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Título : Bis(azobenzene)-Based Photoswitchable, Prochiral, Cα-Tetrasubstituted α-Amino Acids for Nanomaterials Applications
Autor : Fatás, Paola, Crisma, Marco, Toniolo, Claudio, Jiménez, Ana I., Cativiela, Carlos
Fecha de publicación : 2011
Editor: Wiley-VCH
Citación : Chemistry - A European Journal 17(45): 12606-12611 (2011)
Resumen: 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).
Identificadores: doi: 10.1002/chem.201102609
issn: 0947-6539
e-issn: 1521-3765
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