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And exchange reactions

Synthesis and Exchange Reactions of 2- Bis(morpholino)phosphinoyloxy -3ff-l,4-benzodiazepines... [Pg.409]

Linear enzyme concentration dependence is observed for both the phosphorylation and exchange reaction over a 1000-fold enzyme concentration range, pM to nM, if the reactions are run in 25 mM Tris, 5mM Mg, pH 7.6. Under these conditions, the enzyme is associated. [Pg.144]

In the context of synthesis and exchange reactions of biodegradable drug-binding matrices, starch trisuccinic acid was loaded via imidazolides with amines such as n-butylamine, morpholine, 4-aminobenzoic acid, or 3,4-dihydroxyphenylalanine to prepare the respective amides in high yields [160] an example is presented below. [Pg.127]

Hydrogen addition and exchange reactions between a bituminous coal and a donor solvent or a nondonor solvent were investigated using fully-deutrated Tetralin and naphthalene. In the experiments conducted with coal, Tetralin-di2 and deuterium at 400°C, the ratio of hydrogen exchange to addition was on the average 2.0. [Pg.358]

Hydrolysis of formed hydroperoxide and exchange reaction with H02 formation ... [Pg.577]

He also observed and described base exchange in soil, which would later be understood to be cation exchange. However, this understanding had to wait until further development of chemistry and the concepts of ions and exchange reactions. [Pg.24]

Fig. 8-39. Electron state density in an electrode metal, Du, a semiconductor film, Dt, hydrated redox particles, Dredox, and exchange reaction current of redox electrons, t., in electron transfer equilibrium M = exchange current at a bare metal electrode, M/F= exchange current at a thin-film-covered metal electrode. Fig. 8-39. Electron state density in an electrode metal, Du, a semiconductor film, Dt, hydrated redox particles, Dredox, and exchange reaction current of redox electrons, t., in electron transfer equilibrium M = exchange current at a bare metal electrode, M/F= exchange current at a thin-film-covered metal electrode.
The trans elimination can take place if the basic sites of the alumina attack the hydrogen from one side of the plane and the hydroxyl group is removed from the opposite side of the plane by the acidic sites of the alumina. This may be possible if the reaction occurs within the pores of molecular dimensions (46) or within the crevices of the aluminas. Crevice sites on silica-alumina catalyst have been proposed by Burwell and co-workers (57) on the basis of racemization and exchange reactions of hydrocarbons. [Pg.61]

A number of features common to hydrogenation and exchange reactions suggest the possibility of a correlation between the two reaction systems in terms of tt complex adsorption, tt Complex adsorption has already been applied to hydrogenation by Rooney (6) who proposes the following reaction scheme ... [Pg.116]

Traditional sample preparation conditions to form SDS-protein complexes prior to electrophoretic analysis included heat treatment at elevated temperatures (e.g., In the case of non-reduced rMAbs, this could lead to sample preparation artifacts in the form of thermally induced fragmentation attributed to disulfide reduction and exchange reactions. Moreover, it was reported that high pH (>9.0) also enhanced the... [Pg.406]

The ability, evidenced by a variety of microorganisms (see Table VI) to activate molecular hydrogen and enable it to undergo oxidation and exchange reactions, has been attributed to an enzyme, or system of en-... [Pg.358]

TTomogeneous catalysis has made considerable progress in the past decade. Even so there is still uncertainty as to the detailed mechanism of many catalytic reactions. This is particularly true of Pd (II) catalysis. The advances in organic synthesis by Pd (II) catalytic chemistry have been impressive a recent review (I) of two volumes had few references before 1963. However the advances have mainly been in synthetic chemistry, and relatively little effort has been expended on studies of mechanism in this chemistry. To fill this gap we have undertaken a systematic study of the basic mechanisms of Pd (II) catalysis. Some choice of the many catalytic reactions available for study had to be made. For several reasons the reactions chosen for initial study were olefin oxidation and exchange reactions of vinylic and allylic esters and chlorides. Work has concentrated on the PdCl2-NaCl or LiCl systems in... [Pg.42]

The mechanism of molecular recognition reactions (kinetics and mechanism of substitution and exchange reactions with participation of polycomplexes and free chains) is considered. [Pg.139]


See other pages where And exchange reactions is mentioned: [Pg.1504]    [Pg.104]    [Pg.718]    [Pg.157]    [Pg.175]    [Pg.253]    [Pg.409]    [Pg.596]    [Pg.374]    [Pg.12]    [Pg.654]    [Pg.31]    [Pg.285]    [Pg.48]    [Pg.53]    [Pg.123]    [Pg.407]    [Pg.6]    [Pg.138]    [Pg.112]    [Pg.127]    [Pg.487]    [Pg.361]    [Pg.296]    [Pg.53]    [Pg.590]    [Pg.718]    [Pg.279]    [Pg.139]   
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A Swarts reaction and related processes (halogen exchange using HF)

And water exchange reactions

Complex Formation and Ligand-Exchange Reactions

Dissociation, disproportionation, dismutation and exchange reactions

Enamines as intermediates in isotope exchange and halogenation reactions

Exchange and Substitution Reactions

Exchange reactions and decomposition

Exchange reactions and equilibria

Exchange reactions between hydrogen and deuterium

Exchange reactions between niobium metal and ion-oxidisers

Exchange, Extraction (Guest Release), Rearrangement, and Decomposition Reactions

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

Formation and exchange reactions of metal complexes

Hydrogen Exchange Reaction of Arenium Ions and their Precursors

Knoevenagel and Michael Reactions on Cation-exchanged Zeolites

NMR Spectroscopy and Chemical Exchange Reactions

Reactions and Electron-Exchange Rates

Structures, Bonding, and Exchange Reactions

Substitution and Exchange Reactions of CO Ligands

Substitutions for Arenes and Arene Exchange Reactions

Vibrational Relaxation via Long-Lived Complexes and in Symmetric Exchange Reactions

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