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Noncovalent Grafting of a DyIII2 Single-Molecule Magnet onto Chemically Modified Multiwalled Carbon Nanotubes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F18%3A73587951" target="_blank" >RIV/61989592:15310/18:73587951 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.acs.org/doi/10.1021/acs.inorgchem.8b00472" target="_blank" >https://pubs.acs.org/doi/10.1021/acs.inorgchem.8b00472</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.inorgchem.8b00472" target="_blank" >10.1021/acs.inorgchem.8b00472</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Noncovalent Grafting of a DyIII2 Single-Molecule Magnet onto Chemically Modified Multiwalled Carbon Nanotubes

  • Original language description

    While synthetic methods for the grafting of nanoparticles or photoactive molecules onto carbon nanotubes (CNTs) have been developed in the last years, a very limited number of reports have appeared on the grafting of single molecule magnets (SMMs) onto CNTs. There are many potential causes, mainly focused on the fact that the attachment of molecules on surfaces remains not trivial and their magnetic properties are significantly affected upon attachment. Nevertheless, demanding fields such as spintronic devices makes of utmost implementation of this particular type of hybrid material in importance the investigation of new synthetic protocols for effective grafting. In this paper, we demonstrate a new experimental protocol for the noncovalent grafting of Dili, SMM, [Dy-2(NO3)(2)(saph)(2)(DMF)(4)], where H(2)saph = N-salicylidene-o-aminophenol and DMF = N,N-dimethylformamide, onto the surface of functionalized multiwalled CNTs (MWCNTs). We present a simple wet chemical method, followed by an extensive washing protocol, where the cross-referencing of data from high -resolution transmission electron microscopy combined with electron energy loss spectroscopy, conventional magnetic measurements (direct and alternating current), X-ray photoelectron spectroscopy, and Raman spectroscopy was used to investigate the physical properties, chemical nature, and overall magnetic behavior of the resulting hybrids. A key point to the whole synthesis involves the functionalization of MWCNTs with carboxylic groups, which proved to be a powerful strategy for enhancing the ability to process MWCNTs and facilitating the preparation of hybrid composites. While in the majority of analogous hybrid materials the raw carbon material (multiwalled or single -walled nanotubes) is heavily treated to minimize the contribution of contaminant traces of magnetic nanoparticles with important effects on their electronic properties, this method can lead easily to elimination of the largest part of the impurities and provide an effective way to investigate/discriminate the magnetic contribution of the SMM molecules.

  • 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

    10403 - Physical chemistry

Result continuities

  • Project

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

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    INORGANIC CHEMISTRY

  • ISSN

    0020-1669

  • e-ISSN

  • Volume of the periodical

    57

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    6391-6400

  • UT code for WoS article

    000434491700024

  • EID of the result in the Scopus database

    2-s2.0-85048297179