The syntheses of methacrylic monomers of the general structure [GRAPHICS] where n is 3, 4, 5, or 6, were performed by the reaction of the corresponding alcohol ethers with methacryloyl chloride. The alcohol ethers were previously prepared by different synthetic procedures involving the monoetherification of the starting glycols. The polymerizations kinetics of the monomers were examined at several temperatures in the bulk and in dioxane solutions. NMR spectroscopy and electron paramagnetic resonance techniques were used to study the kinetics of polymerization. The polymerization rate parameter, expressed as (2f)(1/2)k(p)/(1/2), and the values of the propagation rate coefficient k(p) and the termination rate coefficient /f, where f is the efficiency factor of the initiator, were determined. The reactivity of the monomers depended on the size of the ester residue in such a way that the longer the lateral chain was, the higher the polymerization rate was and the lower the termination rate coefficient was. On the contrary, the dependence of k(p) on the chemical structure was very small. In the solution polymerizations of all these monomers (monomer concentration = 1 mol L-1), the radical concentrations remained almost constant until very high conversions, whereas in the bulk, a different behavior was observed that depended on the number of oxyethylene units in the side chain of the monomer. In this sense, for n = 4, 5, or 6, the radical concentration remained almost invariable with the reaction time, whereas for n = 3, a moderate increase occurred at low conversions, contrasting with the important increase observed at similar conversions for n = 1. This showed that the gel effect in these methacrylic monomers was greatly dependent on the number of bonds of the lateral chain. (C) 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polyrn Chem 41: 1567-1579, 2003.