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Pentamethylbismuth
Pentamethylbismuth (or pentamethylbismuthorane) is an organometalllic compound containing five methyl groups bound to a bismuth atom with formula Bi(CH3)5. It is an example of a hypervalent compound. The molecular shape is trigonal bipyramid. Production Pentamethylbismuth is produced in a two step process. First, trimethylbismuth is reacted with sulfuryl chloride to yield dichloro trimethylbismuth, which is then reacted with two equivalents of methyllithium dissolved in ether. The blue solution is cooled to −110 °C to precipitate the solid product. :Bi(CH3)3 + SO2Cl2 → Bi(CH3)3Cl2 + SO2 :Bi(CH3)3Cl2 + 2LiCH3 → Bi(CH3)5 + 2LiCl Properties At -110 °C, Bi(CH3)5 is a blue-violet solid. The methyl groups are arranged in a trigonal bipyramid, and the bond-lengths of methyl with bismuth are all the same. However, the molecule is not rigid, as can be determined from the nuclear magnetic resonance spectrum that shows all methyl groups are equivalent. It is stable as a solid, ...
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Pentamethylbismuth Energy States
Pentamethylbismuth (or pentamethylbismuthorane) is an organometalllic compound containing five methyl groups bound to a bismuth atom with formula Bi(CH3)5. It is an example of a hypervalent compound. The molecular shape is trigonal bipyramid. Production Pentamethylbismuth is produced in a two step process. First, trimethylbismuth is reacted with sulfuryl chloride to yield dichloro trimethylbismuth, which is then reacted with two equivalents of methyllithium dissolved in ether. The blue solution is cooled to −110 °C to precipitate the solid product. :Bi(CH3)3 + SO2Cl2 → Bi(CH3)3Cl2 + SO2 :Bi(CH3)3Cl2 + 2LiCH3 → Bi(CH3)5 + 2LiCl Properties At -110 °C, Bi(CH3)5 is a blue-violet solid. The methyl groups are arranged in a trigonal bipyramid, and the bond-lengths of methyl with bismuth are all the same. However, the molecule is not rigid, as can be determined from the nuclear magnetic resonance spectrum that shows all methyl groups are equivalent. It is stable as a sol ...
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Pentamethylantimony
Pentamethylantimony or pentamethylstiborane is an organometalllic compound containing five methyl groups bound to an antimony atom with formula Sb(CH3)5. It is an example of a hypervalent compound. The molecular shape is trigonal bipyramid. Some other antimony(V) organometallic compounds include pentapropynylantimony (Sb(CCCH3)5) and pentaphenyl antimony (Sb(C6H5)5). Other known pentamethyl-pnictides include pentamethylbismuth and pentamethylarsenic. Production Pentamethylantimony can be made by reacting Sb(CH3)3Br2 with two equivalents of methyl lithium. Another production route is to convert trimethylstibine to the trimethyl antimony dichloride, and then replace the chlorine with methyl groups with methyl lithium. :Sb(CH3)3 + Cl2 → Sb(CH3)3Cl2 :Sb(CH3)3Cl2 + 2LiCH3 → Sb(CH3)5 + 2LiCl Properties Pentamethylantimony is colourless. At -143 °C it crystallizes in the orthorhombic system with space group ''Ccmm''. Unit cell dimensions are a=6.630 Å b=11.004  ...
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Pentamethyltantalum
Pentamethyltantalum is a homoleptic organotantalum compound. It has a propensity to explode when it is melted. Its discovery was part of a sequence that lead to Richard R. Schrock's Nobel Prize discovery in olefin metathesis. Production Pentamethyltantalum can be made from the reaction of methyllithium with Ta(CH3)3Cl2. Ta(CH3)3Cl2 is in turn made from tantalum pentachloride and dimethylzinc. The preparation was inspired by the existence of pentaalkyl compounds of phosphorus and arsenic, and the discovery of hexamethyltungsten. The discoverer, Richard R. Schrock considered tantalum to be a metallic phosphorus, and tried the use of methyllithium. Properties The pentamethyltantalum adopts a square pyramid shape. Ignoring the C-H bonds, the molecule has ''C''4v symmetry. The four carbon atoms at the base of the pyramid are called basal, and the carbon atom at the top is called apical or apex. The distance from tantalum to the apical carbon atom is 2.11 Å, and to the basal car ...
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Pentamethylarsenic
Pentamethylarsenic (or pentamethylarsorane)is an organometalllic compound containing five methyl groups bound to an arsenic atom with formula As(CH3)5. It is an example of a hypervalent compound. The molecular shape is trigonal bipyramid. History The first claim to make pentamethylarsenic was in 1862 in a reaction of tetramethylarsonium iodide with dimethylzinc by A. Cahours. For many years all the reproductions of this proved fruitless, so the production proved not to be genuine. It was actually discovered by Karl-Heinz Mitschke and Hubert Schmidbaur in 1973. Production Trimethylarsine is chlorinated to trimethylarsine dichloride, which then reacts with methyl lithium to yield pentamethylarsenic. :As(CH3)3 + Cl2 → As(CH3)3Cl2 :As(CH3)3Cl2 + 2LiCH3 → As(CH3)5 + 2LiCl Side products include As(CH3)4Cl and As(CH3)3=CH2. Pentamethylarsenic is not produced by biological organisms. Properties Pentamethylarsenic smells the same as pentamethylantimony, but is otherwise uniqu ...
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Methyllithium
Methyllithium is the simplest organolithium reagent with the empirical formula CH3Li. This s-block organometallic compound adopts an oligomeric structure both in solution and in the solid state. This highly reactive compound, invariably used in solution with an ether as the solvent, is a reagent in organic synthesis as well as organometallic chemistry. Operations involving methyllithium require anhydrous conditions, because the compound is highly reactive toward water. Oxygen and carbon dioxide are also incompatible with MeLi. Methyllithium is usually not prepared, but purchased as a solution in various ethers. Synthesis In the direct synthesis, methyl bromide is treated with a suspension of lithium in diethyl ether. :2 Li + MeBr → LiMe + LiBr The lithium bromide forms a complex with the methyllithium. Most commercially available methyllithium consists of this complex. "Halide-free" methyllithium is prepared from methyl chloride. Lithium chloride precipitates from the diethyl ...
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Organobismuth Compounds
Organobismuth chemistry is the chemistry of organometallic compounds containing a carbon to bismuth chemical bond. Applications are few. The main bismuth oxidation states are Bi(III) and Bi(V) as in all higher group 15 elements. The energy of a bond to carbon in this group decreases in the order P > As > Sb > Bi. The first reported use of bismuth in organic chemistry was in oxidation of alcohols by Challenger in 1934 (using Ph3Bi(OH)2). Knowledge about methylated species of bismuth in environmental and biological media is limited. Discovery Triethylbismuth, the first known organobismuth compound, is prepared in 1850 by Löwig and Schweizer from iodoethane and a potassium–bismuth alloy. As with most trialkylbismuth compounds, BiEt3 has an extremely pungent and unpleasant odor, and is spontaneously oxidized in air. The chemistry of these complexes first begin receiving significant attention when Grignard reagents and organolithium compounds become available. OrganoBi(III) compo ...
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HOMO
''Homo'' () is the genus that emerged in the (otherwise extinct) genus ''Australopithecus'' that encompasses the extant species ''Homo sapiens'' ( modern humans), plus several extinct species classified as either ancestral to or closely related to modern humans (depending on the species), most notably ''Homo erectus'' and ''Homo neanderthalensis''. The genus emerged with the appearance of '' Homo habilis'' just over 2 million years ago. ''Homo'', together with the genus '' Paranthropus'', is probably sister to ''Australopithecus africanus'', which itself had previously split from the lineage of '' Pan'', the chimpanzees. ''Homo erectus'' appeared about 2 million years ago and, in several early migrations, spread throughout Africa (where it is dubbed ''Homo ergaster'') and Eurasia. It was likely that the first human species lived in a hunter-gatherer society and was able to control fire. An adaptive and successful species, ''Homo erectus'' persisted for more than a million ye ...
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Pnictogen
A pnictogen ( or ; from grc, πνῑ́γω "to choke" and -gen, "generator") is any of the chemical elements in group 15 of the periodic table. Group 15 is also known as the nitrogen group or nitrogen family. Group 15 consists of the elements nitrogen (N), phosphorus (P), arsenic (As), antimony (Sb), bismuth (Bi), and moscovium (Mc). Since 1988, IUPAC calls it Group 15. Before that, in America it was called Group VA, owing to a text by H. C. Deming and the Sargent-Welch Scientific Company, while in Europe it was called Group VB and IUPAC recommended that in 1970. (Pronounced "group five A" and "group five B"; "V" is the Roman numeral 5). In semiconductor physics, it is still usually called Group V. The "five" ("V") in the historical names comes from the " pentavalency" of nitrogen, reflected by the stoichiometry of compounds such as N2O5. They have also been called the pentels. Characteristics Chemical Like other groups, the members of this family show similar patterns ...
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Nuclear Magnetic Resonance
Nuclear magnetic resonance (NMR) is a physical phenomenon in which nuclei in a strong constant magnetic field are perturbed by a weak oscillating magnetic field (in the near field) and respond by producing an electromagnetic signal with a frequency characteristic of the magnetic field at the nucleus. This process occurs near resonance, when the oscillation frequency matches the intrinsic frequency of the nuclei, which depends on the strength of the static magnetic field, the chemical environment, and the magnetic properties of the isotope involved; in practical applications with static magnetic fields up to ca. 20  tesla, the frequency is similar to VHF and UHF television broadcasts (60–1000 MHz). NMR results from specific magnetic properties of certain atomic nuclei. Nuclear magnetic resonance spectroscopy is widely used to determine the structure of organic molecules in solution and study molecular physics and crystals as well as non-crystalline materials. ...
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Trigonal Bipyramid
In geometry, the triangular bipyramid (or dipyramid) is a type of hexahedron, being the first in the infinite set of face-transitive bipyramids. It is the dual of the triangular prism with 6 isosceles triangle faces. As the name suggests, it can be constructed by joining two tetrahedra along one face. Although all its faces are congruent and the solid is face-transitive, it is not a Platonic solid because some vertices adjoin three faces and others adjoin four. The bipyramid whose six faces are all equilateral triangles is one of the Johnson solids, (). As a Johnson solid with all faces equilateral triangles, it is also a deltahedron. Formulae The following formulae for the height (H), surface area (A) and volume (V) can be used if all faces are regular, with edge length L: :H = L\cdot \frac \approx L\cdot 1.632993162 :A = L^2 \cdot \frac \approx L^2\cdot 2.598076211 :V = L^3 \cdot \frac \approx L^3\cdot 0.235702260 Dual polyhedron The dual polyhedron of the ...
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Sulfuryl Chloride
Sulfuryl chloride is an inorganic compound with the formula SO2Cl2. At room temperature, it is a colorless liquid with a pungent odor. Sulfuryl chloride is not found in nature, as can be inferred from its rapid hydrolysis. Sulfuryl chloride is commonly confused with thionyl chloride, SOCl2. The properties of these two sulfur oxychlorides are quite different: sulfuryl chloride is a source of chlorine whereas thionyl chloride is a source of chloride ions. An alternative IUPAC name is sulfuroyl dichloride. Structure Sulfur is tetrahedral in SO2Cl2 and the oxidation state of the sulfur atom is +6, as in sulfuric acid. Synthesis SO2Cl2 is prepared by the reaction of sulfur dioxide and chlorine in the presence of a catalyst, such as activated carbon. :SO2 + Cl2 → SO2Cl2 The product can be purified by fractional distillation. Legacy routes Sulfuryl chloride was first prepared in 1838 by the French chemist Henri Victor Regnault. Legacy routes include oxidation of thionyl ch ...
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