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A novel molecular conjugate (1) that combines radical scavenging properties to light‐regulated release of nitric oxide (NO) has been designed and synthesized by a straightforward procedure. This compound integrates a catecholic unit and a suitable NO photodonor, separated by an alkyl spacer, into the same molecular skeleton. The radical scavenging properties of 1 were evaluated by investigating its...
Chalcone, flavone, and arylideneflavanone derivatives bearing one or two 3,5-di-tert-butyl-4-hydroxyphenyl groups were synthesized from 2′,4′-dihydroxyacetophenone and 3,5-di-tert-butyl-4-hydroxybenzaldehyde. These flavonoids were converted into the corresponding malonates and then reacted with C 60 to yield the title compounds. The O–H bond dissociation enthalpies (BDE) and the chain-breaking...
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