The polyiodides are a class of polyhalogen anions composed entirely of iodine atoms.[1][2] The most common member is the triiodide ion, I
3
. 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 I
3
building blocks.

Preparation

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The polyiodides can be made by addition of stoichiometric amounts of I2 to solutions containing I and I
3
, 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

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The 14-membered ring array of iodine atoms in [([16]aneS4)PdIPd([16]aneS4)][I11]
 
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 I
3
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)+
3
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 [I
3
·I2·I
8
] or [I
3
·I
5
]
[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 I
3
and I2 units
[I10]2− [Cd(12-crown-4)2]2+; Theophyllinium twisted ring configuration with two I
3
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 (I
3
·I2·I·I2·I·I2·I
3
)[12]
[I16]2− [Me2Ph2N]+ centrosymmetric arrangement of [I
7
·I2·I
7
]
[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 112 of the I2 molecules
[I29]3− Cp2Fe+ an anionic 3D network with a cage-like structure of [{(I
5
)12·I2}·{(I2−
12
)12·I2}·I2], with [Cp2Fe]+ ions interacting with the anion in the cavities[13]
[I]δ− Pyrroloperylene+• Infinite polyiodide homopolymer.[14]
 
Structures of some polyiodide ions.

Reactivity

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Polyiodide compounds are generally sensitive to light.

Triiodide, I
3
, undergoes unimolecular photodissociation.[15][16] Polyiodide has been used to improve the scalability in the synthesis of halide perovskite photovoltaic materials.[17]

Conductivity

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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

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References

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  1. ^ Housecroft, Catherine E.; Sharpe, Alan G. (2008). "Chapter 17: The group 17 elements". Inorganic Chemistry (3rd ed.). Pearson. p. 547. ISBN 978-0-13-175553-6.
  2. ^ Kloo, Lars (2021), "Catenated compounds in Group 17—Polyhalides", Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, Elsevier, pp. 1021–1049, doi:10.1016/b978-0-12-823144-9.00013-3, ISBN 978-0-12-409547-2, S2CID 242567501, retrieved 2022-03-28
  3. ^ Brauer, G., ed. (1963). "Potassium triiodide". Handbook of Preparative Inorganic Chemistry. Vol. 1 (2nd ed.). New York: Academic Press. p. 294.
  4. ^ Svensson, Per H.; Gorlov, Mikhail; Kloo, Lars (2008-12-15). "Dimensional Caging of Polyiodides". Inorganic Chemistry. 47 (24): 11464–11466. doi:10.1021/ic801820s. ISSN 0020-1669. PMID 19053351.
  5. ^ García, Marcos D.; Martí-Rujas, Javier; Metrangolo, Pierangelo; Peinador, Carlos; Pilati, Tullio; Resnati, Giuseppe; Terraneo, Giancarlo; Ursini, Maurizio (2011). "Dimensional caging of polyiodides: cation-templated synthesis using bipyridinium salts". CrystEngComm. 13 (13): 4411. doi:10.1039/c0ce00860e. ISSN 1466-8033.
  6. ^ King, R. Bruce (2005). "Chlorine, Bromine, Iodine, & Astatine: Inorganic Chemistry". Encyclopedia of Inorganic Chemistry (2nd ed.). Wiley. p. 747. ISBN 9780470862100.
  7. ^ Rzepa, Henry (May 16, 2009). "The mystery of the Finkelstein reaction". Chemistry with a twist.
  8. ^ Howie, R. Alan; Wardell, James L. (2003-05-15). "Polymeric tris(μ2-acetone-κ2O:O)sodium polyiodide at 120 K". Acta Crystallographica Section C Crystal Structure Communications. 59 (5): m184–m186. doi:10.1107/S0108270103006395. ISSN 0108-2701. PMID 12743392.
  9. ^ Svensson, Per H.; Kloo, Lars (2003). "Synthesis, Structure, and Bonding in Polyiodide and Metal Iodide–Iodine Systems". Chem. Rev. 103 (5): 1649–84. doi:10.1021/cr0204101. PMID 12744691.
  10. ^ Reiss, Guido J.; Van Megen, Martin (2013). "I62− Anion Composed of Two Asymmetric Triiodide Moieties: A Competition between Halogen and Hydrogen Bond". Inorganics. 1 (1): 3–13. doi:10.3390/inorganics1010003.
  11. ^ Reiss, Guido J. (2019-06-26). "A cyclic I102− anion in the layered crystal structure of theophyllinium pentaiodide, C7H9I5N4O2". Zeitschrift für Kristallographie – New Crystal Structures. 234 (4): 737–739. doi:10.1515/ncrs-2019-0082. ISSN 2197-4578.
  12. ^ Reiss, Guido J.; Megen, Martin van (2012). "Two New Polyiodides in the 4,4′-Bipyridinium Diiodide/Iodine System". Zeitschrift für Naturforschung B. 67 (1): 5–10. doi:10.1515/znb-2012-0102. ISSN 1865-7117. S2CID 5857644.
  13. ^ Tebbe, Karl-Friedrich; Buchem, Rita (1997-06-16). "Das bisher iodreichste Polyiodid: Herstellung und Struktur von Fc3I29". Angewandte Chemie (in German). 109 (12): 1403–1405. Bibcode:1997AngCh.109.1403T. doi:10.1002/ange.19971091233.
  14. ^ Madhu, Sheri; Evans, Hayden A.; Doan-Nguyen, Vicky V. T.; Labram, John G.; Wu, Guang; Chabinyc, Michael L.; Seshadri, Ram; Wudl, Fred (4 July 2016). "Infinite Polyiodide Chains in the Pyrroloperylene–Iodine Complex: Insights into the Starch-Iodine and Perylene-Iodine Complexes". Angewandte Chemie International Edition. 55 (28): 8032–8035. doi:10.1002/anie.201601585. PMID 27239781. S2CID 30407996.
  15. ^ Hoops, Alexandra A.; Gascooke, Jason R.; Faulhaber, Ann Elise; Kautzman, Kathryn E.; Neumark, Daniel M. (May 2004). "Two- and three-body photodissociation of gas phase I3−". The Journal of Chemical Physics. 120 (17): 7901–7909. doi:10.1063/1.1691017. hdl:2440/34955. ISSN 0021-9606. PMID 15267705.
  16. ^ Nakanishi, Ryuzo; Saitou, Naoya; Ohno, Tomoyo; Kowashi, Satomi; Yabushita, Satoshi; Nagata, Takashi (2007-05-28). "Photodissociation of gas-phase I3−: Comprehensive understanding of nonadiabatic dissociation dynamics". The Journal of Chemical Physics. 126 (20): 204311. doi:10.1063/1.2736691. ISSN 0021-9606. PMID 17552766.
  17. ^ Turkevych, Ivan; Kazaoui, Said; Belich, Nikolai A.; Grishko, Aleksei Y.; Fateev, Sergey A.; Petrov, Andrey A.; Urano, Toshiyuki; Aramaki, Shinji; Kosar, Sonya; Kondo, Michio; Goodilin, Eugene A. (January 2019). "Strategic advantages of reactive polyiodide melts for scalable perovskite photovoltaics". Nature Nanotechnology. 14 (1): 57–63. doi:10.1038/s41565-018-0304-y. ISSN 1748-3395. PMID 30478274. S2CID 53784226.
  18. ^ Alvarez, Santiago; Novoa, Juan; Mota, Fernando (1986-12-26). "The mechanism of electrical conductivity along polyhalide chains". Chemical Physics Letters. 132 (6): 531–534. doi:10.1016/0009-2614(86)87118-4.
  19. ^ Yu, Hongtao; Yan, Lijia; He, Yaowu; Meng, Hong; Huang, Wei (2017). "An unusual photoconductive property of polyiodide and enhancement by catenating with 3-thiophenemethylamine salt". Chemical Communications. 53 (2): 432–435. doi:10.1039/C6CC08595D. ISSN 1359-7345. PMID 27965990.
  20. ^ Poręba, Tomasz; Ernst, Michelle; Zimmer, Dominik; Macchi, Piero; Casati, Nicola (2019-05-13). "Pressure-Induced Polymerization and Electrical Conductivity of a Polyiodide". Angewandte Chemie International Edition. 58 (20): 6625–6629. doi:10.1002/anie.201901178. ISSN 1433-7851. PMID 30844119. S2CID 73514885.