Related Experiment Video
Updated: May 30, 2025

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
Published on: August 2, 2012
Open Rotaxane Surgery: What Molecular Editing Can Offer to Supramolecular Chemistry?
Jędrzej P Perdek1, Rafał A Grzelczak1, Bartosz Szyszko1
1Faculty of Chemistry, University of Wrocław, 14 F. Joliot-Curie St., 50-383, Wrocław, Poland.
Abstract:
The skeletal editing approach represents a paradigm shift in organic synthesis by directly targeting the molecular skeleton instead of relying on often long and complicated series of organic transformations. Recent advancements in nitrogen atom deletion reactions have enabled unprecedented late-stage, precise modifications of bioactive compounds and complex natural products, influencing a seemingly distant field such as supramolecular chemistry. In a recent contribution, the Leigh group demonstrated the extrusion of a nitrogen atom from an axle of a [2]rotaxane, extending the applicability of molecular editing to complex, mechanically interlocked architectures. This highlight seeks to examine the significance of the skeletal editing method in supramolecular chemistry, address its challenges, and offer an outlook on future directions in this emerging field.
Related Concept Videos
Radical Reactivity: Overview
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Radical Reactivity: Intramolecular vs Intermolecular
Radical Reactivity: Steric Effects
Along with electronic...
Radical Formation: Overview
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
Cycloaddition Reactions: MO Requirements for Thermal Activation
![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)
