We report a rigorous ab initio study of the ground and low-lying excit
ed-state potential-energy surfaces (PESs) of the Cl-2 radical at CASSC
F, CASPT2, and MRSDCI levels of theory. The ground state has two Cl ..
. Cl-2 van der Waals complexes, (X) over tilde L and (X) over tilde'B.
The linear asymmetric minimum ((X) over tilde L) is (II)-I-2, with a
Cl-Cl distance r = 3.90 bohr, and a Cl-M (M: the Cl-2 center-of-mass)
distance R = 8.70 bohr. The bent asymmetric minimum ((X) over tilde'B)
is of (2)A' symmetry, with r = 3.90 bohr, R = 6.85 bohr, and the angl
e between (r) over cap and (R) over cap, gamma = 68.4 degrees. Spin-or
bit CI (configuration interaction) predicts that the global minimum is
linear (X) over tilde L ((II3/2)-I-2) with a bond dissociation energy
of D-e(Cl-2((X) over tilde)-Cl) of 280 cm(-1). Low-lying doublet exci
ted states have only one strongly bound structure, a linear symmetric
(A) over tilde L (1 (IIg)-I-2) state with a bond distance of 4.67 bohr
. This state is bound by similar to 4300cm(-1) with respect to the Cl-
2((II3/2)-I-3)+Cl asymptote, and its minimum lies about 8700 cm(-1) ab
ove the (X) over tilde L van der Waals minimum. Transition dipole mome
nt calculations show that the (A) over tilde-(X) over tilde transition
is fully allowed. Two bound quartet minima were located. The most dee
ply bound was QD3h (1 (4)A(1)') With a D-3h equilibrium geometry (r =
5.00 bohr) about 11 300 cm(-1) above (X) over tilde L. The other state
, QC2v (1 (4)A(2)) had a C-2v equilibrium geometry (r(1) = 4.83 bohr a
nd theta = 101.7 degrees) and an energy of about 13 500 cm(-1) relativ
e to (X) over tilde L. Although Cl-3((X) over tilde) is shown to be un
stable, the present results support the notion that Cl-3 participates
in Cl atom recombination processes. However, the energies and transiti
on moments of the low-lying excited states are not consistent with ele
ctronic spectra that have been tentatively assigned to Cl-3. (C) 1998
American Institute of Physics.