From the results of an infrared-far infrared double resonance experime
nt on (NH3)(2) complexes in a supersonic slit nozzle expansion, it was
possible to characterize the tunneling dynamics, occurring within the
ammonia dimer (Havenith et al., Chem. Phys. Letters 193 (1992) 261).
In the current paper we present additional infrared-far infrared doubl
e resonance spectra. These confirm the former analysis and give a stat
e specific explanation of the overall infrared spectrum of (NH3)(2) as
measured by Snels et al. (Chem. Phys. 115 (1987) 79). The interchange
motion is shown to be quenched from 20 cm(-1) in the ground state to
less than 1 cm(-1) in the infrared excited state. This confirms the as
sumption of Olthof et al. (J. Mel. Struct. THEOCHEM 307 (1994) 201) th
at the barrier for interchange tunneling is very small in (NH3)(2).