4.6 Article

Synthesis, Physical Properties, and Anion Recognition of Two Novel Larger Azaacenes: Benzannelated Hexazaheptacene and Benzannelated N,N-Dihydrohexazaheptacene

Journal

CHEMISTRY-AN ASIAN JOURNAL
Volume 8, Issue 7, Pages 1574-1578

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.201300208

Keywords

anion recognition; heteroacenes; nitrogen heterocycles; semiconductors; sensors

Funding

  1. AcRF Tier 1 from MOE [RG 18/09]
  2. AcRF Tier 2 from MOE [ARC 20/12]
  3. CREATE program (Nanomaterials for Energy and Water Management) from NRF
  4. New Initiative Fund from NTU, Singapore

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Two novel larger azaacenes with six or ten N atoms in their backbones, benzannelated 9,11,13,22,24,26-hexazatetrabenzo[a,c,l,n]heptacene (HATBH, 1) and benzannelated 9,26-dihydro-9,11,13,22,24,26-hexaza-tetrapyrido[3,2-a: 2,3-c: 3,2-l: 2,3-n]heptacene (DHATPH, 2), have been successfully synthesized in two steps. The theoretical band gaps estimated through DFT calculations for HATBH (1) and DHATPH (2) are 1.949eV and 2.278eV, which are close to the experimentally obtained optical band gaps (2.14eV and 2.39eV). Interestingly, HATBH (1) can act as efficient anion sensor for F- and H2PO4-, while DHATPH (2) selectively responds to F- among the ten different anions used (F-, Cl-, Br-, I-, PF6-, HSO4-, NO3-, BF4-, AcO-, and H2PO4-). Our synthetic strategy could offer a promising and easy way to obtain even larger azaacenes.

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