| Literature DB >> 33784461 |
Matthew B Minus1,2, Sarah R Moor2, Fathima F Pary3, L P T Nirmani3, Malgorzata Chwatko4, Brandon Okeke2, Josh E Singleton1, Toby L Nelson3, Nathaniel A Lynd4, Eric V Anslyn2.
Abstract
Typically, Suzuki couplings used in polymerizations are performed at raised temperatures in inert atmospheres. As a result, the synthesis of aromatic materials that utilize this chemistry often demands expensive and specialized equipment on an industrial scale. Herein, we describe a bimetallic methodology that exploits the distinct reactivities of palladium and copper to perform high yielding aryl-aryl dimerizations and polymerizations that can be performed on a benchtop under ambient conditions. These couplings are facile and can be performed by simple mixing in the open vessel. To demonstrate the utility of this method in the context of polymer synthesis: polyfluorene, polycarbazole, polysilafluorene, and poly(6,12-dihydro-dithienoindacenodithiophene) were created at ambient temperature and open to air.Entities:
Year: 2021 PMID: 33784461 PMCID: PMC8982272 DOI: 10.1021/acs.orglett.1c00479
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005