Norbornadiene End-Capping of Cross-Coupling Polymerizations: A Facile Route to Triblock Polymers
The potential use of conjugated polymers in device applications is often limited by their less than optimal physicochemical properties. This work describes an efficient protocol to end-cap conjugated polymers synthesized via palladium-catalyzed cross-coupling polymerizations with norbornene groups....
Main Authors: | , , , |
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Other Authors: | , , |
Format: | Article |
Language: | English |
Published: |
American Chemical Society (ACS),
2012-10-24T19:40:42Z.
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Subjects: | |
Online Access: | Get fulltext |
Summary: | The potential use of conjugated polymers in device applications is often limited by their less than optimal physicochemical properties. This work describes an efficient protocol to end-cap conjugated polymers synthesized via palladium-catalyzed cross-coupling polymerizations with norbornene groups. Specifically, the hydroarylation of norbornadiene is shown to be a high-yielding end-capping method. These strained bicyclic alkenyl end groups can be transformed into macroinitiators via ring-opening metathesis polymerization and can polymerize other strained monomers, such as norbornene, yielding elastomeric triblock copolymers. United States. Army Research Office (Contract W911NF-07-D-004) United States. Air Force Office of Scientific Research (FA9550-10-1-0395) |
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