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Line-sequential scheme

Consider the SXGA display for monitor usage (see Fig. 5.2.1). In the case of the SXGA display, the number of scamiing electrodes is 1024, or the duty ratio is 1/1024. Fbr the usual line-sequential scheme, the fi-ame frequency of the LCD is 60 Hz, or 60 pictures are formed every second. So, the period of one frame (frame rate) or... [Pg.163]

Had it been convenient to use a sequential scheme then as each primer was tested the total T of the observations to date would be calculated and plotted on a chart with suitable boundary lines. It will be found in practice that if p0 is large compared with 6 these boundary lines will rise very steeply and appear to be very close together, so that the chart will be difficult to use. Since the test is to detect a difference, it will not be affected if a constant amount is subtracted from each observation. For purposes of convenience, therefore, instead of considering the actual density we consider the amount by which the density exceeds 1.40, that is to say, 1.40 is subtracted from each observation. Then ... [Pg.48]

In the present work it has been shown that on-line coupling of flowthrough fractionation in RCC with ICP-EAS detection enables not only the fast and efficient fractionation of trace elements (TE) in environmental solids to be achieved but allows real-time studies on the leaching process be made. A novel five-step sequential extraction scheme was tested in on-line mode. The optimal conditions for the fractionation were chosen. Investigating elution curves provides important information on the efficiency of the reagents used, the leaching time needed for the separation of each fraction, and the potential mobility of HM forms. [Pg.459]

A fourfold anionic sequence which is not initiated by a Michael but an aldol reaction has been reported by the group of Suginome and Ito (Scheme 2.129) [295]. In this approach, the borylallylsilane 2-573 reacts selectively in the presence of TiCl4 with two different aldehydes which are added sequentially to the reaction mixture. First, a Lewis acid-mediated allylation of the aldehyde with 2-573 takes place to form a homoallylic alcohol which reacts with the second aldehyde under formation of the oxenium ion 2-574. The sequence is terminated by a Prins-type cyclization of 2-574 and an intramolecular Friedel-Crafts alkylation of the intermediate 2-575 with formation of the fraws-1,2-be rizoxadeca lines 2-576 as single diastereomers. [Pg.137]

We assume that our program scheme P is written in linear sequential form with the first instruction in line 1. We use the convention that in a test statement the first transfer address is the transfer for positive (TRUE) outcome of the test. We can assume that P has input variables x, ...,x disjoint from program variables, ...,ym and an output variable z which is neither an input for a program variable and only appears in a halting sequence z + u STOP. [Pg.232]

A procedure used to assist in identifying sequential mechanisms when the double-reciprocal plots exhibit parallel lines ". In some cases, bireactant mechanism can have various collections of rate constants that result in so-called parallel line kinetics, even though the mechanism is not ping pong. However, if the concentrations of A and B are kept in constant ratio with respect to each other, a sequential mechanism in a 1/v v. 1/[A] plot would be nonlinear (since in the denominator the last term of the double-reciprocal form of the rate expression contains [A] for example, for the steady-state ordered Bi Bi reaction scheme in which [B] = a[A], the double-reciprocal rate expression becomes 1/v =... [Pg.166]

Optically active namral and unnamral amino acids as well as various cyclic amino alcohols have been utilized in the synthesis of a wide variety of bis(oxazo-line) ligands. As previously mentioned, the first bis(oxazoline) ligands, py-box la-d, were synthesized by Nishiyama and co-workers in 1989. The common material for their syntheses was pyridine 2,6-dicarboxylic acid 19. Conversion of 19 to the acid chloride was achieved by treatment with thionyl chloride, as illustrated in Figure 9.4. This was followed by condensation with (5)-valinol in the presence of triethylamine. Conversion of the resulting bis(amidodiol) 20 to py-box-ip lb was achieved by sequential treatment of 20 with thionyl chloride at 50 °C followed by cyclization with aqueous sodium hydroxide in methanol to afford py-box-/p lb in 60% overall yield. The same synthetic scheme can be used to obtain the other... [Pg.534]

Wang, J. and E.H. Hansen. 2003. On-line sample-pre-treatment schemes for trace-level determinations of metals by coupling floe injection or sequential injection with ICP-MS. Trends Anal. Chem. 22 836-845. [Pg.463]

Scheme 55 Polyunsaturated y-alkylidene butenolides by sequential Sonogashira coupling-cyclization [111] (newly formed bonds drawn in bold lines)... Scheme 55 Polyunsaturated y-alkylidene butenolides by sequential Sonogashira coupling-cyclization [111] (newly formed bonds drawn in bold lines)...
Treatment of the aldehyde 19 with amines in the presence of TiCU furnished the precursor 20, which was converted to the 2-pyrrolines 21. The products 21 could thereafter be exposed to methoxide, leading to the corresponding /3-chloropyrroles after elimination of cyanide (Scheme 3) <2005T2879>. A series of pyrroles has also been prepared by a procedure featuring acid-induced cyclization of precursors constructed by sequential lithiation and alkylation of 1-benzylbenzotriazoles with 2-bromoacetaldehyde diethyl acetal and A -benzylideneani-line <1997JHC1379>. [Pg.271]


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See also in sourсe #XX -- [ Pg.163 ]




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