Photo- and Metallo-responsive N-Alkyl α-Bisimines as Orthogonally Addressable Main-Chain Functional Groups in Metathesis Polymers

Lutz Greb, Hatice Mutlu, Christopher Barner-Kowollik*, Jean-Marie Lehn*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

43 Citations (Scopus)

Abstract

N-alkyl α-bisimines were employed as main-chain functional groups in acyclic diene metathesis (ADMET)-polymers, conferring dual responsiveness for the controlled switching of the polymeric particle shape with light and metal ions. Photochemical Z/E-isomerization leads to a significant and reversible change in hydrodynamic volume, thus introducing simple imines as novel photoswitches for light-responsive materials. Mild imine-directed CH activation by Pd(OAc)2 is demonstrated as a new single-chain nanoparticle (SCNP) folding process, enabling a controlled atom- and step-economic SCNP synthesis. The combination of light- and metallo-responsiveness in the same polymer provides the ability for orthogonal switching, a valuable tool for advanced functional material design.
Original languageEnglish
Pages (from-to)1142-1145
JournalJournal of the American Chemical Society
Volume138
Issue number4
Online published23 Dec 2015
DOIs
Publication statusPublished - 3 Feb 2016
Externally publishedYes

Fingerprint

Dive into the research topics of 'Photo- and Metallo-responsive N-Alkyl α-Bisimines as Orthogonally Addressable Main-Chain Functional Groups in Metathesis Polymers'. Together they form a unique fingerprint.

Cite this