| Literature DB >> 30998349 |
Kabali Senthilkumar1, Mateusz Kondratowicz1, Tadeusz Lis1, Piotr J Chmielewski1, Joanna Cybińska1,2, José L Zafra3, Juan Casado3, Thomas Vives4, Jeanne Crassous5, Ludovic Favereau5, Marcin Stępień1.
Abstract
A cycloparaphenylene-based molecular lemniscate (CPPL) was obtained in a short synthesis involving masked p-phenylene equivalents. The strained figure-eight geometry of CPPL is sustained by the incorporated 9,9'-bicarbazole subunit, which also acts as a stereogenic element. The shape of the distorted [16]cycloparaphenylene nanohoop embedded in CPPL is accurately approximated with a Booth lemniscate. The structure of CPPL, investigated using NMR and Raman spectroscopic methods, revealed strain-dependent features, consistent with the variable curvature of the ring. The electronic and optical properties of CPPL combine features more characteristic of smaller cycloparaphenylenes, such as a reduced optical bandgap and red-shifted fluorescence. CPPL was resolved into enantiomers, which are configurationally stable and provide strong chiroptical responses, including circularly polarized luminescence.Entities:
Year: 2019 PMID: 30998349 DOI: 10.1021/jacs.9b01797
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419