O. Dopfer et al., Microsolvation of the water cation in neon: Infrared spectra and potentialenergy surface of the H2O+-Ne open-shell ionic complex, J CHEM PHYS, 114(16), 2001, pp. 7081-7093
The intermolecular potential of the H2O+-Ne open-shell ionic dimer in its d
oublet electronic ground state has been investigated by infrared spectrosco
py in the vicinity of the O-H stretch vibrations (nu (1) and nu (3)) and ab
initio calculations at the unrestricted Moller-Plesset second-order (MP2)
level with a basis set of aug-cc-pVTZ quality. The rovibrational structure
of the photodissociation spectrum is consistent with a proton-bound planar
H-O-H-Ne structure and a Ne-H separation of R-0=1.815(5) Angstrom. The comp
lexation-induced redshifts are Delta nu (1)=-69 cm(-1) and Delta nu (3)=-6
cm(-1), respectively. Tunneling splittings observed in the perpendicular co
mponent of the nu (3) hybrid band of H2O+-Ne are attributed to hindered int
ernal rotation between the two equivalent proton-bound equilibrium structur
es. The interpretation of the H2O+-Ne spectrum is supported by the spectrum
of the monodeuterated species, for which both the proton-bound and the deu
teron-bound isomers are observed (DOH+-Ne, HOD+-Ne). The equilibrium struct
ure of the calculated potential energy surface of H2O+-Ne has a slightly tr
anslinear proton bond, which is characterized by a Ne-H separation of R-e=1
.77 Angstrom, a bond angle of phi (e)=174 degrees, and dissociation energie
s of D-e=756 cm(-1) and D-0=476 cm(-1). According to the calculated potenti
al, the exchange tunneling between the two equivalent minima occurs via the
planar bridged transition state with C-2v symmetry and a barrier of 340 cm
(-1). In general, the calculated properties of H2O+-Ne show good agreement
with the experimental data. Initial steps in the microsolvation of the wate
r cation in neon are discussed by comparing the calculated and experimental
properties of H2O+-Ne-n (n=0-2) with neon matrix isolation data (n --> inf
inity). (C) 2001 American Institute of Physics.