Polycarbonate-based polymers with a well-defined architecture have become interesting materials due to their large range of applications. Ring opening polymerization (ROP) has been largely applied to make branched polycarbonates. The polymer architectures obtained via this method are strictly related with the polymerization mechanisms involved which depend on the polymerization conditions chosen. Hereby, we evaluate the catalytic activity of three acids, fumaric, trifluoroacetic, and methanesulfonic on the Cationic ROP of trimethylene carbonate (TMC) over a trifunctional initiator, trimethylol propane (TMP), under different reaction conditions. In-detail characterization of the polymers showed the co-existence of two polymerization mechanisms: the activated monomer (AM), which produces a tri-armed branched polycarbonate with inclusion of the TMP initiator (TMP-PTMC), and a combined AM/Activated Chain End (ACE) mechanism, which produces a linear polycarbonate (L-PTMC). Such mixtures were identified for nearly all the reaction variables investigated, together with other side reactions. Upon optimization of the synthesis, the polymerizations in toluene with TFA at 35 °C and equimolar acid/initiator ratio were optimal, avoiding side reactions, but still resulting in a polymer mixture composed of ∼69% TMP-PTMC and 31% of a polycarbonate linear polymer. The occurrence of such mixed polymer architectures is commonly overlooked in literature regarding CROP of branched polycarbonates. We demonstrate the importance of performing a full characterization for a successful detection of polymer mixtures having different (number of) end-functionalities, which are critical for further use in advanced applications, such as in the biomedical or pharmaceutical filed.
|Tijdschrift||Journal of Polymer Science, Part A: Polymer Chemistry|
|Nummer van het tijdschrift||9|
|Status||Gepubliceerd - 1 mei 2017|