Abstract

Dynamic macroscopically chiral nanocomposites are prepared by combining silver nanoparticles (AgNPs) and dynamic helical poly(phenylacetylene)s (PPAs) bearing pendants functionalized with amino groups. These amino groups provide the nanocomposite with the ability to disperse in water along with high stability due to the interaction between the ammonium group and the AgNP. Moreover, the equilibrium between NH3+/NH2 produces a "blinking" contact between the PPA and the AgNPs, which allows total control of the dynamic helical behavior of the polymer. The use of acidic or neutral pH allows controlling the morphology of the nanocomposite, which consists of a nanosphere that has trapped inside it a single AgNP (pH = 2) or several AgNPs (pH = 7) with ca. 30 nm of diameter. These nanocomposites combine the optical and chiroptical stimuli-responsive properties of both components, AgNPs and PPAs. Thus, the controlled aggregation of the nanocomposite produced variations in the LSPR band of the AgNPs in a reversible manner. In turn, given that the chiral coating is selective to Ba2+, the presence of this metal ion caused a helical inversion of the chiral coating of the nanocomposite detected by electronic circular dichroism. Moreover, it is possible to distinguish between three metal ions in different oxidation states, such as Ce4+, Fe3+, and Hg2+, which produce different responses of the nanocomposite when oxidizing the AgNP to Ag+.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.