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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/52348
Title: Bis(azobenzene)-Based Photoswitchable, Prochiral, Cα-Tetrasubstituted α-Amino Acids for Nanomaterials Applications
Authors: Fatás, Paola; Crisma, Marco; Toniolo, Claudio; Jiménez, Ana I.; Cativiela, Carlos
Issue Date: 2011
Publisher: Wiley-VCH
Citation: Chemistry - A European Journal 17(45): 12606-12611 (2011)
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).
URI: http://hdl.handle.net/10261/52348
Identifiers: doi: 10.1002/chem.201102609
issn: 0947-6539
e-issn: 1521-3765
DOI: 10.1002/chem.201102609
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