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Unique reactivity of an alpha-ketiminopyridine ligand with metal-alkyls: Synthesis and ROP of epsilon-caprolactone

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F21%3A39917683" target="_blank" >RIV/00216275:25310/21:39917683 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlelanding/2021/nj/d0nj05498d" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2021/nj/d0nj05498d</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d0nj05498d" target="_blank" >10.1039/d0nj05498d</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Unique reactivity of an alpha-ketiminopyridine ligand with metal-alkyls: Synthesis and ROP of epsilon-caprolactone

  • Original language description

    The reaction of an alpha-ketimininopyridine ligand 2-((Me)C = N(C6H3-2,6-iPr(2)))-6-(OMe)C5H3N (L-1) with metal-alkyls, such as MeLi, Et2Zn, Me3Al and Me2AlCl, was studied. The reaction of L-1 with MeLi led exclusively to the formation of [2-((H2C)C-N(C6H3-2,6-iPr(2)))-6-(OMe)C5H3N]Li center dot(THF)(2) (1 center dot(THF)(2)) with a deprotonated ketimine methyl group as a product of methane elimination. The treatment of L-1 with Et2Zn provided, at the first stage, only complex [2-((Me)C = N(C6H3-2,6-iPr(2)))-6-(OMe)C5H3N]ZnEt2 (2). The nonstability of 2 led to ethane elimination along with the deprotonation of a ketimine methyl group, which further yielded [2-((H2C)C-N(C6H3-2,6-iPr(2)))-6-(OMe)C5H3N]ZnEt (3). In contrast, Me3Al reacted with L-1 in a carboalumination fashion and [2-((Me)(2)C-N(C6H3-2,6-iPr(2)))-6-(OMe)C5H3N]AlMe2 (4) was isolated. In the case of Me2AlCl, an ionic species {[2-((Me)C = N(C6H3-2,6-iPr(2)))-6-(OMe)C5H3N]AlMe2}(+) {Me2AlCl2}(-) (5) was formed as a result of a spontaneous dissociation of Me2AlCl initiated by the ligand L-1. Since compounds 2-5 contain a metal-alkyl fragment, they were used as pre-catalysts in ROP of epsilon-caprolactone, as well as compound 1 center dot(THF)(2).

  • 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

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

    <a href="/en/project/GA20-10417S" target="_blank" >GA20-10417S: Auto-ionizated Main Group Cations as Catalysts for Ring-Opening Polymerization reactions</a><br>

  • Continuities

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

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    New Journal of Chemistry

  • ISSN

    1144-0546

  • e-ISSN

  • Volume of the periodical

    45

  • Issue of the periodical within the volume

    8

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    9

  • Pages from-to

    3800-3808

  • UT code for WoS article

    000623596600006

  • EID of the result in the Scopus database

    2-s2.0-85101854908