Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Transition metal manganese

Consider the alkaline earth metal strontium and the transition metal manganese. [Pg.551]

Chiu GN, Abraham SA, Ickenstein LM, et al. Encapsulation of doxorubicin into thermosensitive liposomes via complexation with the transition metal manganese. J Control Release 2005 104 271. [Pg.50]

The criterion of abundance knocks out aU the alternatives but magnesium. Strontium and barium suffer the same fate as most of the bottom half of the periodic table, being too large to be abundant in the universe. In the transition metals, manganese has a size and shape similar to calcium, but it is also too rare to be used in quantity. [Pg.214]

Manganese is the third most abundant transition metal, and is widely distributed in the earth s crust. The most important ore is pyrolusite, manganese(IV) oxide. Reduction of this ore by heating with aluminium gives an explosive reaction, and the oxide Mn304 must be used to obtain the metal. The latter is purified by distillation in vacuo just above its melting point (1517 K) the pure metal can also he obtained by electrolysis of aqueous manganese(II) sulphate. [Pg.384]

Metal Complex. Complexation gas chromatography was first introduced by V. Schurig in 1980 (118) and employs transition metals (eg, nickel, cobalt, manganese or rhodium) complexed with chiral terpenoid ketoenolate ligands such as 3-ttifluoroacetyl-lR-camphorate (6),... [Pg.70]

The Acetaldehyde Oxidation Process. Liquid-phase catalytic oxidation of acetaldehyde (qv) can be directed by appropriate catalysts, such as transition metal salts of cobalt or manganese, to produce anhydride (26). Either ethyl acetate or acetic acid may be used as reaction solvent. The reaction proceeds according to the sequence... [Pg.76]

Metals. Transition-metal ions, such as iron, copper, manganese, and cobalt, when present even in small amounts, cataly2e mbber oxidative reactions by affecting the breakdown of peroxides in such a way as to accelerate further attack by oxygen (36). Natural mbber vulcani2ates are especially affected. Therefore, these metals and their salts, such as oleates and stearates, soluble in mbber should be avoided. [Pg.246]

Most commercial sorbic acid is produced by a modification of this route. Catalysts composed of metals (2inc, cadmium, nickel, copper, manganese, and cobalt), metal oxides, or carboxylate salts of bivalent transition metals (2inc isovalerate) produce a condensation adduct with ketene and crotonaldehyde (22—24), which has been identified as (5). [Pg.283]

Metal-Catalyzed Oxidation. Trace quantities of transition metal ions catalyze the decomposition of hydroperoxides to radical species and greatiy accelerate the rate of oxidation. Most effective are those metal ions that undergo one-electron transfer reactions, eg, copper, iron, cobalt, and manganese ions (9). The metal catalyst is an active hydroperoxide decomposer in both its higher and its lower oxidation states. In the overall reaction, two molecules of hydroperoxide decompose to peroxy and alkoxy radicals (eq. 5). [Pg.223]

Although trialkyl- and triarylbismuthines are much weaker donors than the corresponding phosphoms, arsenic, and antimony compounds, they have nevertheless been employed to a considerable extent as ligands in transition metal complexes. The metals coordinated to the bismuth in these complexes include chromium (72—77), cobalt (78,79), iridium (80), iron (77,81,82), manganese (83,84), molybdenum (72,75—77,85—89), nickel (75,79,90,91), niobium (92), rhodium (93,94), silver (95—97), tungsten (72,75—77,87,89), uranium (98), and vanadium (99). The coordination compounds formed from tertiary bismuthines are less stable than those formed from tertiary phosphines, arsines, or stibines. [Pg.131]

Carbides of the Iron Group Metals. The carbides of iron, nickel, cobalt, and manganese have lower melting points, lower hardness, and different stmctures than the hard metallic materials. Nonetheless, these carbides, particularly iron carbide and the double carbides with other transition metals, are of great technical importance as hardening components of alloy steels and cast iron. [Pg.453]

Cobalt. Without a doubt cobalt 2-ethyIhexanoate [136-52-7] is the most important and most widely used drying metal soap. Cobalt is primarily an oxidation catalyst and as such acts as a surface or top drier. Cobalt is a transition metal which can exist in two valence states. Although it has a red-violet color, when used at the proper concentration it contributes very Httie color to clear varnishes or white pigmented systems. Used alone, it may have a tendency to cause surface wrinkling therefore, to provide uniform drying, cobalt is generally used in combination with other metals, such as manganese, zirconium, lead, calcium, and combinations of these metals. [Pg.221]

The highest halide of each metal is of course a fluoride Rep7 (the only thermally stable heptahalide of a transition metal), TcFg, and MnF4. This again indicates the diminished ability of manganese to attain high oxidation states when compared not only to Tc and Re but also to... [Pg.1051]

The distinction between the first member of the group and the two heavier members, which was seen to be so sharp in the early groups of transition metals, is much less obvious here. The only unsubstituted, discrete oxoanions of the heavier pair of metals are the tetrahedral [Ru 04] and [Ru 04]. This behaviour is akin to that of iron or, even more, to that of manganese, whereas in the osmium analogues the metal always increases its coordination number by the attachment of extra OH ions. If RUO4 is dissolved in cold dilute KOH, or aqueous K2RUO4 is oxidized by chlorine, virtually black crystals of K[Ru 04] ( permthenate ) are deposited. These are unstable unless dried and are reduced by water, especially if alkaline, to the orange... [Pg.1082]


See other pages where Transition metal manganese is mentioned: [Pg.179]    [Pg.240]    [Pg.2966]    [Pg.14]    [Pg.183]    [Pg.340]    [Pg.27]    [Pg.110]    [Pg.6]    [Pg.468]    [Pg.465]    [Pg.324]    [Pg.45]    [Pg.69]    [Pg.179]    [Pg.240]    [Pg.2966]    [Pg.14]    [Pg.183]    [Pg.340]    [Pg.27]    [Pg.110]    [Pg.6]    [Pg.468]    [Pg.465]    [Pg.324]    [Pg.45]    [Pg.69]    [Pg.361]    [Pg.389]    [Pg.392]    [Pg.393]    [Pg.67]    [Pg.134]    [Pg.26]    [Pg.510]    [Pg.527]    [Pg.286]    [Pg.280]    [Pg.349]    [Pg.157]    [Pg.243]    [Pg.345]    [Pg.419]    [Pg.217]    [Pg.216]    [Pg.245]    [Pg.310]    [Pg.30]    [Pg.1062]   
See also in sourсe #XX -- [ Pg.1088 ]




SEARCH



First-Row Transition Metal Elements Scandium to Manganese

Metals manganese

Transition metal complexes, manganese

Transition metal compounds chiral manganese complex

© 2024 chempedia.info