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Reversible swaps

Reversible swaps—which allow one party to reverse the direction of the swap. For example, the party could switch from being the fixed-rate payer to being the fixed-rate receiver. This might happen if a company was able to repay its borrowing prematurely, was now a net investor, and rates had fallen substantially. [Pg.547]

The purpose of a tabu restriction is to prevent a move from being reversed during the length of the short-term memory, which is a number of future moves specified by the variable tabu size. If, at a given iteration, jobs p(i) and p(j) are swapped, then any move that places job p(i) earlier in the sequence than position i is tabu, until tabu size iterations have occurred or the aspiration level is exceeded. To keep track of which moves are tabu and to free those moves from their tabu status, Laguna et al. define the following data structures... [Pg.395]

Total mRNAs from confrol and induced cells were labeled using reverse franscripfase wifh fhe incorporation of fluorescene-dCTP (control, green label) or Cy5-dCTP (induced, red label). The two populations were hybridized to separate arrays. However, the labels were also swapped to verify fhaf any differences in labeling efficiency did not affect the result. [Pg.148]

We are finally ready to consider the effect of the selective 180° lH pulse on the downfield component of the H doublet (auac Pn c transition). We know that the 180° H pulse reverses ( inverts ) the spin state of each proton in the sample every proton in the a state is converted to the p state and every proton in the p state is converted to the a state. Looking at the energy diagram for the pair, we see that the 180° lH pulse swaps the entire... [Pg.259]

Covalent bonding depends on the presence of two atomic receptor sites. When the electron reaches one of these sites its behaviour, while in the vicinity of the atom, is described by an atomic wave function, such as the ip(ls), (l = 0), ground-state function of the H atom. Where two s-type wave functions serve to swap the valence electron the interaction is categorized as of a type. The participating wave functions could also be of p, (l = 1), or d, (/ = 2) character to form 7r or 6 bonds respectively. The quantum number l specifies the orbital angular momentum of the valence electron. A common assumption in bonding theory is that a valence electron with zero angular momentum can be accommodated in a p or d state if a suitable s-state is not available. The reverse situation is not allowed. [Pg.178]

Figure 5.26 shows an LB film that regulates electron transfer. Monolayers of an electron donor layer, an insulating fatty acid layer and an electron acceptor layer were transferred in a defined sequence. In this hetero-layered LB film, electron transfer only occurs from the inside to the outside, and the structure of the insulator layer determines the efficiency of electron transfer. Swapping aroimd the donor layer and the acceptor layer reverses the direction of electron transfer. Simply controlling the layering structure therefore enables us to modulate the direction and efficiency of electron flow. [Pg.162]

A swap of the methyl carbon with nitrogen in aza-AdoMet leads to sinefungin (see Fig. 2g)—a natural nucleoside antibiotic found in Streptomyces griseolus. Such reverse chemistry additionally enhances the chemical stability of cofactor. Because of the positive charge of the protonated amine and correct chirahty at the carbon center, sinefungin has an extremely high inhibitory potential for AdoMet-dependent methyltransferases. [Pg.1101]

Additionally, the reverse capture protocol employs a two-slide dye-swap method in which the dye/sample pairings used on one microarray slide are reversed and applied to a second, parallel slide. This component of the protocol facilitates the normalization of data, and controls for differences in the labeling efficiencies of the different dyes, as well as differences in antihody-hinding efficiencies following the labeling reactions. [Pg.177]

A third methodology uses a simplified approach to get an approximation of the convexity bias. The mean reversion rate, a, typically varies from O.OOf for negligible effects to O.f for high mean reversion. For example, Bloomberg assumes a constant mean reversion rate of 0.03. Observed volatilities of interest rate caps are multiplied by their corresponding swap rates to get an estimate of o. [Pg.642]

A usual MDGC procedure may require multiple heartcuts. If these are transferred to then each of the peaks in these zones will have an input peakwidth equal to the dispersion they have experienced on D. Also, peaks that swap positions on compared with their elution order may suffer worsened resolution on the two-column set, as they try to establish their reversed elution order as they travel along D. It is normally preferred that a cryofocusing event is used at the head of to provide essentially a sharp band injection into D. [Pg.1843]

A peculiar specificity of the thermal energy compared to other energy varieties is that the capacitive relationship is not exactly the same. It differs mainly in the respective roles of the two capacitive state variables, basic quantity and effort, which are symmetrically swapped. For instance, the simplest model that corresponds to an ideal thermal pole uses the same exponential function as in the other energy varieties, but in a reversed way. In other words, this is the reciprocal relationship, called elastive relationship, that is written with the exponential function instead of the capacitive one in aU other varieties. [Pg.81]

The aspect of a reversible reaction of fluorinase was of major importance for further optimizations and by addition of the enzyme L-amino acid oxidase (L-AAO) the oxidative removal of formed L-methionine was enabled. In this way, the equilibrium of the reaction was pulled toward 5 -[ F]FDA and allowed very high radiochemical yields of 95% within 1-2 h. Accordingly, the F-labeled compounds 5 -[ F]fluoro-5 -deoxyinosine (5 -[ F]FDI) (O Fig. 42.30h), 5 -[ F]fluoro-5 -deoxyribose phosphate (O Fig. 42.30c)y and 5 -[ F]fluoro-5 -deoxyribose (O Fig. 42.30d) were successfully produced from 5 -[ F]fluoro-5 -deoxyadenosine (Deng et al. 2006, Onega et al 2009, 2010). In the base-swap strategy, the 5 [i F]fluoro-5 -deoxyribose phosphate O Fig. 42.30c) could be further transformed into... [Pg.2062]

There is another gate which can be used to prove reversible computation. It is the Fredkin gate it performs a controlled swap operation between two bits [6]. [Pg.20]


See other pages where Reversible swaps is mentioned: [Pg.26]    [Pg.26]    [Pg.152]    [Pg.693]    [Pg.73]    [Pg.186]    [Pg.282]    [Pg.88]    [Pg.281]    [Pg.251]    [Pg.142]    [Pg.77]    [Pg.219]    [Pg.4207]    [Pg.434]    [Pg.132]    [Pg.508]    [Pg.202]    [Pg.651]    [Pg.175]    [Pg.186]    [Pg.53]    [Pg.130]    [Pg.67]    [Pg.211]    [Pg.251]    [Pg.882]    [Pg.301]    [Pg.311]    [Pg.439]    [Pg.2375]    [Pg.2030]    [Pg.432]    [Pg.54]    [Pg.392]   
See also in sourсe #XX -- [ Pg.547 ]




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