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”

An adamantane-based disubstituted binding motif with picomolar dissociation constants for cucurbit[n]urils in water and related quaternary assemblies

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28610%2F16%3A43874881" target="_blank" >RIV/70883521:28610/16:43874881 - isvavai.cz</a>

  • Alternative codes found

    RIV/70883521:28110/16:43874881

  • Result on the web

    <a href="http://dx.doi.org/10.1039/c6ra23524g" target="_blank" >http://dx.doi.org/10.1039/c6ra23524g</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c6ra23524g" target="_blank" >10.1039/c6ra23524g</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    An adamantane-based disubstituted binding motif with picomolar dissociation constants for cucurbit[n]urils in water and related quaternary assemblies

  • Original language description

    A non-axial centerpiece based on 1,3-disubstituted adamantane was designed, and three new guests were prepared. In the structure of the heterotritopic guests, the central adamantane site was combined with two terminal butyl or 1-adamantyl sites. The new central binding motif displayed an extraordinarily high affinity towards CB8'(K-a = (5.3 +/- 0.3) x 10(12) M-1 in water) to allow formation of quaternary assemblies with geometries which are dependent on the nature of macrocycles. Based on the individual binding strengths, the replacement of CB7 by CB8 led to inverse arrangements of the quaternary assemblies; i.e., b-CD is capped at the central site by two CB7 units, while the CB8 prefers the central site to be capped with two b-CD units.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    RSC Advances: an international journal to further the chemical sciences

  • ISSN

    2046-2069

  • e-ISSN

  • Volume of the periodical

    6

  • Issue of the periodical within the volume

    107

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    105146-105153

  • UT code for WoS article

    000388116500026

  • EID of the result in the Scopus database

    2-s2.0-84994515724