Synthesis and Characterization of Azadipyrromethene-alt-p

Sep 13, 2012 - X-ray diffraction of the polymers in the solid state showed a lamellar spacing .... André Bessette , Mihaela Cibian , Janaina G. Ferre...
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Article pubs.acs.org/Macromolecules

Synthesis and Characterization of Azadipyrromethene-altp‑Phenylene Ethynylene Conjugated Polymers and Their Chelates Lei Gao,† Saide Tang,‡ Lei Zhu,‡ and Geneviève Sauvé*,† †

Department of Chemistry, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, Ohio 44106, United States Department of Macromolecular Science and Engineering, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, Ohio 44106, United States



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ABSTRACT: Several n-type conjugated polymers incorporating azadipyromethene (aza-DIPY) dyes in the main chain were synthesized by Sonogashira coupling of bisiodo(tetraphenylazadipyrromethene)s with 1,4-bis((2-ethylhexyl)oxy)-2,5-diethynylbenzene. Using branched alkoxy groups on the diethynylbenzene comonomer resulted in polymers with higher molecular weight and higher solubility in organic solvents than our previous report with dodecylalkoxy groups. The physical properties of these polymers were further tuned by coordination of the aza-DIPY moiety with BF2, Cu(I)PEt3, or Ag(I)PEt3 via a postpolymerization reaction. Coordination with the electron-deficient BF2 resulted in improved solubility in organic solvents, higher electron affinity (∼4.5 eV), lower LUMO energy levels (