The rotationally resolved spectrum of the dimer (N2O)(2) has been reco
rded in the region of the monomer N2O nu(3) vibrational band using a d
iode laser absorption spectrometer which incorporates a multiple-pass
cell and a pulsed-jet expansion. A double-modulation technique involvi
ng a fast modulation of the laser frequency and a slow modulation of t
he gas pulse has been developed in the experiments. The spectrum is co
mpletely analysed and the rotational constants and effective structure
s are accurately determined for both the ground and the excited vibrat
ional states. The centrosymmetric slipped parallel structure of (N2O)(
2) is well explained by an intermolecular potential containing a combi
nation of electrostatic interactions between distributed multipoles of
different monomers and atom-atom Lennard-Jones potentials to describe
the repulsion and dispersion interactions.