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Exchange compounds

Zeohtes (qv), ion-exchange compounds, have been researched to some extent and have been proposed to improve NPN utilisation (25). However, no improvement in NPN utilisation was found with lambs fed seoHtes (26). [Pg.157]

The nitrogen atom in quinolizidine derivatives behaves as a tertiary amine and hence it can undergo quaternization by reaction with alkyl halides. For instance, berberine derivative 101 was transformed into 102 by treatment with 3-iodopropanol followed by anion exchange. Compound 102 was then transformed into intermediate 103, which was employed as a precursor for the the preparation of bis-ammonium salt 104 (Scheme 10). This compound showed ultrashort curare-like activity in rhesus monkeys <2001JOC3495>. [Pg.18]

We now turn to reagents which are important in context with the element/halogen exchange Compounds of the type 8 would be interesting reagents for nucleophilic halomethylation but are quite unstable due to carbene formation. Compound 9 would be an attractive synthetic equivalent for the synthons 8. As will be shown... [Pg.119]

Development of proton exchange compound membranes and innovative electrode configuration for PEM fuel cells. Activity leader University of Rome "La Sapienza". Estimated activity cost 6.2 million. [Pg.143]

Sekine et al. [72] studied CsNbTiOs, CsNbTi207 and proton-exchanged compounds for hydrogen evolution from aqueous methanol and oxygen evolution from aqueous AgNOg solution. Flat-band potentials for these materials were determined... [Pg.2879]

Complexation is one of several ways to favorably enhance the physicochemical properties of pharmaceutical compounds. It may loosely be defined as the reversible association of a substrate and ligand to form a new species. Although the classification of complexes is somewhat arbitrary, the differentiation is usually based on the types of interactions and species involved, e.g., metal complexes, molecular complexes, inclusion complexes, and ion-exchange compounds. Cyclodextrins (CDs) are classic examples of compounds that form inclusion complexes. These complexes are formed when a guest molecule is partially or fully included inside a host molecule e.g., CD with no covalent bonding. When inclusion complexes are formed, the physicochemical parameters of the guest molecule are disguised or altered and improvements in the molecule s solubility, stability, taste, safety, bioavailability, etc., are commonly seen. [Pg.671]

Carbonates are examples of builders that precipitate out the calcium ions in the form of calcium carbonate. Precipitating builders can leave behind insoluble deposits on clothes and washing machine components. Aluminosilicates such as zeolites are ion exchange compounds they remove (predominantly) calcium and magnesium ions and exchange them with sodium ions. [Pg.261]

Complex zeolites or base-exchanging compounds such as have been proposed as catalysts for the oxidation of naphthalene may also be used for this decarboxylating reaction.71... [Pg.430]

The first attempt to employ ion exchange for commercial purposes was in 1896 by F. Harm, a German agricultural chemist, to remove Na and from sugar beet juice. The first synthetic ion exchange compounds were aluminum silicates called zeolites and were available commercially about 1903. [Pg.270]

Figure 23-3. p. 271, shows a diagram of a portion of a natural inorganic ion exchange compound, sodalite. [Pg.270]

Heparinoids and Mucopolysaccharides as Complexes, Clathrates, Ion-Exchange Compounds... [Pg.171]

Protein-mediated transport systems, whether facilitative or active, are classified as antiports if they specifically exchange compounds of similar charge across a membrane they are called symports or cotransporters if they simultaneously transport two molecules across the membrane in the same direction. Band 3 in the red blood cell membrane, which exchanges chloride ion for bicarbonate, provides an example of an antiport. [Pg.166]

Fig. 22.8. Malate-aspartate shuttle. NADH produced by glycolysis reduces oxaloacetate (OAA) to malate, which crosses the mitochondrial membrane and is reoxidized to OAA. The mitochondrial NADH donates electrons to the electron transpwrt chain, with 2.5 ATPs generated for each NADH. To complete the shuttle, oxaloacetate must return to the cytosol, although it cannot be directly transported on a translocase. Instead, it is transaminated to aspartate, which is then transported out to the cytosol, where it is transaminated back to oxaloacetate. The translocators exchange compounds in such a way that the shuttle is completely balanced. TA = transamination reaction. a-KG = a-ketoglutarate. Fig. 22.8. Malate-aspartate shuttle. NADH produced by glycolysis reduces oxaloacetate (OAA) to malate, which crosses the mitochondrial membrane and is reoxidized to OAA. The mitochondrial NADH donates electrons to the electron transpwrt chain, with 2.5 ATPs generated for each NADH. To complete the shuttle, oxaloacetate must return to the cytosol, although it cannot be directly transported on a translocase. Instead, it is transaminated to aspartate, which is then transported out to the cytosol, where it is transaminated back to oxaloacetate. The translocators exchange compounds in such a way that the shuttle is completely balanced. TA = transamination reaction. a-KG = a-ketoglutarate.
Hydrogen has two stable isotopes, protium and deuterium. According to the lUPAC classification, deuterium is denoted as or D. The natural abundance of deuterium is very low, about 156 ppm, and restricts the large-scale application of deuterium-exchanged compounds. However, deuterium-exchanged compounds are very useful and often easily obtainable model molecules for various investigations. [Pg.246]

W. A. England, M. G. Cross, A. Hamnett, P. J. Wiseman and J. B. Goodenough, Fast Proton Conduction in Inorganic Ion Exchange Compounds, Solid State Ionics, 1 (1980) 231-49. [Pg.610]

Oscillometric or high-frequency titration was invented simultaneously and independently by Foreman and Crisp and also by Jensen and Parrak in 1946. Inorganic ion-selective heterogeneous membrane electrodes were introduced for electrometric titrations by Pungor in 1961 and those with neutral organic complexing or ion-exchange compounds by Simon in 1966. [Pg.2091]

An important aspect of the physics of double exchange compounds is the interaction between the electron distribution and the movement of the nuclei by vibronic coupling in complexes or electron-phonon interaction in extended systems. This goes beyond the scope of this book and we refer the interested reader to Ref. [5] for further reading. [Pg.187]

Liquid-membrane electrodes include classical ion-exchange, liquid ion-exchange, and electroneutral ionophore-based liquid monbrane electrodes. Of particular interest are systems where the ion-exchanging compounds are dissolved macrocyclic compounds that have a strong selectivity to alkali metals. The stability of the formed complexes in nonpolar solvents far exceeds that found in water and allows for the fabrication of membrane-free micropipettes where the nonpolar/water interface is the membrane. Unfortunately, this leads to higher resistance than that exhibited by crystalline micropipettes and requires the addition of lipophilic salt to the nonpolar solvent to decrease the pipette resistance. [Pg.492]

CfN, CfAs, CfSb. Only susceptibility measurements are available (Nave et al. 1986). The preparation and measurements of these compounds require admirable experimental skill. CfN is a ferromagnet (Tq = 25 K), CfAs and CfSb are antiferro-magnets with Neel temperatures of 17.5 and 25 K, respectively. The paramagnetic moments are practically identical with the free-ion value, which is 10.26/Ib- The susceptibility curves show the typical features of isotropic-exchange compounds. [Pg.341]


See other pages where Exchange compounds is mentioned: [Pg.220]    [Pg.122]    [Pg.40]    [Pg.769]    [Pg.146]    [Pg.142]    [Pg.182]    [Pg.280]    [Pg.2886]    [Pg.359]    [Pg.71]    [Pg.487]    [Pg.420]    [Pg.438]    [Pg.83]    [Pg.234]    [Pg.448]    [Pg.3683]    [Pg.458]    [Pg.185]    [Pg.116]    [Pg.118]    [Pg.537]    [Pg.480]    [Pg.599]   


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Albumin, ligand exchange reactions with compounds

Ammonia, liquid, isotope exchange reactions of organic compounds

Anion exchange acidic compounds

Anion-exchange chromatography arsenic compounds

Aromatic compounds hydrogen isotope exchange reactions

Aromatic compounds nucleophilic exchange reactions

Carbonyl compounds deuterium exchange

Cyclopropyl compounds, 1-bromosynthesis via lithium-halogen exchange

Deuterium exchange, in carbonyl compounds

Exchange Reactions of Group III Alkyl Addition Compounds

Exchange reactions bonded compounds

Exchange reactions organometallic compounds

Exchange reactions, hydrogen isotope, of organic compounds in liquid ammonia

Exchange reactions, oxygen isotope organic compounds

Exchange reactions, oxygen isotope, of organic compounds

Fast Exchange Reactions of Group I, II, and III Organometallic Compounds

Group exchange, organolithium compounds

Halogen-lithium exchange reactions functionalized compounds

Hydrogen exchange electrophilic, in aromatic compounds

Hydrogen-lithium exchange with aromatic compounds

Inclusion compounds guest exchange

Ion exchange compounds

Ligand exchange between dialkylmagnesium compounds

Ligand exchange processes carbonyl compound

Olefinic compounds, exchange labeling

Organoaluminum compounds, exchange

Organoaluminum compounds, exchange reactions

Organolithium compounds, exchange reactions

Organomagnesium compounds exchange with

Organomagnesium compounds, reaction exchange

Organomercury compounds exchange with

Organometallic Compounds Substitution 1 Exchange Reactions

Organometallic compounds alkyl group exchange

Organometallic compounds halogen-metal exchange reactions

Organozinc compounds exchange

Partial rate factors for hydrogen exchange in some substituted aromatic compounds

Preparation of Tritium-Labeled Compounds by Isotope Exchange Reactions

Proton exchange membrane fuel cell compounds

Sulfur exchange via HDS of thioaromatic compounds

The Exchange of Carbonyl Compounds with Water

The Exchange of Hydroxylic Compounds with Water

The Exchange of Other Organic Compounds containing Oxygen with Water

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