Potassium Trithiocarbonate
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Potassium Trithiocarbonate
Potassium trithiocarbonate is the inorganic compound with the chemical formula . It is the potassium salt of trithiocarbonic acid. It consists of two potassium cations and the trigonal planar trithiocarbonate dianion . It is a white solid, although impure samples often appear brown. It is prepared by the reaction of potassium sulfide or potassium hydrosulfide with carbon disulfide. : Potassium trithiocarbonate reacts with alkylating agents to give trithiocarbonate esters: :{{chem2, K2CS3 + 2 RX → (RS)2CS + 2 KX (X = halogen, R = monovalent organyl In organic and organometallic chemistry, an organyl group (commonly denoted by the letter " R") is an organic substituent with one (sometimes more) free valence electron(s) at a carbon atom.. The term is often used in chemical patent literatur ... group) References Inorganic carbon compounds Inorganic sulfur compounds Thiocarbonyl compounds ...
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Thiocarbonic Acid
Thiocarbonic acid is an acid with the chemical formula (or ). It is an analog of carbonic acid (or ), in which all oxygen atoms are replaced with sulfur atoms. It is an unstable hydrophobic red oily liquid. It is often referred to as trithiocarbonic acid so as to differentiate it from other carbonic acids containing sulfur, such as monothiocarbonic ''O'',''O''-acid , monothiocarbonic ''O'',''S''-acid , dithiocarbonic ''O'',''S''-acid and dithiocarbonic ''S'',''S''-acid (see thiocarbonates). Discovery and synthesis It was first reported in brief by Zeise in 1824 and later in more detail by Berzelius in 1826, in both cases it was produced by the action of carbon disulfide on a hydrosulfide salt (e.g. potassium hydrosulfide). : Treatment with acids liberates the thiocarbonic acid as a red oil: : Both the acid and many of its salts are unstable and decompose via the release of carbon disulfide, particularly upon heating: : An improved synthesis involves addition of barium tr ...
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Carbon Disulfide
Carbon disulfide (also spelled as carbon disulphide) is an inorganic compound with the chemical formula and structure . It is also considered as the anhydride of thiocarbonic acid. It is a colorless, flammable, neurotoxic liquid that is used as a building block in organic synthesis. Pure carbon disulfide has a pleasant, ether- or chloroform-like odor, but commercial samples are usually yellowish and are typically contaminated with foul-smelling impurities.. History In 1796, the German chemist Wilhelm August Lampadius (1772–1842) first prepared carbon disulfide by heating pyrite with moist charcoal. He called it "liquid sulfur" (''flüssig Schwefel''). The composition of carbon disulfide was finally determined in 1813 by the team of the Swedish chemist Jöns Jacob Berzelius (1779–1848) and the Swiss-British chemist Alexander Marcet (1770–1822). Their analysis was consistent with an empirical formula of CS2. Occurrence, manufacture, properties Small amounts of carbon ...
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Inorganic Carbon Compounds
An inorganic compound is typically a chemical compound that lacks carbon–hydrogen bonds⁠that is, a compound that is not an organic compound. The study of inorganic compounds is a subfield of chemistry known as ''inorganic chemistry''. Inorganic compounds comprise most of the Earth's crust, although the compositions of the deep mantle remain active areas of investigation. All allotropes (structurally different pure forms of an element) and some simple carbon compounds are often considered inorganic. Examples include the allotropes of carbon (graphite, diamond, buckminsterfullerene, graphene, etc.), carbon monoxide , carbon dioxide , carbides, and salts of inorganic anions such as carbonates, cyanides, cyanates, thiocyanates, isothiocyanates, etc. Many of these are normal parts of mostly organic systems, including organisms; describing a chemical as inorganic does not necessarily mean that it cannot occur within living things. History Friedrich Wöhler's conversion of ...
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Organyl
In organic and organometallic chemistry, an organyl group (commonly denoted by the letter " R") is an organic substituent with one (sometimes more) free valence electron(s) at a carbon atom.. The term is often used in chemical patent literature to protect claims over a broad scope. Examples * Acetonyl group * Acyl group (e.g. acetyl group, benzoyl group) * Alkyl group (e.g., methyl group, ethyl group) * Alkenyl group (e.g., vinyl group, allyl group) * Alkynyl group ( propargyl group) * Benzyloxycarbonyl group (Cbz) * '' tert'' -butoxycarbonyl group (Boc) * Carboxyl group In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group () attached to an R-group. The general formula of a carboxylic acid is often written as or , sometimes as with R referring to an organyl group (e.g. ... References Functional groups {{organic-chem-stub ...
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Valence (chemistry)
In chemistry, the valence (US spelling) or valency (British spelling) of an atom is a measure of its combining capacity with other atoms when it forms chemical compounds or molecules. Valence is generally understood to be the number of chemical bonds that each atom of a given chemical element typically forms. Double bonds are considered to be two bonds, triple bonds to be three, quadruple bonds to be four, quintuple bonds to be five and sextuple bonds to be six. In most compounds, the valence of hydrogen is 1, of oxygen is 2, of nitrogen is 3, and of carbon is 4. Valence is not to be confused with the related concepts of the coordination number, the oxidation state, or the number of valence electrons for a given atom. Description The valence is the combining capacity of an atom of a given element, determined by the number of hydrogen atoms that it combines with. In methane, carbon has a valence of 4; in ammonia, nitrogen has a valence of 3; in water, oxygen has a valence of 2; ...
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Halogen
The halogens () are a group in the periodic table consisting of six chemically related elements: fluorine (F), chlorine (Cl), bromine (Br), iodine (I), and the radioactive elements astatine (At) and tennessine (Ts), though some authors would exclude tennessine as its chemistry is unknown and is theoretically expected to be more like that of gallium. In the modern IUPAC nomenclature, this group is known as group 17. The word "halogen" means "salt former" or "salt maker". When halogens react with metals, they produce a wide range of salts, including calcium fluoride, sodium chloride (common table salt), silver bromide and potassium iodide. The group of halogens is the only periodic table group that contains elements in three of the main states of matter at standard temperature and pressure, though not far above room temperature the same becomes true of groups 1 and 15, assuming white phosphorus is taken as the standard state.This could also be the case for group 12, al ...
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Trithiocarbonate Ester
Thiocarbonate describes a family of anions with the general chemical formula (''x'' = 0, 1, or 2): *for ''x'' = 2 it is monothiocarbonate ion *for ''x'' = 1 it is dithiocarbonate ion *for ''x'' = 0 it is trithiocarbonate ion Like the carbonate dianion, the thiocarbonate ions are trigonal planar, with carbon atom at the center of triangle, and oxygen and sulfur atoms at the peaks of the triangle. The average bond order between C and S or O is . The state of protonation is usually not specified. These anions are good nucleophiles and good ligands. Thiocarbonates refer to salts of those ions as well (e.g. potassium trithiocarbonate, ). Thiocarbonates refer to esters of those ions as well (e.g. dimethyl trithiocarbonate, ). They contain trigonal planar divalent functional groups similar to these anions (''x'' = 0, 1, or 2, R is organyl group). Esters with the formula are also called xanthates, while esters with the formula are also called thioxanthates. Thiocarbonates also refe ...
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Alkylating Agents
Alkylation is a chemical reaction that entails transfer of an alkyl group. The alkyl group may be transferred as an alkyl carbocation, a free radical, a carbanion, or a carbene (or their equivalents). Alkylating agents are reagents for effecting alkylation. Alkyl groups can also be removed in a process known as dealkylation. Alkylating agents are often classified according to their nucleophilic or electrophilic character. In oil refining contexts, alkylation refers to a particular alkylation of isobutane with olefins. For upgrading of petroleum, alkylation produces a premium blending stock for gasoline. In medicine, alkylation of DNA is used in chemotherapy to damage the DNA of cancer cells. Alkylation is accomplished with the class of drugs called alkylating antineoplastic agents. Nucleophilic alkylating agents Nucleophilic alkylating agents deliver the equivalent of an alkyl anion ( carbanion). The formal "alkyl anion" attacks an electrophile, forming a new covalent bond ...
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Potassium Sulfide
Potassium sulfide is an inorganic compound with the formula K2 S. The colourless solid is rarely encountered, because it reacts readily with water, a reaction that affords potassium hydrosulfide (KSH) and potassium hydroxide (KOH). Most commonly, the term potassium sulfide refers loosely to this mixture, not the anhydrous solid. Structure It adopts an antifluorite structure, which means that the small K+ ions occupy the tetrahedral (F−) sites in fluorite, and the larger S2− centers occupy the eight-coordinate sites. Li2S, Na2S, and Rb2S crystallize similarly.Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. . Synthesis and reactions It can be produced by heating K2SO4 with carbon ( coke): :K2SO4 + 4 C → K2S + 4 CO In the laboratory, pure K2S may be prepared by the reaction of potassium and sulfur in anhydrous ammonia. Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. ...
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Potassium Hydrosulfide
Potassium hydrosulfide is an inorganic compound with the formula KSH. This colourless salt consists of the cation and the bisulfide anion . It is the product of the half-neutralization of hydrogen sulfide with potassium hydroxide. The compound is used in the synthesis of some organosulfur compounds. Aqueous solutions of potassium sulfide consist of a mixture of potassium hydrosulfide and potassium hydroxide. The structure of the potassium hydrosulfide resembles that of potassium chloride. Their structure is however complicated by the non-spherical symmetry of the anion An ion () is an atom or molecule with a net electrical charge. The charge of an electron is considered to be negative by convention and this charge is equal and opposite to the charge of a proton, which is considered to be positive by conven ...s, but these tumble rapidly in the solid. The addition of sulfur gives dipotassium pentasulfide. Synthesis It is prepared by neutralizing aqueous KOH with . R ...
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Inorganic Compound
An inorganic compound is typically a chemical compound that lacks carbon–hydrogen bonds⁠that is, a compound that is not an organic compound. The study of inorganic compounds is a subfield of chemistry known as ''inorganic chemistry''. Inorganic compounds comprise most of the Earth's crust, although the compositions of the deep Mantle (geology), mantle remain active areas of investigation. All allotropes (structurally different pure forms of an element) and some simple carbon compounds are often considered inorganic. Examples include the allotropes of carbon (graphite, diamond, buckminsterfullerene, graphene, etc.), carbon monoxide , carbon dioxide , carbides, and salt (chemistry), salts of inorganic anions such as carbonates, cyanides, cyanates, thiocyanates, isothiocyanates, etc. Many of these are normal parts of mostly organic systems, including organisms; describing a chemical as inorganic does not necessarily mean that it cannot occur within life, living things. History ...
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Potassium Sulfide
Potassium sulfide is an inorganic compound with the formula K2 S. The colourless solid is rarely encountered, because it reacts readily with water, a reaction that affords potassium hydrosulfide (KSH) and potassium hydroxide (KOH). Most commonly, the term potassium sulfide refers loosely to this mixture, not the anhydrous solid. Structure It adopts an antifluorite structure, which means that the small K+ ions occupy the tetrahedral (F−) sites in fluorite, and the larger S2− centers occupy the eight-coordinate sites. Li2S, Na2S, and Rb2S crystallize similarly.Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. . Synthesis and reactions It can be produced by heating K2SO4 with carbon ( coke): :K2SO4 + 4 C → K2S + 4 CO In the laboratory, pure K2S may be prepared by the reaction of potassium and sulfur in anhydrous ammonia. Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. ...
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