The vibronic transition probability of the P-6(7/2) --> S-8(7/2) trans
ition of Eu2+ in KMgF3 crystals is reported and compared with those of
Eu2+ in LiBaF3 and of Gd3+ in some fluoride compounds. The difference
s in A(vib) can be attributed to the differences in admixture of the o
pposite parity 4f(6)5d states. For the first time the 6I emission of E
u2+ is reported. 6I emission can be observed because the lowest energe
tic 4f(6)5d level is situated above the I-6(7/2) level of Eu2+. The hi
gh energetic position of the lowest 4f(6)5d level is explained by the
small crystal-field splitting and the energetically high position of t
he centre of gravity of the 4f(6)5d states. The decay time of the 6I e
mission at 4.2 K is 96 mus. Above 25 K the 6I emission is completely q
uenched via the lowest 4f(6)5d level, which is at some 50 cm-1 above t
he I-6(7/2) level and some 3350 cm-1 above the P-6(7/2) level.