Organic compounds, metal-catalyzed hydrolysis

B. Metal-Catalyzed Hydrolysis of Organic Compounds 1. General... 

Dissolved metals and metal-containing surfaces play an important role in the transformation of organic contaminants in the subsurface environment. Metal ions can catalyze hydrolysis in a way similar to acid catalysis. Organic hydrolyzable compounds susceptible to metal ion catalysis include carboxylic acids, esters, amides, anilides, and phosphate-containing esters. Metal ions and protons... 

PROBABLE FATE photolysis photooxidation definitely occurs, photooxidation half-life in water 3.2-160 days photooxidation half-life in air 1.19-11.9 hrs oxidation metal-catalyzed oxidation occurs in aerated surface waters, oxidation by peroxy radicals is important, photochemically produced hydroxyl radicals degrades compound in daylight hours, half-life 8 hrs hydrolysis not an important process volatilization not an important process sorption slight potential for adsorption onto organic materials, adsorption to sediment will be moderate biological processes biodegradation can occur other reactions/interactions chlorine present in water could chlorinate the eompound can be washed out by rain... 

For the construction of artificial metalloproteins, protein scaffolds should be stable, both over a wide range of pH and organic solvents, and at high temperature. In addition, crystal structures of protein scaffolds are crucial for their rational design. The proteins reported so far for the conjugation of metal complexes are listed in Fig. 1. Lysozyme (Ly) is a small enzyme that catalyzes hydrolysis of polysaccharides and is well known as a protein easily crystallized (Fig. la). Thus, lysozyme has been used as a model protein for studying interactions between metal compounds and proteins [13,14,42,43]. For example, [Ru(p-cymene)] L [Mn(CO)3l, and cisplatin are regiospecificaUy coordinated to the N = atom of His 15 in hen egg white lysozyme [14, 42, 43]. Serum albumin (SA) is one of the most abundant blood proteins, and exhibits an ability to accommodate a variety of hydrophobic compounds such as fatty acids, bilirubin, and hemin (Fig. lb). Thus, SA has been used to bind several metal complexes such as Rh(acac)(CO)2, Fe- and Mn-corroles, and Cu-phthalocyanine and the composites applied to asymmetric catalytic reactions [20, 28-30]. 

Polymerizing gel routes. Precursor metal organic compounds, e.g., alkoxides such as TEOS (tetraethylorthosilicate). Process acid catalyzed hydrolysis and condensation reactions to form gel. Pore sizes 1 to 5 nm. 

The three types of solids, metals, covalent semiconductors or insulators, and ionic compounds (including oxides) have characteristic surface reactions. In organic catalysis only metals and ionics are considered (Table 6.5), while in CVD all three types of solid surfaces are of interest. Metals absorb hydrogen and nitrogen dissociatively while ionic substrates have redox reactions or acid/base reactions with molecules. Oxidation of gases is often catalyzed by the surface of metal oxides. So is deposition of oxides by oxidation and hydrolysis of metal-containing precursors. When mixed oxides (e.g., perovskites) are deposited care must be taken to ensure a sufficient availability of the separate components. 

Chemical reactions between biochemical compounds are enhanced by biological catalysts called enzymes, which consist mostly or entirely of globular proteins. In many cases a cofactor is needed to combine with an otherwise inactive protein to produce the catalytically active enzyme complex. The two distinct varieties of cofactors are coenzymes, which are complex organic molecules, and metal ions. Enzymes catalyze six major classes of reactions 1) Oxidoreductases (oxidation-reduction reactions), 2) Transferases (transfer of functional groups), 3) Hydrolases (hydrolysis reactions), 4) Lyases (addition to double bonds, 5) Isomerases (isomerization reactions) and 6) Ligases (formation of bonds with ATP (adenosine triphosphate) cleavage) [1]. 

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