Abstract
Merrifield and Wang resins were successfully converted to supported vinyl-functionalized solid supports with excellent yields by reacting the Cl or OH functionality with an α,ω-difunctional spacer bearing a carboxylic acid group and a terminal alkene. The ruthenium initiator (PCy3)2Cl2Ru = CHPh (Grubbs I catalyst) was then immobilized on the resins via cross metathesis (alkylidene exchange) and was used to initiate ROMP of norbornene. Number-average molecular weight and polydispersity index of the grafted polymers were determined after cleavage of the ester link between the resin and the spacer. The results showed a competition between ROMP and intramolecular "ring-closing" metathesis and/or intermolecular "cross" metathesis, which leads to an overestimated ruthenium initiator loading. © 2007 Elsevier B.V. All rights reserved.
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Lapinte, V., Montembault, V., Houdayer, A., & Fontaine, L. (2007). Surface initiated ring-opening metathesis polymerization of norbornene onto Wang and Merrifield resins. Journal of Molecular Catalysis A: Chemical, 276(1–2), 219–225. https://doi.org/10.1016/j.molcata.2007.06.028
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