1. Phosphite ozonides will decompose to give singlet oxygen: 2. In addition to the superoxide and the ozonide , several brightly coloured suboxides have also been studied. 3. Dichloromethane is often used as a 1 : 1 cosolvent to facilitate timely cleavage of the ozonide . 4. Lithium and sodium ozonide are extremely unstable and must be prepared by low-temperature ion exchange starting from CsO 3. 5. After completing the addition a reagent is then added to convert the intermediate ozonide to a carbonyl derivative . buffer the reaction. 6. When 17 O-labelled benzaldehyde reacts with carbonyl oxides, the label ends up exclusively in the ether linkage of the ozonide . 7. A third method liberates singlet oxygen via phosphite ozonides , which are, in turn, generated " in situ ." 8. Its molecular structure is uncommon for pharmacological compounds in that it has both a ozonide ( trioxolane ) group and an adamantane substituent. 9. The oxide and aldehyde or ketone react again in a 1, 3-dipolar cycloaddition or produce a relatively stable ozonide intermediate ( a trioxolane ). 10. The compound hydrogen ozonide ( HO 3 ) is not known, although some of its alkali metal ozonide salts are; these have the formula MO 3.
Mobile