Triplet Energy Dissipation in Methylenecyclopropane Rearrangement

Certain 1,1-dimethyl-2-aryl-3-methylenecyclopropanes containing carbonyl substituents undergo rearrangement when irradiated with 350 nm light. These rearrangements occur via the (n,π*) triplet state, which fragments the strained cyclopropane bond. Intersystem crossing followed by ring closure gives the observed products. No photoreduction is seen in i-PrOH. Potential Norrish type II processes are also bypassed. It is suggested that the cyclopropane bond fragmentation dissipates the triplet energy and that the new intermediates are not energetic enough to abstract hydrogen atoms in an intramolecular fashion or from solvent. Nitro substituted systems undergo analogous photoinitiated rearrangements. Benzophenone sensitization of naphthyl, biphenyl, styrene, and phenylacetylene analogues also leads to rearrangement, presumably via the sensitized generation of triplet states. When triplet states cannot be accessed by direct irradiation or by sensitized processes, methylenecyclopropane rearrangements do not occur. An exception is the ferrocenyl analogue, which does not photorearrange, presumably due to the very short lifetime of the triplet intermediate.