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Chiral Amplification by L‐ Cysteine‐Capped Gold Nanoparticles in Lyotropic Chromonic Liquid Crystals
Author(s) -
Bergquist Leah,
Hegmann Torsten
Publication year - 2017
Publication title -
chemnanomat
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.947
H-Index - 32
ISSN - 2199-692X
DOI - 10.1002/cnma.201700286
Subject(s) - lyotropic , chirality (physics) , liquid crystal , nanoparticle , materials science , colloidal gold , molecule , nanoscopic scale , lyotropic liquid crystal , nanotechnology , adsorption , chemical physics , chemistry , organic chemistry , liquid crystalline , chiral symmetry breaking , optoelectronics , physics , quantum mechanics , nambu–jona lasinio model , quark
Transfer of chirality from an adsorbed molecule to a metal nanoparticle surface, and from the resulting chiral nanoparticle to its surroundings, depends on numerous factors – structure of the adsorbed molecule, its size and shape, and its interactions with its specific environment – but is often difficult to understand and even more difficult to measure, visualize, and quantify. This severely limits the potential of chiral nanoparticles in a range of emerging applications as optical metamaterials, enantioselective catalysts, or chiral discriminators for biomacromolecules. We examine if chirality at the nanoscale (i. e. in gold nanoparticles capped with chiral ligand molecules) is uniquely able to generate more intense responses than their organic chiral counterparts in soft condensed matter utilizing lyotropic chromonic liquid crystals (LCLCs) forming the nematic phase. As a powerful manifestation of nanoscale chiral amplification, we show that L ‐cysteine capped gold nanoparticles induce a tighter chiral twist within, and similar among, stacks of nematic LCLCs with several orders of magnitude fewer chiral L ‐cysteine ligands in comparison to the free molecular L ‐amino acid.