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  2. Free radical damage to DNA - Wikipedia

    en.wikipedia.org/wiki/Free_radical_damage_to_DNA

    Radiolysis of intracellular water by ionizing radiation creates peroxides, which are relatively stable precursors to hydroxyl radicals. 60%–70% of cellular DNA damage is caused by hydroxyl radicals, [3] yet hydroxyl radicals are so reactive that they can only diffuse one or two molecular diameters before reacting with cellular components.

  3. Radical (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Radical_(chemistry)

    In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron. [1] [2] With some exceptions, these unpaired electrons make radicals highly chemically reactive. Many radicals spontaneously dimerize. Most organic radicals have short lifetimes.

  4. Free-radical addition - Wikipedia

    en.wikipedia.org/wiki/Free-radical_addition

    Chain propagation: A radical reacts with a non-radical to produce a new radical species; Chain termination: Two radicals react with each other to create a non-radical species; In a free-radical addition, there are two chain propagation steps. In one, the adding radical attaches to a multiply-bonded precursor to give a radical with lesser bond ...

  5. Hydroxyl radical - Wikipedia

    en.wikipedia.org/wiki/Hydroxyl_radical

    Skeletal formulae of 1-hydroxy-2()-pyridinethione and its tautomer. The hydroxyl radical, • HO, is the neutral form of the hydroxide ion (HO –).Hydroxyl radicals are highly reactive and consequently short-lived; however, they form an important part of radical chemistry.

  6. Radical disproportionation - Wikipedia

    en.wikipedia.org/wiki/Radical_disproportionation

    Due to the reactive nature of radical molecules, disproportionation proceeds rapidly and requires little to no activation energy. [1] The most thoroughly studied radical disproportionation reactions have been conducted with alkyl radicals, but there are many organic molecules that can exhibit more complex, multi-step disproportionation reactions.

  7. Reactivity–selectivity principle - Wikipedia

    en.wikipedia.org/wiki/Reactivity–selectivity...

    The sulfur radical was found to be more reactive (6*10 8 vs. 1*10 7 M −1.s −1) and less selective (selectivity ratio 76 vs 1200) than the carbon radical. In this case, the effect can be explained by extending the Bell–Evans–Polanyi principle with a factor δ {\displaystyle \delta \,} accounting for transfer of charge from the reactants ...

  8. Unpaired electron - Wikipedia

    en.wikipedia.org/wiki/Unpaired_electron

    In organic chemistry they typically only occur briefly during a reaction on an entity called a radical; however, they play an important role in explaining reaction pathways. Radicals are uncommon in s- and p-block chemistry, since the unpaired electron occupies a valence p orbital or an sp, sp 2 or sp 3 hybrid orbital.

  9. Reactive oxygen species production in marine microalgae

    en.wikipedia.org/wiki/Reactive_oxygen_species...

    Indirectly, the hydroxyl radical can result in significant biogeochemical changes in marine systems by influencing the cycling of dissolved organic matter and trace metal speciation. Both intracellular and extracellular reactive oxygen species can be removed from the environment by antioxidants produced biologically as a defense mechanism.