A highly versatile new strategy for manipulating the molecular weight profiles, including breadth, asymmetry (skewness) and modal nature (mono-, bi-, and multimodal), of a variety of different polyolefins is reported. It involves temporal control over two- and three-state living coordinative chain transfer polymerization (LCCTP) of olefins in a programmable way. By changing the identity of the R' groups of the chain transfer agent, ER'n , with time, different populations of chains within a bi- or multimodal polyolefin product can be selectively tagged with different end-groups. By changing the nature of the main-group metal of the CTA, programmed manipulation of the relative magnitudes of the dispersities of the different maxima that make up the final MWD profile can be achieved. This strategy can be implemented with existing LCCTP materials and conventional reactor methods to provide access to scalable and practical quantities of an unlimited array of new polyolefin materials.
Keywords: coordinative chain transfer; living polymerization; molecular weight distribution; polyolefins.
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