Abstract
The potential control over monomer sequence in the ring-opening metathesis polymerization of functional norbornenes is explored based on the difference in reactivity of endo and exo isomers. This kinetic approach allows the rapid consumption of the exo-norbornene and insertion onto the growing poly(norbornene) chain within a narrow region of the overall polymer chain, whilst maintaining a homogeneous backbone. We herein demonstrate that this can be achieved using a range of functional monomers easily derived from commercially available precursors while their polymerization is carried out in a controlled manner. This journal is © the Partner Organisations 2014.
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CITATION STYLE
Moatsou, D., Hansell, C. F., & O’Reilly, R. K. (2014). Precision polymers: A kinetic approach for functional poly(norbornenes). Chemical Science, 5(6), 2246–2250. https://doi.org/10.1039/c4sc00752b
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