ABSTRACT:The reversible addition-fragmentation chain transfer-chain length dependent termination (RAFT-CLD-T) method has allowed us to answer a number of fundamental questions regarding the mechanism of diffusion-controlled bimolecular termination in free-radical polymerization (FRP). We carried out RAFTmediated polymerizations of methyl acrylate (MA) in the presence of a star matrix to develop an understanding of the effect of polymer matrix architecture on the termination of linear polyMA radicals and compared this to polystyrene, polymethyl methacrylate, and polyvinyl acetate systems. It was found that the matrix architecture had little or no influence on termination in the dilute regime.However, due to the smaller hydrodynamic volumes of the stars in solution compared to linear polymer of the same molecular weight, the gel onset point occurred at greater conversions, and supported the postulate that chain overlap (or c*) is the main cause for the observed autoacceleration observed in FRP. Other theories based on \short-long" termination or free-volume should be disregarded. Additionally, since our systems are well below the entanglement molecular weight, entanglements should also be disregarded as the cause of the gel onset. The semidilute regime occurs over a small conversion range and is difficult to quantify. However, we obtain accurate dependencies for termination in the concentrated regime, and observed that the star polymers (through the tethering of the arms) provided constriction points in the matrix that significantly slow the diffusion of linear polymeric radicals. Although, this could at first sight be postulated to be due to reptation, the dependencies showed that reptation could be considered only at very high conversions (close to the glass transition regime). In general, we find from our data that the polymer matrix is much more mobile than what is expected if reptation were to dominate.