Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Aug 13;57(33):10515-10519.
doi: 10.1002/anie.201802392. Epub 2018 Jun 15.

Light-Gated Rotation in a Molecular Motor Functionalized with a Dithienylethene Switch

Affiliations

Light-Gated Rotation in a Molecular Motor Functionalized with a Dithienylethene Switch

Diederik Roke et al. Angew Chem Int Ed Engl. .

Abstract

A multiphotochromic hybrid system is presented in which a light-driven overcrowded alkene-based molecular rotary motor is connected to a dithienylethene photoswitch. Ring closing of the dithienylethene moiety, using an irradiation wavelength different from the wavelength applied to operate the molecular motor, results in inhibition of the rotary motion as is demonstrated by detailed 1 H-NMR and UV/Vis experiments. For the first time, a light-gated molecular motor is thus obtained. Furthermore, the excitation wavelength of the molecular motor is red-shifted from the UV into the visible-light region upon attachment of the dithienylethene switch.

Keywords: alkenes; diarylethenes; molecular motors; molecular switches; photochromism.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Scheme 1
Scheme 1
a) A full 360° rotary cycle of molecular motors 1 and 2 (note that the isomer generated after 180° rotation is identical to the starting isomer, but has a different viewpoint). b) Representation of light‐gated rotary motion through switching between the open and closed form of the appending DTE moiety.
Figure 1
Figure 1
1H‐NMR spectra of 2 in CD2Cl2. i) Before irradiation; ii) PSS 455 nm; iii) PSS 312 nm; iv) sample from (iii) irradiated with 455 nm; v) sample from (ii) irradiated with 312 nm.
Scheme 2
Scheme 2
Photochemical and thermal isomerization steps of hybrid 2.
Figure 2
Figure 2
UV/Vis spectra of hybrid 2 in CH2Cl2 (c=1.8×10−4m). a) After irradiation with 455 nm (−9 °C) followed by 312 nm (−9 °C) and 528 nm (20 °C). b) After irradiation with 312 nm (20 °C) followed by 455 nm (−9 °C) and 528 nm (20 °C).

Similar articles

Cited by

References

    1. Sauvage J.-P., Acc. Chem. Res. 1998, 31, 611–619.
    1. Balzani V., Credi A., Raymo F. M., Stoddart J. F., Angew. Chem. Int. Ed. 2000, 39, 3348–3391; - PubMed
    2. Angew. Chem. 2000, 112, 3484–3530.
    1. Browne W. R., Feringa B. L., Nat. Nanotechnol. 2006, 1, 25–35. - PubMed
    1. Molecular Devices and Machines: Concepts and Perspectives for the Nanoworld, Second ed (Eds.: V. Balzani, A. Credi, M. Venturi), Wiley-VCH, Weinheim, 2008.
    1. Coskun A., Banaszak M., Astumian R. D., Stoddart J. F., Grzybowski B. A., Chem. Soc. Rev. 2012, 41, 19–30. - PubMed

Publication types

LinkOut - more resources