Interhalogen

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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.

Contents

Most interhalogen compounds known are binary (composed of only two distinct elements). Their formulae are generally XYn, 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, [1] although a few books claim that IFCl2 and IF2Cl have been obtained, [2] [3] [4] [5] and theoretical studies seem to indicate that some compounds in the series BrClF
n
are barely stable. [6]

Some interhalogens, such as BrF3, IF5, and ICl, are good halogenating agents. BrF5 is too reactive to generate fluorine. Beyond that, iodine monochloride has several applications, including helping to measure the saturation of fats and oils, and as a catalyst for some reactions. A number of interhalogens, including IF7, are used to form polyhalides. [1]

Similar compounds exist with various pseudohalogens, such as the halogen azides ( FN3 , ClN3 , BrN3 , and IN3 ) and cyanogen halides ( FCN , ClCN , BrCN , and ICN ).

Types of interhalogens

F
F2
Cl
Cl2
Br Br2
I
IF, IF3, IF5, IF7
IBr, IBr3
I2
At
unknown
AtBr
AtI
At2(?)
FClBrIAt

Diatomic interhalogens

Iodine monochloride Iodine-monochloride-3D-vdW.png
Iodine monochloride

The interhalogens of form XY have physical properties intermediate between those of the two parent halogens. The covalent bond between the two atoms has some ionic character, the less electronegative halogen, X, being oxidised and having a partial positive charge. All combinations of fluorine, chlorine, bromine, and iodine that have the above-mentioned general formula are known, but not all are stable. Some combinations of astatine with other halogens are not even known, and those that are known are highly unstable.

Br2(l) + F2(g) → 2 BrF(g)

Bromine monofluoride dissociates like this:

3 BrF → Br2 + BrF3
Astatine chloride Astatine-chloride-3D-vdW.png
Astatine chloride
Astatine bromide Astatine-bromide-3D-vdW.png
Astatine bromide
Astatine iodide Astatine-iodide-3D-vdW.svg
Astatine iodide

No astatine fluorides have been discovered yet. Their absence has been speculatively attributed to the extreme reactivity of such compounds, including the reaction of an initially formed fluoride with the walls of the glass container to form a non-volatile product. [lower-alpha 1] Thus, although the synthesis of an astatine fluoride is thought to be possible, it may require a liquid halogen fluoride solvent, as has already been used for the characterization of radon fluorides. [10] [11]

In addition, there exist analogous molecules involving pseudohalogens, such as the cyanogen halides.

Tetratomic interhalogens

Chlorine trifluoride Chlorine-trifluoride-3D-vdW.png
Chlorine trifluoride
I2 + 3  XeF2 → 2 IF3 + 3  Xe
can be used. Not much is known about iodine trifluoride as it is so unstable.

Hexatomic interhalogens

Bromine pentafluoride Bromine-pentafluoride-3D-vdW.png
Bromine pentafluoride

All stable hexatomic and octatomic interhalogens involve a heavier halogen combined with five or seven fluorine atoms. Unlike the other halogens, fluorine atoms have high electronegativity and small size which is able to stabilize them.

Octatomic interhalogens

Iodine heptafluoride Iodine-heptafluoride-3D-vdW.png
Iodine heptafluoride

Properties

Typically, interhalogen bonds are more reactive than diatomic halogen bonds—because interhalogen bonds are weaker than diatomic halogen bonds, except for F2. If interhalogens are exposed to water, they convert to halide and oxyhalide ions. With BrF5, this reaction can be explosive. If interhalogens are exposed to silicon dioxide, or metal oxides, then silicon or metal respectively bond with one of the types of halogen, leaving free diatomic halogens and diatomic oxygen. Most interhalogens are halogen fluorides, and all but three (IBr, AtBr, and AtI) of the remainder are halogen chlorides. Chlorine and bromine can each bond to five fluorine atoms, and iodine can bond to seven. AX and AX3 interhalogens can form between two halogens whose electronegativities are relatively close to one another. When interhalogens are exposed to metals, they react to form metal halides of the constituent halogens. The oxidation power of an interhalogen increases with the number of halogens attached to the central atom of the interhalogen, as well as with the decreasing size of the central atom of the compound. Interhalogens containing fluorine are more likely to be volatile than interhalogens containing heavier halogens. [1]

Interhalogens with one or three halogens bonded to a central atom are formed by two elements whose electronegativities are not far apart. Interhalogens with five or seven halogens bonded to a central atom are formed by two elements whose sizes are very different. The number of smaller halogens that can bond to a large central halogen is guided by the ratio of the atomic radius of the larger halogen over the atomic radius of the smaller halogen. A number of interhalogens, such as IF7, react with all metals except for those in the platinum group. IF7, unlike interhalogens in the XY5 series, does not react with the fluorides of the alkali metals. [1]

ClF3 is the most reactive of the XY3 interhalogens. ICl3 is the least reactive. BrF3 has the highest thermal stability of the interhalogens with four atoms. ICl3 has the lowest. Chlorine trifluoride has a boiling point of −12 °C. Bromine trifluoride has a boiling point of 127 °C and is a liquid at room temperature. Iodine trichloride melts at 101 °C. [1]

Most interhalogens are covalent gases. Some interhalogens, especially those containing bromine, are liquids, and most iodine-containing interhalogens are solids. Most of the interhalogens composed of lighter halogens are fairly colorless, but the interhalogens containing heavier halogens are deeper in color due to their higher molecular weight. In this respect, the interhalogens are similar to the halogens. The greater the difference between the electronegativities of the two halogens in an interhalogen, the higher the boiling point of the interhalogen. All interhalogens are diamagnetic. The bond length of interhalogens in the XY series increases with the size of the constituent halogens. For instance, ClF has a bond length of 1.628  Å, and IBr has a bond length of 2.47 Å. [1]

Production

It is possible to produce larger interhalogens, such as ClF3, by exposing smaller interhalogens, such as ClF, to pure diatomic halogens, such as F2. This method of production is especially useful for generating halogen fluorides. At temperatures of 250 to 300 °C, this type of production method can also convert larger interhalogens into smaller ones. It is also possible to produce interhalogens by combining two pure halogens at various conditions. This method can generate any interhalogen save for IF7. [1]

Smaller interhalogens, such as ClF, can form by direct reaction with pure halogens. For instance, F2 reacts with Cl2 at 250 °C to form two molecules of ClF. Br2 reacts with diatomic fluorine in the same way, but at 60 °C. I2 reacts with diatomic fluorine at only 35 °C. ClF and BrF can both be produced by the reaction of a larger interhalogen, such as ClF3 or BrF3 and a diatomic molecule of the element lower in the periodic table. Among the hexatomic interhalogens, IF5 has a higher boiling point (97 °C) than BrF5 (40.5 °C), although both compounds are liquids at room temperature. The interhalogen IF7 can be formed by reacting palladium iodide with fluorine. [1]

See also

Notes

  1. An initial attempt to fluoridate astatine using chlorine trifluoride resulted in formation of a product which became stuck to the glass. Chlorine monofluoride, chlorine, and tetrafluorosilane were formed. The authors called the effect "puzzling", admitting they had expected formation of a volatile fluoride. [7] Ten years later, the compound was predicted to be non-volatile, out of line with the other halogens but similar to radon difluoride; [8] by this time, the latter had been shown to be ionic. [9]

Related Research Articles

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Bromine is a chemical element; it has symbol Br and atomic number 35. It is a volatile red-brown liquid at room temperature that evaporates readily to form a similarly coloured vapour. Its properties are intermediate between those of chlorine and iodine. Isolated independently by two chemists, Carl Jacob Löwig and Antoine Jérôme Balard, its name was derived from the Ancient Greek βρῶμος (bromos) meaning "stench", referring to its sharp and pungent smell.

<span class="mw-page-title-main">Chlorine</span> Chemical element, symbol Cl and atomic number 17

Chlorine is a chemical element; it has symbol Cl and atomic number 17. The second-lightest of the halogens, it appears between fluorine and bromine in the periodic table and its properties are mostly intermediate between them. Chlorine is a yellow-green gas at room temperature. It is an extremely reactive element and a strong oxidising agent: among the elements, it has the highest electron affinity and the third-highest electronegativity on the revised Pauling scale, behind only oxygen and fluorine.

<span class="mw-page-title-main">Halogen</span> Group of chemical elements

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.

<span class="mw-page-title-main">Iodine</span> Chemical element, symbol I and atomic number 53

Iodine is a chemical element; it has symbol I and atomic number 53. The heaviest of the stable halogens, it exists at standard conditions as a semi-lustrous, non-metallic solid that melts to form a deep violet liquid at 114 °C (237 °F), and boils to a violet gas at 184 °C (363 °F). The element was discovered by the French chemist Bernard Courtois in 1811 and was named two years later by Joseph Louis Gay-Lussac, after the Ancient Greek Ιώδης 'violet-coloured'.

<span class="mw-page-title-main">Haloalkane</span> Group of chemical compounds derived from alkanes containing one or more halogens

The haloalkanes are alkanes containing one or more halogen substituents. They are a subset of the general class of halocarbons, although the distinction is not often made. Haloalkanes are widely used commercially. They are used as flame retardants, fire extinguishants, refrigerants, propellants, solvents, and pharmaceuticals. Subsequent to the widespread use in commerce, many halocarbons have also been shown to be serious pollutants and toxins. For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl bromide is a controversial fumigant. Only haloalkanes that contain chlorine, bromine, and iodine are a threat to the ozone layer, but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated the compound a non-ozone layer depleter. For more information, see Halomethane. Haloalkane or alkyl halides are the compounds which have the general formula "RX" where R is an alkyl or substituted alkyl group and X is a halogen.

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<span class="mw-page-title-main">Chlorine pentafluoride</span> Chemical compound

Chlorine pentafluoride is an interhalogen compound with formula ClF5. This colourless liquid 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.

<span class="mw-page-title-main">Bromine trifluoride</span> Chemical compound

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.

<span class="mw-page-title-main">Bromine pentafluoride</span> Chemical compound

Bromine pentafluoride, BrF5, is an interhalogen compound and a fluoride of bromine. It is a strong fluorinating agent.

Iodine pentafluoride is an interhalogen compound with chemical formula IF5. It is one of the fluorides of iodine. It is a colorless liquid, although impure samples appear yellow. It is used as a fluorination reagent and even a solvent in specialized syntheses.

<span class="mw-page-title-main">Iodine heptafluoride</span> Chemical compound

Iodine heptafluoride, also known as iodine(VII) fluoride, is an interhalogen compound with the chemical formula IF7. It has an unusual pentagonal bipyramidal structure, as predicted by VSEPR theory. The molecule can undergo a pseudorotational rearrangement called the Bartell mechanism, which is like the Berry mechanism but for a heptacoordinated system. It forms colourless crystals, which melt at 4.5 °C: the liquid range is extremely narrow, with the boiling point at 4.77 °C. The dense vapor has a mouldy, acrid odour. The molecule has D5h symmetry.

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

Selenium tetrafluoride (SeF4) is an inorganic compound. It is a colourless liquid that reacts readily with water. It can be used as a fluorinating reagent in organic syntheses (fluorination of alcohols, carboxylic acids or carbonyl compounds) and has advantages over sulfur tetrafluoride in that milder conditions can be employed and it is a liquid rather than a gas.

<span class="mw-page-title-main">Iodine monochloride</span> Chemical compound

Iodine monochloride is an interhalogen compound with the formula ICl. 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+. Discovered in 1814 by Gay-Lussac, iodine monochloride is the first interhalogen compound discovered.

Bromine compounds are compounds containing the element bromine (Br). These compounds usually form the -1, +1, +3 and +5 oxidation states. Bromine is intermediate in reactivity between chlorine and iodine, and is one of the most reactive elements. Bond energies to bromine tend to be lower than those to chlorine but higher than those to iodine, and bromine is a weaker oxidising agent than chlorine but a stronger one than iodine. This can be seen from the standard electrode potentials of the X2/X couples (F, +2.866 V; Cl, +1.395 V; Br, +1.087 V; I, +0.615 V; At, approximately +0.3 V). Bromination often leads to higher oxidation states than iodination but lower or equal oxidation states to chlorination. Bromine tends to react with compounds including M–M, M–H, or M–C bonds to form M–Br bonds.

Iodine compounds are compounds containing the element iodine. Iodine can form compounds using multiple oxidation states. Iodine is quite reactive, but it is much less reactive than the other halogens. For example, while chlorine gas will halogenate carbon monoxide, nitric oxide, and sulfur dioxide, iodine will not do so. Furthermore, iodination of metals tends to result in lower oxidation states than chlorination or bromination; for example, rhenium metal reacts with chlorine to form rhenium hexachloride, but with bromine it forms only rhenium pentabromide and iodine can achieve only rhenium tetraiodide. By the same token, however, since iodine has the lowest ionisation energy among the halogens and is the most easily oxidised of them, it has a more significant cationic chemistry and its higher oxidation states are rather more stable than those of bromine and chlorine, for example in iodine heptafluoride.

<span class="mw-page-title-main">Bromine monofluoride</span> Chemical compound

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:

Polyhalogen ions are a group of polyatomic cations and anions containing halogens only. The ions can be classified into two classes, isopolyhalogen ions which contain one type of halogen only, and heteropolyhalogen ions with more than one type of halogen.

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">Astatine compounds</span>

Astatine compounds are compounds that contain the element astatine (At). As this element is very radioactive, few compounds have been studied. Less reactive than iodine, astatine is the least reactive of the halogens. Its compounds have been synthesized in nano-scale amounts and studied as intensively as possible before their radioactive disintegration. The reactions involved have been typically tested with dilute solutions of astatine mixed with larger amounts of iodine. Acting as a carrier, the iodine ensures there is sufficient material for laboratory techniques to work. Like iodine, astatine has been shown to adopt odd-numbered oxidation states ranging from −1 to +7.

References

  1. 1 2 3 4 5 6 7 8 Saxena, P. B. (2007). Chemistry Of Interhalogen Compounds. ISBN   978-81-8356-243-0 . Retrieved February 27, 2013.
  2. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 824. ISBN   978-0-08-037941-8.
  3. Meyers, Robert A., ed. (2001). Encyclopedia of Physical Science and Technology: Inorganic Chemistry (3rd ed.). Academic Press. ISBN   978-0-12-227410-7. A few ternary compounds, such as IFCl
    2
    and IF
    2
    Cl
    , are also known [no source given].
  4. Murthy, C. Parameshwara (2008). University Chemistry. Vol. 1. New Age International. p. 675. ISBN   978-81-224-0742-6. The only two interhalogen compounds are IFCl
    2
    and IF
    2
    Cl
    [no source given].
  5. Sahoo, Balaram; Nayak, Nimai Charan; Samantaray, Asutosh; Pujapanda, Prafulla Kumar (2012). Inorganic Chemistry. PHI Learning. ISBN   978-81-203-4308-5. Only a few ternary interhalogen compounds such as IFCl
    2
    and IF
    2
    Cl
    have been prepared [no source given].
  6. Ignatyev, Igor S.; Schaefer, Henry F. III (1999). "Bromine Halides: The Neutral Molecules BrClF
    n
    (n = 1–5) and Their Anions — Structures, Energetics, and Electron Affinities". Journal of the American Chemical Society. 121 (29): 6904–6910. doi:10.1021/ja990144h.
  7. Appelman, E. H.; Sloth, E. N.; Studier, M. H. (1966). "Observation of astatine compounds by time-of-flight mass spectrometry". Inorganic Chemistry. 5 (5): 766–769. doi:10.1021/ic50039a016.
  8. Pitzer, K. S. (1975). "Fluorides of radon and element 118". Journal of the Chemical Society, Chemical Communications. 5 (18): 760b–761. doi:10.1039/C3975000760B.
  9. Bartlett, N.; Sladky, F. O. (1973). "The chemistry of krypton, xenon and radon". In Bailar, J. C.; Emeléus, H. J.; Nyholm, R.; et al. (eds.). Comprehensive Inorganic Chemistry. Vol. 1. Pergamon. pp. 213–330. ISBN   0-08-017275-X.
  10. Zuckerman & Hagen 1989, p. 31.
  11. Kugler & Keller 1985, pp. 112, 192–193.

Bibliography