Metals lanthanum carbonate

In this article the term organometallic compound includes alkyl and aryl derivatives of the rare earths—the transition metals of group III, scandium, yttrium, lanthanum and the lanthanides cerium to liitetium with covalent metal-to-carbon a-bonds, as well as the so-called 77-complexes with more than monohapto metal-to-carbon bonds, for example cyclopentadienyl and olefin complexes, metal acetylides, but not carbonyls, cyanides and isocyanide complexes. Derivatives of scandium, yttrium and lanthanum are included and discussed together with the compounds of the lanthanides, because of many similarities in the synthesis and the chemistry of these organometallic derivatives of the rare earths. 

Lanthanide metal ions, Ln +, can exchange with, and mimic the function of, Ca + ions in the human body. Lanthanum carbonate is administered as chewable tablets under the tradename of Fosrenol to patients with particularly high levels of phosphate ions in the blood. However, there are significant gastrointestinal side-effects, and more soluble... 

Reactions with Transition Metals Forming Carbon-Carbon Bonds. The combination of certain lanthanides and TMS-Br has been found to produce lanthanum halides (LaX n = 2 or 3) that are very active reducing reagents (eq 19). So far, the only metals to be used in these reactions are samarium (Sm) and ytterbium (Yb). In addition to TMS-Br, these reactions have been accomplished using Sm/TMS-Cl/Nal under similar conditions with corr5>arable yields. 

Bina Selenides. Most biaary selenides are formed by beating selenium ia the presence of the element, reduction of selenites or selenates with carbon or hydrogen, and double decomposition of heavy-metal salts ia aqueous solution or suspension with a soluble selenide salt, eg, Na2Se or (NH 2S [66455-76-3]. Atmospheric oxygen oxidizes the selenides more rapidly than the corresponding sulfides and more slowly than the teUurides. Selenides of the alkah, alkaline-earth metals, and lanthanum elements are water soluble and readily hydrolyzed. Heavy-metal selenides are iasoluble ia water. Polyselenides form when selenium reacts with alkah metals dissolved ia hquid ammonia. Metal (M) hydrogen selenides of the M HSe type are known. Some heavy-metal selenides show important and useful electric, photoelectric, photo-optical, and semiconductor properties. Ferroselenium and nickel selenide are made by sintering a mixture of selenium and metal powder. 

Sihca is reduced to siUcon at 1300—1400°C by hydrogen, carbon, and a variety of metallic elements. Gaseous siUcon monoxide is also formed. At pressures of >40 MPa (400 atm), in the presence of aluminum and aluminum haUdes, siUca can be converted to silane in high yields by reaction with hydrogen (15). SiUcon itself is not hydrogenated under these conditions. The formation of siUcon by reduction of siUca with carbon is important in the technical preparation of the element and its alloys and in the preparation of siUcon carbide in the electric furnace. Reduction with lithium and sodium occurs at 200—250°C, with the formation of metal oxide and siUcate. At 800—900°C, siUca is reduced by calcium, magnesium, and aluminum. Other metals reported to reduce siUca to the element include manganese, iron, niobium, uranium, lanthanum, cerium, and neodymium (16). 

Lanthanum is a soft silvery-white metal that, when cut with a knife, forms an oxide with the air (tarnishes) on the exposed area. It is the most reactive of the elements in the series. It reacts slightly with cold water but rapidly with hot water, producing hydrogen gas (H ) and lanthanum oxide (La O ). It directly interacts with several other elements, including nitrogen, boron, the halogens, carbon, sulfur, and phosphorus. 

Lanthanum fluoride is used in phosphor lamp coating. Mixed with other rare earths, it is used in carbon arc electrodes and lasers. Also, the fluoride is used in the production of lanthanum metal, an intermediate step in the manufacture of high purity metal. 

One of the aspects that has been of interest is the incorporation of an external atom in the spheroidal cavity. A variety of metal atoms can, in principle, be trapped in this cavity. Some of the studies have claimed that it is possible to push atoms such as lanthanum, iron and helium inside the spheroidal cavity of CgQ and other fullerenes. Substitution of the carbon in CgQ by boron and nitrogen has been attempted. Interestingly, nitrogen not only substitutes for carbon in the cage but also adds on to Cgo and C-iq. 

Another reaction in which the cleavage of a carbon-hydrogen bond is important is the bromination of ketones. In the bromination of ethyl acetoacetate and 2-carboethoxycyclopentanone, it was shown that multivalent cations are catalysts. In the latter reaction, cupric, nickelous, lanthanum, zinc, plumbous, manganous, cadmium, magnesium, and calcium ions were effective (45). One can interpret the effect of the metal ion in terms of its catalysis of the proton transfer from the ester to a base, whether the reaction is carried out in dilute hydrochloric acid solution (acid-catalyzed bromination) or in acetate buffer (base-catalyzed bromination). 

Mischmetal is produced commercially by electrolysis, The usual starting ingredient is the dehydrated rare earth chloride produced from monazite or bastnasite. The mixed rare earth chloride is fused in an iron, graphite, or ceramic crucible with the aid of electrolyte mixtures made up of potassium, barium, sodium, or calcium chlorides. Carbon anodes are immersed in the molten salt. As direct current flows through the cell, molten mischmetal huilcls up in the bottom of the crucible. This method is also used to prepare lanthanum and cerium metals. 

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