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Active Esters as Pseudostoppers for Slippage Synthesis of [2]Pseudorotaxane Building Blocks: A Straightforward Route to Multi‐Interlocked Molecular Machines
Authors:Dr Thibaut Legigan  Benjamin Riss‐Yaw  Dr Caroline Clavel  Dr Frédéric Coutrot
Institution:1. www.glycorotaxane.fr;2. Supramolecular Machines and ARchitectures Team, Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS, Université Montpellier - ENSCM, case courrier 1706, Batiment Chimie (17), 3ème étage, Faculté des Sciences, Montpellier cedex 5, France
Abstract:The efficient synthesis and very easy isolation of dibenzo24]crown‐8‐based 2]pseudorotaxane building blocks that contain an active ester motif at the extremity of the encircled molecular axle and an ammonium moiety as a template for the dibenzo24]crown‐8 is reported. The active ester acts both as a semistopper for the 2]pseudorotaxane species and as an extensible extremity. Among the various investigated active ester moieties, those that allow for the slippage process are given particular focus because this strategy produces fewer side products. Extension of the selected N‐hydroxysuccinimide ester based pseudorotaxane building block by using either a mono‐ or a diamino compound, both containing a triazolium moiety, is also described. These provide a pH‐dependent two‐station 2]rotaxane molecular machine and a palindromic 3]rotaxane molecular machine, respectively. Molecular machinery on both interlocked compounds through variation of pH was studied and characterized by means of NMR spectroscopy.
Keywords:crown compounds  kinetics  molecular machines  rotaxanes  thermodynamics
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