Csaba Fehér
University of Pannonia
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Publication
Featured researches published by Csaba Fehér.
Green Chemistry | 2012
Csaba Fehér; Eszter Kriván; Jenő Hancsók; Rita Skoda-Földes
Bronsted acidic ionic liquids, supported on silica gel, have been used effectively in oligomerisation of isobutene. The supported catalysts could be used several times without loss of activity or change in selectivity. The ratio of the products could be influenced by the proper choice of the ionic liquid component of the catalyst and the reaction temperature.
Monatshefte Fur Chemie | 2014
Csaba Fehér; Ivan Habuš; Johan Wouters; Rita Skoda-Földes
The palladium-catalyzed carbonylation of iodoferrocene was investigated in the presence of 2-aminopyrimidine derivatives as nucleophiles. 2-Amino-4-hydroxy-6-methylpyrimidine was found to act both as an O- and an N-nucleophile, leading to an ester and an amide derivative, respectively. Together with other spectroscopic methods, the structure of both products was proved by X-ray crystallography. 2-(Ferrocenoylamino)-4-chloro-6-alkylpyrimidines were obtained during carbonylation of iodoferrocene and 2-amino-4-chloro-6-alkylpyrimidines. The formation of a dimeric product via two subsequent carbonylation steps was also observed. The products may have practical importance as electrochemically detectable biosensors or building blocks for supramolecular assemblies.Graphical abstract
Hungarian Journal of Industrial Chemistry | 2011
Csaba Fehér; R. Skoda-Földes; E. Kriván; Jenő Hancsók
In the petrochemical industry, the C4 stream including isobutene is an important raw material that can be upgraded. Oligomerization of isobutene is a very promising reaction, as the hydrogenation products of dimers and trimers, obtained from isobutene, can be used as gasoline and diesel additives, respectively. In the present paper, our results concerning the use of Bronsted acidic ionic liquids as oligomerization catalysts are presented. The ionic liquids were supported on silica. Most of the solid catalysts were reused several times without loss of activity. By the proper choice of the ionic liquid and reaction conditions, good selectivity towards either C8 or C12+ products could be achieved.
Advances in Asymmetric Autocatalysis and Related Topics | 2017
Csaba Fehér; Máté Papp; Béla Urbán; Rita Skoda-Földes
Supported ionic liquids (SILPs), prepared via the immobilization of ionic liquids on solid material, can efficiently be used in catalytic reactions as catalysts, or as supports for transition metal catalysts. The SILP concept combines the advantages of homogeneous catalysis with those of heterogeneous systems. In the present paper, this is demonstrated with two examples. In the first application, acidic SILPs are shown to be selective and recyclable catalyst for the trimerization of isobutene. In the second example, neutral SILPs are proved to be excellent supports stabilizing palladium catalysts for carbonylation reactions, as well as ensuring effective catalyst recycling.
Journal of Organometallic Chemistry | 2009
Csaba Fehér; Árpád Kuik; László Márk; László Kollár; Rita Skoda-Földes
Journal of Molecular Catalysis A-chemical | 2013
Csaba Fehér; Eszter Kriván; József Kovács; Jenő Hancsók; Rita Skoda-Földes
Tetrahedron Letters | 2010
Csaba Fehér; Béla Urbán; László Ürge; Ferenc Darvas; József Bakos; Rita Skoda-Földes
Organometallics | 2016
Csaba Fehér; Máté Papp; Ágnes Gömöry; Lívia Nagy; Johan Wouters; György Lendvay; Rita Skoda-Földes
Archive | 2014
Csaba Fehér; Eszter Kriván; Zoltán Eller; Jenő Hancsók; RitaSkoda-Földes
Tetrahedron | 2011
Csaba Fehér; Béla Urbán; László Ürge; Ferenc Darvas; József Bakos; Rita Skoda-Földes