Polyhalogen ions

Not to be confused with Polyhalite.

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.

Introduction

Numerous polyhalogen ions have been found, with their salts isolated in the solid state and structurally characterized. The following tables summarize the species found so far.^[1]^[2]^[3]^[4]^[5]

Isopolyhalogen cations
Diatomic species	*[Cl₂]⁺, [Br₂]⁺, [I₂]⁺
Triatomic species	[Cl₃]⁺, [Br₃]⁺, [I₃]⁺
Tetraatomic species	[Cl₄]⁺, [I₄]²⁺
Pentaatomic species	[Br₅]⁺, [I₅]⁺
Heptaatomic species	^[I₇]⁺
Higher species	[I₁₅]³⁺

Notes: *[Cl₂]⁺ can only exist as [Cl₂O₂]²⁺ at low temperatures, a charge-transfer complex from O₂ to [Cl₂]⁺.^[2] Free [Cl₂]⁺ is only known from its electronic band spectrum obtained in a low-pressure discharge tube.^[3] ^The existence of [I₇]⁺ is possible but still uncertain.^[1]

Heteropolyhalogen cations
Triatomic species	[ClF₂]⁺, [Cl₂F]⁺, [BrF₂]⁺, [IF₂]⁺, [ICl₂]⁺, [IBrCl]⁺, [IBr₂]⁺, [I₂Cl]⁺, [I₂Br]⁺
Pentaatomic species	[ClF₄]⁺, [BrF₄]⁺, [IF₄]⁺, [I₃Cl₂]⁺
Heptaatomic species	[ClF₆]⁺, [BrF₆]⁺, [IF₆]⁺

Isopolyhalogen anions
Triatomic species	[Cl₃]⁻, [Br₃]⁻, [I₃]⁻
Tetraatomic species	[Br₄]²⁻, [I₄]²⁻
Pentaatomic species	[I₅]⁻
Heptaatomic species	[I₇]⁻
Octaatomic species	[Br₈]²⁻, [I₈]²⁻
Higher species	[I₉]⁻, [I₁₀]²⁻, [I₁₀]⁴⁻, [I₁₁]⁻, [I₁₂]²⁻, [I₁₃]³⁻, [I₁₆]²⁻, [I₂₂]⁴⁻, [I₂₆]³⁻, [I₂₆]⁴⁻, [I₂₈]⁴⁻, [I₂₉]³⁻

Heteropolyhalogen anions
Triatomic species	[ClF₂]⁻, [BrF₂]⁻, [BrCl₂]⁻, [IF₂]⁻, [ICl₂]⁻, [IBrF]⁻, [IBrCl]⁻, [IBr₂]⁻, [I₂Cl]⁻, [I₂Br]⁻, [AtBrCl]⁻, [AtBr₂]⁻, [AtICl]⁻, [AtIBr]⁻, [AtI₂]⁻
Pentaatomic species	[ClF₄]⁻, [BrF₄]⁻, [IF₄]⁻, [ICl₃F]⁻, [ICl₄]⁻, [IBrCl₃]⁻, [I₂Cl₃]⁻, [I₂BrCl₂]⁻, [I₂Br₂Cl]⁻, [I₂Br₃]⁻,[I₄Cl]⁻, [I₄Br]⁻
Hexaatomic species	[IF₅]²⁻
Heptaatomic species	[ClF₆]⁻, [BrF₆]⁻, [IF₆]⁻, [I₃Br₄]⁻
Nonaatomic species	[IF₈]⁻

Structure

Structures of some isopolyhalogen cations

Solid state structures of the polyhalogen ions [BrF₂]⁺, [ClF₂]⁺, [ICl₂]⁺ in their [SbF₆]⁻ salts.

Solid state structure of [I₃Cl₂]⁺ in [I₃Cl₂]⁺[AsCl₆]⁻.

Structure of the [I₂F₁₂]⁻ dimer present in [Me₄N]⁺[IF₆]⁻.

Most of the structures of the ions have been determined by IR spectroscopy, Raman spectroscopy and X-ray crystallography. The polyhalogen ions always have the heaviest and least electronegative halogen present in the ion as the central atom, making the ion asymmetric in some cases. For example, [Cl₂F]⁺ has a structure of [Cl–Cl–F]⁻ but not [Cl–F–Cl]⁻.

In general, the structures of most heteropolyhalogen ions and lower isopolyhalogen ions were in agreement with the VSEPR model. However, there were exceptional cases. For example, when the central atom is heavy and has seven lone pairs, such as [BrF₆]⁻ and [IF₆]⁻, they have a regular octahedral arrangement of fluoride ligands instead of a distorted one due to the presence of a stereochemically inert lone pair. More deviations from the ideal VSEPR model were found in the solid state structures due to strong cation-anion interactions, which also complicates interpretation of vibrational spectroscopic data. In all known structures of the polyhalogen anion salts, the anions make very close contact, via halogen bridges, with the counter-cations.^[4] For example, in the solid state, [IF₆]⁻ is not regularly octahedral, as solid state structure of [Me₄N]⁺[IF₆]⁻ reveals loosely bound [I₂F₁₁]²⁻ dimers. Significant cation-anion interactions were also found in [BrF₂]⁺[SbF₆]⁻, [ClF₂]⁺[SbF₆]⁻, [BrF₄]⁺[Sb₆F₁₁]⁻.^[2]

General structures of selected heteropolyhalogen ions
Linear (or almost linear)	[ClF₂]⁻, [BrF₂]⁻, [BrCl₂]⁻, [IF₂]⁻, [ICl₂]⁻, [IBr₂]⁻, [I₂Cl]⁻, [I₂Br]⁻
Bent	[ClF₂]⁺, [Cl₂F]⁺, [BrF₂]⁺, [IF₂]⁺, [ICl₂]⁺, [I₂Cl]⁺, [IBr₂]⁺, [I₂Br]⁺, [IBrCl]⁺
Square planar	[ClF₄]⁻, [BrF₄]⁻, [IF₄]⁻, [ICl₄]⁻
Disphenoidal (or seesaw)	[ClF₄]⁺, [BrF₄]⁺, [IF₄]⁺
Pentagonal planar	#[IF₅]²⁻
Octahedral	[ClF₆]⁺, [BrF₆]⁺, [IF₆]⁺, §[ClF₆]⁻, [BrF₆]⁻, [IF₆]⁻
Square antiprismatic	[IF₈]⁻

Note: #[IF₅]²⁻ is one of the two XY_n-type species known to have the rare pentagonal planar geometry, the other being [XeF₅]⁻. §[ClF₆]⁻ is distorted octahedral as the stereochemical inert pair effect is not significant in the chlorine atom.

The [I₃Cl₂]⁺ and [I₃Br₂]⁺ ions have a trans-Z-type structure, analogous to that of [I₅]⁺.

Solid state structure of [BrF₄]⁺ in [BrF₄]⁺[Sb₂F₁₁]⁺.

Higher polyiodides

Main article: Polyiodide

The polyiodide ions have much more complicated structures. Discrete polyiodides usually have a linear sequence of iodine atoms and iodide ions, and are described in terms of association between I₂, I⁻ and I₃⁻ units, which reflects the origin of the polyiodide. In the solid states, the polyiodides can interact with each other to form chains, rings, or even complicated two-dimensional and three-dimensional networks.

Bonding

The bonding in polyhalogen ions mostly invoke the predominant use of p-orbitals. Significant d-orbital participation in the bonding is improbable as much promotional energy will be required, while scant s-orbital participation is expected in iodine-containing species due to the inert pair effect, suggested by data from Mössbauer spectroscopy. However, no bonding model has been capable of reproducing such wide range of bond lengths and angles observed so far.^[3]

As expected from the fact that an electron is removed from the antibonding orbital when X₂ is ionized to [X₂]⁺, the bond order as well as the bond strength in [X₂]⁺ gets higher, consequently the interatomic distances in the molecular ion is less than those in X₂.

Linear or nearly linear triatomic polyhalides have weaker and longer bonds compared with that in the corresponding diatomic interhalogen or halogen, consistent with the additional repulsion between atoms as the halide ion is added to the neutral molecule. Another model involving the use of resonance theory exists, for example, [ICl₂]⁻ can be viewed as the resonance hybrid of the following canonical forms:

Evidence supporting this theory comes from the bond lengths (255pm in [ICl₂]⁻ and 232pm in ICl(g)) and bond stretching wavenumbers (267 and 222 cm⁻¹ for symmetric and asymmetric stretching in [ICl₂]⁻ compared with 384 cm⁻¹ in ICl), which suggests a bond order of about $\tfrac{1}{2}$ for each I–Cl bonds in [ICl₂]⁻, consistent with the interpretation using the resonance theory. Other triatomic species [XY₂]⁻ can be similarly interpreted.^[2]

Synthesis

The formation of polyhalogen ions can be viewed as the self-dissociation of their parent interhalogens or halogens:

2 XY_n [XY_n-1]⁺ + [XY_n+1]⁻
3 X₂ [X₃]⁺ + [X₃]⁻
4 X₂ [X₅]⁺ + [X₃]⁻
5 X₂ 2 [X₂]⁺ + 2 [X₃]⁻

Polyhalogen cations

There are two general strategies for preparing polyhalogen cations:

By reacting the appropriate interhalogen with a lewis acid (such as the halides of B, Al, P, As, Sb) either in an inert or oxidizing solvent (such as anhydrous HF) or without one, to give a heteropolyhalogen cation.

XY_n + MY_m → [XY_n-1]⁺ + [MY_m+1]⁻

By an oxidative process, in which the halogen or interhalogen is reacted with an oxidizer and a lewis acid to give the cation:

Cl₂ + ClF + AsF₅ → [Cl₃]⁺[AsF₆]⁻

In some cases the lewis acid (the fluoride acceptor) itself act as an oxidant:

3 I₂ + 3 SbF₅ → 2 [I₃]⁺[SbF₆]⁻ + SbF₃

Usually the first method is employed for preparing heteropolyhalogen cations, and the second one is applicable to both. The oxidative process is useful in the preparation of the cations [IBr₂]⁺, [ClF₆]⁺, [BrF₆]⁺, as their parent interhalogens, IBr₃, ClF₇, BrF₇ respectively, has never been isolated:

Br₂ + IOSO₂F → [IBr₂]⁺[SO₃F]⁻

2 ClF₅ + 2 PtF₆ → [ClF₆]⁺[PtF₆]⁻ + [ClF₄]⁺[PtF₆]⁻

BrF₅ + [KrF]⁺[AsF₆]⁻ → [BrF₆]⁺[AsF₆]⁻ + Kr

The preparation of some individual species are briefly summarized in the table below with equations:^[1]^[2]^[3]^[4]

Synthesis of some polyhalogen cations
Species	Relevant chemical equation	Additional conditions required
[Cl₂]⁺ (as [Cl₂O₂]⁺)	Cl₂ + [O₂]⁺[SbF₆]⁻ → [Cl₂O₂]⁺[SbF₆]⁻	in anhydrous HF at low temperatures
[Br₂]⁺	Br₂ (in BrSO₃F) + 3 SbF₅ → [Br₂]⁺[Sb₃F₁₆]⁻ (not balanced)	at room temperature
[I₂]⁺	2 I₂ + S₂O₆F₂ → 2 [I₂]⁺[SO₃F]⁻	in HSO₃F
[Cl₃]⁺	Cl₂ + ClF + AsF₅ → [Cl₃]⁺[AsF₆]⁻	at a temperature of 195K
[Br₃]⁺	3 Br₂ + 2 [O₂]⁺[AsF₆]⁻ → 2 [Br₃]⁺[AsF₆]⁻ + 2 O₂
[I₃]⁺	3 I₂ + S₂O₆F₂ → 2 [I₃]⁺[SO₃F]⁻
[Cl₄]⁺	2 Cl₂ + IrF₆ → [Cl₄]⁺[IrF₆]⁻	in anhydrous HF, at a temperature of <193K
[I₄]²⁺	2 I₂ + 3 AsF₅ → [I₄]²⁺[AsF₆⁻]₂ + AsF₃	in liquid SO₂
[Br₅]⁺	8 Br₂ + 3 [XeF]⁺[AsF₆]⁻ → 3 [Br₅]⁺[AsF₆]⁻ + 3 Xe + BrF₃
[I₅]⁺	2 I₂ + ICl + AlCl₃ → [I₅]⁺[AlCl₄]⁻
[I₇]⁺	7 I₂ + S₂O₆F₂ → 2 I₇SO₃F
[ClF₂]⁺	ClF₃ + AsF₅ → [ClF₂]⁺[AsF₆]⁻
[Cl₂F]⁺	2 ClF + AsF₅ → [Cl₂F]⁺[AsF₆]⁻	at a temperature of <197K
[BrF₂]⁺	5 BrF₃ + 2 Au → 3 BrF + 2 [BrF₂]⁺[AuF₄]⁻	with excess BrF₃ required
[IF₂]⁺	IF₃ + AsF₅ → [IF₂]⁺[AsF₆]⁻
[ICl₂]⁺	ICl₃ + SbCl₅ → [ICl₂]⁺[SbCl₆]⁻
[IBr₂]⁺	Br₂ + IOSO₂F → [IBr₂]⁺[SO₃F]⁻
[ClF₄]⁺	ClF₅ + SbF₅ → [ClF₄]⁺[SbF₆]⁻
[BrF₄]⁺	BrF₅ + AsF₅ → [BrF₄]⁺[AsF₆]⁻
[IF₄]⁺	IF₅ + 2 SbF₅ → [IF₄]⁺[Sb₂F₁₁]⁻
[ClF₆]⁺	‡Cs₂NiF₆ + 5 AsF₅ + ClF₅ → [ClF₆]⁺[AsF₆]⁻ + Ni[AsF₆]₂ + 2 CsAsF₆
[BrF₆]⁺	[KrF]⁺[AsF₆]⁻ + BrF₅ → [BrF₆]⁺[AsF₆]⁻ + Kr
[IF₆]⁺	IF₇ + BrF₃ → [IF₆]⁺[BrF₄]⁻

‡In this reaction, the active oxidizing species is [NiF₃]⁺, which is formed in situ in the Cs₂NiF₆/AsF₅/HF system. It is an even more powerful oxidizing and fluorinating agent than PtF₆.

Polyhalogen anions

For polyhalogen anions, there are two general preparation strategies as well:

By reacting an interhalogen or halogen with a lewis base, most likely a fluoride:

[Et₄N]⁺Y⁻ + XY_n → [Et₄N]⁺[XY_n+1]⁻

X₂ + X⁻ → X₃⁻

By oxidation of simple halides:

KI + Cl₂ → K⁺[ICl₂]⁻

The preparation of some individual species are briefly summarized in the table below with equations:^[1]^[2]^[3]^[4]

Synthesis of some polyhalogen anions
Species	Relevant chemical equation	Additional conditions required
[Cl₃]⁻, [Br₃]⁻, [I₃]⁻	X₂ + X⁻ → [X₃]⁻ (X = Cl, Br, I)
[Br₃]⁻	Br₂ + [ⁿBu₄N]⁺Br⁻ → [ⁿBu₄N]⁺[Br₃]⁻	in 1,2-dichloroethane or liquid sulfur dioxide. [Br₃]⁻ does not exist in solution and is only formed when the salt crystallizes out.
[Br₅]⁻	2 Br₂ + [ⁿBu₄N]⁺Br⁻ → [ⁿBu₄N]⁺[Br₅]⁻	in 1,2-dichloroethane or liquid sulfur dioxide, with excess Br₂
[ClF₂]⁻	ClF + CsF → Cs⁺[ClF₂]⁻
[BrCl₂]⁻^[6]	Br₂ + Cl₂ + 2 CsCl → 2 Cs⁺[BrCl₂]⁻
[ICl₂]⁻^[7]	KI + Cl₂ → K⁺[ICl₂]⁻
[IBr₂]⁻^[8]	CsI + Br₂ → Cs⁺[IBr₂]⁻
[AtBr₂]⁻, [AtICl]⁻, [AtIBr]⁻, [AtI₂]⁻	AtY + X⁻ → [AtXY]⁻ (X = I, Br, Cl; Y = I, Br)
[ClF₄]⁻	NOF + ClF₃ → [NO]⁺[ClF₄]⁻
[BrF₄]⁻	6 KCl + 8 BrF₃ → 6 K⁺[BrF₄]⁻ + 3 Cl₂ + Br₂	excess BrF₅ needed
[IF₄]⁻	2 XeF₂ + [Me₄N]⁺I⁻ → [Me₄N]⁺[IF₄]⁻ + 2 Xe	the reactants were mixed at 242K, then warmed to 298K for the reaction to proceed
[ICl₄]⁻^[9]	KI + ICl₃ → K⁺[ICl₄]⁻
[IF₅]²⁻	IF₃ + 2 [Me₄N]⁺F⁻ → [Me₄N⁺]₂[IF₅]²⁻
[IF₆]⁻	IF₅ + CsF → Cs⁺[IF₆]⁻
[I₃Br₄]⁻	[PPh₄]⁺Br⁻ + 3 IBr → [PPh₄]⁺[I₃Br₄]⁻
[IF₈]⁻	IF₇ + [Me₄N]⁺F⁻ → [Me₄N]⁺[IF₈]⁻	in acetonitrile

The higher polyiodides were formed upon crystallization of solutions containing various concentrations of I⁻ and I₂. For instance, the monohydrate of KI₃ crystallizes when a saturated solution containing appropriate amounts of I₂ and KI is cooled.^[10]

Properties

Stability

In general, a large counter cation or anion (such as Cs⁺, [SbF₆]⁻) can help stabilize the polyhalogen ions formed in the solid state from lattice energy considerations, as the packing efficiency was increased.

The polyhalogen cations are strong oxidizing agents, as indicated by the fact that they can only be prepared in oxidative liquids as a solvent, such as oleum. The most oxidizing and therefore most unstable ones are the species [X₂]⁺ and [XF₆]⁺ (X = Cl, Br), followed by [X₃]⁺ and [IF₆]⁺.

The stability of the [X₂]⁺ salts (X = Br, I) are thermodynamically quite stable. However, their stability in solution depends on the superacid solvent. For example, [I₂]⁺ is stable in HF of highest highest acidity (HF with 0.2N SbF₅, H₀ = -20.65), but disproportionates to [I₃]⁺, [I₅]⁺ and I₂ as acidity is decreased by adding different amounts of NbF₅, TaF₅ or NaF.^[4]

14 [I₂]⁺ + 5 F⁻ → 9 [I₃]⁺ + IF₅

For polyhalogen anions with the same cation, the more stable ones are those with a heavier halogen at the center, symmetric ions are also more stable than asymmetric ones. therefore the stability of the anions decrease in the order:

[I₃]⁻ > [IBr₂]⁻ > [ICl₂]⁻ > [I₂Br]⁻ > [Br₃]⁻ > [BrCl₂]⁻ > [Br₂Cl]⁻

Heteropolyhalogen ions with a coordination number larger than or equal to four can only exist with fluoride ligands.

Color

Most polyhalogen ions are intensely colored, with deepened color as the atomic weight of the constituent element increases. The well-known starch-iodine complex has a deep blue color due to the linear [I₅]⁻ ions present in the amylose helix.^[4] Some colors of the common species were listed below:^[3]

fluorocations tend to be colorless or pale yellow, other heteropolyhalogen ions are orange, red or deep purple^[4]
compounds of [ICl₂]⁺ are wine red to bright orange; while that of [I₂Cl]⁺ are dark brown to purplish black
[Cl₃]⁺ is yellow
[Cl₄]⁺ is blue^[2]
[Br₂]⁺ is cherry red
[Br₃]⁺ is brown
[Br₅]⁺ is dark brown
[I₂]⁺ is bright blue
[I₃]⁺ is dark brown to black
[I₄]²⁺ is red to brown
[I₅]⁺ is green or black, the salt [I₅]⁺[AlCl₄]⁻ exists as greenish-black needles, but appears brown-red in thin sections
[I₇]⁺ is black, if its existence in the compound I₇SO₃F has been firmly established
[I₁₅]³⁺ is black^[5]
[ICl₄]⁻ is golden-yellow
polyiodides have very dark colors, either dark brown or dark blue

Chemical properties

The heteropolyhalogen cations are explosively reactive oxidants, and the cations often have higher reactivity than their parent interhalogens and decompose by reductive pathways. As expected from the highest oxidation state of +7 in [ClF₆]⁺, [BrF₆]⁺ and [IF₆]⁺, these species are extremely strong oxidizing agents, demonstrated by the reactions shown below:

2 O₂ + 2 [BrF₆]⁺[AsF₆]⁻ →2 [O₂]⁺[AsF₆]⁻ + 2 BrF₅ + F₂

Rn + [IF₆]⁺[SbF₆]⁻ →[RnF]⁺[SbF₆]⁻ + IF₅

Polyhalogen cations with lower oxidation states tend to disproportionate. For example, [Cl₂F]⁺ is unstable in solution and disproportionate completely in HF/SbF₅ even at 197K:

2 [Cl₂F]⁺ → [ClF₂]⁺ + [Cl₃]⁺

[I₂]⁺ reversibly dimerizes at 193K, and is observed as the blue color of paramagnetic [I₂]⁺ dramatically shifts to the red-brown color of diamagnetic [I₂]⁺, together with a drop in paramagnetic susceptibility and electrical conductivity when the solution is cooled to below 193K:^[2]

2 [I₂]⁺

[I₄]²⁺

The dimerization can be attributed to the overlapping of the half-filled π* orbitals in two [I₂]⁺.

[Cl₄]⁺ in [Cl₄]⁺[IrF₆]⁻ is structurally analogous to [I₄]²⁺, but decomposes at 195K to give salts of [Cl₃]⁺ instead of [Cl₂]⁺ and Cl₂.^[2]

Attempts to prepare ClF₇ and BrF₇ by fluorinating [ClF₆]⁺ and [BrF₆]⁺ using NOF have met with failure, instead the following reactions occurred:^[3]

[ClF₆]⁺[PtF₆]⁻ + NOF →[NO]⁺[PtF₆]⁻ + ClF₅ + F₂

[BrF₆]⁺[AsF₆]⁻ + 2 NOF →[NO]⁺[AsF₆]⁻ + [NO]⁺[BrF₆]⁻ + F₂

The anions are less reactive compared to the cations, and are generally weaker oxidants than their parent interhalogens. They are less reactive towards organic compounds, and some salts are of quite high thermal stability. Salts containing polyhalogen anions of the type M⁺[X_mY_nZ_p]⁻ (where m+n+p = 3, 5, 7, 9...) tend to dissociate into simple monohalide salts between M⁺ and the most electronegative halogen, so that the monohalide has the highest lattice energy. An interhalogen is usually formed as the other product. The salt [Me₄N]⁺[ClF₄]⁻ decomposes at about 100 °C, and salts of [ClF₆]⁻ are thermally unstable and can explode even at -31 °C.^[4]

References

1 2 3 4 R. Bruce King (2005). "Chlorine, Bromine, Iodine, & Astatine: Inorganic Chemistry". Encyclopedia of Inorganic Chemistry, 2nd edition. Wiley. p. 747. ISBN 9780470862100.
1 2 3 4 5 6 7 8 9 Catherine E. Housecroft; Alan G. Sharpe (2008). "Chapter 17: The group 17 elements". Inorganic Chemistry, 3rd Edition. Pearson. p. 547. ISBN 978-0-13-175553-6.
1 2 3 4 5 6 7 Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 835. ISBN 0-08-037941-9.
1 2 3 4 5 6 7 8 F. Albert Cotton; Geoffrey Wilkinson; Carlos A. Murillo; Manfred Bochmann (1999). Advanced Inorganic Chemistry, 6th Edition. Wiley. ISBN 978-0471199571.
1 2 Wiberg, Egon; Wiberg, Nils and Holleman, Arnold Frederick (2001). Inorganic chemistry. Academic Press. pp. 419–420. ISBN 0-12-352651-5.
↑ "Cesium dichlorobromide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 294.
↑ "Potassium dichloroiodide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 295.
↑ "Cesium dibromoiodide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 297.
↑ "Potassium tetrachloroiodide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 298.
↑ "Potassium triiodide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 294.

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