Copolymerization of two AB(2)-type monomers that incorporate spacer segments of similar lengths but different flexibility permitted, for the first time, the preparation of a range of hyperbranched copolymers, wherein the backbone rigidity was varied while maintaining similar branching densities. The copolymers were prepared via a recently developed melt trans etherification methodology to yield moderately high molecular weight polymers, with molecular weights ranging from 20 000 to 50 000. H-1 NMR spectroscopic studies revealed that the composition of the copolymers varied linearly with monomer composition, confirming the formation of truly random copolymers. Analogous linear copolymers based on suitably designed AB-type monomers, containing the same two spacers, were also prepared for comparison. Thermal analysis of these copolymers using DSC indicated that the T-g's of both linear copolymers and hyperbranched copolymers varied with composition in a manner that was in complete accordance with the Fox equation, although all the linear copolymers exhibited significantly higher T-g values than their hyperbranched counterparts. It is interesting that, despite their very different topology and the presence of large number of chain ends, hyperbranched copolymers exhibit a similar T-g variation as their linear analogues. The generality of this observation in the broader context of hyperbranched copolymers, such as those possessing different branching densities and terminal functionalities, remains to be tested.