Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Erika, Samoľová"'
Publikováno v:
Crystals, Vol 13, Iss 10, p 1460 (2023)
Mixed-ligand complexes featuring a carboxylato ligand and bidentate chelate N,N′-donor ligands along with a single halogenido ligand are rarely subjected to studies despite their interesting physical, chemical and biological properties. A direct sy
Externí odkaz:
https://doaj.org/article/5ea5cba2857846499f1e93718f564734
Autor:
Ján Gettler, Tomáš Čarný, Martin Markovič, Peter Koóš, Erika Samoľová, Ján Moncoľ, Tibor Gracza
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 12, p 10331 (2023)
A versatile strategy for the enantioselective synthesis of a benzo[c]oxepine structural core containing natural secondary metabolites was developed. The key steps of the synthetic approach include ring-closing alkene metathesis for seven-member ring
Externí odkaz:
https://doaj.org/article/5acac42d6707472690948078e0241e1c
Autor:
Michaela Harmošová, Martin Kello, Michal Goga, Ľudmila Tkáčiková, Mária Vilková, Danica Sabolová, Simona Sovová, Erika Samoľová, Miroslava Litecká, Veronika Kuchárová, Juraj Kuchár, Ivan Potočňák
Publikováno v:
Inorganics, Vol 11, Iss 2, p 60 (2023)
Two tetranuclear [Zn4Cl2(ClQ)6]·2DMF (1) and [Zn4Cl2(ClQ)6(H2O)2]·4DMF (2), as well as three dinuclear [Zn2(ClQ)3(HClQ)3]I3 (3), [Zn2(dClQ)2(H2O)6(SO4)] (4) and [Zn2(dBrQ)2(H2O)6(SO4)] (5), complexes (HClQ = 5-chloro-8-hydroxyquinoline, HdClQ = 5,7
Externí odkaz:
https://doaj.org/article/68b98665207b46c9bb7e653b50987a91
Publikováno v:
IUCrData, Vol 6, Iss 4, p x210356 (2021)
In the title compound, C22H20O3, the dihedral angle between the aromatic rings linked by the methine group is 81.265 (4)° and the ethoxy side chain adopts an extended conformation [C—O—C—C = 177.24 (10)°]. In the crystal, weak C—H...π and
Externí odkaz:
https://doaj.org/article/b45a43d4793d4bb6b8124bfce2f33b46
Publikováno v:
IUCrData, Vol 6, Iss 4, p x210335 (2021)
The new title Schiff base compound, C11H15BrN2O2, crystallizes in the monoclinic space group P21 with two independent molecules in the asymmetric unit. It was prepared by the condensation reaction of 5-bromo-2-hydroxybenzaldehyde and aminoethylethano
Externí odkaz:
https://doaj.org/article/8f4dd8d8ee3a45cab3fa6a63cc79fbc2
Autor:
Romana Mičová, Cyril Rajnák, Ján Titiš, Erika Samoľová, Michal Zalibera, Alina Bieńko, Roman Boča
Publikováno v:
Chemical Communications. 59:2612-2615
AC susceptibility confirms a field supported slow magnetic relaxation in which the over-barrier Orbach relaxation process does not play a role. Both systems possess two or three slow relaxation channels.
Autor:
Dušan S. Dimić, Goran N. Kaluđerović, Edina H. Avdović, Dejan A. Milenković, Marko N. Živanović, Ivan Potočňák, Erika Samoľová, Milena S. Dimitrijević, Luciano Saso, Zoran S. Marković, Jasmina M. Dimitrić Marković
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 2, p 1001 (2022)
In this contribution, four new compounds synthesized from 4-hydroxycoumarin and tyramine/octopamine/norepinephrine/3-methoxytyramine are characterized spectroscopically (IR and NMR), chromatographically (UHPLC-DAD), and structurally at the B3LYP/6-31
Externí odkaz:
https://doaj.org/article/a4178c5fb34b43fd8ab79a1b76ad7807
Autor:
Gracza, Ján Gettler, Tomáš Čarný, Martin Markovič, Peter Koóš, Erika Samoľová, Ján Moncoľ, Tibor
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 12; Pages: 10331
A versatile strategy for the enantioselective synthesis of a benzo[c]oxepine structural core containing natural secondary metabolites was developed. The key steps of the synthetic approach include ring-closing alkene metathesis for seven-member ring
Autor:
Romana Mičová, Zuzana Bielková, Cyril Rajnák, Ján Titiš, Milan Gembický, Franz Renz, Ondřej Malina, Erika Samoľová, Jana Nováčiková, Roman Boča
Publikováno v:
New Journal of Chemistry. 46:18083-18089
A new series of Fe(iii) mononuclear complexes of the [Fe(Lam)(X)] type {where X = Cl (1), NCSe (2), NCS (3), N3 (4), and NCO (5)} have been prepared and characterized in detail.
Publikováno v:
Dalton Transactions.
Complexes under study exhibit field-supported SMR. For 1, the relaxation time at T = 2.0 K is τHF = 20 and 2 ms at the applied field BDC = 0.15 and 0.35 T, respectively. For 2 at T = 2.0 K and BDC = 0.1 T, the relaxation time is τHF = 6 ms.