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Signal attributes

Model-wide utilities Ports and subsystems Signal attributes Signal routing Sinks Sources... [Pg.151]

At first, the dimeric nature of the base isolated from 3-ethyl-2-methyl-4-phenylthiazolium was postulated via a chemical route. Indeed the adduct of ICH, on a similar 2-ethylidene base is a 2-isopropylthiazolium salt in the case of methylene base it is an anilinovinyl compound identified by its absorption spectrum and chemical reactivity (45-47). This dimeric structure of the molecule has been definitively established by its NMR spectrum. It is very similar to the base issued from 2.3-dimethyl-benzo thiazolium (48). It corresponds to 2-(3 -ethyl-4 -phenyl-2 -methylenethiazolinilydene)2-methyl-3-ethyl-4-phenylthiazoline (13). There is only one methyl signal (62 = 2.59), and two series of signals (63= 1.36-3.90, 63= 1.12-3.78) correspond to ethyl groups. Three protons attributed to positions T,5,5 are shifted to a lower field 5.93, 6.58, and 8.36 ppm. The bulk of the ten phenyl protons is at 7.3 ppm (Scheme 22). [Pg.39]

This attribute of rapid accumulation of spectra leads to excellent reproducibility and better signal-to-noise characteristics, and it makes full use of small quantities of sample. [Pg.401]

The F nmr spectrum of this compound gives only one signal over a wide range of temperatures, a result attributed to Berry pseudorotation (144). No alkyl- or aryltetrabromoarsorane has been reported. There is, however, an early report on the preparation of tetraiodomethylarsorane from methylarsonic acid and hydriodic acid (145). [Pg.339]

Figure 2.36 A shows a typical low-loss spectrum taken from boron nitride (BN). The structure of BN is similar to that of graphite, i. e. sp -hybridized carbon. For this reason the low-loss features are quite similar and comprise a distinct plasmon peak at approximately 27 eV attributed to collective excitations of both n and a electrons, whereas the small peak at 7 eV comes from n electrons only. Besides the original spectrum the zero-loss peak and the low-loss part derived by deconvolution are also drawn. By calculating the ratio of the signal intensities hot and Iq a relative specimen thickness t/2 pi of approximately unity was found. Owing to this specimen thickness there is slight indication of a second plasmon. Figure 2.36 A shows a typical low-loss spectrum taken from boron nitride (BN). The structure of BN is similar to that of graphite, i. e. sp -hybridized carbon. For this reason the low-loss features are quite similar and comprise a distinct plasmon peak at approximately 27 eV attributed to collective excitations of both n and a electrons, whereas the small peak at 7 eV comes from n electrons only. Besides the original spectrum the zero-loss peak and the low-loss part derived by deconvolution are also drawn. By calculating the ratio of the signal intensities hot and Iq a relative specimen thickness t/2 pi of approximately unity was found. Owing to this specimen thickness there is slight indication of a second plasmon.
Many events signaled the beginning of a lengthy transition period for the utility industry in general, and more specifically, for the facility planning activity. The timeline m many instances was blurred, with some of the blurring attributable to a reluctance to change. [Pg.1201]

Ward (Ref 15) and Brown and Williams (Ref 16) studied nitrobenzene with radiation > 3300A using tetrahydrofuran (THF) as solvent in degassed solns. The effects of low temp were also studied. An ESR signal, attributed to the C6HsN(02)H radical, was obtained with THF as solvent. No ESR signal was obtained when perfluoronaphthalene was added. They concluded that the triplet state of nitrobenzene was an intermediate... [Pg.736]

In some crystalline polymers chemical shift differences between crystalline and amorphous phases have been observed and interpreted and for several crystalline forms the signals to be attributed to nuclei in different conformational environments have been identified [111, 112]. [Pg.209]

Shipping analysis is an extremely sensitive electrochemical technique for measuring trace metals (19,20). Its remarkable sensitivity is attributed to the combination of an effective preconcentration step with advanced measurement procedures that generate an extremely favorable signal-to-background ratio. Since the metals are preconcentrated into the electrode by factors of 100 to 1000, detection limits are lowered by 2 to 3 orders of magnitude compared to solution-phase voltammetric measurements. Hence, four to six metals can be measured simultaneously in various matrices at concentration levels down to 10 10 i. utilizing relatively inexpensive... [Pg.75]

There are two notable features of the quantitative performance of this type of interface. It has been found that non-linear responses are often obtained at low analyte concentrations. This has been attributed to the formation of smaller particles than at higher concentrations and their more easy removal by the jet separator. Signal enhancement has been observed due to the presence of (a) coeluting compounds (including any isotopically labelled internal standard that may be used), and (b) mobile-phase additives such as ammonium acetate. It has been suggested that ion-molecule aggregates are formed and these cause larger particles to be produced in the desolvation chamber. Such particles are transferred to the mass spectrometer more efficiently. It was found, however, that the particle size distribution after addition of ammonium acetate, when enhancement was observed, was little different to that in the absence of ammonium acetate when no enhancement was observed. [Pg.150]


See other pages where Signal attributes is mentioned: [Pg.87]    [Pg.139]    [Pg.2]    [Pg.87]    [Pg.139]    [Pg.2]    [Pg.38]    [Pg.39]    [Pg.160]    [Pg.173]    [Pg.875]    [Pg.1292]    [Pg.90]    [Pg.250]    [Pg.394]    [Pg.56]    [Pg.30]    [Pg.30]    [Pg.200]    [Pg.249]    [Pg.46]    [Pg.127]    [Pg.171]    [Pg.288]    [Pg.320]    [Pg.465]    [Pg.718]    [Pg.1268]    [Pg.135]    [Pg.275]    [Pg.128]    [Pg.397]    [Pg.441]    [Pg.526]    [Pg.39]    [Pg.68]    [Pg.203]    [Pg.163]    [Pg.186]    [Pg.1027]    [Pg.235]    [Pg.83]    [Pg.157]    [Pg.478]   
See also in sourсe #XX -- [ Pg.169 , Pg.314 ]




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