Lanthanide ions dissolved in low vibrational frequency inorganic liqui
ds have potential applications in laser systems requiring long non rad
iative lifetimes such as mid infrared and up conversion lasers. The us
e of liquids, whilst presenting some thermal and technological problem
s, avoids costly crystal growth and fabrication and gives great flexib
ility in varying lanthanide species, doping levels and co-doping. We r
eport an extensive study of solvent systems based on POCl3, PSCl3, PBr
3, PCl3, AsCl3, SbCl3 and SbBr3. The relatively well known POCl3 syste
m is found to show a far more complex behaviour than the early literat
ure suggests because of formation of the adduct 2POCl(3):SnCl4. The ot
her species except for PBr3 and PCl3 prove unsuitable owing to the rea
dy production of absorbing species. PBr3 and PCl3 produce solvent syst
ems when combined with the Lewis acids AlBr3 and SbBr3 or AlCl3 and Sb
Cl3 respectively. The energy levels of all laser relevant lanthanide i
ons below similar to 20000 cm(-1) were determined in the PBr, solvent
system, and correlations between the required Lewis acid concentration
and the lanthanide element found. Comparison of the spectra in variou
s solvents leads to preliminary conclusions about the lanthanide ion c
oordination.