4.8 Article

2,7-and 4,9-Dialkynyldihydropyrene Molecular Switches: Syntheses, Properties, and Charge Transport in Single-Molecule Junctions

Journal

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c02289

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Funding

  1. Australian Research Councils [DP 150104117, DP 200101659]
  2. School of Physical Sciences Postdoctoral Development Award of the University of Liverpool
  3. Leverhulme Trust [ECF-2018-375]
  4. Royal Society [MR/S015329/2]
  5. University, State and Commonwealth Governments
  6. UKRI Future Leaders Fellowship [URF\R1\191241]

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This paper describes the synthesis methods of several functionalized dihydropyrene (DHP) molecular switches with different substitution patterns and demonstrates their molecular properties and switching capabilities through experiments. The performance of DHPs was assessed by light irradiation experiments, spectroelectrochemistry, and cyclic voltammetry. The molecular structures were elucidated by X-ray single-crystal diffraction. Charge-transport behavior was evaluated by combining density functional theory (DFT) calculations and single-molecule scanning tunneling microscope (STM) measurements.
This paper describes the syntheses of several functionalized dihydropyrene (DHP) molecular switches with different substitution patterns. Regioselective nucleophilic alkylation of a 5-substituted dimethyl isophthalate allowed the development of a workable synthetic protocol for the preparation of 2,7-alkyne-functionalized DHPs. Synthesis of DHPs with surface-anchoring groups in the 2,7- and 4,9-positions is described. The molecular structures of several intermediates and DHPs were elucidated by X-ray single-crystal diffraction. Molecular properties and switching capabilities of both types of DHPs were assessed by light irradiation experiments, spectroelectrochemistry, and cyclic voltammetry. Spectroelectrochemistry, in combination with density functional theory (DFT) calculations, shows reversible electrochemical switching from the DHP forms to the cyclophanediene (CPD) forms. Charge-transport behavior was assessed in single-molecule scanning tunneling microscope (STM) break junctions, combined with density functional theory-based quantum transport calculations. All DHPs with surface-contacting groups form stable molecular junctions. Experiments show that the molecular conductance depends on the substitution pattern of the DHP motif. The conductance was found to decrease with increasing applied bias.

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