An electron paramagnetic resonance study of a synthetic single crystal of C
r-doped LiScGeO4 was carried out at the X- and Q-bands at 300 K and at the
broad band (70-370 GHz) at 4.2 K. It was established that the EPR spectra w
ith the magnetic multiplicity K-M = 2 observed in all the frequency bands a
re due to the Cr3+ substituted for Sc3+ at the mirror symmetry octahedral s
ite. The angular dependences of the two symmetry-related spectra of Cr3+ in
the three crystallographic planes were fitted with the spin Hamiltonian (S
= 3/2) of monoclinic symmetry. The zero-field splitting of the ground stat
e energy levels was determined as 1.309(5) cm(-1) which compares well with
that for Cr3+ in forsterite and alexandrite crystals with similar olivine-l
ike structure. Additional weak lines due to Mn2+ and Fe3+ at the mirror sym
metry sites were also identified in the X- and Q-band spectra.