In strongly disordered solids the complex conductivity has a remarkably uni
form dependence on the number of carriers, temperature and frequency. Still
, as we illustrate for randomly packed molecular cluster compounds, it is p
ossible to derive the relevant hopping parameters. In particular the analys
is of the transition from phonon- to photon-assisted hopping in the pair li
mit, when combined with the low-frequency data, yields precise information.
In polymer blends and conjugated polymers the charge mobility behaves in a
qualitatively similar way, but its temperature and frequency dependences d
eviate from the almost universal behaviour in the fully random systems. We
show how these differences relate to the mesoscopic structure.