Laser spectroscopy of (ν=0,R=1)10F and (ν=0,R=1)10G states ofH2: A test of the polarization model

Abstract
Rydberg states of H2 consisting of a 10F or 10G electron bound to the ν=0,R=1 state of H2+ are studied using Doppler-tuned laser spectroscopy of Rydberg-Rydberg transitions. The positions of all such states are measured to a precision of better than 0.01 cm1 and are compared with the predictions of the polarization model. The polarization model is derived from first principles. Nonadiabatic corrections to the dipole polarization energies, calculated for the first time, are found to be expressible in terms of the S3-moment functions of H2+. Higher-order adiabatic polarization energies are estimated from calculated higher-order H2+ polarizabilities.