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:
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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.
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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.
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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.
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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.
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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.
2011
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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, -
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
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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, -
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, -
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,