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Tris(tert-butoxy)silanethiol
Tris(''tert''-butoxy)silanethiol is a silicon compound containing three ''tert''-butoxy groups and a rare Si–S–H functional group. This colourless compound serves as an hydrogen donor in radical chain reactions. It was first prepared by alcoholysis of silicon disulfide Silicon disulfide is the inorganic compound with the formula Silicon, SiSulfur, S2. Like silicon dioxide, this material is polymeric, but it adopts a 1-dimensional structure quite different from the usual polymorphism (materials science), forms o ... and purified by distillation: :3 (CH3)3COH + SiS2 → CH3)3COsub>3SiSH + H2S Since 1962 it was thoroughly studied including its acid-base properties and coordination chemistry with metal ions. It coordinates to metal ions via the sulfur and oxygen donor atoms.A. Pladzyk, A. Ozarowski, Ł. Ponikiewski: Crystal and electronic structures of Ni(II) silanethiolates containing flexible diamine ligands. Inorg. Chim. Acta 440 (2016) 84-93. References {{D ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tert-butyl Alcohol
''tert''-Butyl alcohol is the simplest tertiary alcohol, with a formula of (CH3)3COH (sometimes represented as ''t''-BuOH). Its isomers are 1-butanol, isobutanol, and butan-2-ol. ''tert''-Butyl alcohol is a colorless solid, which melts near room temperature and has a camphor-like odor. It is miscible with water, ethanol and diethyl ether. Natural occurrence ''tert''-Butyl alcohol has been identified in beer and chickpeas. It is also found in cassava, which is used as a fermentation ingredient in certain alcoholic beverages. Preparation ''tert''-Butyl alcohol is derived commercially from isobutane as a coproduct of propylene oxide production. It can also be produced by the catalytic hydration of isobutylene, or by a Grignard reaction between acetone and methylmagnesium chloride. Purification cannot be performed by simple distillation due to formation of an azeotrope with water, although initial drying of the solvent containing large amounts of water is performed by adding benz ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Functional Group
In organic chemistry, a functional group is a substituent or moiety in a molecule that causes the molecule's characteristic chemical reactions. The same functional group will undergo the same or similar chemical reactions regardless of the rest of the molecule's composition. This enables systematic prediction of chemical reactions and behavior of chemical compounds and the design of chemical synthesis. The reactivity of a functional group can be modified by other functional groups nearby. Functional group interconversion can be used in retrosynthetic analysis to plan organic synthesis. A functional group is a group of atoms in a molecule with distinctive chemical properties, regardless of the other atoms in the molecule. The atoms in a functional group are linked to each other and to the rest of the molecule by covalent bonds. For repeating units of polymers, functional groups attach to their nonpolar core of carbon atoms and thus add chemical character to carbon chains. Fun ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Radical Chain Reaction
Radical may refer to: Politics and ideology Politics *Radical politics, the political intent of fundamental societal change * Radicalism (historical), the Radical Movement that began in late 18th century Britain and spread to continental Europe and Latin America in the 19th century * Radical Party (other), several political parties * Radicals (UK), a British and Irish grouping in the early to mid-19th century *Radicalization Ideologies *Radical chic, a term coined by Tom Wolfe to describe the pretentious adoption of radical causes * Radical feminism, a perspective within feminism that focuses on patriarchy *Radical Islam, or Islamic extremism * Radical veganism, a radical interpretation of veganism, usually combined with anarchism * Radical Reformation, an Anabaptist movement concurrent with the Protestant Reformation Science and mathematics Science *Radical (chemistry), an atom, molecule, or ion with unpaired valence electron(s) *Radical surgery, where diseased tissue or ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Alcoholysis
In chemistry, solvolysis is a type of nucleophilic substitution (S1/S2) or elimination reaction, elimination where the nucleophile is a solvent molecule. Characteristic of S1 reactions, solvolysis of a chirality (chemistry), chiral reactant affords the racemate. Sometimes however, the stereochemical course is complicated by intimate ion pairs, whereby the leaving anion remains close to the carbocation, effectively shielding it from an attack by the nucleophile. Particularly fast reactions can occur by neighbour group participation, with nonclassical ions as intermediates or transition states. Examples For certain nucleophiles, solvolysis reactions are classified. Solvolysis involving water (molecule), water is called hydrolysis. Related terms are alcoholysis (Alcohol (chemistry), alcohols) and specifically methanolysis (methanol), acetolysis, ammonolysis (ammonia), and aminolysis (alkyl amines). Glycolysis is however an older term for the multistep conversion of glucose to pyruvat ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Silicon Disulfide
Silicon disulfide is the inorganic compound with the formula Silicon, SiSulfur, S2. Like silicon dioxide, this material is polymeric, but it adopts a 1-dimensional structure quite different from the usual polymorphism (materials science), forms of SiO2. Synthesis, structure, and properties The material is formed by heating silicon and sulfur or by the exchange reaction between Silicon dioxide, SiO2 and Aluminium sulfide, Al2S3. The material consists of chains of edge-shared tetrahedra, Si(μ-S)2Si(μS)2, etc. Like other silicon sulfur-compounds (e.g., bis(trimethylsilyl)sulfide) SiS2 hydrolyzes readily to release H2S. In liquid ammonia it is reported to form the imide Si(NH)2 and NH4SH, but a recent report has identified crystalline (NH4)2[SiS3(NH3)]·2NH3 as a product which contains the tetrahedral thiosilicate anion, SiS3(NH3). Reaction with ethanol gives the alkoxide tetraethyl orthosilicate and H2S. With bulky tert-butanol, alcoholysis gives tris(tert-butoxy)silanethiol: :3 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Hydrogen Compounds
Hydrogen compounds are compounds containg the element hydrogen. In these compounds, hydrogen can form in the +1 and -1 oxidation states. Hydrogen can form compounds both ionically and in covalent substances. It is a part of many organic compounds such as hydrocarbons as well as water and other organic substances. The ion is often called a proton because it has one proton and no electrons, although the proton does not move freely. Brønsted–Lowry acids are capable of donating ions to bases. Covalent and organic compounds While is not very reactive under standard conditions, it does form compounds with most elements. Hydrogen can form compounds with elements that are more electronegative, such as halogens (F, Cl, Br, I), or oxygen; in these compounds hydrogen takes on a partial positive charge. When bonded to a more electronegative element, particularly fluorine, oxygen, or nitrogen, hydrogen can participate in a form of medium-strength noncovalent bonding with another elect ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Silicon Compounds
Silicon is a chemical element with the symbol Si and atomic number 14. It is a hard, brittle crystalline solid with a blue-grey metallic luster, and is a tetravalent metalloid and semiconductor. It is a member of group 14 in the periodic table: carbon is above it; and germanium, tin, lead, and flerovium are below it. It is relatively unreactive. Because of its high chemical affinity for oxygen, it was not until 1823 that Jöns Jakob Berzelius was first able to prepare it and characterize it in pure form. Its oxides form a family of anions known as silicates. Its melting and boiling points of 1414 °C and 3265 °C, respectively, are the second highest among all the metalloids and nonmetals, being surpassed only by boron. Silicon is the eighth most common element in the universe by mass, but very rarely occurs as the pure element in the Earth's crust. It is widely distributed in space in cosmic dusts, planetoids, and planets as various forms of silicon dioxide ( ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tert-butyl Compounds
In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula , derived from either of the two isomers (''n''-butane and isobutane) of butane. The isomer ''n''-butane can connect in two ways, giving rise to two "-butyl" groups: * If it connects at one of the two terminal carbon atoms, it is normal butyl or ''n''-butyl: (preferred IUPAC name: butyl) * If it connects at one of the non-terminal (internal) carbon atoms, it is secondary butyl or ''sec''-butyl: (preferred IUPAC name: butan-2-yl) The second isomer of butane, isobutane, can also connect in two ways, giving rise to two additional groups: * If it connects at one of the three terminal carbons, it is isobutyl: (preferred IUPAC name: 2-methylpropyl) * If it connects at the central carbon, it is tertiary butyl, ''tert''-butyl or ''t''-butyl: (preferred IUPAC name: ''tert''-butyl) Nomenclature According to IUPAC nomenclature, "isobutyl", "''sec''-butyl", and "''tert''-b ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
