4.3 Article

Formation of Two-dimensionally Ordered Diarylethene Annulated Isomer at the Liquid/HOPG Interface upon In Situ UV Irradiation

Journal

CHEMISTRY LETTERS
Volume 42, Issue 12, Pages 1537-1539

Publisher

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.130705

Keywords

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Funding

  1. NEXT program from JSPS, Japan [GR062]
  2. [25810048]
  3. Grants-in-Aid for Scientific Research [25810048] Funding Source: KAKEN

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A unique photoinduced change in the molecular ordering of a photochromic diarylethene derivative having amide groups was investigated at the liquid/highly oriented pyrolytic graphite (HOPG) interface by scanning tunneling microscopy (STM). Ordering of the diarylethene was stabilized by the hydrogen-bonded network of amide groups. The open- and the closed isomers formed characteristic stripe-patterned orderings; a different hydrogen-bonding network was formed in each case. In situ UV irradiation resulted in the exclusive formation of a third molecular ordering gamma that is composed of the photoirreversible annulated isomer. No photoisomerized molecule was detected in the 2-D orderings, i.e., the open-ring isomer in the ordering of the closed-ring isomer and vice versa, despite the similarity in their molecular structures.

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