All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Anion recognition using meta-substituted ureidocalix[4]arene receptors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F24%3A00599919" target="_blank" >RIV/61388955:_____/24:00599919 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985858:_____/24:00600604 RIV/60461373:22310/24:43930889

  • Result on the web

    <a href="https://hdl.handle.net/11104/0357328" target="_blank" >https://hdl.handle.net/11104/0357328</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d4ob01441c" target="_blank" >10.1039/d4ob01441c</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Anion recognition using meta-substituted ureidocalix[4]arene receptors

  • Original language description

    Calix[4]arenes bearing urea units at the meta position(s) of the upper rim of the macrocyclic skeleton were prepared by the reaction of the corresponding amines with aryl isocyanates. As shown by the H-1 NMR and UV/vis titration experiments, these systems are capable of effectively complexing selected anions even in a highly competitive environment (such as DMSO-d(6)). While the monoureido derivatives showed approximately the same complexation ability irrespective of the substitution (para vs. meta isomers), the bisureas at the upper rim demonstrated interesting differences in complexation. The meta,meta and para,para isomers were shown to prefer 2 : 1 complexes (anion : receptor) regardless of the anion tested, while the analogous meta,para isomer formed 1 : 1 complexes with strongly coordinated anions (e.g. H2PO4-) based on synchronous complexation by both ureido groups. This suggests that the regioselective introduction of urea units into the upper rim of calix[4]arene brings with it the possibility of ´´tuning´´ the complexation properties depending on the substitution pattern of the functional groups.

  • 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

    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

    Organic & Biomolecular Chemistry

  • ISSN

    1477-0520

  • e-ISSN

    1477-0539

  • Volume of the periodical

    22

  • Issue of the periodical within the volume

    43

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    8669-8678

  • UT code for WoS article

    001331669600001

  • EID of the result in the Scopus database

    2-s2.0-85206557610