Nitroxide‐mediated synthesis of styrenic‐based segmented and tapered block copolymers using poly(lactide)‐functionalized TEMPO macromediators |
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Authors: | Rifat Jabbar Andres Graffe Benoît Lessard Milan Mari? |
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Affiliation: | Department of Chemical Engineering, McGill Institute of Advanced Materials (MIAM), Centre for Self‐Assembled Chemical Structures (CSACS), McGill University, Montréal, Québec, Canada H3A 2B2 |
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Abstract: | Poly(styrene)‐poly(lactide) (PS‐PLA), poly (tert‐butyl styrene)‐poly(lactide) (PtBuS‐PLA) diblocks, and poly(tert‐butyl styrene)‐poly(styrene)‐poly(lactide) (PtBuS‐PS‐PLA) segmented and tapered triblocks of controlled segment lengths were synthesized using nitroxide‐mediated controlled radical polymerization. Well‐defined PLA‐functionalized macromediators derived from hydroxyl terminated TEMPO (PLAT) of various molecular weights mediated polymerizations of the styrenic monomers in bulk and in dimethylformamide (DMF) solution at 120–130°C. PS‐PLA and PtBuS‐PLA diblocks were characterized by narrow molecular weight distributions (polydispersity index (Mw/Mn) < 1.3) when using the PLAT mediator with the lowest number average molecular weight Mn= 6.1 kg/mol while broader molecular weight distributions were exhibited (Mw/Mn = 1.47‐1.65) when using higher molecular weight mediators (Mn = 7.4 kg/mol and 11.3 kg/mol). Segmented PtBuS‐PS‐PLA triblocks were initiated cleanly from PtBuS‐PLA diblocks although polymerizations were very rapid with PS segments ~ 5–10 kg/mol added within 3–10 min of polymerization at 130°C in 50 wt % DMF solution. Tapering from the PtBuS to the PS segment in semibatch mode at a lower temperature of 120°C and in 50 wt % DMF solution was effective in incorporating a short random segment of PtBuS‐ran‐PS while maintaining a relatively narrow monomodal molecular weight distribution (Mw/Mn ≈ 1.5). © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008 |
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Keywords: | block copolymers polystyrene ring‐opening polymerization radical polymerization templates |
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