Making and Breaking Helical Open‐Chain Oligopyrroles

Author:

Urban Adrian1,De Feyter Steven1

Affiliation:

1. Division of Molecular Imaging and Photonics Department of Chemistry Katholieke Universiteit Leuven Celestijnenlaan 200 F 3001 Leuven Belgium

Abstract

AbstractClosed‐chain oligopyrroles such as porphyrins or corroles have been well‐established in literature and experience a steadily strong interest by several fields of science. However, their open‐chain derivatives are comparatively underrepresented, despite their intriguing properties and promising applications. Here, we aim to review typical synthetic routes, as well as point towards several emergent properties, marking them as interesting candidates for various fields of study. The review focuses on two traditional methods (each starting from highly symmetric metalloporphyrins) and then expands its scope towards more recent variations before moving on to more exotic and recent highlights that have yet to be included into the canon. Key chemical reactivities (ring closure, substitution and fragmentation) are then followed by notable physicochemical properties, placing special emphasis on potential uses in molecular electronics and sensors.

Publisher

Wiley

Subject

General Chemistry

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