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Iodine chlorides

Chlorine also forms BrCl (see bromine halides) and ICl and ICI3 (see iodine chlorides). See also inierhalogen compounds. [Pg.93]

Iodine monochlorlde may be prepared as follows. Pass dry chlorine into 127 g. of iodine contained in a 125 ml. distilling flask until the weight has increased by 34-6 g. The chlorine should be led in at or below the surface of the iodine whilst the flask is gently shaken it is essential to have an excess of iodine. Distil the iodine chloride in an ordinary distillation apparatus use a filter flask, protected from atmospheric moisture by a calcium chloride (or cotton wool) guard tube, as a receiver. Collect the fraction b.p. 97-105° the jdeld is 140 g. Preserve the iodine monochloride in a dry, glass-stoppered bottle. [Pg.974]

Iodine reacts with sulfuryl chloride ia the presence of aluminum chloride as catalyst-forming iodine chlorides. Sulfuryl chloride reacts with anhydrous ammonia yielding a series of sulfamides of the general formula NH2S02(NHS02) NH2, where n > 0. A cycHc compound of the formula... [Pg.142]

Hydrochloric acid digestion takes place at elevated temperatures and produces a solution of the mixed chlorides of cesium, aluminum, and other alkah metals separated from the sUiceous residue by filtration. The impure cesium chloride can be purified as cesium chloride double salts such as cesium antimony chloride [14590-08-0] 4CsCl SbCl, cesium iodine chloride [15605 2-2], CS2CI2I, or cesium hexachlorocerate [19153 4-7] Cs2[CeClg] (26). Such salts are recrystaUized and the purified double salts decomposed to cesium chloride by hydrolysis, or precipitated with hydrogen sulfide. Alternatively, solvent extraction of cesium chloride direct from the hydrochloric acid leach Hquor can be used. [Pg.375]

Iodine chloride of sufficient purity for this preparation... [Pg.53]

Stenc effects are presumably also responsible for the surprising formation of a chlorinated product from reaction of a hindered fluorinated olefin with potassium fluoride and iodine chloride [U6] (equation 18). [Pg.67]

Table 5. Reactions of Iodine Chloride viith Fluorodienes in Methylene Chloride at -S C under Argon [ll ... Table 5. Reactions of Iodine Chloride viith Fluorodienes in Methylene Chloride at -S C under Argon [ll ...
Terminal (perfluoroalkyl)alkynes react with iodine or iodine chloride to yield syn addition products bearing iodine on the terminal carbon [16 (equation 9). [Pg.369]

Chlor-jod, n. iodine chloride, specif, iodine monochloride, -kali, n. chloride of potash (potassium hypochlorite) potassium chloride. -kalilOsung, /. Pharm.) solution of chlorinated potassa, Javelle water, -kalium, n. potassium chloride. [Pg.91]

When iodine chloride is heated to 27°C, the weak intermolecular forces are unable to keep the molecules rigidly aligned, and the solid melts. Dipole forces are still important in the liquid state, because the polar molecules remain close to one another. Only in the gas, where the molecules are far apart, do the effects of dipole forces become negligible. Hence boiling points as well as melting points of polar compounds such as Id are somewhat higher than those of nonpolar substances of comparable molar mass. This effect is shown in Table 9.3. [Pg.237]

Iodine chloride decomposes at high temperatures to iodine and chlorine gases. [Pg.348]

The liberated iodine and the excess of iodide is determined by titration with standard potassium iodate solution the hydrochloric acid concentration must not be allowed to fall below 7JVf in order to prevent re-oxidation of the vanadium compound by iodine chloride. [Pg.404]

ICUWUZ Dimethyl 2-thioxo-l,3-dithiole-4,5-dicarboxylate-S-iodine chloride 2.591 2.603 176.11 A... [Pg.92]

Chlorine fluoride Aluminium Iodine chloride Metals Iodine heptafluoride Metals Iodine pentafluoride Metals... [Pg.34]

See Chromium pentafluoride Phosphorus trichloride Chromyl chloride Non-metal halides Fluorine Phosphorus halides Iodine chloride Phosphorus trichloride... [Pg.1456]

Sodium ignites in fluorine gas but is inert in the liquefied gas [1]. Cold sodium ignites in moist chlorine [2] but may be distilled unchanged in the dry gas [1]. Sodium and liquid bromine appear to be unreactive on prolonged contact [3], but mixtures may be detonated violently by mechanical shock [4]. Finely divided sodium luminesces in bromine vapour [1], Iodine bromide or iodine chloride react slowly with sodium, but mixtures will explode under a hammer-blow [1]. Interaction of iodine pentafluoride with solid sodium is initially vigorous, but soon slows with film-formation, while that with molten sodium is explosively violent... [Pg.1818]

Trialkylstannyl chlorides undergo dealkylation in the presence of iodine chloride, as shown in reaction 27. The alkyl iodide product reacts further very slowly in the case of primary alkyl groups, however, reaction 28 proceeds readily for R = i -Pr. The mechanism involves a charge transfer complex that can be detected in the reaction mixture. The compounds involved in the process can be analysed by GC, NMR and UVV spectroscopy282. [Pg.408]

Iodine bromide, 0254 Iodine chloride, 4013 Iodine heptafluoride, 4378 Iodine pentafluoride, 4355 Iodine trichloride, 4139... [Pg.207]


See other pages where Iodine chlorides is mentioned: [Pg.219]    [Pg.296]    [Pg.63]    [Pg.63]    [Pg.186]    [Pg.204]    [Pg.204]    [Pg.52]    [Pg.53]    [Pg.53]    [Pg.230]    [Pg.314]    [Pg.402]    [Pg.97]    [Pg.284]    [Pg.137]    [Pg.20]    [Pg.92]    [Pg.92]    [Pg.1370]    [Pg.196]    [Pg.565]    [Pg.486]    [Pg.632]    [Pg.285]   
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