The absorption spectrum of H2S has been investigated in the range 11 9
30-12 300 cm(-1) by means of an externally frequency modulated tunable
diode laser and a multipath absorption cell. Approximately 290 lines
have been assigned to rovibrational transitions of the 3 nu(1) + 2 nu(
3) and 2 nu(1) + 3 nu(3) bands which are in strong interaction. The ro
tational structure of the corresponding excited vibrational states has
been satisfactorily reproduced using a Hamiltonian model which takes
explicitly into account the strong Coriolis interaction coupling the l
evels of(302) with those of (203), as well as weaker anharmonic and Co
riolis-type interactions between the levels of(302) and (203) and thos
e of (222) and (321). Precise band centers and rotational and coupling
constants have been derived and the local mode behavior of the energy
levels was clearly observed. (C) 1995 Academic Press, Inc.