Search results

  1. 1.
    0431916 - ÚMCH 2015 ES eng A - Abstract
    Plachý, T. - Sedlačík, M. - Pavlinek, V. - Stejskal, Jaroslav - Pedro Graça, M. - Cadillon Costa, L.
    Temperature dependent electrorheological effect and its description with respect to dielectric spectra.
    Book of Abstracts. Granada: Universidad de Granada, 2014. s. 170.
    [International Conference on Electrorheological Fluids and Magnetorheological Suspensions /14./ - ERMR2014. 07.07.2014-11.07.2014, Granada]
    Institutional support: RVO:61389013
    Keywords : electrorheology * polymer systems
    Subject RIV: CD - Macromolecular Chemistry
    Permanent Link: http://hdl.handle.net/11104/0236948
     
     
  2. 2.
    0431914 - ÚMCH 2015 ES eng A - Abstract
    Plachý, T. - Sedlačík, M. - Pavlinek, V. - Stejskal, Jaroslav
    Electrorheology of suspensions based on carbonized poly(p-phenylenediamine) particles.
    Book of Abstracts. Granada: Universidad de Granada, 2014. s. 71.
    [International Conference on Electrorheological Fluids and Magnetorheological Suspensions /14./ - ERMR2014. 07.07.2014-11.07.2014, Granada]
    Institutional support: RVO:61389013
    Keywords : electrorheology * poly(p-phenylenediamine) particles
    Subject RIV: CD - Macromolecular Chemistry
    Permanent Link: http://hdl.handle.net/11104/0236946
     
     
    0369984 - ÚOCHB 2012 RIV DE eng J - Journal Article
    Dejmek, Milan - Hřebabecký, Hubert - Šála, Michal - Dračínský, Martin - Nencka, Radim
    Microwave- assisted solvent-free Diels-Alder reaction – a fast and simple route to various 5,6-substituted norbornenes and polychlorinated norbornenes.
    Synthesis. -, č. 24 (2011), s. 4077-4083. ISSN 0039-7881. E-ISSN 1437-210X
    R&D Projects: GA MŠMT 1M0508
    Institutional research plan: CEZ:AV0Z40550506
    Keywords : Diels-Alder reaction * polychlorinated norbornanes * norbornene
    Subject RIV: CC - Organic Chemistry
    Impact factor: 2.466, year: 2011

    A series of 5,6-substituted norbornenes and 5,6-substituted polychlorinated norbornenes was prepared using microwave assisted Diels-Alder reaction. This procedure proved very versatile, fast and easy to work up and therefore suitable even for large-scale synthesis.


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