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”

Synthesis, catalytic activity and medium fluorous recycle of fluorous analogues of PEPPSI catalysts

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F20%3A43921654" target="_blank" >RIV/60461373:22310/20:43921654 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388963:_____/20:00525654

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0022113920302864" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0022113920302864</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jfluchem.2020.109588" target="_blank" >10.1016/j.jfluchem.2020.109588</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis, catalytic activity and medium fluorous recycle of fluorous analogues of PEPPSI catalysts

  • Original language description

    PEPPSI complexes are air and moisture stable Pd catalysts, which can be used conveniently in many coupling reactions. With the aim to obtain Pd catalysts recyclable by fluorous separation methods, we modified the structure of commercial PEPPSI complexes by per- or polyfluoroalkylation in various positions. The modifications included the use of a linear polyfluoroalkyl group instead of one aryl group on the NHC ligand, perfluoroalkylation of pyridine ligand, and substitution of chloride ligands on Pd for perfluoroalkanoates or perfluoropolyoxaalkanoates. Comparison of catalytic activity of commercial catalysts with the modified ones in Suzuki-Miyaura cross-coupling reactions showed that the fluorous modifications mostly resulted in the increase of catalytic activity. Moreover, polyfluoroalkylation enabled efficient medium fluorous recycle of the modified catalysts using a two phase aqueous DMF/HFE 7500 ether system.

  • 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

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GAP207%2F10%2F1533" target="_blank" >GAP207/10/1533: Fluorous carbenes, complexes and ionic liquids based on perfluoropolyether-substituted imidazolium salts and their applications</a><br>

  • Continuities

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

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Fluorine Chemistry

  • ISSN

    0022-1139

  • e-ISSN

  • Volume of the periodical

    236

  • Issue of the periodical within the volume

    109588

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    14

  • Pages from-to

    1-14

  • UT code for WoS article

    000551145100016

  • EID of the result in the Scopus database

    2-s2.0-85086442977