The 1-cyclopropylcyclopentyl radical (114a) and 1-cyclopropylcyclohexyl radical (114b) were generated in the presence of PhSH via 366 nm photolysis of azo-1-cyclopropylcyclopentane and azo-1-cyclopropylcyclohexane respectively. These radicals undergo cyclopropylcarbinyl (CPC) rearrangement to primary homoallylic radicals 115a and 115b, respectively, at rates of 1.45 × 10\sp7 s\sp−1 and 1.1 × 10\sp7 s\sp−1 based on competitive trapping with PhSH. These rates are 6-9 times slower than the parent CPC radical. E\sba for 114a$\to115awasfoundtobe7.0kcal/molandlogA=12.3.Deuteriumlabelingstudiesshowthathomoallylicradical115areclosesto114awithk\sb{\rm rr}$ = 5.5 × 10\sp4 s\sp−1. Unsymmetrical triplet biradical 1-cyclopropyl-1,3-cyclopentanediyl (104T) is produced from the triplet sensitized photolysis of 1-cyclopropyl-2,3-diazabicyclo (2.2.1) hept-2-ene (123). Biradical 104T undergoes CPC rearrangement to a pair of 1,6-biradicals 105E and 105Z the latter of which undergoes rapid intramolecular disproportionation to Z-3-propylidenecyclopentene (108Z). On account of its geometry, 105E cannot lead directly to a stable product; hence, it recloses to 104T (k\sbra = 1.2 × 10\sp5 s\sp−1) but interestingly, not to 104S. If the CPC rearrangement rate of 104T is taken as that of 114a, we calculate from the product distribution that the lifetime (τ = 1/k\sbisc) of 104T is 59 ns. This figure is only one half the lifetime of the parent 1,3-cyclopentanediyl and is close to τ = 42 ns for 1,3-dimethyl-1,3-cyclopentanediyl, showing that the effect of the cyclopropyl group is similar to that of methyl. ISC of 104T displays linear Arrhenius behavior over 3.4-61.0\sp∘C. Activation parameters for ISC of 104T were determined via competition with the CPC rearrangement and were found to be E\sba (ISC) = 1.6 kcal/mol and log A = 8.4. Thus 104T is shown to be a ground state triplet and the low value of log A is characteristic of spin-forbidden ISC.