Polyiodide

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Template:Short description The polyiodides are a class of polyhalogen anions composed entirely of iodine atoms.[1][2] The most common member is the triiodide ion, Template:Chem/link. Other known larger polyiodides include [I4]2−, [I5], [I6]2−, [I7], [I8]2−, [I9], [I10]2−, [I10]4−, [I11]3−, [I12]2−, [I13]3−, [I14]4-, [I16]2−, [I22]4−, [I26]3−, [I26]4−, [I28]4− and [I29]3−. All these can be considered as formed from the interaction of the I, I2, and Template:Chem/link building blocks.

Preparation

The polyiodides can be made by addition of stoichiometric amounts of I2 to solutions containing I and Template:Chem/link, with the presence of large countercations to stabilize them. For example, KI3·H2O can be crystallized from a saturated solution of KI when a stoichiometric amount of I2 is added and cooled.[3]

Structure

File:Solid state structure of the (I11)3- ion in (((16)aneS4)PdIPd((16)aneS4))(I11).png
The 14-membered ring array of iodine atoms in [([16]aneS4)PdIPd([16]aneS4)][I11]
File:Solid state structure of (I26)4- in (DMFc)4(I26).png
The primitive cubic lattice of iodide ions bridge by I2 molecules, present in [Cp*2Fe]4[I26]

Polyiodides adopt diverse structures. Most can be considered as associations of I2, I, and Template:Chem/link units. Discrete polyiodides are usually linear. The more complex two- or three-dimensional network structures of chains and cages are formed as the ions interact with each other, with their shapes depending on their associated cations quite strongly, a phenomenon named dimensional caging.[4][5] The table below lists the polyiodide salts which have been structurally characterized, along with their counter-cation.[6]

Structure of higher polyiodides
Anion Counter-cation Structural description
[I2] Na(C3H6O)Script error: No such module "Su". linear[7][8]
[I3] Cs+, (C4H9)4N+ linear
[I4]2− [Cu(NH3)4]2+ symmetric linear array of iodine atoms[9]
[I5] [EtMe3N]+ V-shaped with polymeric layers
[EtMePh2N]+ V-shaped with isolated [I5] ions
[I6]2− [NH3(CH2)8NH3]2+ almost linear [[10]]
[I7] [Ag(18aneS6)]+ an anionic network derived from a primitive rhombohedral lattice of iodide ions bridged by I2 molecules
[I8]2− [Ni(phen)3]2+ regular anionic shapes, can be described as [Template:Chem/link·I2·Template:Chem/link] or [Template:Chem/link·Template:Chem/link]
[I9] [Me2iPrPhN]+ 14-membered ring tied by two I2 bridges to give 10-membered rings
[Me4N]+ non-octahedral, but a twisted "h"-like arrangement of Template:Chem/link and I2 units
[I10]2− [Cd(12-crown-4)2]2+; Theophyllinium twisted ring configuration with two Template:Chem/link units linked by two I2 molecules[11]
[I11]3− [(16aneS4)PdIPd(16aneS4)]3+ 14-membered ring (9.66 × 12.64 Å) around the complex cation, with the rings interlink further to give an infinite 2D sheet
[I12]2− [Ag2(15aneS5)2]2+ extended 3D spiral superstructure supported by Ag–I bonds and weak I···S interactions
[Cu(Dafone)3]2+ planar configuration
[I13]3− [Me2Ph2N]+ consists of zigzag chains of I and I2
[I14]4− 4,4′-bipyridinium double hook (Template:Chem/link·I2·I·I2·I·I2·Template:Chem/link)[12]
[I16]2− [Me2Ph2N]+ centrosymmetric arrangement of [Template:Chem/link·I2·Template:Chem/link]
[iPrMe2PhN]+ the anion forms 14-membered rings catenated by I2 molecules, which further link into layers with 10- and 14-membered rings
[I22]4− [MePh3P]+ two L-shaped [I5] units linked by an I2 molecule and completed by two end-on [I5] groups
[I26]3− [Me3S]+ consists of [I5] and [I7] ions with intercalated I2 molecules
[I26]4− Cp*2Fe+ an anionic network derived from a primitive cubic lattice built from I ions, with I2 bridges on all edges and systematically removing <templatestyles src="Fraction/styles.css" />112 of the I2 molecules
[I29]3− Cp2Fe+ an anionic 3D network with a cage-like structure of [{(Template:Chem/link)Template:1/2·I2}·{(Template:Chem/link)Template:1/2·I2}·I2], with [Cp2Fe]+ ions interacting with the anion in the cavities[13]
[I]δ− Pyrroloperylene+• Infinite polyiodide homopolymer.[14]
File:Structures of some polyiodide ions.png
Structures of some polyiodide ions.

Reactivity

Polyiodide compounds are generally sensitive to light.

Triiodide, Template:Chem/link, undergoes unimolecular photodissociation.[15][16] Polyiodide has been used to improve the scalability in the synthesis of halide perovskite photovoltaic materials.[17]

Conductivity

Solid state compounds containing linear-chain polyiodide ions exhibit enhanced conductivity[18][19] than their simple iodide counterparts. The conductivity can be drastically modified by external pressure, which changes the interatomic distances between iodine moieties and the charge distribution.[20]

See also

References

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