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Charge-transfer complexation: A highly effective way towards chiral nanoparticles endowed by intrinsically chiral helicene and enantioselective SERS detection

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985858%3A_____%2F23%3A00575451" target="_blank" >RIV/67985858:_____/23:00575451 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22310/23:43928177 RIV/60461373:22340/23:43928177

  • Result on the web

    <a href="https://hdl.handle.net/11104/0345237" target="_blank" >https://hdl.handle.net/11104/0345237</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.snb.2023.134332" target="_blank" >10.1016/j.snb.2023.134332</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Charge-transfer complexation: A highly effective way towards chiral nanoparticles endowed by intrinsically chiral helicene and enantioselective SERS detection

  • Original language description

    An ordered chiral gold nanoparticle (AuNPs) array was prepared by the treatment of achiral sphere-shaped gold nanoparticles endowed with electron-accepting dinitro-phenyl (DNP) groups complexing with enantiomers of [6]helicene representing electron donors with strong chiroptical properties. Such surface-functionalization utilizes the principles of charge-transfer (CT) interaction. The incorporation of [6]helicene molecules with unique electronic and optical properties and subsequent arrangement of AuNPs caused chirality induction to intrinsically non-chiral plasmon-active nanostructures. The created nanostructures enabled the excitation of chiral plasmon and its application in highly sensitive enantioselective detection of small chiral molecules by surface-enhanced Raman spectroscopy (SERS). The chiral plasmonic response of such a system was shown to be fully controlled via the helicity of the parent [6]helicene. Upon calibration, it allowed us to directly determine the enantiomeric composition of non-racemic mixtures of (R)/(S)− 1-phenylethanol and (R)/(S)− 2-butanol.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Sensors and Actuators B - Chemical

  • ISSN

    0925-4005

  • e-ISSN

    0925-4005

  • Volume of the periodical

    394

  • Issue of the periodical within the volume

    1 NOV

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    11

  • Pages from-to

    134332

  • UT code for WoS article

    001158796700001

  • EID of the result in the Scopus database

    2-s2.0-85167440292