Calorimetric and dielectric results for crystallizable poly(n-alkyl methacrylates) (PnAMA) with C = 12, 16 and 18 alkyl carbons per side chain are presented. Degree of crystallization D-cal and melting peak temperature T-M are estimated from conventional DSC measurements. For poly(n-hexadecyl methacrylate) (C = 16) the influence of isothermal crystallization is studied by DSC as well as TMDSC. Changes in dielectric relaxation strength Deltaepsilon and alpha peak shape during crystallization are investigated. Effects of side chain crystallization on the complex dynamics of PnAMA are discussed. The results are related to the relaxation behavior of lower nanophase-separated PnAMA with two co-existing glass transitions, the conventional glass transition (alpha or alpha) and the polyethylene-like glass transition (alpha(PE)) within alkyl nanodomains formed by aggregated alkyl rests. It is shown that amorphous as well as semicrystalline PnAMA can be understood as nanophase- separated polymers with alkyl nanodomains having a typical dimension of 1-2 nm. The results are compared with the predictions of simple morphological pictures for side chain polymers. X-ray scattering data for the amorphous and semicrystalline PnAMA are included in the discussion. Common aspects of nanophase-separated systems in both states as well as differences caused by crystallization are discussed. Indications for the existence of rigid amorphous regions are compiled. Different approaches to explain a similar increase of T-g(alpha(PE))-the glass temperature of the amorphous alkyl nanodomains-and T-M-the melting temperature of crystalline alkyl nanodomains-with side chain length are considered. Pros and cons of both approaches, based on increasing order within the alkyl nanodomains and confinement effects in nanophase-separated systems, are discussed. Main trends concerning crystallization and cooperative dynamics are compared with those in other systems with self-assembled nanometer confinements like microphase-separated blockcopolymers or semicrystalline main chain polymers. (C) 2003 Elsevier Science B.V. All rights reserved.