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Organoiodine chemistry is the study of the synthesis and properties of organoiodine compounds, or organoiodides, organic compounds that contain one or more carbon–iodine bonds. They occur widely in organic chemistry, but are relatively rare in nature. The thyroxine hormones are organoiodine compounds that are required for health and the reason for government-mandated iodization of salt.

Structure, bonding, general properties

Almost all organoiodine compounds feature iodide connected to one carbon center. These are usually classified as derivatives of I. Some organoiodine compounds feature iodine in higher oxidation states.

The C–I bond is the weakest of the carbon–halogen bonds. These bond strengths correlate with the electronegativity of the halogen, decreasing in the order F > Cl > Br > I. This periodic order also follows the atomic radius of halogens and the length of the carbon-halogen bond. For example, in the molecules represented by CH₃X, where X is a halide, the carbon-X bonds have strengths, or bond dissociation energies, of 115, 83.7, 72.1, and 57.6 kcal/mol for X = fluoride, chloride, bromide, and iodide, respectively. Of the halides, iodide usually is the best leaving group. Because of the weakness of the C–I bond, samples of organoiodine compounds are often yellow due to an impurity of I₂.

A noteworthy aspect of organoiodine compounds is their high density, which arises from the high atomic weight of iodine. For example, one millilitre of methylene iodide weighs 3.325 g.

Industrial applications

Few organoiodine compounds are important industrially, at least in terms of large scale production. Iodide-containing intermediates are common in organic synthesis on the laboratory scale because of the easy formation and cleavage of the C–I bond. But the same lability of the C-I bond limits the applications of organoiodine compounds as drugs.

Industrially significant organoiodine compounds, often used as disinfectants or pesticides, are iodoform (CHI₃), methylene iodide (CH₂I₂), and methyl iodide (CH₃I). Although methyl iodide is not an industrially important product, it is an important intermediate, being a transiently generated intermediate in the industrial production of acetic acid and acetic anhydride. The potential for methyl iodide to replace the ubiquitous dependence on methyl bromide as a soil fumigant has been considered, however limited information is available on environmental behavior of the former. Ioxynil (3,5-diiodo-4-hydroxybenzonitrile), which inhibits photosynthesis at photosystem II, is among the very few organoiodine herbicides. A member of the hydroxybenzonitrile herbicide class, ioxynil is an iodinated analog of the brominated herbicide, bromoxynil (3,5-dibromo-4-hydroxybenzonitrile).

Iodinated and brominated organic compounds are of concern as environmental contaminants owing to very limited information available on environment fate behavior. However, recent reports have shown promise in biological detoxification of these classes of contaminants. For example, Iodotyrosine deiodinase is a mammalian enzyme with the unusual function of aerobic reductive dehalogenation of iodine- or bromine-substituted organic substrates. Bromoxynil and ioxynil herbicides have been shown to undergo a variety of environmental transformations, including reductive dehalogenation by anaerobic bacteria.

Polyiodoorganic compounds are sometimes employed as X-ray contrast agents, in fluoroscopy, a type of medical imaging. This application exploits the X-ray absorbing ability of the heavy iodine nucleus. A variety of agents are available commercially, many are derivatives of 1,3,5-triiodobenzene and contain about 50% by weight iodine. For most applications, the agent must be highly soluble in water and, of course, non-toxic and readily excreted. A representative reagent is Ioversol (Figure to right), which has water-solubilizing diol substituents. Typical applications include urography and angiography.

Organoiodine lubricants can be used with titanium, stainless steels, and other metals which tend to seize up with conventional lubricants: organoiodine lubricants can be used in turbines and spacecraft, and as a cutting oil in machining.

• Methyl iodide, intermediate in the industrial routes to acetic acid.
• Erythrosine, a common food dye.
• Ioversol, an organoiodine compound used as an X-ray contrast agent, the dominant iodine compound of commerce.
• Thyroxine (T₄), a hormone.
• Triiodothyronine (T₃), another thyroid hormone.
• Idoxuridine an anti-herpesvirus antiviral drug, is a rare iodine-containing drug.]]

Biological role

In terms of human health, the most important organoiodine compounds are the two thyroid hormones thyroxine ("T₄") and triiodothyronine ("T₃"). Marine natural products are rich sources of organoiodine compounds, like the recently discovered plakohypaphorines from the sponge Plakortis simplex.

The sum of iodomethane produced by the marine environment, microbial activity in rice paddies, and the burning of biological material is estimated to be 214 kilotonnes per year. The volatile iodomethane is broken up by oxidation reactions in the atmosphere and a global iodine cycle is established. More than 3000 organoiodine compounds have been identified.

Methods for preparation of the C–I bond

From I₂

Organoiodine compounds are prepared by numerous routes, depending on the degree and regiochemistry of iodination sought as well as the nature of the precursors. The direct iodination with I₂ is employed with unsaturated substrates:

RHC=CH₂ + I₂ → RHIC-CIH₂

This reaction is used to determine the iodine number, an indicator of the unsaturation of fats and related samples.

From I sources

The iodide anion is a good nucleophile and will displace chloride, tosylate, bromide and other leaving groups, as in the Finkelstein reaction.

Alcohols can be converted to the corresponding iodides using phosphorus triiodide. Illustrative is the conversion of methanol to iodomethane:

PI₃ + 3 CH
₃OH → 3 CH
₃I + "H
₃PO
₃"

For bulky alcohol substrates, the methiodide of triphenylphosphite has been used.

I + ROH → RI + CH₃(C₆H₅O)₂PO + C₆H₅OH

Aromatic iodides may be prepared via a diazonium salt by treatment with potassium iodide:

${\displaystyle {\ce {C6H5N2+ + KI -> C6H5I + K+ + N2}}}$

From I sources

Benzene can be iodinated with a combination of iodide and nitric acid. Iodine monochloride is a reagent that is sometimes used to deliver the equivalent of "I".

See also

• Organofluorine compounds
• Organochlorine compounds
• Organobromine compounds
• Iodanes
• Periodinanes

References

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2. Blanksby SJ, Ellison GB (April 2003). "Bond dissociation energies of organic molecules". Acc. Chem. Res. 36 (4): 255–63. CiteSeerX 10.1.1.616.3043. doi:10.1021/ar020230d. PMID 12693923.
3. Kaiho, Tatsuo (2014). "Pharmaceuticals". Iodine Chemistry and Applications. pp. 433–437. doi:10.1002/9781118909911.ch23. ISBN 978-1-118-46629-2.
4. Phyllis A. Lyday. "Iodine and Iodine Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a14_381. ISBN 978-3527306732.
5. Allard, A.S. and A. H. Neilson 2003 Degradation and transformation of organic bromine and iodine compounds: comparison with their chlorinated analogues. The Handbook of Environmental Chemistry 3:1-74.
6. McTamney, P.M. and S.E. Rokita 2010. A mammalian reductive deiodinase has broad power to dehalogenate chlorinated and brominated substrates. J Am Chem Soc. 131(40): 14212–14213.
7. Cupples, A. M., R. A. Sanford, and G. K. Sims. 2005. Dehalogenation of Bromoxynil (3,5-Dibromo-4-Hydroxybenzonitrile) and Ioxynil (3,5-Diiodino-4-Hydroxybenzonitrile) by Desulfitobacterium chlororespirans. Appl. Env. Micro. 71(7):3741-3746.
8. Ulrich Speck, Ute Hübner-Steiner "Radiopaque Media" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. doi:10.1002/14356007.a22_593
9. "Key Lubrication Ingredient: Iodine Moves to Space Age", Schenectady Gazette, November 17, 1965.
10. Wilhelmus KR (January 2015). "Antiviral treatment and other therapeutic interventions for herpes simplex virus epithelial keratitis". The Cochrane Database of Systematic Reviews. 1 (1): CD002898. doi:10.1002/14651858.CD002898.pub5. PMC 4443501. PMID 25879115.
11. Gribble, G. W. (1996). "Naturally occurring organohalogen compounds - A comprehensive survey". Progress in the Chemistry of Organic Natural Products. 68 (10): 1–423. doi:10.1021/np50088a001. PMID 8795309.
12. N. Bell; L. Hsu; D. J. Jacob; M. G. Schultz; D. R. Blake; J. H. Butler; D. B. King; J. M. Lobert & E. Maier-Reimer (2002). "Methyl iodide: Atmospheric budget and use as a tracer of marine convection in global models". Journal of Geophysical Research. 107 (D17): 4340. Bibcode:2002JGRD..107.4340B. doi:10.1029/2001JD001151. hdl:11858/00-001M-0000-0012-0250-1. S2CID 18327103.
13. V.M. Dembitsky; G.A. Tolstikov . (2003). "Naturally occurring organohalogen compounds - A comprehensive survey". Nauka Press, Novosibirsk.
14. King, C. S.; Hartman, W. W. (1933). "Methyl Iodide". Organic Syntheses. 13: 60. doi:10.15227/orgsyn.013.0060.
15. H. N. Rydon (1971). "Alkyl Iodides: Neopentyl Iodide and Iodocyclohexane". Organic Syntheses. 51: 44. doi:10.15227/orgsyn.051.0044.
16. Lucas, H. J.; Kennedy, E. R. (1939). "Iodobenzene". Organic Syntheses. 19: 55. doi:10.15227/orgsyn.019.0055.
17. F. B. Dains and R. Q. Brewster (1929). "Iodobenzene". Organic Syntheses. 9: 46. doi:10.15227/orgsyn.009.0046.

v t e Compounds of carbon with other elements in the periodic table
CH He CLi CBe CB CC CN CO CF Ne CNa CMg CAl CSi CP CS CCl CAr CK CCa CSc CTi CV CCr CMn CFe CCo CNi CCu CZn CGa CGe CAs CSe CBr CKr CRb CSr CY CZr CNb CMo CTc CRu CRh CPd CAg CCd CIn CSn CSb CTe CI CXe CCs CBa CLu CHf CTa CW CRe COs CIr CPt CAu CHg CTl CPb CBi CPo CAt Rn Fr CRa Lr Rf Db CSg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og   CLa CCe CPr CNd CPm CSm CEu CGd CTb CDy CHo CEr CTm CYb Ac CTh CPa CU CNp CPu CAm CCm CBk CCf CEs Fm Md No
Legend	Chemical bonds to carbon Core organic chemistry Many uses in chemistry Academic research, no widespread use Bond unknown

• Organoiodides