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Amphiphilic Block Copolymers Containing Regioregular Poly(3-hexylthiophene) and Poly(2-ethyl-2-oxazoline)

Poly(3‐hexylthiophene)‐block‐poly(2‐ethyl‐2‐oxazoline) amphiphilic rod–coil diblock copolymers have been synthesized by a combination of Grignard metathesis (GRIM) and ring‐opening cationic polymerization. Diblock copolymers containing 5, 15, and 30 mol‐% poly(2‐ethyl‐2‐oxazoline) have been synthesi...

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Bibliographic Details
Published in:Macromolecular chemistry and physics 2010-06, Vol.211 (12), p.1291-1297
Main Authors: Alemseghed, Mussie G., Servello, John, Hundt, Nadia, Sista, Prakash, Biewer, Michael C., Stefan, Mihaela C.
Format: Article
Language:English
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Summary:Poly(3‐hexylthiophene)‐block‐poly(2‐ethyl‐2‐oxazoline) amphiphilic rod–coil diblock copolymers have been synthesized by a combination of Grignard metathesis (GRIM) and ring‐opening cationic polymerization. Diblock copolymers containing 5, 15, and 30 mol‐% poly(2‐ethyl‐2‐oxazoline) have been synthesized and characterized. The synthesized rod–coil block copolymers display nanofibrillar morphology where the density of the nanofibrills is dependent on the concentration of the poly(2‐ethyl‐2‐oxazoline) coil segment. The conductivity of the diblock copolymers was lowered from 200 to 35 S · cm−1 with an increase in the content of the insulating poly(2‐ethyl‐2‐oxazoline) block. By contrast, the field‐effect mobility decreased by 2–3 orders of magnitude upon the incorporation of the poly(2‐ethyl‐2‐oxazoline) insulating segment. Hydrophobic semiconducting poly(3‐hexylthiophene) has been incorporated in block copolymers with hydrophilic poly(2‐ethyl‐2‐oxazoline). The synthesized block‐copolymers have good conductivities. By contrast, the incorporation of hydrophilic insulating poly(2‐ethyl‐2‐oxazoline) resulted in the decrease of field‐effect mobilities by 2–3 orders of magnitude. Solvatochromic behavior of the poly(3‐hexylthiophene)‐block‐poly(2‐ethyl‐2‐oxazoline) diblock copolymers have been observed in tetrahydrofuran/water mixtures.
ISSN:1022-1352
1521-3935
DOI:10.1002/macp.200900725