Fluorescence from films as well as from a solid solution of a ladder-type p
oly(para-phenylene) has been studied as a function of pump energy upon exci
tation at variable spectral positions within the inhomogeneously broadened
absorption band. Photoinduced transmission changes following excitation wit
h 200 fs laser pulses at 25000 cm(-1) have been recorded at variable delay
time, The latter testify on the occurrence of optical gain in the spectral
range of spontaneous emission and of absorption bleaching. The initial deca
y time of the gain is on the order of 1 ps. Above a certain pump power a 18
0 cm(-1) broad emission feature emerges from the inhomogeneously broadened
fluorescence spectrum of the film. Upon exciting within the low energy tail
of the S-1 <-- S-0 0-0 absorption band sharp (7-9 cm(-1)) emission feature
s show up, off-set from the laser line by the energies of the dominant vibr
ational modes of the polymer. The phenomenon is identified as amplified spo
ntaneous emission induced by spontaneous emission from polymer segments pri
or to the depopulation by energy transfer towards lower energy sites. [S016
3-1829(99)12805-4].