4.8 Article

Decarboxylative Polymerization of 2,6-Naphthalenedicarboxylic Acid at Surfaces

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 136, Issue 27, Pages 9658-9663

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja5033875

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Funding

  1. Deutsche Forschungsgemeinschaft [SFB 858, TRR 61]
  2. Alexander von Humboldt Foundation

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Metal-catalyzed polymerization of 2,6-naphthalenedicarboxylic acid (NDCA) to form poly-2,6-naphthalenes at various surfaces is reported. Polymerizations occur via initial formal dehydrogenation of self-assembled diacids with subsequent decarboxylation to give polymeric bisnaphthyl-Cu species at elevated temperature as intermediate structures (<160 degrees C). Further temperature increase eventually leads to poly-naphthalenes via reductive elimination. It is demonstrated that the Cu( iii) surface works most efficiently to conduct such polymerizations as compared to the Au(111), Ag(111), Cu(100), and Cu(110) surfaces. Poly-2,6-naphthalene with a chain length of over 50 nm is obtained by using this approach. The decarboxylative coupling of aromatic diacids is a very promising tool which further enlarges the portfolio of reactions allowing for on-surface polymerizations and novel organometallic systems preparations.

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