Chlorofluoromethane

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Chlorofluoromethane
Chlorofluoromethane.png
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Names
Preferred IUPAC name
Chloro(fluoro)methane
Other names
Chlorofluoromethane
Fluorochloromethane
Chloro-fluoro-methane
Methylene chloride fluoride
Monochloromonofluoromethane
CFM
Khladon 31
Freon 31
CFC 31
R 31
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.008.914 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 209-803-2
KEGG
PubChem CID
UNII
Properties
CH2ClF
Molar mass 68.48 g/mol
AppearanceGas
Density 1.271 kg/m3 at 20 °C
Melting point −133.0 °C (−207.4 °F; 140.2 K)
Boiling point −9.1 °C (15.6 °F; 264.0 K)
0.15 mol.kg−1.bar−1
Hazards
Main hazards Carc. Cat. 3
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Chlorofluoromethane or Freon 31 is the hydrochlorofluorocarbon (HCFC) with the formula CH2ClF. It is a colorless, odorless, flammable gas. [1]

Contents

Uses

Pyrolysis of a mixture of dichlorofluoromethane and chlorofluoromethane gives hexafluorobenzene: [1]

3 CHCl2F + 3 CH2ClF → C6F6 + 9 HCl

It was used as a refrigerant and has an ozone depletion potential of 0.02.

Additional data

Its crystal structure is monoclinic with space group P21 and lattice constants a = 6.7676, b = 4.1477, c = 5.0206 (0.10−1 nm), β = 108.205°. [2]

At an altitude of 22 km, traces of chlorofluoromethane occur (148 ppt). [3]

Related Research Articles

Chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs) are fully or partly halogenated paraffin hydrocarbons that contain only carbon (C), hydrogen (H), chlorine (Cl), and fluorine (F), produced as volatile derivative of methane, ethane, and propane. They are also commonly known by the DuPont brand name Freon.

The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring. Friedel–Crafts reactions are of two main types: alkylation reactions and acylation reactions. Both proceed by electrophilic aromatic substitution.

Zinc chloride

Zinc chloride is the name of chemical compounds with the formula ZnCl2 and its hydrates. Zinc chlorides, of which nine crystalline forms are known, are colorless or white, and are highly soluble in water. This white salt is hygroscopic and even deliquescent. Samples should therefore be protected from sources of moisture, including the water vapor present in ambient air. Zinc chloride finds wide application in textile processing, metallurgical fluxes, and chemical synthesis. No mineral with this chemical composition is known aside from the very rare mineral simonkolleite, Zn5(OH)8Cl2·H2O.

Cobalt(II) chloride

Cobalt(II) chloride is an inorganic compound of cobalt and chlorine, with the formula CoCl
2
. It is a sky blue crystalline solid.

Chromium(III) chloride

Chromium(III) chloride (also called chromic chloride) describes any of several compounds of with the formula CrCl3 • xH2O, where x can be 0, 5, and 6. The anhydrous compound with the formula CrCl3 is a violet solid. The most common form of the trichloride is the dark green hexahydrate, CrCl3 • 6H2O. Chromium chlorides find use as catalysts and as precursors to dyes for wool.

The phosphonium cation describes polyatomic cations with the chemical formula PR+
4
. They are tetrahedral and generally colorless.

Rhodium(III) chloride

Rhodium(III) chloride refers to inorganic compounds with the formula RhCl3(H2O)n, where n varies from 0 to 3. These are diamagnetic solids featuring octahedral Rh(III) centres. Depending on the value of n, the material is either a dense brown solid or a soluble reddish salt. The soluble trihydrated (n = 3) salt is widely used to prepare compounds used in homogeneous catalysis, notably for the industrial production of acetic acid and hydroformylation.

Caesium chloride

Caesium chloride or cesium chloride is the inorganic compound with the formula CsCl. This colorless salt is an important source of caesium ions in a variety of niche applications. Its crystal structure forms a major structural type where each caesium ion is coordinated by 8 chlorine ions. Caesium chloride dissolves in water. CsCl changes to NaCl structure on heating. Caesium chloride occurs naturally as impurities in carnallite, sylvite and kainite. Less than 20 tonnes of CsCl is produced annually worldwide, mostly from a caesium-bearing mineral pollucite.

Diazonium compound

Diazonium compounds or diazonium salts are a group of organic compounds sharing a common functional group R−N+
2
X
where R can be any organic group, such as an alkyl or an aryl, and X is an inorganic or organic anion, such as a halogen.

Ruthenium(III) chloride

Ruthenium(III) chloride is the chemical compound with the formula RuCl3. "Ruthenium(III) chloride" more commonly refers to the hydrate RuCl3·xH2O. Both the anhydrous and hydrated species are dark brown or black solids. The hydrate, with a varying proportion of water of crystallization, often approximating to a trihydrate, is a commonly used starting material in ruthenium chemistry.

Triflic acid

Triflic acid, is the short name for trifluoromethanesulfonic acid, TFMS, TFSA, HOTf or TfOH, is a sulfonic acid with the chemical formula CF3SO3H. It is one of the strongest acids. Triflic acid is mainly used in research as a catalyst for esterification. It is a hygroscopic, colorless, slightly viscous liquid and is soluble in polar solvents.

Titanocene dichloride

Titanocene dichloride is the organotitanium compound with the formula (η5-C5H5)2TiCl2, commonly abbreviated as Cp2TiCl2. This metallocene is a common reagent in organometallic and organic synthesis. It exists as a bright red solid that slowly hydrolyzes in air. It shows antitumour activity and was the first non-platinum complex to undergo clinical trials as a chemotherapy drug.

Tebbes reagent

Tebbe's reagent is the organometallic compound with the formula (C5H5)2TiCH2ClAl(CH3)2. It is used in the methylenation of carbonyl compounds, that is it converts organic compounds containing the R2C=O group into the related R2C=CH2 derivative. It is a red solid that is pyrophoric in the air, and thus is typically handled with air-free techniques. It was originally synthesized by Fred Tebbe at DuPont Central Research.

1,2-Bis(diphenylphosphino)ethane

1,2-Bis(diphenylphosphino)ethane (dppe) is an organophosphorus compound with the formula (Ph2PCH2)2 (Ph = phenyl). It is a commonly used bidentate ligand in coordination chemistry. It is a white solid that is soluble in organic solvents.

Tetrathiafulvalene Chemical compound

Tetrathiafulvalene is an organosulfur compound with the formula (H2C2S2C)2. Studies on this heterocyclic compound contributed to the development of molecular electronics. TTF is related to the hydrocarbon fulvalene, (C5H4)2, by replacement of four CH groups with sulfur atoms. Over 10,000 scientific publications discuss TTF and its derivatives.

1,2-Bis(dimethylarsino)benzene

1,2-Bis(dimethylarsino)benzene (diars) is the organoarsenic compound with the formula C6H4(As(CH3)2)2. The molecule consists of two dimethylarsino groups attached to adjacent carbon centers of a benzene ring. It is a chelating ligand in coordination chemistry. This colourless oil is commonly abbreviated "diars."

Dichlorofluoromethane

Dichlorofluoromethane or Freon 21 or R 21 is a halomethane or hydrochlorofluorocarbon with the formula CHCl2F. It is a colorless and odorless gas. It is produced by fluorination of chloroform using a catalyst such as antimony trifluoride:

Isomer

In chemistry, isomers are molecules or polyatomic ions with identical molecular formulas — that is, same number of atoms of each element — but distinct arrangements of atoms in space. Isomerism is existence or possibility of isomers.

Xenon monochloride (XeCl) is an exciplex which is used in excimer lasers and excimer lamps emitting near ultraviolet light at 308 nm. It is most commonly used in medicine. Xenon monochloride was first synthesized in the 1960s. Its kinetic scheme is very complex and its state changes occur on a nanosecond timescale. In the gaseous state, at least two kinds of xenon monochloride are known: XeCl and Xe
2
Cl
, whereas complex aggregates form in the solid state in noble gas matrices. The excited state of xenon resembles halogens and it reacts with them to form excited molecular compounds.

Transition metal chloride complex Coordination complex

In chemistry, a transition metal chloride complex is a coordination complex that consists of a transition metal coordinated to one or more chloride ligand. The class of complexes is extensive.

References

  1. 1 2 Dagani, M. J.; = Barda, H. J.; Benya, T. J.; Sanders, D. C. "Bromine Compounds". Ullmann's Encyclopedia of Industrial Chemistry . Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_405.
  2. Binbrek O. S.; Torrie B. H.; Swainson I. P. (2002). "Neutron powder-profile study of chlorofluoromethane". Acta Crystallographica C . 58 (11): 672–674. doi:10.1107/S0108270102017328. PMID   12415178.
  3. C. Lippens; et al. (1981). "Atmospheric nitric acid and chlorofluoromethane 11 from interferometric spectra obtained at the Observatoire du Pic du Midi". Journal of Optics . 12 (5): 331–336. Bibcode:1981JOpt...12..331L. doi:10.1088/0150-536X/12/5/007.