| Abstract: | Block copolymers have become an integral part of the preparation of complex architectures through self‐assembly. The use of reversible addition–fragmentation chain transfer (RAFT) allows blocks ranging from functional to nonfunctional polymers to be made with predictable molecular weight distributions. This article models block formation by varying many of the kinetic parameters. The simulations provide insight into the overall polydispersities (PDIs) that will be obtained when the chain‐transfer constants in the main equilibrium steps are varied from 100 to 0.5. When the first dormant block [polymer–S? C(Z)?S] has a PDI of 1 and the second propagating radical has a low reactivity to the RAFT moiety, the overall PDI will be greater than 1 and dependent on the weight fraction of each block. When the first block has a PDI of 2 and the second propagating radical has a low reactivity to the RAFT moiety, the PDI will decrease to around 1.5 because of random coupling of two broad distributions. It is also shown how we can in principle use only one RAFT agent to obtain block copolymers with any desired molecular weight distribution. We can accomplish this by maintaining the monomer concentration at a constant level in the reactor over the course of the reaction. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5643–5651, 2005 |
