Chiral Dibenzopentalene‐Based Conjugated Nanohoops through Stereoselective Synthesis. Issue 19 (23rd March 2021)

• Record Type: Journal Article
• Authors: Hermann, Mathias; Wassy, Daniel; Kohn, Julia; Seitz, Philipp; Betschart, Martin U.; Grimme, Stefan; Esser, Birgit
• Is Part Of: Angewandte Chemie international edition. Volume 60:Issue 19(2021)
• Page Start: 10680
• Page End: 10689
• Publication Date: 2021-03-23
• Subjects: antiaromaticity -- chiral macrocycles -- chiral resolution -- cycloparaphenylenes -- fullerenes; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202016968
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Conjugated nanohoops allow to investigate the effect of radial conjugation and bending on the involved π‐systems. They can possess unexpected optoelectronic properties and their radially oriented π‐system makes them attractive for host–guest chemistry. Bending the π‐subsystems can lead to chiral hoops. Herein, we report the stereoselective synthesis of two enantiomers of chiral conjugated nanohoops by incorporating dibenzo[ a, e ]pentalenes (DBPs), which are generated in the last synthetic step from enantiomerically pure diketone precursors. Owing to its bent shape, this diketone unit was used as the only bent precursor and novel "corner unit" in the synthesis of the hoops. The [6]DBP[4]Ph‐hoops contain six antiaromatic DBP units and four bridging phenylene groups. The small HOMO–LUMO gap and ambipolar electrochemical character of the DBP units is reflected in the optoelectronic properties of the hoop. Electronic circular dichroism spectra and MD simulations showed that the chiral hoop did not racemize even when heated to 110 °C. Due to its large diameter, it was able to accommodate two C60 molecules, as binding studies indicate. Abstract : Chiral, dibenzo[ a, e ]pentalene‐based conjugated nanohoops were synthesized in a stereoselective way from enantiomerically pure diketone precursors. The hoop shows ambipolar electrochemical behavior due to the antiaromaticity of the dibenzopentalene units and can accommodate two fullerene molecules. Circular dichroism measurements and molecular dynamics simulations indicated no racemization even at 110 °C.