Linear polyurethane, linear segmented polyurethane, polyurethane networks, and polyurethane acrylate networks of various composition were synthesized. The variation of T-g with the type of macrodiol, its length, and the chemical composition of the polymer were studied in relation with the percentage of soft segments, the molar mass between crosslinks, and the concentration of urethane bonds. In this work, the networks were considered as composed of chain segments of various composition between point-like crosslinks. The chemical heterogeneities of the networks were not taken into account. For polyurethanes, it was shown that T-g values are essentially controlled by the amount of urethane bonds. For polyurethane acrylates, the T-g values are dependent on the amount of urethane bonds but also on the presence of crosslinks whose number is varying with the excess of diisocyanate of the first step three times faster for PUA compared with PU. No clear relation was observed between T-g and the molar mass between point-like crosslinks. Another approach considering the network heterogeneities is indispensable and will be used in a following work.