The Na+-NO adsorption complex in zeolite NaA was investigated in a wide tem
perature range from 4 to 300 K by electron paramagnetic resonance (EPR) spe
ctroscopy. The ground state of the adsorbed NO molecules and the rotational
ground state of the (2)Pi(3/2) State of desorbed gaseous NO could be obser
ved. At low temperatures the NO molecules were found to be coordinated to t
he sodium ion in a bent complex structure. The EPR spectra are subjected to
motional averaging by a two-site jump process between two chemically ident
ical complex structures at T > 30 K. Desorption processes of the NO molecul
es from the Lewis acid centres manifest themselves in homogeneous line broa
dening effects in the EPR spectra of the distorted (2)Pi(1/2) state of NO i
n the Na+-NO adsorption complex at higher temperatures. In this model, the
homogeneous linewidths are determined by the lifetime of the adsorption com
plex and provide a direct measure of the adsorption energy of NO at the sod
ium cation sites. Furthermore, desorption of the nitric oxide from the zeol
ite was monitored simultaneously by the EPR signal of the (2)Pi(3/2) state
of free NO molecules in the gas phase to support this approach. Copyright (
C) 1999 John Wiley & Sons, Ltd.