532]    [Pg.328]    [Pg.24]    [Pg.162]    [Pg.339]   


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