Step-growth polymerization of supracolloidal chains from patchy micelles of diblock copolymers

Hypothesis: The formation of supracolloidal chains from the patchy micelles of diblock copolymers bears a close resemblance to traditional step-growth polymerization of difunctional monomers in many aspects, including chain-length evolution, size distribution, and initial-concentration dependence. Thus, understanding the colloidal polymerization based on the step-growth mechanism can offer potential control over the formation of supracolloidal chains in terms of chain structure and reaction rate.Experiments: We analyzed the size evolution of supracolloidal chains of patchy micelles of PS-b-P4VP by investigating a large number of colloidal chains visualized in SEM images. We varied the initial concentration of patchy micelles to achieve a high degree of polymerization and a cyclic chain. To manipulate the polymerization rate, we also changed the ratio of water to DMF and adjusted the patch size by employing PS(25)-b-P4VP(7) and PS(145)-b-P4VP(40).Findings: We confirmed the step-growth mechanism for the formation supracolloidal chains from patchy micelles of PS-b-P4VP. Based on this mechanism, we were able to achieve a high degree of polymerization early in the reaction by increasing the initial concentration and form cyclic chains by diluting the solution. We also accelerated colloidal polymerization by increasing the ratio of water to DMF in the solution and patch size by using PS-b-P4VP with a larger molecular weight.

Automated summary

Through experiments, we confirmed the step-growth mechanism for the formation of supracolloidal chains from PS-b-P4VP patchy micelles. Based on this mechanism, we were able to achieve high degrees of polymerization early in the reaction by increasing the initial concentration and form cyclic chains by diluting the solution. We also accelerated colloidal polymerization by increasing the ratio of water to DMF in the solution and patch size by using PS-b-P4VP with a larger molecular weight.