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Interhalogen
In chemistry, an interhalogen compound is a molecule which contains two or more different halogen atoms (fluorine, chlorine, bromine, iodine, or astatine) and no atoms of elements from any other group. Most interhalogen compounds known are binary (composed of only two distinct elements). Their formulae are generally , where ''n'' = 1, 3, 5 or 7, and X is the less electronegative of the two halogens. The value of ''n'' in interhalogens is always odd, because of the odd valence of halogens. They are all prone to hydrolysis, and ionize to give rise to polyhalogen ions. Those formed with astatine have a very short half-life due to astatine being intensely radioactive. No interhalogen compounds containing three or more different halogens are definitely known, although a few books claim that and have been obtained, and theoretical studies seem to indicate that some compounds in the series are barely stable. Some interhalogens, such as , , and , are good halogenating agents. is to ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Halogen
The halogens () are a group in the periodic table consisting of five or six chemically related elements: fluorine (F), chlorine (Cl), bromine (Br), iodine (I), astatine (At), and tennessine (Ts). 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. All of the halogens form acids when bonded to hydrogen. Most halogens are typically produced from minerals or salts. The middle halogens—chlorine, bromine, and iodine—are often used as disinfectants. Organobromides are the most important class of flame retardants, while elemental halogens are dangerous and can be toxic. History The fl ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bromine Trifluoride
Bromine trifluoride is an interhalogen compound with the formula BrF3. At room temperature, it is a straw-coloured liquid with a pungent odor which decomposes violently on contact with water and organic compounds. It is a powerful fluorinating agent and an ionizing inorganic solvent. It is used to produce uranium hexafluoride (UF6) in the processing and reprocessing of nuclear fuel. Synthesis Bromine trifluoride was first described by Paul Lebeau in 1906, who obtained the material by the reaction of bromine with fluorine at 20 °C: : The disproportionation of bromine monofluoride also gives bromine trifluoride: : Structure Like ClF3 and IF3, the BrF3 molecule is T-shaped and planar. In the VSEPR formalism, the bromine center is assigned two electron pairs. The distance from the bromine each axial fluorine is 1.81 Å and to the equatorial fluorine is 1.72 Å. The angle between an axial fluorine and the equatorial fluorine is slightly smaller than 90° — the 86.2° ang ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chlorine Trifluoride
Chlorine trifluoride is an interhalogen compound with the formula ClF3. This colorless, poisonous, corrosive, and extremely reactive gas condenses to a pale-greenish yellow liquid, the form in which it is most often sold (pressurized at room temperature). The compound is primarily of interest in plasmaless cleaning and etching operations in the semiconductor industry, in nuclear reactor fuel processing, as a component in rocket fuels, and other industrial operations. Preparation, structure, and properties It was first reported in 1930 by Ruff and Krug who prepared it by fluorination of chlorine; this also produced ClF (chlorine monofluoride) and the mixture was separated by distillation. :3 F2 + Cl2 → 2 ClF3 The molecular geometry of ClF3 is approximately T-shaped, with one short bond (1.598 Å) and two long bonds (1.698 Å). This structure agrees with the prediction of VSEPR theory, which predicts lone pairs of electrons as occupying two equatorial positions o ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bromine Pentafluoride
Bromine pentafluoride, Br F5, is an interhalogen compound and a fluoride of bromine. It is a strong fluorinating agent. BrF5 finds use in oxygen isotope analysis. Laser ablation of solid silicates in the presence of BrF5 releases O2 for subsequent analysis. It has also been tested as an oxidizer in liquid rocket propellants and is used as a fluorinating agent in the processing of uranium. Preparation BrF5 was first prepared in 1931 by the direct reaction of bromine and fluorine. This reaction is suitable for the preparation of large quantities, and is carried out at temperatures over with an excess of fluorine: :Br2 + 5 F2 → 2 BrF5 For the preparation of smaller amounts, potassium bromide is used: :KBr + 3 F2 → KF + BrF5 This route yields BrF5 almost completely free of trifluorides and other impurities. Reactions BrF5 reacts with water to form bromic acid and hydrofluoric acid: :BrF5 + 3 H2O → HBrO3 + 5 HF It is an extremely effective fluorinating agent, being able ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bromine Monofluoride
Bromine monofluoride is a quite unstable interhalogen compound with the chemical formula BrF. It can be produced through the reaction of bromine trifluoride (or bromine pentafluoride) and bromine. Due to its lability, the compound can be detected but not isolated: :BrF3 + Br2 → 3 BrF :BrF5 + 2 Br2 → 5 BrF :Br2(l) + F2(g) → 2 BrF(g) It is usually generated in the presence of cesium fluoride. Bromine monofluoride decomposes at normal temperature through dismutation to bromine trifluoride, bromine pentafluoride, and free bromine. See also * Bromine trifluoride, BrF3 * Bromine pentafluoride Bromine pentafluoride, Br F5, is an interhalogen compound and a fluoride of bromine. It is a strong fluorinating agent. BrF5 finds use in oxygen isotope analysis. Laser ablation of solid silicates in the presence of BrF5 releases O2 for subsequ ..., BrF5 References Fluorides Bromine(I) compounds Interhalogen compounds {{Inorganic-compound-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chlorine Pentafluoride
Chlorine pentafluoride is an interhalogen compound with formula ClF5. This colourless gas is a strong oxidant that was once a candidate oxidizer for rockets. The molecule adopts a square pyramidal structure with C4v symmetry, as confirmed by its high-resolution 19F NMR spectrum. It was first synthesized in 1963. Preparation Some of the earliest research on the preparation was classified. It was first prepared by fluorination of chlorine trifluoride at high temperatures and high pressures: :ClF3 + F2 → ClF5 :ClF + 2F2 → ClF5 :Cl2 + 5F2 → 2ClF5 :CsClF4 + F2 → CsF + ClF5 NiF2 catalyzes this reaction. Certain metal fluorides, MClF4 (i.e. KClF4, RbClF4, CsClF4), react with F2 to produce ClF5 and the corresponding alkali metal fluoride. Reactions In a highly exothermic reaction, ClF5 reacts with water to produce chloryl fluoride and hydrogen fluoride: : + 2 → + 4 It is also a strong fluorinating agent. At room temperature it reacts readil ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chlorine Monofluoride
Chlorine monofluoride is a volatile interhalogen compound with the chemical formula ClF. It is a colourless gas at room temperature and is stable even at high temperatures. When cooled to −100 °C, ClF condenses as a pale yellow liquid. Many of its properties are intermediate between its parent halogens, Cl2 and F2. Reactivity Chlorine monofluoride is a versatile fluorinating agent, converting metals and non-metals to their fluorides and releasing Cl2 in the process. For example, it converts tungsten to tungsten hexafluoride and selenium to selenium tetrafluoride: :W + 6 ClF → WF6 + 3 Cl2 :Se + 4 ClF → SeF4 + 2 Cl2 FCl can also chlorofluorinate compounds, either by addition across a multiple bond or via oxidation. For example, it adds fluorine and chlorine to the carbon of carbon monoxide, yielding carbonyl chloride fluoride: :CO + ClF → See also *Chlorine fluoride A chlorine fluoride is an interhalogen compound containing only chlorine and fluorine. {, class= ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Fluorine Azide
Fluorine azide or triazadienyl fluoride is a yellow green gas composed of nitrogen and fluorine with formula . It is counted as an interhalogen compound, as the azide functional group is termed a pseudohalogen. It resembles , , and in this respect. The bond between the fluorine atom and the nitrogen is very weak, leading to this substance being very unstable and prone to explosion. Calculations show the F–N–N angle to be around 102° with a straight line of 3 nitrogen atoms. The gas boils at –30° and melts at –139 °C. It was first made by John F. Haller in 1942. Reactions Fluorine azide can be made by reacting hydrazoic acid and fluorine gas. Another way to form it is by reacting sodium azide with fluorine. Fluorine azide decomposes without explosion at normal temperatures to make dinitrogen difluoride: :. At higher temperatures such as 1000 °C fluorine azide breaks up into nitrogen monofluoride radical: : The FN itself dimerizes on cooling. : Sol ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pseudohalogen
Pseudohalogens are polyatomic analogues of halogens, whose chemistry, resembling that of the true halogens, allows them to substitute for halogens in several classes of chemical compounds. Pseudohalogens occur in pseudohalogen molecules, inorganic molecules of the general forms ''Ps''–''Ps'' or ''Ps''–X (where ''Ps'' is a pseudohalogen group), such as cyanogen; pseudohalide anions, such as cyanide ion; inorganic acids, such as hydrogen cyanide; as ligands in coordination complexes, such as ferouscyanide; and as functional groups in organic molecules, such as the nitrile group. Well-known pseudohalogen functional groups include cyanide, cyanate, thiocyanate, and azide. Common pseudohalogens and their nomenclature Many pseudohalogens are known by specialized common names according to where they occur in a compound. Well-known ones include (the true halogen chlorine is listed for comparison): Au− is considered to be a pseudohalogen ion due to its disproportionation reactio ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Iodine Monochloride
Iodine monochloride is an interhalogen compound with the formula . It is a red-brown chemical compound that melts near room temperature. Because of the difference in the electronegativity of iodine and chlorine, this molecule is highly polar and behaves as a source of I+. Preparation Iodine monochloride is produced simply by combining the halogens in a 1:1 molar ratio, according to the equation : When chlorine gas is passed through iodine crystals, one observes the brown vapor of iodine monochloride. Dark brown iodine monochloride liquid is collected. Excess chlorine converts iodine monochloride into iodine trichloride in a reversible reaction: : Polymorphs has two polymorphs; α-ICl, which exists as black needles (red by transmitted light) with a melting point of 27.2 °C, and β-ICl, which exists as black platelets (red-brown by transmitted light) with a melting point 13.9 °C.Brisbois, R. G.; Wanke, R. A.; Stubbs, K. A.; Stick, R. V. "Iodine Monochloride" ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyanogen
Cyanogen is the chemical compound with the formula ( C N)2. It is a colorless and highly toxic gas with a pungent odor. The molecule is a pseudohalogen. Cyanogen molecules consist of two CN groups – analogous to diatomic halogen molecules, such as Cl2, but far less oxidizing. The two cyano groups are bonded together at their carbon atoms: N≡C‒ C≡N, although other isomers have been detected. The name is also used for the CN radical, and hence is used for compounds such as cyanogen bromide (NCBr) (but see also ''Cyano radical''.) Cyanogen is the anhydride of oxamide: :H2NC(O)C(O)NH2 → NCCN + 2 H2O although oxamide is manufactured from cyanogen by hydrolysis: :NCCN + 2 H2O → H2NC(O)C(O)NH2 Preparation Cyanogen is typically generated from cyanide compounds. One laboratory method entails thermal decomposition of mercuric cyanide: :2 Hg(CN)2 → (CN)2 + Hg2(CN)2 Alternatively, one can combine solutions of copper(II) salts (such as copper(II) sulfate) ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Iodine Azide
Iodine azide () is an explosive inorganic compound, which in ordinary conditions is a yellow solid. Formally, it is an inter-pseudohalogen. Preparation Iodine azide can be prepared from the reaction between silver azide and elemental iodine: : Since silver azide can only be handled safely while moist, but even small traces of water cause the iodine azide to decompose, this synthesis is done by suspending the silver azide in dichloromethane and adding a drying agent before reaction with the iodine. In this way, a pure solution of iodine azide results, which can then be carefully evaporated to form needle-shaped golden crystals. This reaction was used in the original synthesis of iodine azide in 1900, where it was obtained as unstable solutions in ether and impure crystals contaminated by iodine. Iodine azide can also be generated ''in situ'' by reacting iodine monochloride and sodium azide under conditions where it is not explosive. Properties In the solid state, io ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
