| Title | Norbornadiene End-Capping of Cross-Coupling Polymerizations: A Facile Route to Triblock Polymers |
| Publication Type | Journal Article |
| Year of Publication | 2012 |
| Authors | Cox, JR, Kang, HA, Igarashi, T, Swager, TM |
| Journal | ACS Macro Letters |
| Volume | 1 |
| Pagination | 334–337 |
| Date Published | feb |
| ISSN | 2161-1653 |
| Keywords | norbornadiene crosscoupling ring opening metathesi, norbornene copolymer macroinitiator hydroarylation |
| Abstract | The potential use of conjugated polymers in device applications is often limited by their less than optimal physicochem. properties. This work describes an efficient protocol to end-cap conjugated polymers synthesized via palladium-catalyzed cross-coupling polymns. 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 polymn. and can polymerize other strained monomers, such as norbornene, yielding elastomeric triblock copolymers. [on SciFinder(R)] |
| URL | http://pubs.acs.org/doi/abs/10.1021/mz200205k |
| DOI | 10.1021/mz200205k |