Nonstoichiometric Direct Arylation Polymerization of Octafluorobiphenyl with 2,7-Diiodofluorene for Regulating CH Terminals of π-Conjugated Polymer

Macromol Rapid Commun. 2024 Jan;45(1):e2300225. doi: 10.1002/marc.202300225. Epub 2023 Jun 9.

Abstract

Nonstoichiometric direct arylation polycondensation of 2,2',3,3',5,5',6,6'-octafluorobiphenyl with excess of 2,7-diiodo-9,9-dioctyl-9H-fluorene is demonstrated. Pd/Ag dual-catalyst system under water/2-methyltetrahydrofuran biphasic conditions enables direct arylation under mild conditions and promotes the intramolecular transfer of a Pd catalyst walking through the fluorene moiety. The nonstoichiometric direct arylation polycondensation under the optimized reaction conditions produces the corresponding π-conjugated polymer with a high molecular weight and terminal octafluorobiphenyl units at both ends.

Keywords: conjugated polymers; direct arylation; intramolecular catalyst transfer; nonstoichiometric polycondensation.

MeSH terms

  • Catalysis
  • Fluorenes*
  • Hydrocarbons, Fluorinated / chemistry
  • Palladium / chemistry
  • Polymerization
  • Polymers*

Substances

  • fluorene
  • Fluorenes
  • Polymers
  • Palladium
  • Hydrocarbons, Fluorinated