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14977-61-8[Cl-].[Cl-].[Cr+6].[O-2].[O-2]AHXGRMIPHCAXFP-UHFFFAOYSA-L14977-61-8Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
VerwendenHighly spin-polarized chromium dioxide (CrO2) thin films were deposited on 100 TiO2 substrates by chemical vapor deposition using chromyl chloride as a precursor. Chromyl chloride (Cr02C12) reacts with cyclohexane solvent at 75 OC to give a dark precipitate along with chlorocyclohexane and a small amount of cyclohexene (in 10.0 and ca. 0.3% yields based on chromium). Chromyl chloride, CrO2C12, oxidizes cyclooctane, isobutane, and toluene under mild conditions (25-60" C). The reactions give chlorinated products (chlorocyclooctane, tert- butyl chloride, and benzyl chloride) and a dark chromium-containing precipitate. Used for Organic oxidations and chlorination, chromium coordination complexes, catalyst for polymerization of olefins. Chromyl chloride in carbon tetrachloride solution reacts in the cold with cyclohexene, cyclopentene, and 1-hexene to give the various isomeric chlorohydrins as the major products.
synthetischeChromyl chloride is prepared by reacting chromium(III) chloride with hydrochloric acid: CrO3 + 2HCl → CrO2Cl2 + H2O Also, it may be prepared by warming potassium dichromate with potassium chloride in concentrated sulfuric acid: K2Cr2O7 + 4KCl + 3H2SO4 → 2Cr2O2Cl2 + 3K2SO4 + 3H2O.
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DefinitionA dark red covalent liquid prepared either by distilling a dry mixture of potassium dichromate and sodium chloride with concentrated sulfuric acid or by the action of concentrated sulfuric acid on chromium(VI) oxide dissolved in concentrated hydrochloric acid. Chromyl chloride is hydrolyzed by water, and with solutions of alkalis it undergoes immediate hydrolysis to produce chromate ions. It is used as an oxidizing agent in organic chemistry. Chromyl chloride oxidizes methyl groups at the ends of aromatic side chains to aldehyde groupings (étard’s reaction).