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Bis(azobenzene)-Based Photoswitchable, Prochiral, Cα-Tetrasubstituted α-Amino Acids for Nanomaterials Applications
Journal article   Peer reviewed

Bis(azobenzene)-Based Photoswitchable, Prochiral, Cα-Tetrasubstituted α-Amino Acids for Nanomaterials Applications

P Fatas, Edoardo Longo, Federico Rastrelli, Marco Crisma, Claudio Toniolo, AI Jimenez, Carlo Cativiela and Alessandro Moretto
Chemistry - A European Journal, Vol.17(45), pp.12606-12611
17
04/11/2011
Handle:
https://hdl.handle.net/10863/34004
PMID: 21956889

Abstract

Light-driven chirality: Sequential light-driven isomerization of prochiral, bis(azobenzene)-containing amino acids results in the formation of chiral entities that have been characterized by different techniques. Metal nanoparticles conjugated with these amino acids retain the photoswitching properties and show conformation-dependent magnetic susceptibility that can be reversibly controlled by irradiation (see figure).
url
https://onlinelibrary.wiley.com/doi/full/10.1002/chem.201102609View

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