Hypervalent Iodine Compounds

Iodine is element 53, in the 5th period, Group VIIa, halogens of the periodic table. Iodine is a large-sized halogen element, easily polarizable, and low in electronegativity. It forms hypervalent organoiodanes beyond the octet theory by readily extending its valence. For example, hypervalent organoiodane with three ligands is a 10-I-3 type compound as shown in the figure. The central iodine atom forms a plane with two lone pairs and one σ-bond, and furthermore, this iodine atom coordinates two ligands with larger electronegativity in an apical position orthogonal to the plane resulting in the formation of a linear three center-four electron bond. The I-L bond in the apical position is weaker and longer than the covalent bond. For example, the I-O bond lengths in PhI(OAc)2 are longer than the sum of their covalent bond radii (1.99Å) and these bond lengths have a range of 2.15~2.16Å.

The stability and reactivity of hypervalent organoiodanes exhibit a greater dependence on the character of hypervalent bonds in the apical position. The hypervalent bonds in the apical position are easily cleaved, and the cleavage causes trivalent iodines with 10 electrons to be reduced to monovalent iodines of a more stable octet structure. For this reason it exhibits good elimination and oxidation rate and finds application in organic syntheses.1~3)
(Diacetoxyiodo)benzene, the most typical trivalent iodine compounds, which is attempted to support the polymers. For example, Togo and co-workers have demonstrated several oxidative functional group conversion reactions using poly[4-(diacetoxyiodo)styrene].4) After reaction, this polymer-supported reagent can be recovered by filtration and reused after re-oxidation with peracetic acid. Therefore, it is expected to be used as environmentally-friendly chemical conversion reagent in the near future.

P1081 P1081 P1080 P1080 P1659 P1659
P1082 P1082 B2121 B2121 I0073 I0073
I0591 I0591 B2359 B2359 D2045 D2045
D2372 D2372 D2356 D2356 D2248 D2248
D2238 D2238 D2373 D2373 D2357 D2357
D2243 D2243 D2253 D2253 D2503 D2503
E0467 E0467 I0330 I0330 I0479 I0479
P1620 P1620 P1415 P1415 P1239 P1239
B1175 B1175 B1616 B1616 P1298 P1298
P1015 P1015
P1081 (Perfluoro-n-octyl)phenyliodonium Trifluoromethanesulfonate
P1080 (Perfluorohexyl)phenyliodonium Trifluoromethanesulfonate
P1659 (Perfluoroisopropyl)phenyliodonium Trifluoromethanesulfonate
P1082 (Perfluoropropyl)phenyliodonium Trifluoromethanesulfonate
B2121 1-(tert-Butylperoxy)-1,2-benziodoxol-3(1H)-one
I0073 2-Iodosobenzoic Acid
I0591 4-Isopropyl-4'-methyldiphenyliodonium Tetrakis(pentafluorophenyl)borate
B2359 Bis(2,4,6-trimethylpyridine)iodonium Hexafluorophosphate
D2045 Dess-Martin Periodinane
D2372 Diphenyliodonium Bromide
D2356 Diphenyliodonium Chloride
D2248 Diphenyliodonium Hexafluoroarsenate
D2238 Diphenyliodonium Hexafluorophosphate
D2373 Diphenyliodonium Iodide
D2357 Diphenyliodonium Nitrate
D2243 Diphenyliodonium Perchlorate
D2253 Diphenyliodonium Trifluoromethanesulfonate
D2503 Diphenyliodonium-2-carboxylate Monohydrate
E0467 Ethynyl(phenyl)iodonium Tetrafluoroborate [Ethynylating Reagent]
I0330 Iodobenzene Diacetate
I0479 Iodomesitylene Diacetate
P1620 Phenyl[2-(trimethylsilyl)phenyl]iodonium Trifluoromethanesulfonate
P1415 Poly[4-(diacetoxyiodo)styrene]
P1239 Trimethylsilylethynyl(phenyl)iodonium Tetrafluoroborate
B1175 [Bis(trifluoroacetoxy)iodo]benzene
B1616 [Bis(trifluoroacetoxy)iodo]pentafluorobenzene
P1298 [Hydroxy(methanesulfonyloxy)iodo]benzene
P1015 [Hydroxy(tosyloxy)iodo]benzene

Many hypervalent organoiodanes may decompose violently when exposed to heat, shock, and friction, etc.. Sufficient safety measures, such as usage of safety shield, wearing of protective equipment, and extreme caution should be taken, when using this compound, from the opening up to the disposal of the reagents.

Literature

1) A. Varvoglis, Synthesis, 1984, 709.
2) P. J. Stang, V. V. Zhdankin, Chem. Rev., 1996, 96, 1123.
3) M. Ochiai, TCIMAIL, 1999, 104, 2.
4) H. Togo, K. Sakuratani, Kagaku To Kogyo (Tokyo), 2002, 55, 1018.
H. Togo, K. Sakuratani, Synlett, 2002, 1966.
Tokyo Kasei Kogyo Co., Ltd., JP Patent, 2003-113131.


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