Abstract
Photochemically induced grafting (1) and graft polymerization (2) from N,N‐dimethylformamide solutions of four acryloxy‐substituted aromatic diazenes, chosen as model molecules of acryloxy azo dyes, were investigated kinetically at 25°C onto polypropylene, polycaprolactam, and poly(ethylene terephtalate) films, by polychromatic irradiations. Quantum efficiencies at zero concentration of dyes and lifetimes of excited states for processes (1) and (2) were evaluated from experimental data by Stern–Volmer plots. The surface density of grafted molecules at the end of process (1) was not affected by the concentration of dyes in solution, but varied sensibly with the chemical nature of polymers and dyes. The relevant parameters are discussed on the basis of the proposed mechanism.