Ivan Nemec

Email: ivan.nemec@upol.cz
Adresa:
17. listopadu 12, 771 46 Olomouc
Telefon: (+420) 58 563 4354
Fax: (+420) 58 563 4357

 
Kvalifikace:
Anorganická chémia, Fakultachemickej a potravinárskej technológie, Slovenská technická univerzita v Bratislave – Ing.
Anorganická chémia, Fakulta chemickej a potravinárskej technológie, Slovenská technická univerzita v Bratislave – Ph.D.   
od 2010   -   Junior Researcher, Regionální centrum pokročilých technologií a materiálů PřF UP v Olomouci

Oblast výzkumu: 
Koordinační chemie, Magnetochemie, Komplexy přechodných kovů (Fe, Co, Mn, Ni, Cr, Cu), Monokrystalová rentgenová strukturní analýza, Spin-crossover, Molekulové magnety

Publikační aktivita:
Počet publikací (WoS): 7
Počet citací (WoS): 7
H-index: 2

Zahraniční pobyty:
2006: USA, 4 měsíce, skupina prof. Philipa Coppensa, The State University of New York – University at Buffalo
2008-2010: Německo, více 3-6ti týdenních stází u prof. Hartmuta Fuessa, Darmstadt University of Technology, Institute of Materiál Science
2008-2009: Rakousko, 2 x 2,5 měsíce, Prof. Wolfgang Linert, Institute of Applied Synthetic Chemistry, Vienna University of Technology

Další aktivity:
Časopisecké recenze: Dalton Transaction, CrystEngComm

Vybrané publikace:

  1. Nemec, I.; Boča, R.; Gembický, M.; Dlháň, L.; Herchel, R.; Renz, F., High-spin Schiff-base dinuclear iron(III) complexes bridged by N-oxide ligands. Inorganica Chimica Acta 2009, 362 (13), 4754-4759.
  2. Nemec, I.; Boča, R.; Herchel, R.; Trávníček, Z.; Gembický, M.; Linert, W., Dinuclear Fe(III) complexes with spin crossover. Mon. Chem. 2009, 140 (7), 815-828.
  3. Nemec, I.; Herchel, R.; Boča, R.; Trávníček, Z.; Svoboda, I.; Fuess, H.; Linert, W., Tuning of spin crossover behaviour in iron(iii) complexes involving pentadentate Schiff bases and pseudohalides. Dalton Transactions 2011, 40 (39), 10090-10099.
  4. Nemec, I.; Herchel, R.; Boča, R.; Svoboda, I.; Trávníček, Z.; Dlháň, L.; Matelková, K.; Fuess, H., Heterobimetallic assemblies of Ni(II) complexes with a tetradentate amine ligand and diamagnetic cyanidometallates. Inorganica Chimica Acta 2011, 366 (1), 366-372.
  5. Šalitroš, I.; Boča, R.; Dlháň, L.; Gembický, M.; Kožíšek, J.; Linares, J.; Moncol, J.; Nemec, I.; Perašínová, L.; Renz, F.; Svoboda, I.; Fuess, H., Unconventional spin crossover in dinuclear and trinuclear iron(III) complexes with cyanido and metallacyanido bridges. European Journal of Inorganic Chemistry 2009,  (21), 3141-3154.

 

 

Show publications

Publications

2011

  • [DOI] I. Nemec, R. Herchel, R. Boca, I. Svoboda, Z. Travnicek, L. Dlhan, K. Matelkova, and H. Fuess, “Heterobimetallic assemblies of Ni(II) complexes with a tetradentate
    amine ligand and diamagnetic cyanidometallates,” INORGANICA CHIMICA ACTA, vol. 366, iss. 1, pp. 366-372, 2011.
    [Bibtex]
    @article ISI:000285994200049,
    Author = Nemec, Ivan and Herchel, Radovan and Boca, Roman and Svoboda, Ingrid and
       Travnicek, Zdenek and Dlhan, Lubor and Matelkova, Kristina and Fuess,
       Hartmut,
    Title = Heterobimetallic assemblies of Ni(II) complexes with a tetradentate
       amine ligand and diamagnetic cyanidometallates,
    Journal = INORGANICA CHIMICA ACTA,
    Year = 2011,
    Volume = 366,
    Number = 1,
    Pages = 366-372,
    Month = JAN 30,
    Abstract = Syntheses and crystal structures of nickel(II) complexes containing teta
       (teta = N,N'-bis(2-aminoethyl)ethane-1,2-diamine) as a tetradentate
       blocking ligand and cyanidometallic bridging complexes are described.
       The complexes [Ni(teta)(cis-mu(2)-Ni(CN)(4))] (1) and
       [\Ni(teta)\(3)(mu(6)-Co(CN)(6))] (ClO(4))(3) (2) exhibit a
       1D-polymeric structure whereas the heterometallic trinuclear complex
       [Ni(teta)(mu(1)-Ag(CN)(2))(2)] (3) forms a unique network. The weak
       antiferromagnetic exchange was found in polymeric species 1 and 2 by
       analyzing the magnetic data with several models in which either only
       susceptibility was treated or simultaneous fitting of temperature and
       magnetic field dependences of the magnetization was applied using the
       finite-size closed ring approach. Moreover, an effect of the zero-field
       splitting phenomenon (ZFS) was considered for 2 by advanced modeling of
       magnetic properties for varying axial ZFS parameter/isotropic exchange
       (D/J) ratios. (C) 2010 Elsevier B.V. All rights reserved.,
    DOI = 10.1016/j.ica.2010.11.028,
    ISSN = 0020-1693,
    Unique-ID = ISI:000285994200049,
    
  • [DOI] I. Nemec, R. Herchel, R. Boca, Z. Travnicek, I. Svoboda, H. Fuess, and W. Linert, “Tuning of spin crossover behaviour in iron(III) complexes involving
    pentadentate Schiff bases and pseudohalides,” DALTON TRANSACTIONS, vol. 40, iss. 39, pp. 10090-10099, 2011.
    [Bibtex]
    @article ISI:000295843100018,
    Author = Nemec, Ivan and Herchel, Radovan and Boca, Roman and Travnicek, Zdenek
       and Svoboda, Ingrid and Fuess, Hartmut and Linert, Wolfgang,
    Title = Tuning of spin crossover behaviour in iron(III) complexes involving
       pentadentate Schiff bases and pseudohalides,
    Journal = DALTON TRANSACTIONS,
    Year = 2011,
    Volume = 40,
    Number = 39,
    Pages = 10090-10099,
    Abstract = Investigations on a series of eight novel mononuclear iron(III) Schiff
       base complexes with the general formula [Fe(L(5))(L(1))]center dot S
       (where H(2)L(5) = pentadentate Schiff-base ligand, L(1) = a pseudohalido
       ligand, and S is a solvent molecule) are reported. Several different
       aromatic 2-hydroxyaldehyde derivatives were used in combination with a
       non-symmetrical triamine 1,6-diamino-4-azahexane to synthesize the
       H(2)L(5) Schiff base ligands. The consecutive reaction with iron(III)
       chloride resulted in the preparation of the [Fe(L(5))Cl] precursor
       complexes which were left to react with a wide range of the L(1)
       pseudohalido ligands. The low-spin compounds were prepared using the
       cyanido ligand: [Fe(3m-salpet)(CN)]center dot CH(3)OH (1a),
       [Fe(3e-salpet)(CN)]center dot H(2)O (1b), while the high-spin
       compounds were obtained by the reaction of the pseudohalido (other than
       cyanido) ligands with the [Fe(L(5))Cl] complex arising from
       salicylaldehyde derivatives: [Fe(3Bu5Me-salpet)(NCS)] (2a),
       [Fe(3m-salpet)(NCO)]center dot CH(3)OH (2b) and
       [Fe(3m-salpet)-(N(3))] (2c). The compounds exhibiting spin-crossover
       phenomena were prepared only when L(5) arose from
       2-hydroxy-1-naphthaldehyde (H(2)L(5) = H(2)napet):
       [Fe(napet)(NCS)]center dot CH(3)CN (3a, T(1/2) = 151 K),
       [Fe(napet)(NCSe)]center dot CH(3)CN (3b, T(1/2) = 170 K),
       [Fe(napet)(NCO)] (3c, T(1/2) = 155 K) and [Fe(napet)(N(3))], which,
       moreover, exhibits thermal hysteresis (3d, T(1/2)up arrow = 122 K,
       T(1/2)down arrow = 117 K). These compounds are the first examples of
       octahedral iron(III) spin-crossover compounds with the coordinated
       pseudohalides. We report the structure and magnetic properties of these
       complexes. The magnetic data of all the compounds were analysed using
       the spin Hamiltonian formalism including the ZFS term and in the case of
       spin-crossover, the Ising-like model was also applied.,
    DOI = 10.1039/c1dt10696a,
    ISSN = 1477-9226,
    Unique-ID = ISI:000295843100018,
    

2009

  • [DOI] I. Nemec, R. Boca, M. Gembicky, L. Dlhan, R. Herchel, and F. Renz, “High-spin Schiff-base dinuclear iron(III) complexes bridged by N-oxide
    ligands,” INORGANICA CHIMICA ACTA, vol. 362, iss. 13, pp. 4754-4759, 2009.
    [Bibtex]
    @article ISI:000270168500015,
    Author = Nemec, Ivan and Boca, Roman and Gembicky, Milan and Dlhan, Lubor and
       Herchel, Radovan and Renz, Franz,
    Title = High-spin Schiff-base dinuclear iron(III) complexes bridged by N-oxide
       ligands,
    Journal = INORGANICA CHIMICA ACTA,
    Year = 2009,
    Volume = 362,
    Number = 13,
    Pages = 4754-4759,
    Month = OCT 15,
    Abstract = Synthesis and structure of dinuclear complexes
       [\Fe(III)(L(5))\b\Fe(III)(L(5))\](BPh(4))(2), where L(5) is a
       pentadentate Schiff-base ligand, b is a bidentate N-oxide bridging
       ligand based on bipyridine, is reported. Magnetic behavior is
       investigated in terms of the magnetic susceptibility, magnetization, and
       Mossbauer spectroscopy revealing that the complexes are high-spin over
       the whole temperature region. (C) 2009 Elsevier B. V. All rights
       reserved.,
    DOI = 10.1016/j.ica.2009.06.057,
    ISSN = 0020-1693,
    Unique-ID = ISI:000270168500015,
    
  • [DOI] R. Boca, I. Nemec, I. Salitros, J. Pavlik, R. Herchel, and F. Renz, “Interplay between spin crossover and exchange interaction in iron(III)
    complexes,” PURE AND APPLIED CHEMISTRY, vol. 81, iss. 8, pp. 1357-1383, 2009.
    [Bibtex]
    @article ISI:000269408000002,
    Author = Boca, Roman and Nemec, Ivan and Salitros, Ivan and Pavlik, Jan and
       Herchel, Radovan and Renz, Franz,
    Title = Interplay between spin crossover and exchange interaction in iron(III)
       complexes,
    Journal = PURE AND APPLIED CHEMISTRY,
    Year = 2009,
    Volume = 81,
    Number = 8,
    Pages = 1357-1383,
    Month = AUG,
    Abstract = In the dinuclear and polynuclear metal complexes exhibiting the low-spin
       (LS) to high-spin (HS) transition, the spin-crossover phenomenon
       interferes with the magnetic exchange interaction. The latter manifests
       itself in forming spin-multiplets, which causes a possible overlap of
       the band originating in different reference spin states (ILL, LH, HL,
       and HH). A series of dinuclear Fe(III) complexes has been prepared; the
       iron centers are linked by a bidentate bridge (CN(-), and diamagnetic
       metallacyanates \Fe(CN)(5)(NO)\, \Ni(CN)(4)\ \Pt(CN)(4)\, and
       \Ag(CN)(2)\). Magnetic measurements confirm that the spin crossover
       proceeds on the thermal propagation. This information has been completed
       also by the Mossbauer spectral (MS) data. A theoretical model has been
       developed that allows a simultaneous fitting of all available
       experimental data (magnetic susceptibility, magnetization, HS mole
       fraction) on a common set of parameters.,
    DOI = 10.1351/PAC-CON-08-07-20,
    ISSN = 0033-4545,
    Unique-ID = ISI:000269408000002,
    
  • [DOI] I. Nemec, R. Boca, R. Herchel, Z. Travnicek, M. Gembicky, and W. Linert, “Dinuclear Fe(III) complexes with spin crossover,” MONATSHEFTE FUR CHEMIE, vol. 140, iss. 7, pp. 815-828, 2009.
    [Bibtex]
    @article ISI:000266926500011,
    Author = Nemec, Ivan and Boca, Roman and Herchel, Radovan and Travnicek, Zdenek
       and Gembicky, Milan and Linert, Wolfgang,
    Title = Dinuclear Fe(III) complexes with spin crossover,
    Journal = MONATSHEFTE FUR CHEMIE,
    Year = 2009,
    Volume = 140,
    Number = 7,
    Pages = 815-828,
    Month = JUL,
    Abstract = A series of dinuclear Fe(III) complexes was synthesized in which the
       Schiff-base blocking ligand L(5) coordinates each of the centers which
       are linked by a bidentate, bipyridine-type ligand. For these systems,
       [L(5)Fe(III)\bridge\ Fe(III)L(5)](BPh(4))(2), thermally induced spin
       crossover is observed. The corollary of the systems is that the spin
       crossover interferes with the magnetic exchange interaction. The overlap
       of the energy bands of the LL and HH reference states (L, low-spin; H,
       high-spin) causes the exchange interaction to act against the spin
       crossover (leading to incompleteness or gradual behavior).,
    DOI = 10.1007/s00706-008-0096-0,
    ISSN = 0026-9247,
    Unique-ID = ISI:000266926500011,