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  2. Hypervalent organoiodine compounds - Wikipedia

    en.wikipedia.org/wiki/Hypervalent_organoiodine...

    In iodane chemistry, carbon is considered more electronegative than iodine, despite the Pauling electronegativities of those respective atoms. [2] Thus iodobenzene (C 6 H 5 I) is an iodine(I) compound, (dichloroiodo)benzene (C 6 H 5 ICl 2) and iodosobenzene (C 6 H 5 IO) iodine(III) compounds, and iodoxybenzene (C 6 H 5 IO 2) an iodine(V) compound.

  3. Samarium(II) iodide - Wikipedia

    en.wikipedia.org/wiki/Samarium(II)_iodide

    Samarium(II) iodide is a reagent for carbon-carbon bond formation, for example in a Barbier reaction (similar to the Grignard reaction) between a ketone and an alkyl iodide to form a tertiary alcohol: [9] R 1 I + R 2 COR 3 → R 1 R 2 C(OH)R 3 Barbier reaction using SmI 2. Typical reaction conditions use SmI 2 in THF in the presence of ...

  4. Carbonyl oxidation with hypervalent iodine reagents - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_oxidation_with...

    One alternative to hypervalent iodine oxidation that does not employ heavy metals is the attack of a metal enolate on dioxygen, followed by reduction of the resulting peroxide (equation ). The most popular method for the α-hydroxylation of carbonyl compounds is the Rubottom oxidation , which employs silyl enol ethers as substrates and peracids ...

  5. (Bis(trifluoroacetoxy)iodo)benzene - Wikipedia

    en.wikipedia.org/wiki/(Bis(trifluoroacetoxy)iodo...

    The reaction can also be carried out under mildly acidic conditions by way of the same intermediate using a hypervalent iodine compound in aqueous solution. [1] An example published in Organic Syntheses is the conversion of cyclobutanecarboxamide , easily synthesized from cyclobutylcarboxylic acid , to cyclobutylamine . [ 2 ]

  6. Iodine - Wikipedia

    en.wikipedia.org/wiki/Iodine

    This is an accepted version of this page This is the latest accepted revision, reviewed on 16 February 2025. This article is about the chemical element. For other uses, see Iodine (disambiguation). Chemical element with atomic number 53 (I) Iodine, 53 I Iodine Pronunciation / ˈ aɪ ə d aɪ n, - d ɪ n, - d iː n / (EYE -ə-dyne, -⁠din, -⁠deen) Appearance lustrous metallic gray solid ...

  7. Diiodine hexaoxide - Wikipedia

    en.wikipedia.org/wiki/Diiodine_hexaoxide

    Structurally, the compound is iodyl periodate, an iodine(V,VII) oxide approximating IO 2 + IO 4 −. [2] As a solid, the compound crystallizes in the space group P 1 (space group no. 2) with the lattice constants a = 500.6 pm, b = 674.1 pm, c = 679.5 pm, α = 97.1°, β = 96.43°, γ = 105.36° with one formula unit per unit cell.

  8. Iodine monochloride - Wikipedia

    en.wikipedia.org/wiki/Iodine_monochloride

    Iodine monochloride is an interhalogen compound with the formula ICl. It is a red-brown chemical compound that melts near room temperature . Because of the difference in the electronegativity of iodine and chlorine , this molecule is highly polar and behaves as a source of I + .

  9. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    Reagents are "substances or compounds that are added to a system in order to bring about a chemical reaction or are added to see if a reaction occurs." [1] Some reagents are just a single element. However, most processes require reagents made of chemical compounds. Some of the most common ones used widely for specific reactive functions are ...