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Synthesis and Properties of pH-Responsive Imidazolium-based Guests

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28110%2F15%3A43873271" target="_blank" >RIV/70883521:28110/15:43873271 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis and Properties of pH-Responsive Imidazolium-based Guests

  • Original language description

    Guest molecules with multiple non-equivalent binding sites are recently extensively studied as important components for complex supramolecular systems. Compounds bearing protondissociable groups (e.g. carboxylate, amine), which pH-affected dissociation can change binding properties of entire molecule, are of a particular interest. Herein, we report a preparation of imidazolium-based guest consisting of adamantane cage, permanently charged (benz)imidazolium cation, and dissociable carboxylic group linkedto the (benz)imidazolium by C5 aliphatic chain. In addition, we examined the binding properties of new guest towards cucurbit[n]urils (CBn, n=6 and 7) and ?-/?-cyclodextrins (CD) using NMR, ITC and ESI-MS techniques. Since the sphere-like adamantane cage perfectly fits the interior of CB7 and ?-CD, these two hosts predominantly occupy the adamantane binding site. On the other hand, the interior cavity of ?-CD and CB6 is too small to include bulky adamantane moiety. Therefore, these host

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2015

  • Confidentiality

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