Conjugated Nanohoops Incorporating Donor, Acceptor, Hetero- or Polycyclic Aromatics

Angew Chem Int Ed Engl. 2021 Jul 12;60(29):15743-15766. doi: 10.1002/anie.202007024. Epub 2021 Mar 22.

Abstract

In the last 13 years several synthetic strategies were developed that provide access to [n]cycloparaphenylenes ([n]CPPs) and related conjugated nanohoops. A number of potential applications emerged, including optoelectronic devices, and their use as templates for carbon nanomaterials and in supramolecular chemistry. To tune the structural or optoelectronic properties of carbon nanohoops beyond the size-dependent effect known for [n]CPPs, a variety of aromatic rings other than benzene were introduced. In this Review, we provide an overview of the syntheses, properties, and applications of conjugated nanohoops beyond [n]CPPs with intrinsic donor/acceptor structure or such that contain acceptor, donor, heteroaromatic or polycyclic aromatic units within the hoop as well as conjugated nanobelts.

Keywords: cyclacenes; cycloparaphenylenes; macrocycles; nanohoops; optoelectronic properties.

Publication types

  • Review