Abstract

We address a central question in the realm of the dynamics of high-n (= 40- 250) Rydberg states of diatomics and large molecules. What is the coupling responsible for the 'global' l mixing, which results in the breakdown of the n 3 scaling law for the non-radiative lifetimes and for the lifetime lengthening (by two to four orders of magnitude) of these states? To explore the implications of intramolecular interactions on l mixing and on electronic-rotational energy exchange we analysed the intramolecular couplings of the ion core dipole, quadrupole and (anisotropic) polarizability with a non-penetrating (l⩾ 3) Rydberg electron, in conjunction with the energy gaps between proximal pairs of energy levels. Calculations of the energy gaps and the couplings were performed for the high-n non-penetrating Rydberg states of NO and for model 'light' (B = 19 cm-1) and 'heavy' (B = 0⋅05 cm-1) polar molecules. All the intramolecular interactions are of the form of a power law proportional to l -η, with η being determined by the nature of the long-range coupling, by the l dependence of the quantum defects for multipole couplings and by the l dependence of angular integrals. We established a bottleneck effect for the intramolecular couplings between non-penetrating (l⩾3) states. For n- and N+-changing dipole, quadrupole and polarizability interactions the energetics ofthe proximalpairs of levels, in conjunction with the bottleneck effect,prohibit the |n, l, N +, N> - |n', l', N +', N>, l (⩾ 3) couplings (with n ╪ n') and the electronic-rotational energy exchange. For n- and N +-conserving quadrupole and polarizability interactions, the l (⩾ 3) mixing (which prevails only for l N ++ N) is also prohibited by the bottleneck effect. 'Global' intramolecular l mixing (with both n ╪ n' and n = n') in diatomics and in large molecules is precluded, implying that the dramatic lengthening of the non-radiative lifetimes of high-n Rydberg states can be induced only by exterior electric field coupling.

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