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Substrate organization

Retention Length of Substrate Organic acid Reaction Cell density... [Pg.204]

X oxidized organic 4 X reduced substrate organic substrate... [Pg.716]

TonB-dependent receptor I (kDa) Additional proteins (kDa) Substrates Organism... [Pg.301]

At the beginning stage of dehydrogenation, the substrate organic hydride is adsorbed onto the catalyst surface from the liquid phase directly and easily. Catalytic reaction processes will succeed it, until the surface sites are filled with the adsorbed reactant and products. Once product desorption starts to form and grow a bubble, product readsorption becomes unfavorable due to the increment of translational entropy of the product molecule in the bubble, if compared with that in the solution, shifting the adsorption equilibrium for the product and suppressing its effect of rate retardation. [Pg.471]

Substrate (Organic solvent) HEAT Homogeneous COOL Product (Organic solvent)... [Pg.147]

The catalytic, asymmetric hydrogenations of alkenes, ketones and imines are important transformations for the synthesis of chiral substrates. Organic dihydropyridine cofactors such as dihydronicotinamide adenine dinucleotide (NADH) are responsible for the enzyme-mediated asymmetric reductions of imines in living systems [86]. A biomimetic alternative to NADH is the Hantzsch dihydropyridine, 97. This simple compound has been an effective hydrogen source for the reductions of ketones and alkenes. A suitable catalyst is required to activate the substrate to hydride addition [87-89]. Recently, two groups have reported, independently, the use of 97 in the presence of a chiral phosphoric acid (68 or 98) catalyst for the asymmetric transfer hydrogenation of imines. [Pg.229]

Substrate organization in membrane mimetic systems leads to altered solvation, ionization and reduction potentials and, hence, to altered reaction rates, paths and stereochemistries. These properties have been advantageously exploited, in turn, for reactivity control, catalysis, drug delivery and artificial photosynthesis (8). There are only limited examples of the utilization of membrane mimetic systems in permeability control. In order to gain insight into this important area, we have initiated a research program in BLMs. A status report of our activities in this area will be summarized in the next section. [Pg.96]

Magnetic metal nanoparticles tend to self-assemble not only for reasons known from nomnagnetic species, namely, van der Waals forces, but especially owing to their intrinsic magnetic nature. Solutions of 4.8mn CoPts particles, spread onto a substrate, organize spontaneously when the solvent is evaporated.Higher concentrations of the solutions easily result in formation of double and triple layers as is indicated in Figure IS. ... [Pg.5954]

In respiration, substrate organic molecules containing carbon-hydrogen bonds (food) and oxygen are absorbed by prokaryotic cells or by the mitochondria of eukaryotic cells. The oxygen reacts with electrons that are derived from metabolic changes to the carbon-hydrogen bonds of the substrates. The final steps of substrate metabolism, the Krebs cycle,... [Pg.9]

These are listed in Table 7. Just as in the case of substrate, organ-specific pH optima have been observed. Thus, for example, purified human placental alkaline phosphatase exhibits an optimum pH of 10.6 in contrast to 9.8 for the human intestinal preparation (Fig. 7). [Pg.274]

All OLEDs were fabricated on indium tin oxide precoated onto glass substrate. Organic layers were vacuum deposited via thermal evaporation in the high-vacuum chamber. Fig. 11 shows the structure of blue OLED device and its energy diagram. The thickness and materials of each layer are same for fabricated devices except ETMs to eliminate another possible luminance attenuating factor. [Pg.53]

Influence of the reaction conditions (pH, temperature, concentration of substrates, organic solvent/cosolvents) on the reaction system and on the equilibrium constant,... [Pg.189]

In the presence of aqueous NaOH, palladium(II) chloride was effective for the transfer hydrogenation of unsaturated acids, azlactones and phenylpyruvic acid (Scheme 3.36) at 65 °C although in quite long reaction times (typically 16 h) [255], For these water-soluble substrates organic solvents were not required. No attempt was made to clarify the nature of the active catalytic species, which -under these conditions- may well be a fine colloid of Pd metal. [Pg.108]

A8. Leidheiser, H., Jr. "Corrosion Control Through a Better Understanding of the Metallic Substrate/Organic Coating Interface" AD/A 095A20, National Technical Information Service Springfield, Va., 1980. [Pg.798]

Sunvold, G.D. G.C. Fahey, Jr. N.R. Merchen G.A. Reinhart. In vitro fermentation of selected fibrous substrates by dog and cat fecal inoculum Influence of diet composition on substrate organic matter disappearance and short-chain fatty acid production./. Anim. Sci. 1995, 73, 1110-1122. [Pg.302]

The ligands bound to a catalytic metal control that metal s reactivity by adjusting the electron density at the metal, opening and closing coordination sites for the substrates and creating a shape to orient the substrate. Organic ligands often require complex syntheses and are difficult to optimize. [Pg.47]

A significant part of OH oxidation of bioorganic materials is dne to the initial dehydro-genization of the substrate organic molecnles RH ... [Pg.857]

Various levels of molstinre In SSF have been reported for different products. About 75% moisture In straw was used for SCP production (2,3,3a) Pereas for aflatoxln production It was 33.3% In rice and 48.4% In straw (JL). Thus moisture level In the SSF depends on the nature of the substrate, organism and the type of end product. [Pg.438]

Growth- substrate/ organism Y (mg cell per mg growth substrate) k (pmole growth substrate per mg cell-day) K (pM) K (pM) b (day ) Refs... [Pg.77]

As well as using a chiral auxiliary or enantiopure substrates, organic chemists have also directed their efforts at achieving an asymmetric version of the MBH... [Pg.104]


See other pages where Substrate organization is mentioned: [Pg.116]    [Pg.341]    [Pg.404]    [Pg.119]    [Pg.116]    [Pg.147]    [Pg.101]    [Pg.226]    [Pg.23]    [Pg.5294]    [Pg.651]    [Pg.53]    [Pg.658]    [Pg.13]    [Pg.75]    [Pg.5293]    [Pg.639]    [Pg.45]    [Pg.368]    [Pg.172]    [Pg.400]    [Pg.531]    [Pg.385]    [Pg.751]    [Pg.494]    [Pg.1027]    [Pg.1027]   


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Organic substrates

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