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Trimethylplatinum Iodide
Trimethylplatinum iodide is the organoplatinum complex with the formula CH3)3PtIsub>4. It is a white, air-stable solid that was one of the first organometallic complexes reported. It arises from the reaction of potassium hexachloroplatinate with methylmagnesium iodide. The complex exists as a tetramer: a cubane-type cluster with four octahedral Pt(IV) centers linked by four iodides as triply bridging ligand In coordination chemistry, a bridging ligand is a ligand that connects two or more atoms, usually metal ions. The ligand may be atomic or polyatomic. Virtually all complex organic compounds can serve as bridging ligands, so the term is usually r ...s.{{cite journal, authors=Ebert, K. H.; Massa, W.; Donath, H.; Lorberth, J.; Seo, B. S.; Herdtweck, E., title=Organoplatinum Compounds: VI. Trimethylplatinum Thiomethylate and Trimethylplatinum Iodide. The Crystal Structures of CH3)3PtS(CH3)sub>4 and CH3)3PtIsub>4·0.5CH3I, journal=J. Organomet. Chem., year=1998, volume=559, i ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Organoplatinum Complex
Organoplatinum chemistry is the chemistry of organometallic compounds containing a carbon to platinum chemical bond, and the study of platinum as a catalyst in organic reactions. Organoplatinum compounds exist in oxidation state 0 to IV, with oxidation state II most abundant. The general order in bond strength is Pt-C (sp) > Pt-O > Pt-N > Pt-C (sp3). Organoplatinum and organopalladium chemistry are similar, but organoplatinum compounds are more stable and therefore less useful as catalysts. Organoplatinum(0) Most organoplatinum(0) compounds contain alkene and alkyne ligands. Carbonyl complexes are rare, and the analogue of Ni(CO)4 is elusive. The alkene and alkyne ligands serve as two-electron donors, for example in the complexes (PPh3)2Pt(C2H4) and (PPh3)2Pt( C2Ph2). The ethylene ligand in (PPh3)2Pt(C2H4) is labile and exchanges with alkynes and electrophilic alkenes, even C60 a fullerene. A general synthetic route to (PPh3)2Pt(un) (un = alkene, alkyne) is reduction of potass ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Potassium Hexachloroplatinate
Potassium hexachloroplatinate is the inorganic compound with the formula K2PtCl6. It is a yellow solid that is an example of a comparatively insoluble potassium salt. The salt features the hexachloroplatinate(IV) dianion, which has octahedral coordination geometry. The precipitation of this compound from solutions of hexachloroplatinic acid was formerly used for the determination of potassium by gravimetric analysis. It is also useful as an intermediate in the recovery of platinum from wastes. Reactions Using salt metathesis reactions, potassium hexachloroplatinate is converted to a variety of quaternary ammonium and related lipophilic salts. These include tetrabutylammonium salt (NBu4)2PtCl6, known as Lukevics catalyst. Reduction of potassium hexachloroplatinate with hydrazine dihydrochloride In chemistry, a hydrochloride is an acid salt resulting, or regarded as resulting, from the reaction of hydrochloric acid with an organic base (e.g. an amine). An alternative name is chlo ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Methylmagnesium Iodide
Methylmagnesium chloride is an organometallic compound with the general formula CH3MgCl. This highly flammable, colorless, and moisture sensitive material is the simplest Grignard reagent and is commercially available, usually as a solution in tetrahydrofuran. Synthesis and reactions Relative to the more commonly encountered methylmagnesium bromide and methylmagnesium iodide, methylmagnesium chloride offers the advantages of low equivalent weight and low cost. It is prepared by the reaction of methyl chloride and magnesium in ethyl ether. left, Structure of CH3MgCl(thf)2, which is representative of the species in donor solvents. As with most Grignard reagents, methylmagnesium chloride is highly solvated by ether solvents via coordination from two oxygen atoms to give a tetrahedrally bonded magnesium center. Like methyllithium, it is the synthetic equivalent to the methyl carbanion synthon. It reacts with water and other protic reagents to give methane, e.g.,: :CH3MgCl + RO ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tetramer
A tetramer () (''tetra-'', "four" + '' -mer'', "parts") is an oligomer formed from four monomers or subunits. The associated property is called ''tetramery''. An example from inorganic chemistry is titanium methoxide with the empirical formula Ti(OCH3)4, which is tetrameric in solid state and has the molecular formula Ti4(OCH3)16. An example from organic chemistry is kobophenol A, a substance that is formed by combining four molecules of resveratrol. In biochemistry, it similarly refers to a biomolecule formed of four units, that are the same (homotetramer), i.e. as in Concanavalin A or different (heterotetramer), i.e. as in hemoglobin. Hemoglobin has 4 similar sub-units while immunoglobulins have 2 very different sub-units. The different sub-units may have each their own activity, such as binding biotin in avidin tetramers, or have a common biological property, such as the allosteric binding of oxygen in hemoglobin. See also * Cluster chemistry; atomic and molecular clusters ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cubane-type Cluster
A cubane-type cluster is an arrangement of atoms in a molecular structure that forms a cube. In the idealized case, the eight vertices are symmetry equivalent and the species has Oh symmetry. Such a structure is illustrated by the hydrocarbon cubane. With chemical formula , cubane has carbon atoms at the corners of a cube and covalent bonds forming the edges. Most cubanes have more complicated structures, usually with nonequivalent vertices. They may be simple covalent compounds or macromolecular or supramolecular cluster compounds. Examples Other compounds having different elements in the corners, various atoms or groups bonded to the corners are all part of this class of structures. Inorganic cubane-type clusters include selenium tetrachloride, tellurium tetrachloride, and sodium silox. Cubane clusters are common throughout bioinorganic chemistry. Ferredoxins containing e4S4iron–sulfur clusters are pervasive in nature. The four iron atoms and four sulfur atoms form an alter ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bridging Ligand
In coordination chemistry, a bridging ligand is a ligand that connects two or more atoms, usually metal ions. The ligand may be atomic or polyatomic. Virtually all complex organic compounds can serve as bridging ligands, so the term is usually restricted to small ligands such as pseudohalides or to ligands that are specifically designed to link two metals. In naming a complex wherein a single atom bridges two metals, the bridging ligand is preceded by the Greek letter mu, μ, with a subscript number denoting the number of metals bound to the bridging ligand. μ2 is often denoted simply as μ. When describing coordination complexes care should be taken not to confuse μ with η ('eta'), which relates to hapticity. Ligands that are not bridging are called terminal ligands. List of bridging ligands Virtually all ligands are known to bridge, with the exception of amines and ammonia. Common bridging ligands include most of the common anions. Many simple organic ligands form str ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Organoplatinum Compounds
Organoplatinum chemistry is the chemistry of organometallic compounds containing a carbon to platinum chemical bond, and the study of platinum as a catalyst in organic reactions. Organoplatinum compounds exist in oxidation state 0 to IV, with oxidation state II most abundant. The general order in bond strength is Pt-C (sp) > Pt-O > Pt-N > Pt-C (sp3). Organoplatinum and organopalladium chemistry are similar, but organoplatinum compounds are more stable and therefore less useful as catalysts. Organoplatinum(0) Most organoplatinum(0) compounds contain alkene and alkyne ligands. Carbonyl complexes are rare, and the analogue of Ni(CO)4 is elusive. The alkene and alkyne ligands serve as two-electron donors, for example in the complexes (PPh3)2Pt(C2H4) and (PPh3)2Pt( C2Ph2). The ethylene ligand in (PPh3)2Pt(C2H4) is labile and exchanges with alkynes and electrophilic alkenes, even C60 a fullerene. A general synthetic route to (PPh3)2Pt(un) (un = alkene, alkyne) is reduction of potassium ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
