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Ethylene Bis(dithiocarbamate)
In organic chemistry, a dithiocarbamate is a chemical compound with the general formula . It contains the functional group with the structure . It is the analog of a carbamate in which both oxygen atoms are replaced by sulfur atoms (when only one oxygen is replaced the result is thiocarbamate). Dithiocarbamate also refers to the dithiocarbamate ion and its salts. A common example is sodium diethyldithiocarbamate . Dithiocarbamates and their derivatives are widely used in the vulcanization of rubber. Formation Many secondary amines react with carbon disulfide and sodium hydroxide to form dithiocarbamate salts: : Ammonia reacts with similarly, to give ammonium dithiocarbamate: : Dithiocarbamate salts are pale colored solids that are soluble in water and polar organic solvents. Dithiocarbamic acid A primary amine and carbon disulfide react to give a dithiocarbamic acid: : In the presence of diimides or pyridine, these acids convert to isothiocyanates: : Reactions Dithiocarbam ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dithiocarbamate
In organic chemistry, a dithiocarbamate is a chemical compound with the general formula . It contains the functional group with the Chemical structure, structure . It is the analog of a carbamate in which both oxygen atoms are replaced by sulfur atoms (when only one oxygen is replaced the result is thiocarbamate). Dithiocarbamate also refers to the dithiocarbamate ion and its salts. A common example is sodium diethyldithiocarbamate . Dithiocarbamates and their derivatives are widely used in the vulcanization of rubber. Formation Many secondary amines react with carbon disulfide and sodium hydroxide to form dithiocarbamate salts: : Ammonia reacts with carbon disulfide, similarly, to give ammonium dithiocarbamate: : Dithiocarbamate salts are pale colored solids that are soluble in water and Solvent, polar organic solvents. Dithiocarbamic acid A primary amine and carbon disulfide react to give a dithiocarbamic acid: : In the presence of diimides or pyridine, these acids convert t ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Solvent
A solvent (from the Latin language, Latin ''wikt:solvo#Latin, solvō'', "loosen, untie, solve") is a substance that dissolves a solute, resulting in a Solution (chemistry), solution. A solvent is usually a liquid but can also be a solid, a gas, or a supercritical fluid. Water is a solvent for Chemical polarity#Polarity of molecules, polar molecules, and the most common solvent used by living things; all the ions and proteins in a Cell (biology), cell are dissolved in water within the cell. Major uses of solvents are in paints, paint removers, inks, and dry cleaning. Specific uses for Organic compound, organic solvents are in dry cleaning (e.g. tetrachloroethylene); as paint thinners (toluene, turpentine); as nail polish removers and solvents of glue (acetone, methyl acetate, ethyl acetate); in spot removers (hexane, petrol ether); in detergents (D-limonene, citrus terpenes); and in perfumes (ethanol). Solvents find various applications in chemical, pharmaceutical, oil, and gas ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Manganese
Manganese is a chemical element; it has Symbol (chemistry), symbol Mn and atomic number 25. It is a hard, brittle, silvery metal, often found in minerals in combination with iron. Manganese was first isolated in the 1770s. It is a transition metal with a multifaceted array of industrial alloy uses, particularly in stainless steels. It improves strength, workability, and resistance to wear. Manganese oxide is used as an oxidising agent, as a rubber additive, and in glass making, fertilisers, and ceramics. Manganese sulfate can be used as a fungicide. Manganese is also an essential human dietary element, important in macronutrient metabolism, bone formation, and free radical defense systems. It is a critical component in dozens of proteins and enzymes. It is found mostly in the bones, but also the liver, kidneys, and brain. In the human brain, the manganese is bound to manganese metalloproteins, most notably glutamine synthetase in astrocytes. Manganese is commonly found in labo ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Polyolefin
A polyolefin is a type of polymer with the general formula (CH2CHR)n where R is an alkyl group. They are usually derived from a small set of simple olefins (alkenes). Dominant in a commercial sense are polyethylene and polypropylene. More specialized polyolefins include Polyisobutene, polyisobutylene and polymethylpentene. They are all colorless or white oils or solids. Many copolymers are known, such as polybutene, which derives from a mixture of different butene isomers. The name of each polyolefin indicates the olefin from which it is prepared; for example, polyethylene is derived from ethylene, and polymethylpentene is derived from 4-methyl-1-pentene. Polyolefins are not olefins themselves because the double bond of each olefin monomer is opened in order to form the polymer. Monomers having more than one double bond such as butadiene and isoprene yield polymers that contain double bonds (polybutadiene and polyisoprene) and are usually not considered polyolefins. Polyolefins are ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Crosslink
In chemistry and biology, a cross-link is a bond or a short sequence of bonds that links one polymer chain to another. These links may take the form of covalent bonds or ionic bonds and the polymers can be either synthetic polymers or natural polymers (such as proteins). In polymer chemistry "cross-linking" usually refers to the use of cross-links to promote a change in the polymers' physical properties. When "crosslinking" is used in the biological field, it refers to the use of a probe to link proteins together to check for protein–protein interactions, as well as other creative cross-linking methodologies. Although the term is used to refer to the "linking of polymer chains" for both sciences, the extent of crosslinking and specificities of the crosslinking agents vary greatly. Synthetic polymers : 260px, left, Chemical reactions associated with crosslinking of drying oils, the process that produces curing'' refers to the crosslinking of thermosetting">linoleum. Cros ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Xanthate
A xanthate is a Salt (chemistry), salt or ester of a xanthic acid. The formula of the salt of xanthic acid is (where R is organyl group and M is usually Sodium, Na or Potassium, K). Xanthate also refers to the anion . The formula of a xanthic acid is , such as ethyl xanthic acid, while the formula of a xanthate ester is , where R and R' are organyl groups. The salts of xanthates are sometimes called ''O''-organyl dithioates. The esters of xanthic acid are sometimes called ''O'',''S''-diorganyl esters of Dithiocarbonate, dithiocarbonic acid. The name ''xanthate'' is derived from Ancient Greek (''xanthos'') meaning 'yellowish' or 'golden', and indeed most xanthate salts are yellow. They were discovered and named in 1823 by Danish chemist William Christopher Zeise. These organosulfur compounds are important in two areas: the production of cellophane and related polymers from cellulose and (in mining) for extraction of certain sulphide bearing ores. They are also versatile intermedi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dithiocarboxylate
Dithiocarboxylic acids are organosulfur compounds with the formula . They are the dithia analogues of carboxylic acids. A closely related and better studied family of compounds are the monothiocarboxylic acids, with the formula . Dithiocarboxylic acids are about 3x more acidic than the monothiocarboxylic acids. Thus, for dithiobenzoic acid pKa = 1.92. Such compounds are commonly prepared by the reaction of carbon disulfide with a Grignard reagent: : : This reaction is comparable to the formation of carboxylic acids using a Grignard reagent and carbon dioxide. Dithiocarboxylate salts readily S-alkylate to give dithiocarboxylate esters: : Aryldithiocarboxylic acids, e.g., dithiobenzoic acid, chlorinate to give the thioacyl chlorides. Oxygen transfer to a dithiocarboxylate ester gives a sulfine Sulfinylmethane or sulfine is an organic compound with molecular formula H2CSO. It is the simplest sulfine. Sulfines are chemical compounds with the general structure XY=SO. I ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Transition Metal Dithiocarbamate Complexes
193px, Structure of iron tris(diethyldithiocarbamate). Transition metal dithiocarbamate complexes are coordination complexes containing one or more dithiocarbamate ligand, which are typically abbreviated R2dtc−. Many complexes are known. Several homoleptic derivatives have the formula M(R2dtc)n where n = 2 and 3. Ligand characteristics Dithiocarbamate anions are bidentate ligands that are classified as L-X ligand in the Covalent bond classification method. In the usual electron counting method, they are three-electron ligands. With respect to HSAB theory, they are classified as soft. Because of the pi-donor properties of the amino substituent, the two sulfur centers show enhanced basicity relative to dithiocarboxylates. This situation is represented by the zwitterionic resonance structure that depicts a positive charge on N and negative charges on both sulfurs. This N to C pi-bonding results in partial double bond character for the C-N bond. Consequently, barriers to ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Grignard Reagent
Grignard reagents or Grignard compounds are chemical compounds with the general formula , where X is a halogen and R is an organic group, normally an alkyl or aryl. Two typical examples are methylmagnesium chloride and phenylmagnesium bromide . They are a subclass of the organomagnesium compounds. Grignard compounds are popular reagents in organic synthesis for creating new carbon–carbon bonds. For example, when reacted with another halogenated compound in the presence of a suitable catalyst, they typically yield and the magnesium halide as a byproduct; and the latter is insoluble in the solvents normally used. Grignard reagents are rarely isolated as solids. Instead, they are normally handled as solutions in solvents such as diethyl ether or tetrahydrofuran using air-free techniques. Grignard reagents are complex with the magnesium atom bonded to two ether ligands as well as the halide and organyl ligands. The discovery of the Grignard reaction in 1900 was recogn ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
