Sulfur trifluoride

Last updated
Sulfur trifluoride
Sulfur trifluoride.svg
Names
Other names
sulfur(III) fluoride
trifluorosulfur radical
Identifiers
3D model (JSmol)
  • InChI=1S/F3S/c1-4(2)3
    Key: PSCXEUSWZWRCMQ-UHFFFAOYSA-N
  • F[S](F)F
Properties
F3S
Molar mass 89.06 g·mol−1
Related compounds
Related compounds
SF2, SF4, SF6, S2F10
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Sulfur trifluoride is the inorganic chemical compound with the formula SF3. It is a radical. [1] [2]

Contents

Structure and synthesis

Sulfur trifluoride is predicted to be pyramidal. [3] [4]

SF3 is generated by irradiation of crystals SF+
3
BF
4
with gamma rays. [1]

SF
3

A derivative formally derived from SF
3
is the coordination complex Ir(Cl)(CO)(F)(SF3)(Et3P)2 obtained by oxidative addition of sulfur tetrafluoride to Ir(Cl)(CO)(PEt3)2 (Et = C2H5). [5] [6]

Related Research Articles

<span class="mw-page-title-main">Iridium</span> Chemical element, symbol Ir and atomic number 77

Iridium is a chemical element; it has symbol Ir and atomic number 77. A very hard, brittle, silvery-white transition metal of the platinum group, it is considered the second-densest naturally occurring metal with a density of 22.56 g/cm3 (0.815 lb/cu in) as defined by experimental X-ray crystallography. It is one of the most corrosion-resistant metals, even at temperatures as high as 2,000 °C (3,630 °F). However, corrosion-resistance is not quantifiable in absolute terms: although only certain molten salts and halogens are corrosive to solid iridium, finely divided iridium dust is much more reactive and can be flammable, whereas gold dust is not flammable but can be attacked by substances that iridium resists, such as aqua regia.

In chemistry, the oxidation state, or oxidation number, is the hypothetical charge of an atom if all of its bonds to other atoms were fully ionic. It describes the degree of oxidation of an atom in a chemical compound. Conceptually, the oxidation state may be positive, negative or zero. While fully ionic bonds are not found in nature, many bonds exhibit strong ionicity, making oxidation state a useful predictor of charge.

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. Despite being famous for its extreme oxidation properties and igniting many things, chlorine trifluoride is not combustible itself. The compound is primarily of interest in plasmaless cleaning and etching operations in the semiconductor industry, in nuclear reactor fuel processing, historically as a component in rocket fuels, and various other industrial operations owing to its corrosive nature.

<span class="mw-page-title-main">Iron(III) fluoride</span> Chemical compound

Iron(III) fluoride, also known as ferric fluoride, are inorganic compounds with the formula FeF3(H2O)x where x = 0 or 3. They are mainly of interest by researchers, unlike the related iron(III) chloride. Anhydrous iron(III) fluoride is white, whereas the hydrated forms are light pink.

<span class="mw-page-title-main">Scandium fluoride</span> Chemical compound

Scandium(III) fluoride, ScF3, is an ionic compound. This salt is slightly soluble in water but dissolves in the presence of excess fluoride to form the ScF63− anion.

<span class="mw-page-title-main">Sulfur tetrafluoride</span> Chemical compound

Sulfur tetrafluoride is the chemical compound with the formula SF4. It is a colorless corrosive gas that releases dangerous HF upon exposure to water or moisture. Despite these unwelcome characteristics, this compound is a useful reagent for the preparation of organofluorine compounds, some of which are important in the pharmaceutical and specialty chemical industries.

<span class="mw-page-title-main">Tungsten oxytetrafluoride</span> Chemical compound

Tungsten oxytetrafluoride is an inorganic compound with the formula WOF4. It is a colorless diamagnetic solid. The compound is one of many oxides of tungsten. It is usually encountered as product of the partial hydrolysis of tungsten hexafluoride.

Osmium compounds are compounds containing the element osmium (Os). Osmium forms compounds with oxidation states ranging from −2 to +8. The most common oxidation states are +2, +3, +4, and +8. The +8 oxidation state is notable for being the highest attained by any chemical element aside from iridium's +9 and is encountered only in xenon, ruthenium, hassium, iridium, and plutonium. The oxidation states −1 and −2 represented by the two reactive compounds Na
2
[Os
4
(CO)
13
]
and Na
2
[Os(CO)
4
]
are used in the synthesis of osmium cluster compounds.

<span class="mw-page-title-main">Transition metal dinitrogen complex</span> Coordination compounds with N2

Transition metal dinitrogen complexes are coordination compounds that contain transition metals as ion centers the dinitrogen molecules (N2) as ligands.

Diboron tetrafluoride is the inorganic compound with the formula (BF2)2. A colorless gas, the compound has a halflife of days at room temperature. It is the most stable of the diboron tetrahalides, and does not appreciably decompose under standard conditions.

<span class="mw-page-title-main">Iridium hexafluoride</span> Chemical compound

Iridium hexafluoride, also iridium(VI) fluoride, (IrF6) is a compound of iridium and fluorine and one of the seventeen known binary hexafluorides. It is one of only a few compounds with iridium in the oxidation state +6.

<span class="mw-page-title-main">Organoiridium chemistry</span> Chemistry of organometallic compounds containing an iridium-carbon bond

Organoiridium chemistry is the chemistry of organometallic compounds containing an iridium-carbon chemical bond. Organoiridium compounds are relevant to many important processes including olefin hydrogenation and the industrial synthesis of acetic acid. They are also of great academic interest because of the diversity of the reactions and their relevance to the synthesis of fine chemicals.

Boron monofluoride or fluoroborylene is a chemical compound with the formula BF, one atom of boron and one of fluorine. It is an unstable gas, but it is a stable ligand on transition metals, in the same way as carbon monoxide. It is a subhalide, containing fewer than the normal number of fluorine atoms, compared with boron trifluoride. It can also be called a borylene, as it contains boron with two unshared electrons. BF is isoelectronic with carbon monoxide and dinitrogen; each molecule has 14 electrons.

Transition metal carbyne complexes are organometallic compounds with a triple bond between carbon and the transition metal. This triple bond consists of a σ-bond and two π-bonds. The HOMO of the carbyne ligand interacts with the LUMO of the metal to create the σ-bond. The two π-bonds are formed when the two HOMO orbitals of the metal back-donate to the LUMO of the carbyne. They are also called metal alkylidynes—the carbon is a carbyne ligand. Such compounds are useful in organic synthesis of alkynes and nitriles. They have been the focus on much fundamental research.

<span class="mw-page-title-main">Disulfur dioxide</span> Chemical compound

Disulfur dioxide, dimeric sulfur monoxide or SO dimer is an oxide of sulfur with the formula S2O2. The solid is unstable with a lifetime of a few seconds at room temperature.

<span class="mw-page-title-main">Thiophosphoryl fluoride</span> Chemical compound

Thiophosphoryl fluoride is an inorganic molecular gas with formula PSF3 containing phosphorus, sulfur and fluorine. It spontaneously ignites in air and burns with a cool flame. The discoverers were able to have flames around their hands without discomfort, and called it "probably one of the coldest flames known". The gas was discovered in 1888.

Fluorine forms a great variety of chemical compounds, within which it always adopts an oxidation state of −1. With other atoms, fluorine forms either polar covalent bonds or ionic bonds. Most frequently, covalent bonds involving fluorine atoms are single bonds, although at least two examples of a higher order bond exist. Fluoride may act as a bridging ligand between two metals in some complex molecules. Molecules containing fluorine may also exhibit hydrogen bonding. Fluorine's chemistry includes inorganic compounds formed with hydrogen, metals, nonmetals, and even noble gases; as well as a diverse set of organic compounds. For many elements the highest known oxidation state can be achieved in a fluoride. For some elements this is achieved exclusively in a fluoride, for others exclusively in an oxide; and for still others the highest oxidation states of oxides and fluorides are always equal.

<span class="mw-page-title-main">Transition metal chloride complex</span> 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.

<span class="mw-page-title-main">Transition metal dithiocarbamate complexes</span>

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.

Iridium compounds are compounds containing the element iridium (Ir). Iridium forms compounds in oxidation states between −3 and +9, but the most common oxidation states are +1, +2, +3, and +4. Well-characterized compounds containing iridium in the +6 oxidation state include IrF6 and the oxides Sr2MgIrO6 and Sr2CaIrO6. iridium(VIII) oxide was generated under matrix isolation conditions at 6 K in argon. The highest oxidation state (+9), which is also the highest recorded for any element, is found in gaseous [IrO4]+.

References

  1. 1 2 Morton, J. R.; Preston, K. F.; Strach, S. J. (1978). "The EPR spectrum of SF3 Trapped in SF3BF4 Crystals". The Journal of Chemical Physics. 69 (4): 1392. Bibcode:1978JChPh..69.1392M. doi:10.1063/1.436766.
  2. Deng, Jianming; Wang, Chaoyang; Li, Qian-shu; Xie, Yaoming; King, R. Bruce; Schaefer, Henry F. (2011). "Trifluorosulfane Ligand as an Analogue of the Nitrosyl Ligand: Highly Exothermic Fluorine Transfer Reactions from Sulfur to Metal in the Chemistry of SF3 Metal Carbonyls of the First Row Transition Metals". Inorganic Chemistry. 50 (7): 2824–2835. doi:10.1021/ic101994k. PMID   21366337.
  3. Irikura, Karl K. (1995). "Structure and thermochemistry of sulfur fluorides SFn (n = 1–5) and their ions SF+
    n
    (n = 1–5)"
    . The Journal of Chemical Physics. 102 (13): 5357–5367. Bibcode:1995JChPh.102.5357I. doi:10.1063/1.469263.
  4. Woon, David E.; Dunning, Thom H. (2009). "Theory of Hypervalency: Recoupled Pair Bonding in SFn (n = 1−6)". The Journal of Physical Chemistry A. 113 (27): 7915–7926. Bibcode:2009JPCA..113.7915W. doi: 10.1021/jp901949b . PMID   19499905.
  5. Cockman, Russell W.; Ebsworth, E. A. V.; Holloway, John H. (1987). "Complexes of iridium(III) containing the novel sulfur trifluoride ligand". Journal of the American Chemical Society. 109 (7): 2194–2195. doi:10.1021/ja00241a055.
  6. Gao, Xiaozhen; Li, Nan; King, R. Bruce (December 2014). "Formation of Difluorosulfane Complexes of the Third Row Transition Metals by Sulfur-to-Metal Fluorine Migration in Trifluorosulfane Metal Complexes: The Anomaly of Trifluorosulfane Iridium Tricarbonyl". Inorganic Chemistry. 53 (23): 12635–12642. doi:10.1021/ic502375q. PMID   25397720.