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Hydrogen bonding and supramolecular assemblies in azocoupled enaminones

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F04%3A00001968" target="_blank" >RIV/00216275:25310/04:00001968 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    čeština

  • Original language name

    Hydrogen bonding and supramolecular assemblies in azocoupled enaminones

  • Original language description

    We found out the structure of the azo coupled enaminones depends on type of their amino group and on starting enaminone. If the amino group is primary, the resulting product exists as in CDCl3 solution as in the solid state predominantly as azo compoundwith intramolecular hydrogen bond between nitrogens of tha amino group and the azo group. The second hydrogen of the amino group in crystal participates in intermolecular hydrogen bonding with carbonyl group of a neighbouring molecule. In CDCl3 solutionthere exists also an isomer with intramolecular hydrogen bond between nitrogen of the amino group and the carbobyl group of the same molecule as minor form.

  • Czech name

    Hydrogen bonding and supramolecular assemblies in azocoupled enaminones

  • Czech description

    We found out the structure of the azo coupled enaminones depends on type of their amino group and on starting enaminone. If the amino group is primary, the resulting product exists as in CDCl3 solution as in the solid state predominantly as azo compoundwith intramolecular hydrogen bond between nitrogens of tha amino group and the azo group. The second hydrogen of the amino group in crystal participates in intermolecular hydrogen bonding with carbonyl group of a neighbouring molecule. In CDCl3 solutionthere exists also an isomer with intramolecular hydrogen bond between nitrogen of the amino group and the carbobyl group of the same molecule as minor form.

Classification

  • Type

    D - Article in proceedings

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA203%2F03%2F0356" target="_blank" >GA203/03/0356: Tautomerism and hydrogen bonding in beta-eneminone derivatives. Multinuclear and X-ray study</a><br>

  • Continuities

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

Others

  • Publication year

    2004

  • Confidentiality

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

Data specific for result type

  • Article name in the collection

    10th Bi-Annual International Conference on Pigments, Dyes and Functional Dyes - COLORCHEM 2004

  • ISBN

    80-85119-01-3

  • ISSN

  • e-ISSN

  • Number of pages

    1

  • Pages from-to

    "P34"

  • Publisher name

    Výzkumný ústav organických syntéz, a.s.

  • Place of publication

    Pardubice

  • Event location

    Špindlerův Mlýn

  • Event date

    May 23, 2004

  • Type of event by nationality

    WRD - Celosvětová akce

  • UT code for WoS article