Metal acetate-iodine

The reduction steps on active Co sites are strongly affected by activated hydrogen transferred from promoter metal particles (Pt and Ru). Several indications for the existence and importance of hetero-bimetallic centers have been obtained.63 [Cp Co(CO)2] in the presence of PEt3 and Mel catalyzes the carbonylation of methanol with initial rates up to 44 mol L 1 h 1 before decaying to a second catalytic phase with rates of 3 mol L 1 h-1.64 HOAc-AcOMe mixtures were prepared by reaction of MeOH with CO in the presence of Co(II) acetate, iodine, and additional Pt or Pd salts, e.g., [(Ph3P)2PdCl2] at 120-80 °C and 160-250 atm.65... 

Hypoiodite reactionThis reaction is usually carried out with iodine and HgO (5, 347-348). A new version uses iodine in combination with this diphenyl-selenurane, and this version gives essentially only cyclic ethers without any iodo-hydrins or other products encountered with other heavy metal acetates. 

Alkyl hypochlorites and hypobromites are relatively stable molecules alkyl hypoiodites can only be prepared in situ, usually by the reaction of alcohols with metal acetates or oxides and iodine or by the reaction of alcohols with a hypervalent iodine compound and iodine.1319 Alkyl hypochlorites and hypoiodites can be utilized in reactions that parallel those of the organic nitrites (Barton reaction Section 6.4.2). For example, the photochemistry of the steroidal hypoiodite 497, prepared by the reaction of the corresponding alcohol with iodine oxide (I2O) generated from mercury(II) oxide and molecular iodine in situ, affords a new five-membered ring via an O I bond fission, 1,5-hydrogen abstraction and substitution (Scheme 6.244).1353... 

Although alkyl hypochlorites and hypobromites are isolable species, alkyl hypoiodites are not isolable. They can only be prepared in situ, either by the reaction of alcohols with metal acetates or oxide and iodine in solution, or by the reaction of alcohols with a hypervalent iodine compound and iodine in... 

Manufacture. Trichloromethanesulfenyl chloride is made commercially by chlorination of carbon disulfide with the careful exclusion of iron or other metals, which cataly2e the chlorinolysis of the C—S bond to produce carbon tetrachloride. Various catalysts, notably iodine and activated carbon, are effective. The product is purified by fractional distillation to a minimum purity of 95%. Continuous processes have been described wherein carbon disulfide chlorination takes place on a granular charcoal column (59,60). A series of patents describes means for yield improvement by chlorination in the presence of dihinctional carbonyl compounds, phosphonates, phosphonites, phosphites, phosphates, or lead acetate (61). 

The Perkin reaction is of importance for the iadustrial production of coumarin and a number of modifications have been studied to improve it, such as addition of a trace of iodine (46) addition of oxides or salts of metals such as iron, nickel, manganese, or cobalt (47) addition of catalytic amounts of pyridine (48) or piperidine (49) replacement of sodium acetate by potassium carbonate (50,51) or by cesium acetate (52) and use of alkaU metal biacetate... 

The reaction is a sensitive one, but is subject to a number of interferences. The solution must be free from large amounts of lead, thallium (I), copper, tin, arsenic, antimony, gold, silver, platinum, and palladium, and from elements in sufficient quantity to colour the solution, e.g. nickel. Metals giving insoluble iodides must be absent, or present in amounts not yielding a precipitate. Substances which liberate iodine from potassium iodide interfere, for example iron(III) the latter should be reduced with sulphurous acid and the excess of gas boiled off, or by a 30 per cent solution of hypophosphorous acid. Chloride ion reduces the intensity of the bismuth colour. Separation of bismuth from copper can be effected by extraction of the bismuth as dithizonate by treatment in ammoniacal potassium cyanide solution with a 0.1 per cent solution of dithizone in chloroform if lead is present, shaking of the chloroform solution of lead and bismuth dithizonates with a buffer solution of pH 3.4 results in the lead alone passing into the aqueous phase. The bismuth complex is soluble in a pentan-l-ol-ethyl acetate mixture, and this fact can be utilised for the determination in the presence of coloured ions, such as nickel, cobalt, chromium, and uranium. 

As mentioned earlier, metal complexation not only allows isolation of the QM derivatives but can also dramatically modify their reactivity patterns.29o-QMs are important intermediates in numerous synthetic and biological processes, in which the exocyclic carbon exhibits an electrophilic character.30-33 In contrast, a metal-stabilized o-QM can react as a base or nucleophile (Scheme 3.16).29 For instance, protonation of the Ir-T 4-QM complex 24 by one equivalent of HBF4 gave the initial oxo-dienyl complex 25, while in the presence of an excess of acid the dicationic complex 26 was obtained. Reaction of 24 with I2 led to the formation of new oxo-dienyl complex 27, instead of the expected oxidation of the complex and elimination of the free o-QM. Such reactivity of the exocyclic methylene group can be compared with the reactivity of electron-rich enol acetates or enol silyl ethers, which undergo electrophilic iodination.34... 

Redox titrants (mainly in acetic acid) are bromine, iodine monochloride, chlorine dioxide, iodine (for Karl Fischer reagent based on a methanolic solution of iodine and S02 with pyridine, and the alternatives, methyl-Cellosolve instead of methanol, or sodium acetate instead of pyridine (see pp. 204-205), and other oxidants, mostly compounds of metals of high valency such as potassium permanganate, chromic acid, lead(IV) or mercury(II) acetate or cerium(IV) salts reductants include sodium dithionate, pyrocatechol and oxalic acid, and compounds of metals at low valency such as iron(II) perchlorate, tin(II) chloride, vanadyl acetate, arsenic(IV) or titanium(III) chloride and chromium(II) chloride. 

A mixture of 1,4-dioxane and water is often used as the solvent for the conversion of aldehydes and ketones by H2Se03 to a-dicarbonyl compounds in one step (Eq. 8.117).331 Dehydrogenation of carbonyl compounds with selenium dioxide generates the a, (i-unsaturated carbonyl compounds in aqueous acetic acid.332 Using water as the reaction medium, ketones can be transformed into a-iodo ketones upon treatment with sodium iodide, hydrogen peroxide, and an acid.333 Interestingly, a-iodo ketones can be also obtained from secondary alcohol through a metal-free tandem oxidation-iodination approach. 

FIGURE 6.21 (A) Removal of trityl and acetamidomethyl from sulfhydryl by oxidative cleavage by iodine. (B) Cleavage of terf-butylsulfanyl by mercury(II) acetate,88 followed by displacement of the metal ion by hydrogen sulfide. 

Black crystaUine solid exists in two modifications stable black needles known as alpha form that produces ruby-red color in transmitted light, and a labile, metastable beta modification consisting of black platelets which appear brownish-red in transmitted light density of alpha form 3.86 g/cm at 0°C density of beta form 3.66 g/cm at 0°C alpha form melts at 27.3°C, vapor pressure being 28 torr at 25°C beta form melts at 13.9°C hquid iodine monochloride has bromine-hke reddish-brown color hquid density 3.10 g/mL at 29°C viscosity 1.21 centipoise at 35°C decomposes around 100°C supercools below its melting point polar solvent as a hquid it dissolves iodine, ammonium chloride and alkali metal chlorides hquid ICl also miscible with carbon tetrachloride, acetic acid and bromine the solid crystals dissolve in ethanol, ether, acetic acid and carbon disulfide solid ICl also dissolves in cone. HCl but decomposes in water or dilute HCl. 

Potassium hydrogen phthalate Potassium hydrogen phthalate Potassium iodate Anhydrous sodium carbonate Zinc metal Standardisation of sodium hydroxide solution Standardisation of acetous perchloric acid Standardisation of sodium thiosulphate solution through generation of iodine Standardisation of hydrochloric acid Standardisation of EDTA solution... 

Treatment of a series of metal acetylacetonates with the N-halogen suc-cinimides in boiling chloroform afforded the trihalogenated metal chelates in high yields. The use of bromine or iodine monochloride in buffered acetic acid also yielded the bromo- and iodochelates (7). 

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