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Dithionitronium Hexachloroantimonate
Dithionitronium hexafloroarsenate is the inorganic compound with the formula . It is the hexafluoroarsenate () salt of S=N=S+. The cation is of interest as the sulfur analogue of nitronium (). Hexafloroarsenate is a weakly coordinating anion. According to X-ray crystallography, S=N=S+ is linear with S-N distances of 146 picometers. Synthesis and reactions Dithionitronium hexafluoroarsenate is prepared from thiazyl chloride using silver hexafluoroarsenate. The hexachloroantimonate salt can be prepared by treating thiazyl chloride with sulfur in the presence of antimony pentachloride according to this idealized equation: : The dithionitronium cation reacts with nitriles to give dithiadiazolium salts: : Addition to alkyne \ce \ce Acetylene \ce \ce \ce Propyne \ce \ce \ce \ce 1-Butyne In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. The simplest acyclic alkynes with only one triple bond and n ...s gives di ...
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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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Hexafluoroarsenate
The hexafluoroarsenate (sometimes shortened to fluoroarsenate) anion is a chemical species with formula . Hexafluoroarsenate is relatively inert, being the conjugate base of the notional superacid hexafluoroarsenic acid (). Synthesis The first undisputed synthesis is due to Otto Ruff, Kurt Stäuber and Hugo Graf, who began with the lower-valent arsenic trifluoride, using silver(I) fluoride as both a fluorine source and oxidant: cites but discounts it as describing an implausibly easy synthesis with a hydrolyzable product. : In the following reaction, one mole of arsenic trifluoride, three moles of silver fluoride, and one mole of nitrosyl chloride are reacted to produce one mole of nitrosyl hexafluoroarsenate, one mole of silver chloride, and two moles of elemental silver. Modern syntheses usually begin with arsenic pentafluoride (), which abstracts fluoride from common donors, such as hydrogen fluoride () or ''cis''- difluorodiazine (). Although the hexafluoroarsenate ...
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Nitronium
The nitronium ion, , is a cation. It is an onium ion because its nitrogen atom has +1 charge, similar to ammonium ion . It is created by the removal of an electron from the paramagnetic nitrogen dioxide molecule A molecule is a group of two or more atoms that are held together by Force, attractive forces known as chemical bonds; depending on context, the term may or may not include ions that satisfy this criterion. In quantum physics, organic chemi ... , or the protonation of nitric acid (with removal of ). It is stable enough to exist in normal conditions, but it is generally reactive and used extensively as an electrophile in the nitration of other substances. The ion is generated '' in situ'' for this purpose by mixing concentrated sulfuric acid and concentrated nitric acid according to the equilibrium: : Structure The nitronium ion is isoelectronic with carbon dioxide and has the same linear structure and bond angle of 180°. For this reason it has ...
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Weakly Coordinating Anion
Anions that interact weakly with cations are termed non-coordinating anions, although a more accurate term is weakly coordinating anion. Non-coordinating anions are useful in studying the reactivity of electrophilic cations. They are commonly found as counterions for cationic metal complexes with an unsaturated coordination sphere. These special anions are essential components of homogeneous alkene polymerisation catalysts, where the active catalyst is a coordinatively unsaturated, cationic transition metal complex. For example, they are employed as counterions for the 14 valence electron cations C5H5)2ZrRsup>+ (R = methyl or a growing polyethylene chain). Complexes derived from non-coordinating anions have been used to catalyze hydrogenation, hydrosilylation, oligomerization, and the living polymerization of alkenes. The popularization of non-coordinating anions has contributed to increased understanding of agostic complexes wherein hydrocarbons and hydrogen serve as ligand ...
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X-ray Crystallography
X-ray crystallography is the experimental science of determining the atomic and molecular structure of a crystal, in which the crystalline structure causes a beam of incident X-rays to Diffraction, diffract in specific directions. By measuring the angles and intensities of the X-ray diffraction, a crystallography, crystallographer can produce a three-dimensional picture of the density of electrons within the crystal and the positions of the atoms, as well as their chemical bonds, crystallographic disorder, and other information. X-ray crystallography has been fundamental in the development of many scientific fields. In its first decades of use, this method determined the size of atoms, the lengths and types of chemical bonds, and the atomic-scale differences between various materials, especially minerals and alloys. The method has also revealed the structure and function of many biological molecules, including vitamins, drugs, proteins and nucleic acids such as DNA. X-ray crystall ...
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Picometer
The picometre (international spelling as used by the International Bureau of Weights and Measures; SI symbol: pm) or picometer ( American spelling) is a unit of length in the International System of Units (SI), equal to , or one trillionth of a metre, which is the SI base unit of length. The picometre is one thousand femtometres, one thousandth of a nanometre ( nm), one millionth of a micrometre (also known as a micron), one billionth of a millimetre, and one trillionth of a metre. The symbol μμ was once used for it. It is also one hundredth of an ångström, an internationally known (but non-SI) unit of length. Use The picometre's length is of an order so small that its application is almost entirely confined to particle physics, quantum physics, chemistry, and acoustics. Atoms are between 62 and 520 pm in diameter, and the typical length of a carbon–carbon single bond is 154 pm. Smaller units still may be used to describe smaller particles (some of which ...
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Thiazyl Chloride
Trithiazyl trichloride is the inorganic compound with the formula . A white solid, it is a precursor to other sulfur nitrides, but has no commercial applications. Structure The molecule is a 6-membered ring of alternating nitrogen and sulfur atoms, where each sulfur atom is attached to one chlorine atom by a single bond. The molecule contains alternating single and double bonds in the core. The molecule has C3v symmetry. The core is slightly ruffled structure with S-N distances of 160.5 pm. The S-Cl distances are 208 pm, and the chlorine atoms are mutually ''cis''. The S centers are tetravalent and pyramidal. In contrast to the NSCl connectivity, nitrosyl chloride has the connectivity ONCl. Synthesis and reactions Trithiazyl trichloride is obtained by chlorination of tetrasulfur tetranitride or thiazyl fluoride monomer: : : At 100 °C in vacuum, thiazyl chloride trimer undergoes cracking to thiazyl chloride monomer, which is a green gas. : In N≡S−Cl, chlorine is bonded to ...
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Hexachloroantimonate
Antimony pentachloride is a chemical compound with the formula SbCl5. It is a colourless oil, but typical samples are yellowish due to dissolved chlorine. Owing to its tendency to hydrolyse to hydrochloric acid, SbCl5 is a highly corrosive substance and must be stored in glass or PTFE containers. Preparation and structure Antimony pentachloride is prepared by passing chlorine gas into molten antimony trichloride: :SbCl3 + Cl2 → SbCl5 Gaseous SbCl5 has a trigonal bipyramidal structure. Reactions This compounds reacts with water to form antimony pentoxide and hydrochloric acid: :2 SbCl5 + 5 H2O → Sb2O5 + 10 HCl The mono- and tetrahydrates are known, SbCl5·H2O and SbCl5·4H2O. This compound forms adducts with many Lewis bases. SbCl5 is a soft Lewis acid and its ECW model parameters are EA = 3.64 and CA = 10.42. It is used as the standard Lewis acid in the Gutmann scale of Lewis basicity. It is also a strong oxidizing agent. For example aromatic ethers are oxidized to ...
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Antimony Pentachloride
Antimony pentachloride is a chemical compound with the formula SbCl5. It is a colourless oil, but typical samples are yellowish due to dissolved chlorine. Owing to its tendency to hydrolyse to hydrochloric acid, SbCl5 is a highly corrosive substance and must be stored in glass or PTFE containers. Preparation and structure Antimony pentachloride is prepared by passing chlorine gas into molten antimony trichloride: :SbCl3 + Cl2 → SbCl5 Gaseous SbCl5 has a trigonal bipyramidal structure. Reactions This compounds reacts with water to form antimony pentoxide and hydrochloric acid: :2 SbCl5 + 5 H2O → Sb2O5 + 10 HCl The mono- and tetrahydrates are known, SbCl5·H2O and SbCl5·4H2O. This compound forms adducts with many Lewis bases. SbCl5 is a soft Lewis acid and its ECW model parameters are EA = 3.64 and CA = 10.42. It is used as the standard Lewis acid in the Gutmann scale of Lewis basicity. It is also a strong oxidizing agent. For example aromatic ethers are oxidize ...
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Nitrile
In organic chemistry, a nitrile is any organic compound that has a functional group. The name of the compound is composed of a base, which includes the carbon of the , suffixed with "nitrile", so for example is called " propionitrile" (or propanenitrile). The prefix '' cyano-'' is used interchangeably with the term ''nitrile'' in industrial literature. Nitriles are found in many useful compounds, including methyl cyanoacrylate, used in super glue, and nitrile rubber, a nitrile-containing polymer used in latex-free laboratory and medical gloves. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons. Inorganic compounds containing the group are not called nitriles, but cyanides instead. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Structure and basic properties The N−C−C geom ...
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Dithiadiazolium
Part of the structure of 1,2‑dithia-3,5‑diazole highlighting the stacking motif common for these compounds. Color code: yellow = S, blue = N, gray = C., 180px In chemistry, dithiadiazoles are a family of heterocyclic compounds with the formula . Two isomers have been studied: the 1,2dithia-3,5diazoles, in which the sulfur atoms are bonded to each other across the ring from the carbon atom, and the 1,3dithia-2,5diazoles, in which nitrogen and sulfur atoms alternate around the ring. In both cases, the neutral species are radicals that are of interest as examples of paramagnetic heterocycles. They have also attracted interest because of the tendency of the neutral species to form linear chain compounds, a theme in molecular electronics. 1,2-Dithia-3,5-diazoles and their oxidized derivatives Structures The structures of both the 1,2-dithia-3,5-diazolium cations and the neutral 1,2-dithia-3,5-diazoles are fairly similar. These are planar five-membered rings. With one electron ...
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Alkyne
\ce \ce Acetylene \ce \ce \ce Propyne \ce \ce \ce \ce 1-Butyne In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. The simplest acyclic alkynes with only one triple bond and no other functional groups form a homologous series with the general chemical formula . Alkynes are traditionally known as acetylenes, although the name ''acetylene'' also refers specifically to , known formally as ethyne using IUPAC nomenclature. Like other hydrocarbons, alkynes are generally hydrophobic. Structure and bonding In acetylene, the H–C≡C bond angles are 180°. By virtue of this bond angle, alkynes are rod-like. Correspondingly, cyclic alkynes are rare. Benzyne cannot be isolated. The C≡C bond distance of 118 picometers (for C2H2) is much shorter than the C=C distance in alkenes (132 pm, for C2H4) or the C–C bond in alkanes (153 pm). : The triple bond is very strong with a bond strength of 839 kJ/mol. ...
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