Recent application of the methods of surface dilational rheology to solutions of the complexes between synthetic polyelectrolytes and oppositely charged surfactants (PSC) gave a possibility to determine some steps of the adsorption layer formation and to discover an abrupt transition connected with the formation of microaggregates at the liquid surface. The kinetic dependencies of the dynamic surface elasticity are always monotonous at low surfactant concentrations but can have one or two local maxima in the range beyond the critical aggregation concentration. The first maximum is accompanied by the generation of higher harmonics of induced surface tension oscillations and caused by heterogeneities in the adsorption layer. The formation of a multilayered structure at the surface for some systems leads to the second maximum in the dynamic surface elasticity. The hydrophobicity and charge density of a polymer chain influence strongly the surface structure, resulting in a variety of dynamic surface properties of PSC solutions. Optical methods and atomic force microscopy give additional information for the systems under consideration. Experimental results and existing theoretical frameworks are reviewed with emphasis on the general features of all studied PSC systems. (C) 2011 Elsevier B.V. All rights reserved.