Journal
MACROMOLECULAR RAPID COMMUNICATIONS
Volume 37, Issue 1, Pages 79-85Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.201500587
Keywords
catalyst transfer; end functionalization; Pd catalyst; pi-conjugated polymer; Suzuki polycondensation; unstoichiometric polycondensation
Categories
Funding
- Japan Society for the Promotion of Science (JSPS) [15H03819]
- MEXT
Ask authors/readers for more resources
The Suzuki-Miyaura coupling polymerization of dibromoarene 1 and arylenediboronic acid (ester) 2 with a Pd catalyst having a high propensity for intramolecular catalyst transfer is reported. The polymerization of excess 1 with 2 affords high-molecular-weight p-conjugated polymer having boronic acid (ester) moieties at both ends, contrary to Flory's principle. This unstoichiometric polycondensation behavior is accounted for by intramolecular transfer of the Pd catalyst on 1. In the polymerization of 1 and 2 having different aryl residues, high-molecular-weight polymer is obtained when the stronger donor aromatic is used as the dibromo monomer and the weaker donor or acceptor aromatic is used as diboronic acid (ester) monomer. The pinacol boronate moieties at both ends of the obtained poly(p-phenylene) (PPP) can be converted to benzoic acid ester, hydroxyl group, and bromine. Furthermore, the reaction of the pinacol boronate-terminated PPP with poly(3-hexylthiophene) (P3HT) having bromine at one end yields a triblock copolymer of P3HT-b-PPP-b-P3HT.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available