We report the first observation of the electronic Raman effect in semi
conducting p-type, isotopically controlled diamonds. The Raman transit
ion between the spin-orbit split Is ground states of boron accepters o
ccurs at Delta' = 2.07(1) and 2.01(1) meV in natural and C-13 diamonds
, respectively. Polarization features show the transition to be predom
inantly Gamma(5) in character, placing an upper limit on the ratio of
the nonspherical Luttinger parameters of the valence band. Host-isotop
e-related self-energy shifts are observed in both the electronic infra
red and Raman spectra.