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Journal articles on the topic 'Triiodide'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Edis, Haj Bloukh, Abu Sara, Bhakhoa, Rhyman, and Ramasami. "“Smart” Triiodide Compounds: Does Halogen Bonding Influence Antimicrobial Activities?" Pathogens 8, no. 4 (2019): 182. http://dx.doi.org/10.3390/pathogens8040182.

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Antimicrobial agents containing symmetrical triiodides complexes with halogen bonding may release free iodine molecules in a controlled manner. This happens due to interactions with the plasma membrane of microorganisms which lead to changes in the structure of the triiodide anion. To verify this hypothesis, the triiodide complex [Na(12-crown-4)2]I3 was prepared by an optimized one-pot synthesis and tested against 18 clinical isolates, 10 reference strains of pathogens and five antibiotics. The antimicrobial activities of this symmetrical triiodide complex were determined by zone of inhibition

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2

Yushina, Irina, Natalya Tarasova, Dmitry Kim, Vladimir Sharutin, and Ekaterina Bartashevich. "Noncovalent Bonds, Spectral and Thermal Properties of Substituted Thiazolo[2,3-b][1,3]thiazinium Triiodides." Crystals 9, no. 10 (2019): 506. http://dx.doi.org/10.3390/cryst9100506.

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The interrelation between noncovalent bonds and physicochemical properties is in the spotlight due to the practical aspects in the field of crystalline material design. Such study requires a number of similar substances in order to reveal the effect of structural features on observed properties. For this reason, we analyzed a series of three substituted thiazolo[2,3-b][1,3]thiazinium triiodides synthesized by an iodocyclization reaction. They have been characterized with the use of X-ray diffraction, Raman spectroscopy, and thermal analysis. Various types of noncovalent interactions have been

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3

Bandara, Madhushi, Khadijatul Kobra, Spencer R. Watts, et al. "Synthesis and Characterization of New Organoammonium, Thiazolium, and Pyridinium Triiodide Salts: Crystal Structures, Polymorphism, and Thermal Stability." Crystals 14, no. 12 (2024): 1020. http://dx.doi.org/10.3390/cryst14121020.

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Triiodide salts are of interest for a variety of applications, including but not limited to electrochemical and photochemical devices, as antimicrobials and disinfectants, in supramolecular chemistry and crystal engineering, and in ionic liquids and deep eutectic solvents. Our work has focused on the design of salt–solvate cocrystals and deep eutectic solvents in which the triiodide anion interacts as a halogen bond acceptor with organoiodine molecules. To understand structure–property relationships in these hybrid materials, it is essential to have benchmark structural and physical data for t

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4

Ledesma, Gabriela N., Ernesto Schulz Lang, and Ulrich Abram. "2,4,6-Triphenylphenyltellurium(IV) triiodide – supramolecular self-assembling in organotellurium triiodides." Journal of Organometallic Chemistry 689, no. 12 (2004): 2092–95. http://dx.doi.org/10.1016/j.jorganchem.2004.03.034.

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5

Parvez, M., M. Wang, and P. M. Boorman. "Tetraphenylphosphonium Triiodide." Acta Crystallographica Section C Crystal Structure Communications 52, no. 2 (1996): 377–78. http://dx.doi.org/10.1107/s0108270195010456.

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6

Zhang, Yuanmin. "Samarium Triiodide." Synlett 2011, no. 11 (2011): 1638–39. http://dx.doi.org/10.1055/s-0030-1260781.

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7

Tornieporth-Oetting, Inis, and Thomas Klapötke. "Nitrogen Triiodide." Angewandte Chemie International Edition in English 29, no. 6 (1990): 677–79. http://dx.doi.org/10.1002/anie.199006771.

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8

Abu Talip, Ruwaida Asyikin, Wan Zaireen Nisa Yahya, and Mohamad Azmi Bustam. "Viscosity and Ionic Conductivity of Imidazolium based Ionic Liquids bearing Triiodide Anion." E3S Web of Conferences 287 (2021): 02015. http://dx.doi.org/10.1051/e3sconf/202128702015.

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In the electrolyte application for dye sensitized solar cells, utilization of ionic liquids is getting the highlights to replace volatile organic solvent thanks to their low volatility, thermal and electrochemical stability. The iodide/triiodide redox electrolyte is the preferred choice for this application, hence numerous iodide-based ionic liquids have been explored and reported. On the contrary, the transport properties of triiodide based ionic liquid is often lack of reporting despite of having an equal influence on the overall viscosity and ionic conductivity of the electrolyte. In this s

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9

Anderson, A., J. A. Campbell, and R. W. G. Syme. "Raman spectra of crystalline antimony triiodide and arsenic triiodide." Journal of Raman Spectroscopy 19, no. 6 (1988): 379–82. http://dx.doi.org/10.1002/jrs.1250190602.

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10

Rudiuk, Vitalii V., Anna M. Shaposhnyk, Vyacheslav M. Baumer, Igor A. Levandovskiy, and Svitlana V. Shishkina. "Salts of 4-[(benzylamino)carbonyl]-1-methylpyridinium and iodide anions with different cation:iodine stoichiometric ratios." Acta Crystallographica Section E Crystallographic Communications 77, no. 12 (2021): 1219–23. http://dx.doi.org/10.1107/s2056989021011300.

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The two iodide salts, 4-[(benzylamino)carbonyl]-1-methylpyridinium iodide–iodine (2/1), C14H15N2O+·I−·0.5I2, I, and 4-[(benzylamino)carbonyl]-1-methylpyridinium triiodide, C14H15N2O+·I3 −, II, with different cation:iodine atoms ratios were studied. Salt I contains one cation, one iodide anion and half of the neutral I2 molecule in the asymmetric unit (cation:iodine atoms ratio is 1:2). Salt II contains two cations, one triiodide anion (I 3 −) and two half triiodide anions (cation:iodine atoms ratio is 1:3). The NH group forms N—H...I hydrogen bonds with the I− anion in the crystal of I or N—H.

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11

Pennington, William, Madhushi Bandara, Andrew Peloquin, and Colin McMillen. "Where are the crystals? X-DES: Deep Eutectic Solvents based on Halogen Bonding." Structural Dynamics 12, no. 2_Supplement (2025): A134. https://doi.org/10.1063/4.0000443.

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As a crystallographer, nothing is sadder than failed crystal growth. As an “experienced” crystallographer (a basketball ref couldn't hand signal my number of years), I’ve thrown away more than my share of oily smudges (always according to established hazardous waste procedures, of course). Fortunately, my students are more curious than I. Recently we reported the first halogen-bonding-based deep eutectic solvent, which consisted of a mixture of 1,3-dithiane and o- diiodotetrafluorobenzene – a system that simply refused to cooperate during crystal growth (Peloquin et al. Angew Chem, Int. Ed.202

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12

Timofte, Tudor, Arash Babai, Gerd Meyer, and Anja-Verena Mudring. "Neodymium triiodide nonahydrate." Acta Crystallographica Section E Structure Reports Online 61, no. 5 (2005): i87—i88. http://dx.doi.org/10.1107/s160053680501216x.

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13

Timofte, Tudor, Arash Babai, Gerd Meyer, and Anja-Verena Mudring. "Praseodymium triiodide nonahydrate." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): i94—i95. http://dx.doi.org/10.1107/s1600536805012857.

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14

Jongen, Liesbet, and Gerd Meyer. "Yttrium triiodide, YI3." Acta Crystallographica Section E Structure Reports Online 61, no. 8 (2005): i151—i152. http://dx.doi.org/10.1107/s1600536805019847.

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15

Alikberova, Ludmila Yu, Dmitry V. Albov, Denis V. Golubev, Valery V. Kravchenko, and Nataliya S. Rukk. "Tetraaquatetraureaneodymium(III) triiodide." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (2007): m3078. http://dx.doi.org/10.1107/s1600536807058643.

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16

Blake, Alexander J., Claudia Caltagirone, Vito Lippolis, Martin Schröder, and Claire Wilson. "(Ferrocenylmethyl)trimethylammonium triiodide." Acta Crystallographica Section E Structure Reports Online 60, no. 1 (2003): m20—m21. http://dx.doi.org/10.1107/s1600536803026084.

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17

Tan, Xue-Jie, Si-Xiu Sun, Shu-Lian Liu, Jian-Ping Ma, and Dian-Xiang Xing. "1,4-Dimethylpyridinium triiodide." Acta Crystallographica Section E Structure Reports Online 61, no. 3 (2005): o756—o757. http://dx.doi.org/10.1107/s1600536805005301.

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18

Savinkina, Elena V., Yana F. Al Ansari, Ilia A. Zamilatskov, Dmitry V. Albov, and Aslan Yu Tsivadze. "Octaureasamarium(III) triiodide." Acta Crystallographica Section E Structure Reports Online 61, no. 4 (2005): m664—m666. http://dx.doi.org/10.1107/s1600536805006781.

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19

Reiss, Guido J., and Martin van Megen. "Two New Polyiodides in the 4,4´-Bipyridinium Diiodide/Iodine System." Zeitschrift für Naturforschung B 67, no. 1 (2012): 5–10. http://dx.doi.org/10.1515/znb-2012-0102.

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The reaction of bipyridine with hydroiodic acid in the presence of iodine gave two new polyiodide-containing salts best described as 4,4´-bipyridinium bis(triiodide), C10H10N2[I3]2, 1, and bis(4,4´-bipyridinium) diiodide bis(triiodide) tris(diiodine) solvate dihydrate, (C10H10N2)2I2[I3]2 · 3 I2 ·2H2O, 2. Both compounds have been structurally characterized by crystallographic and spectroscopic methods (Raman and IR). Compound 1 is composed of I3 − anions forming one-dimensional polymers connected by interionic halogen bonds. These chains run along [101] with one crystallographically independent

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20

Bartashevich, E. V., V. I. Batalov, I. D. Yushina, A. I. Stash, and Y. S. Chen. "Nontypical iodine–halogen bonds in the crystal structure of (3E)-8-chloro-3-iodomethylidene-2,3-dihydro-1,4-oxazino[2,3,4-ij]quinolin-4-ium triiodide." Acta Crystallographica Section C Structural Chemistry 72, no. 4 (2016): 341–45. http://dx.doi.org/10.1107/s2053229616003934.

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Two kinds of iodine–iodine halogen bonds are the focus of our attention in the crystal structure of the title salt, C12H8ClINO+·I3−, described by X-ray diffraction. The first kind is a halogen bond, reinforced by charges, between the I atom of the heterocyclic cation and the triiodide anion. The second kind is the rare case of a halogen bond between the terminal atoms of neighbouring triiodide anions. The influence of relatively weakly bound iodine inside an asymmetric triiodide anion on the thermal and Raman spectroscopic properties has been demonstrated.

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21

Duan, Yanyan, Qunwei Tang, Yuran Chen, et al. "Solid-state dye-sensitized solar cells from poly(ethylene oxide)/polyaniline electrolytes with catalytic and hole-transporting characteristics." Journal of Materials Chemistry A 3, no. 10 (2015): 5368–74. http://dx.doi.org/10.1039/c4ta06393g.

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Iodide/triiodide-incorporated PEO/PANi solid-state electrolyte is realized for dye-sensitized solar cell with the aim of expanding the catalytic event of the triiodide species and shortening the charge diffusion path length, yielding an impressive efficiency of 6.1%.

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22

Lee, Haeri, Eunkyung Choi, Tae Hwan Noh, and Ok-Sang Jung. "Recyclable scavengers for photo-cyclopropanation via an in situ crystallization process." Dalton Transactions 45, no. 46 (2016): 18476–83. http://dx.doi.org/10.1039/c6dt02604d.

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A tripalladium(ii) cyclophane system containing transannular π⋯π interactions acts as an efficient and quantitative triiodide scavenger through in situ crystallization of triiodide-exchanged species during a photoreaction. The recycling behavior can be ascribed to the rigidity and stability of the molecules.

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23

Perez-Benito, Joaquin F., Enrique Brillas, and Conchita Arias. "Iodimetric determinations in organic solvents: Determination of manganese oxidation states in methylene chloride solutions." Canadian Journal of Chemistry 68, no. 1 (1990): 79–81. http://dx.doi.org/10.1139/v90-016.

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An iodimetric technique has been developed to quantitatively analyze the oxidants present in organic solutions. Addition of excess tetrabutylammonium iodide and excess glacial acetic acid results in the formation of tetrabutylammonium triiodide, whose concentration can be measured spectrophotometrically at 295 or 365 nm. Application of this technique to the determination of the final oxidation state of manganese in permanganate reactions in methylene chloride solutions is described. The equilibrium constant for formation of tetrabutylammonium triiodide in methylene chloride has been measured:

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24

Esposito, A., A. Lukas, J. E. Meany, and Y. Pocker. "The reversible enolization and hydration of pyruvate: possible roles of keto, enol, and hydrated pyruvate in lactate dehydrogenase catalysis." Canadian Journal of Chemistry 77, no. 5-6 (1999): 1108–17. http://dx.doi.org/10.1139/v99-071.

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The reversible enolization and hydration of pyruvic acid and pyruvate anion were monitored using spectrophotometric methods at several temperatures. Widely varying values for the equilibrium constant for the enolization of pyruvic acid and pyruvate ion appear in the literature. To accurately determine the position of equilibrium for the enolization reaction, we have developed a method that gives consistent results in which purified samples of sodium pyruvate are first "titrated" with triiodide ion to remove any triiodide-scavenging impurities such as those resulting from aldol condensation rea

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25

Lien, Shui-Yang, Shao-Yu Liu, Wen-Ray Chen, et al. "The Influence of Argon Plasma on Organic Perovskite MAPbI3 Film Doped with Inorganic Perovskite CsPbI3 Quantum Dots (QDs)." Crystals 12, no. 6 (2022): 799. http://dx.doi.org/10.3390/cryst12060799.

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In this study, the inorganic perovskite cesium lead triiodide (CsPbI3) quantum dots (QDs) produced by hot-injection method were added into the hybrid perovskite methylamine lead triiodide (CH3NH3PbI3; MAPbI3) to form composite perovskite film. It is not easy for argon (Ar) to react with perovskite. Therefore, argon plasma was used to optimize the properties of the surface. However, methylamine lead triiodide molecular will be degraded by excessive wattage. Therefore, the influence of plasma power acting on composite perovskite film was investigated. The experimental results show that the light

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26

Kut, D., Ye Mahada, M. Fershal, and M. Kut. "SYNTHESIS OF QUATERNIZED THIAZOLOQUINAZOLINIUM TRIIODIDE AND ITS APPLICATION AS AN ACTIVE SUBSTANCE FOR POTENTIOMETRIC SENSOR." Scientific Bulletin of the Uzhhorod University. Series «Chemistry» 51, no. 1 (2024): 82–95. http://dx.doi.org/10.24144/2414-0260.2024.1.82-95.

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For the first time, the synthesis, isolation, and identification of angular triiodide, 1,2,4,5-tetrahydro-4-ethyl-1-(iodomethyl)-1-methyl-5-oxothiazolo[3,2-a]quinazolin-10-ium, have been achieved. The formation of the triiodide was confirmed by elemental analysis, and its structure was approved by NMR spectra containing signals from the fused thiazolonine ring. The cyclization process was confirmed by the change in signal multiplicity from singlets (thioether) to doublets (thiazole) and a shift to a weaker field in the spectrum of the methyl group from 1.83 ppm to 2.15 ppm. Optimal reaction co

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27

Kobra, Khadijatul, Shaun O’Donnell, Andrew Ferrari, Colin D. McMillen, and William T. Pennington. "Halogen bonding and triiodide asymmetry in cocrystals of triphenylmethylphosphonium triiodide with organoiodines." New Journal of Chemistry 42, no. 13 (2018): 10518–28. http://dx.doi.org/10.1039/c8nj01373j.

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28

Kollitz, Megan R., Allen G. Oliver та A. Graham Lappin. "Structure of Λ(δλλ)-[Co(en)3]I3(I)2". Acta Crystallographica Section E Crystallographic Communications 77, № 4 (2021): 446–49. http://dx.doi.org/10.1107/s2056989021002826.

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The structure of tris(ethane-1,2-diamine-κ2 N,N')cobalt(III) bis(iodide) triiodide, [Co(C2H8N2)3]I3(I)2, at 120 K has orthorhombic (P212121) symmetry. The diamine nitrogen atoms form N—H...I hydrogen bonds throughout the lattice, resulting in a three-dimensional network, which involves the iodide and all atoms in the triiodide anions.

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29

Siczek, Miłosz, Marta S. Krawczyk, and Tadeusz Lis. "trans-Dioxidotetrapyridinerhenium(V) triiodide." Acta Crystallographica Section E Structure Reports Online 65, no. 9 (2009): m1057. http://dx.doi.org/10.1107/s1600536809030724.

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30

Billing, David G., Robert S. Black, and Wonga M. Hexana. "4-Nitroanilinium triiodide monohydrate." Acta Crystallographica Section E Structure Reports Online 66, no. 5 (2010): o1186. http://dx.doi.org/10.1107/s1600536810014674.

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31

Gainsford, Graeme J., and Tim Kemmitt. "Dihydrobis(methylamine)borate triiodide." Acta Crystallographica Section C Crystal Structure Communications 62, no. 10 (2006): o602—o604. http://dx.doi.org/10.1107/s010827010603335x.

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32

Nurtaeva, A. K., G. Hu, and E. M. Holt. "Tetraethylammonium Dicopper(I) Triiodide and (18-Crown-6)potassium Dicopper(I) Triiodide." Acta Crystallographica Section C Crystal Structure Communications 54, no. 5 (1998): 597–600. http://dx.doi.org/10.1107/s0108270197017496.

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33

Reiss, Guido J. "I5– polymers with a layered arrangement: synthesis, spectroscopy, and structure of a new polyiodide salt in the nicotine/HI/I2 system." Zeitschrift für Naturforschung B 70, no. 10 (2015): 735–39. http://dx.doi.org/10.1515/znb-2015-0092.

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AbstractThe reaction of S-nicotine with hydroiodic acid in the presence of iodine gave the new polyiodide-containing salt nicotine-1,1′-diium bis(triiodide)-diiodine (1/1) (C10H16N2) [I3]2·I2 (1). The title compound has been characterised by spectroscopic methods (Raman and IR) and single-crystal X-ray diffraction. The asymmetric unit of the title structure consists of one dication, two triiodide anions, and one iodine molecule, all located in general positions in the non-centrosymmetric space group P1. One of the two crystallographically independent triiodide anions and the doubly protonated

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34

J., P. SAXENA, LODHA VANDANA та KHIVSARA PRITI. "Studies on Quaternary β-Ketoalkyl Iodides and Triiodides of some Heterocyclic Bases". Journal of Indian Chemical Society Vol. 62, Sep 1985 (1985): 684–86. https://doi.org/10.5281/zenodo.6322746.

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Department of Chemistry, University of Jodhpur, Jodhpur-142 001 <em>Manuscript received 29 September 1984, revised 24 June 1985, accepted 11 September 1985</em> Isobutyl methyl ketone reacted with iodine in presence of heterocyclic tertiary bases, <em>viz</em>. pyridine, quinoline, isoquinoline, and α-, β- and \(\gamma\)-picolines using isopropanol as solvent, resulting in the formation of a series of quaternary <em>N</em>-(2-oxopentyl-4-methyl)ammonium iodides. When acetic acid was used as medium of reaction the triiodides of quaternary <em>N</em>-(2-oxopentyl-4-methyl)animoni

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35

Il’inykh, E., and V. Sharutin. "Synthesis and study of the structure of iodine-containing imidazo[2,1-b][1,3]thiazinium systems." Bulletin of the South Ural State University series "Chemistry" 16, no. 1 (2024): 108–17. http://dx.doi.org/10.14529/chem240108.

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Heterocyclization of S-alkenyl derivatives of 1-methylimidazole-2-thiol (1-methyl-2-prenyl-sulfanylimidazole (1), 1-methyl-2-cinnamylsulfanylimidazole (4), and 2-(3-butenyl)sulfanyl-1-methyl-imidazole (7)) has been studied for the first time under the action of iodine (iodocyclization) in various solvents (chloroform, dichloro-methane, glacial acetic acid), and at different substrate and iodine ratios (1 : 1, 1 : 2). It has been found that the interaction of compounds 1, 4, 7 with iodine proceeds regioselectively, regardless of the reaction conditions, and it is accompanied by the linear annel

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36

Farhadi, Khalil, Ramin Maleki, and Mojtaba Shamsipur. "Triiodide Ion-Selective Polymeric Membrane Electrode Based on a Ketoconazole-Triiodide Ion Pair." Electroanalysis 14, no. 11 (2002): 760. http://dx.doi.org/10.1002/1521-4109(200206)14:11<760::aid-elan760>3.0.co;2-q.

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37

Owczarzak, Agata, Anna K. Przybył, and Maciej Kubicki. "Different cationic forms of (–)-cytisine in the crystal structures of its simple inorganic salts." Acta Crystallographica Section C Structural Chemistry 74, no. 11 (2018): 1518–30. http://dx.doi.org/10.1107/s2053229618012585.

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The crystal structures of 13 simple salts of cytisine, an alkaloid isolated from the seeds of Laburnum anagyroides, have been determined, namely cytisinium (6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-11-ium) bromide, C11H15N2O+·Br−, cytisinium iodide, C11H15N2O+·I−, cytisinium perchlorate, C11H15N2O+·ClO4 −, cytisinium iodide triiodide, C11H15N2O+·I−·I3 −, cytisinium chloride monohydrate, C11H15N2O+·Cl−·H2O, cytisinium iodide monohydrate, C11H15N2O+·I−·H2O, cytisinium nitrate monohydrate, C11H15N2O+·NO3 −·H2O, hydrogen dicytisinium tribromide, C22H31N4O2 3+·3Br−, hydrogen dicytisiniu

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38

Sakač, Nikola, Maja Karnaš, Jasminka Dobša, et al. "Application of Spectrophotometric Fingerprint in Cluster Analysis for Starch Origin Determination." Food Technology and Biotechnology 58, no. 1 (2020): 5–11. http://dx.doi.org/10.17113/ftb.58.01.20.6239.

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The botanical origin of starch is of importance in industrial applications and food processing because it may influence the properties of the final product. Current microscopic methods are time-consuming. Starch consists of an origin-dependent amylose/amylopectin ratio. Triiodide ions bind characteristically to the amylose and amylopectin depending on the botanical origin of the starch. The absorbance of the starch-triiodide complex was measured for wheat, potato, corn, rye, barley, rice, tapioca and unknown origin starch, and within the different cultivars. Each starch sample had specific par

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39

Nurtaeva, A. K., and E. M. Holt. "(15-Crown-5)caesium Dicopper(I) Triiodide, (15-Crown-5)potassium Dicopper(I) Triiodide and (15-Crown-5)rubidium Dicopper(I) Triiodide." Acta Crystallographica Section C Crystal Structure Communications 54, no. 5 (1998): 594–97. http://dx.doi.org/10.1107/s0108270197017502.

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40

Martynov, Yaroslav B., Rashid G. Nazmitdinov, Andreu Moià-Pol, et al. "On the efficiency limit of ZnO/CH3NH3PbI3/CuI perovskite solar cells." Physical Chemistry Chemical Physics 19, no. 30 (2017): 19916–21. http://dx.doi.org/10.1039/c7cp03892e.

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41

Kormosh, Z. A., T. I. Savchuk, D. I. Semenishin, S. V. Suprunovich, V. V. Kochubei, and S. I. Korolchuk. "Potentiometric Sensor For Analgin Determination In Pharmaceutical Formulations." Methods and Objects of Chemical Analysis 15, no. 2 (2020): 66–72. http://dx.doi.org/10.17721/moca.2020.66-72.

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Ion associates (IA) of butylrodamine C with triiodide and iod bromide have been synthesized. Their thermal behavior is investigated. Thermolysis synthesized by IA BR+I3¯ passes through a number of intermediate stages, since the C4H9 radical, which is part of the dye, has a significant effect on the process of thermolysis of the ionic associate. IA BR+I3¯ begins to decompose significantly at a temperature higher than 140 єC with an endothermic effect at 240 єC and two small exothermic effects with a maximum at 282 єC and 355 єC (corresponding to the release of 2NH3, 8C2H4, 2HI). In the range of

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42

Janczak, Jan, and Ynara Marina Idemori. "[Phthalocyaninato(2–)]arsenic(III) triiodide." Acta Crystallographica Section E Structure Reports Online 58, no. 1 (2001): m36—m38. http://dx.doi.org/10.1107/s1600536801021365.

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43

Szuromi, Phil. "Healing defects with triiodide ions." Science 356, no. 6345 (2017): 1346.15–1348. http://dx.doi.org/10.1126/science.356.6345.1346-o.

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44

Evans, Gwyndaf, and Gérard Bricogne. "Triiodide derivatization in protein crystallography." Acta Crystallographica Section D Biological Crystallography 59, no. 11 (2003): 1923–29. http://dx.doi.org/10.1107/s0907444903012897.

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Lin, Xiao Lan, Yun Jie Wang, Zhi Rong Chen, and Ji Bo Liu. "2,2′-Bipyridinium 1-oxide triiodide." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4322. http://dx.doi.org/10.1107/s1600536807049215.

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Abstract:

The title compound, C10H9N2O+·I3 −, was obtained unintentionally as the product of an attempted synthesis of an iodoplumbate complex using NaI as a donor to provide I−. The cation is planar (r.m.s. deviation for all non-H atoms is 0.024 Å) and has an intramolecular N—H...O hydrogen bond.

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Reiss, Guido J., and Peer B. Leske. "2-Aminopyridin-1-ium triiodide." Acta Crystallographica Section E Structure Reports Online 69, no. 7 (2013): o1060—o1061. http://dx.doi.org/10.1107/s1600536813015389.

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Son, Jung-Ho, and James D. Hoefelmeyer. "8-Iodoquinolinium triiodide tetrahydrofuran solvate." Acta Crystallographica Section E Structure Reports Online 64, no. 11 (2008): o2077. http://dx.doi.org/10.1107/s1600536808031516.

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Fialho De Assis, E., R. A. Howie, and J. L. Wardell. "2-(2-Pyridyl)pyridinium Triiodide." Acta Crystallographica Section C Crystal Structure Communications 52, no. 4 (1996): 955–57. http://dx.doi.org/10.1107/s0108270195014533.

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Chadha, R. K., John E. Drake, and Mary K. H. Neo. "Crystal structure of methylgermanium triiodide." Journal of Crystallographic and Spectroscopic Research 15, no. 1 (1985): 39–43. http://dx.doi.org/10.1007/bf01185715.

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Kochel, Andrzej. "4-(4-Pyridyl)pyridinium triiodide." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5605—o5606. http://dx.doi.org/10.1107/s1600536806047623.

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