We calculate the L=0 ground and excited state energies for the rare gas tri
mers He-3, Ne-3, and Ar-3. An adiabatic representation is adopted to solve
the nuclear Schrodinger equation, in which the Schrodinger equation in hype
rangular coordinates is solved at a series of fixed hyper-radii using B spl
ines. We compare results obtained in a strict adiabatic approximation with
nonperturbative coupled-adiabatic-channel calculations. Structural properti
es such as the pair and angle distributions are monitored as functions of t
he hyper-radius. These structural studies pinpoint the locus of configurati
onal changes that occur as the trimer fragments into a diatom plus an atom.
Analysis of the angular channel functions and their associated radial comp
onents permits an approximate classification of the vibrational spectrum. (
C) 2000 American Institute of Physics. [S0021-9606(00)00230-0].