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Assembled triphenylamine -urea macrocycles: exploring photodriven electron transfer from host to guests

Absorption of electronic acceptors in the accessible channels of an assembled triphenylamine (TPA) bis -urea macrocycle 1 enabled the study of electron transfer from the walls of the TPA framework to the encapsulated guests. The TPA host is isoskeletal in all host-guest structures analyzed with gues...

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Published in:Physical chemistry chemical physics : PCCP 2021-10, Vol.23 (41), p.23953-2396
Main Authors: Islam, Md Faizul, Sindt, Ammon J, Hossain, Muhammad Saddam, Ayare, Pooja J, Smith, Mark D, Vannucci, Aaron K, Garashchuk, Sophya, Shimizu, Linda S
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container_issue 41
container_start_page 23953
container_title Physical chemistry chemical physics : PCCP
container_volume 23
creator Islam, Md Faizul
Sindt, Ammon J
Hossain, Muhammad Saddam
Ayare, Pooja J
Smith, Mark D
Vannucci, Aaron K
Garashchuk, Sophya
Shimizu, Linda S
description Absorption of electronic acceptors in the accessible channels of an assembled triphenylamine (TPA) bis -urea macrocycle 1 enabled the study of electron transfer from the walls of the TPA framework to the encapsulated guests. The TPA host is isoskeletal in all host-guest structures analyzed with guests 2,1,3-benzothiadiazole, 2,5-dichlorobenzoquinone and I 2 loading in single-crystal-to-single-crystal transformations. Analysis of the crystal structures highlights how the spatial proximity and orientation of the TPA host and the entrapped guests influence their resulting photophysical properties and allow direct comparison of the different donor-acceptor complexes. Diffuse reflectance spectroscopy shows that upon complex formation 1 ·2,5-dichlorobenzoquinone exhibits a charge transfer (CT) transition. Whereas, the 1 ·2,1,3-benzothiadiazole complex undergoes a photoinduced electron transfer (PET) upon irradiation with 365 nm LEDs. The CT absorptions were also identified with the aid of time dependent density functional theory (TD-DFT) calculations. Cyclic voltammetry experiments show that 2,1,3-benzothiadiazole undergoes reversible reduction within the host-guest complex. Moreover, the optical band gaps of the host 1 ·2,5-dichlorobenzoquinone (1.66 eV), and host 1 ·2,1,3-benzothiadiazole (2.15 eV) complexes are significantly smaller as compared to the free host 1 material (3.19 eV). Overall, understanding this supramolecular electron transfer strategy should pave the way towards designing lower band gap inclusion complexes. Absorption of electron acceptors into assembled triphenylamine bis-urea macrocycles lowers the band gap and triggers host to guest electron transfer.
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title Assembled triphenylamine -urea macrocycles: exploring photodriven electron transfer from host to guests
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