Add time:09/29/2019 Source:infona.pl
Two mechanisms for the isomerization of cyclopenta[fg]aceanthrylene to acefluoranthene were revealed. The first pathway occurs via a cyclobutyl intermediate, whereas the second pathway involves a transition state that contains an sp 3-hybridized carbon atom. Both patterns show that the Stone-Wales rearrangement requires extremely high activation energy and indicate that the isomerization process can occur only under a drastic temperature regime. Graphical abstract
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