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Diiodination

There appears to be only one true oxide of iodine, diiodine pentoxide, IjOs- It is a white solid prepared by heating iodic acid(V) to 450 K ... [Pg.337]

These are acids which can be regarded, in respect of their formulae (but not their properties) as hydrates of the hypothetical diiodine heptoxide, liO-j. The acid commonly called periodic acid , I2O7. 5H2O, is written HglO (since the acid is pentabasic) and should strictly be called hexaoxoiodic(VII) acid. It is a weak acid and its salts are hydrolysed in solution. It can be prepared by electrolytic oxidation of iodic(V) acid at low temperatures ... [Pg.342]

M. A. IT insky and G. Knorre proposed l-nitroso-2-naphthol as a reagent for cobalt and Zh.I. lotsich - magnesium diiodine acetylene as a reagent for carbonyl group. F.M. Flavitsky developed a method for qualitative analysis based on solid substances as well as a portable laboratory for qualitative analysis. G.V. Khlopin proposed a method for determining oxygen dissolved in water. [Pg.20]

D.6 Write the formula of (a) dinitrogen tetroxide (b) hydrogen sulfide (c) dichlorine heptoxide (d) nitrogen triiodide (e) sulfur dioxide (f) hydrogen fluoride (g) diiodine hexachloride. [Pg.61]

Electron donors which interact at only one end of the X2 or XY molecule form simple adducts (Fig. 1, mode A), often referred to as a spoke structure. The diiodine complex of tris(diethylamino)phosphine selenide (PAQKIB) [ 135] shown in Fig. 2a is an excellent example of this mode, as the Se- I distance at one end of the I2 molecule is 2.715 A, while at the other end there are no close contacts with any other atom. [Pg.80]

DARZAY0 2,3,5,6-tetrakis(2-Pyridyl)pyrazine hexakis(diiodine) 2.498 2.760 174.46 BA... [Pg.82]

QAMZAF (2-Methyl-l,2-dicarba-cZoso-dodecaboranyl)-bis(isopropyl)-(diiodine)phosphane 2.598 3.021 177.50 A... [Pg.85]

SORPUK Tris(2,4,6-trimethoxyphenyl)(diiodine)phosphine dichloromethane solvate 2.483 3.340 174.50 I... [Pg.85]

DAXXIK Bis(benzimidazole-2-thione)iodonium (benzimidazole-2-thione-diiodine) triiodide 2.670 2.887 178.34 A... [Pg.86]

See other pages where Diiodination is mentioned: [Pg.339]    [Pg.50]    [Pg.453]    [Pg.842]    [Pg.27]    [Pg.281]    [Pg.293]    [Pg.101]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.81]    [Pg.82]    [Pg.82]    [Pg.82]    [Pg.82]    [Pg.82]    [Pg.83]    [Pg.83]    [Pg.85]    [Pg.86]    [Pg.86]    [Pg.86]    [Pg.86]    [Pg.86]    [Pg.86]   
See also in sourсe #XX -- [ Pg.2 , Pg.650 ]



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Amines diiodine basicity

Blue Shift of the Visible Diiodine Transition Upon Halogen Bonding to Pyridines

Carbon monoxide diiodine

Complexation constants diiodine

Diiodine

Diiodine

Diiodine affinity scale

Diiodine arenes

Diiodine basicity scale

Diiodine cation

Diiodine complexation enthalpy

Diiodine drugs

Diiodine ethers

Diiodine haloalkanes

Diiodine hexachloride

Diiodine in aqueous solution

Diiodine inter- and intra-molecular distances

Diiodine methods

Diiodine oxides

Diiodine pentoxide

Diiodine pyridines

Diiodine selenium bases

Diiodine solvent effects

Diiodine sulfides

Diiodine thiophenes

Enthalpy diiodine complexes

Haloalkanes diiodine basicity

Introduction Measuring the Weak Diiodine Basicity of Haloalkanes

Iodination diiodination

Iodine => diiodine

Oxidation diiodine pentoxide

Regioselective diiodination

The Diiodine Affinity Scale

The Diiodine Basicity Scale

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