Abstract
Carboxyl-terminated polystyrene was esterified with 2,2,2-trifluoroethanol using a carbodiimide-mediated room temperature reaction, and hydroxyl-terminated polystyrene was fluoro-derivatized with trifluoroacetic anhydride. The soformed fluorine-containing esters were then quantitatively determined with 19F NMR, using α,α,α-trifluorotoluene as secondary standard. This provides a technique for the reliable determination of carboxylic acid and hydroxyl groups in small samples of polymers.
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CITATION STYLE
Rajan, M., Cotiuga, I., Ma, Y., Picchioni, F., & Agarwal, U. S. (2003). Determination of acid and hydroxyl end-groups in endfunctionalized polystyrenes using 19F NMR. E-Polymers, 3(1). https://doi.org/10.1515/epoly.2003.3.1.608
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