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Coordination-triggered redox activity of early and late lanthanide calix[4]arene complexes.

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F24%3A00584312" target="_blank" >RIV/61388955:_____/24:00584312 - isvavai.cz</a>

  • Result on the web

    <a href="https://hdl.handle.net/11104/0352243" target="_blank" >https://hdl.handle.net/11104/0352243</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d3dt03828a" target="_blank" >10.1039/d3dt03828a</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Coordination-triggered redox activity of early and late lanthanide calix[4]arene complexes.

  • Original language description

    The methylation of p-tert-butylcalix[4]arene in the distal 1,3-phenolic sites provides H2L = {p-tert-butylcalix[4](OMe)2(OH)2arene}. This unit acts as a rigid coordinating ligand to early and late lanthanide metal ions, enabling the construction of two families of mononuclear compounds featuring (N(nBu)4)[LnIIIL(acac)2]·CH3CN (Ln = Pr (1), Nd (2), Ho (3), and Er (4)) and (N(nBu)4)2[LnIIIL{Mo5O13(OMe)4(NO)}]·CH2Cl2 (Ln = Nd (5) and Er (6)). The metal ions adopt distorted bicapped trigonal prismatic coordination environments, resulting in slow relaxation of the magnetization for 4. These compounds exhibit reversible redox waves at positive potentials, centered within the calix[4]arene ligand, representing a new type of calix[n]arene-based electrochemical activity induced by coordination to the metal centers.

  • 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

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

    <a href="/en/project/GA23-06465S" target="_blank" >GA23-06465S: Merging photochemistry and electrochemistry in flavin-based redox catalysis</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Dalton Transactions

  • ISSN

    1477-9226

  • e-ISSN

    1477-9234

  • Volume of the periodical

    53

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    7

  • Pages from-to

    4930-4936

  • UT code for WoS article

    001175442600001

  • EID of the result in the Scopus database

    2-s2.0-85186999973