| 1. | Phosphite ozonides will decompose to give singlet oxygen:
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| 2. | In addition to the superoxide and the ozonide, several brightly coloured suboxides have also been studied.
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| 3. | Dichloromethane is often used as a 1 : 1 cosolvent to facilitate timely cleavage of the ozonide.
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| 4. | Lithium and sodium ozonide are extremely unstable and must be prepared by low-temperature ion exchange starting from CsO 3.
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| 5. | After completing the addition a reagent is then added to convert the intermediate ozonide to a carbonyl derivative . buffer the reaction.
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| 6. | When 17 O-labelled benzaldehyde reacts with carbonyl oxides, the label ends up exclusively in the ether linkage of the ozonide.
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| 7. | A third method liberates singlet oxygen via phosphite ozonides, which are, in turn, generated " in situ ."
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| 8. | Its molecular structure is uncommon for pharmacological compounds in that it has both a ozonide ( trioxolane ) group and an adamantane substituent.
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| 9. | The oxide and aldehyde or ketone react again in a 1, 3-dipolar cycloaddition or produce a relatively stable ozonide intermediate ( a trioxolane ).
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| 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.
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