These are preliminary reports that have not been peer-reviewed. They should not be regarded as conclusive, guide clinical practice/health-related behavior, or be reported in news media as established information. For more information, please see our FAQs.
Xu Porphyrinylene Nanohoop ChemRxiv.pdf (11.47 MB)

Highly Strained, Radially π-Conjugated Porphyrinylene Nanohoops

submitted on 08.08.2019, 09:46 and posted on 08.08.2019, 14:43 by Youzhi Xu, Sebastian Gsänger, Martin B. Minameyer, Inhar Imaz, Daniel Maspoch, Oleksandr Shyshov, Fabian Schwer, Xavi Ribas, Thomas Drewello, Bernd Meyer, Max von Delius

Small π conjugated nanohoops are difficult to prepare, but offer an excellent platform for studying the interplay between strain and optoelectronic properties and increasingly, these shape persistent macrocycles find uses in host guest chemistry and self assembly. We report the synthesis of a new family of radially π conjugated porphyrinylene/phenylene nanohoops. The strain energy in the smallest nanohoop [2]CPT is approx-imately 54 kcal mol-1, which results in a narrowed HOMO LUMO gap and a red shift in the visible part of the absorption spectrum. Due to its high degree of preorganization and a diameter of ca. 13 Å, [2]CPT was found to accommodate C60 with a binding affinity exceeding 108 M-1 despite the fullerene not fully entering the cavity of the host (X Ray crystallography). Moreover, the π extended nanohoops [2]CPTN , [3]CPTN and [3]CPTA (N for 1,4 naphthyl; A for 9,10 anthracenyl) have been prepared using the same strategy, and [2]CPTN has been shown to bind C70 five times more strongly than [2]CPT. Our failed synthesis of [2]CPTA highlights a limitation of the experimental approach most commonly used to prepare strained nanohoops, because in this particular case the sum of aromatization energies no longer outweighs the buildup of ring strain in the final reaction step (DFT calculations). These results indicate that forcing ring strain onto organic semiconductors is a viable strategy to fundamentally influence both optoelectronic and supramolecular properties.


Email Address of Submitting Author


University of Ulm



ORCID For Submitting Author


Declaration of Conflict of Interest

No conflict of interest


Read the published paper

in Journal of the American Chemical Society