Araškov, Jovana

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ec37f1f3-82d8-4ecc-b2e4-f62c2173ce7c
  • Araškov, Jovana (1)
  • Araškov, Jovana B. (1)

Author's Bibliography

Zn(ii) complexes with thiazolyl-hydrazones: structure, intermolecular interactions, photophysical properties, computational study and anticancer activity

Araškov, Jovana B.; Višnjevac, Aleksandar; Popović, Jasminka; Blagojević, Vladimir; Fernandes, Henrique S.; Sousa, Sérgio F.; Novaković, Irena; Padrón, José M.; Holló, Berta Barta; Monge, Miguel; Rodríguez-Castillo, María; López-De-Luzuriaga, José M.; Filipović, Nenad; Todorović, Tamara

(Royal Society of Chemistry, 2022)

TY  - JOUR
AU  - Araškov, Jovana B.
AU  - Višnjevac, Aleksandar
AU  - Popović, Jasminka
AU  - Blagojević, Vladimir
AU  - Fernandes, Henrique S.
AU  - Sousa, Sérgio F.
AU  - Novaković, Irena
AU  - Padrón, José M.
AU  - Holló, Berta Barta
AU  - Monge, Miguel
AU  - Rodríguez-Castillo, María
AU  - López-De-Luzuriaga, José M.
AU  - Filipović, Nenad
AU  - Todorović, Tamara
PY  - 2022
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5431
AB  - Earth-abundant, cheap and non-toxic zinc-based coordination compounds are drawing research attention as promising candidates for various applications, such as photoluminescent materials and anticancer agents. In this paper we report six zinc complexes (1-3-NO3 and 1-3-Cl) with pyridyl-based thiazolyl-hydrazone ligands, which differ in the nature of substituents at the ligands' periphery, anion type, and geometry around the metal ion. The complexes were characterized by single-crystal and powder X-ray diffraction analysis, as well as IR and NMR spectroscopy. The symmetrical complexes 2-Cl and 3-Cl, where zinc atoms are located at a two-fold axis, do not exhibit photophysical properties, unlike their asymmetrical analogs 2-NO3 and 3-NO3 with the same complex cation. Asymmetrical pentacoordinated 1-Cl and hexacoordinated 1-NO3 complexes exhibit photophysical properties. An admixture of allowed intra-ligand (1IL) and chloro (X)-to-ligand charge-transfer (1XLCT) electronic transitions is responsible for the fluorescence of the 1-Cl complex. The origin of the emission of the 1-NO3 complex is ascribed to an admixture of 3IL and ligand-to-ligand charge-transfer (3LLCT) forbidden electronic transitions, while for 3-NO3 most electronic excitations are of LLCT character. The thermal stability of the complexes is in accord with the strength of respective intermolecular interactions. The antiproliferative activity of the complexes was in the nanomolar range on some of the investigated cancer cell lines. Contrary to the increase of antiproliferative activity of the complexes in comparison to the free ligands in cancer cell lines, an acute toxicity determined in the brine shrimp assay follows the opposite trend. The overall results suggest that Zn(ii) thiazoyl-hydrazone complexes have considerable potential as multifunctional materials.
PB  - Royal Society of Chemistry
T2  - CrystEngComm
T1  - Zn(ii) complexes with thiazolyl-hydrazones: structure, intermolecular interactions, photophysical properties, computational study and anticancer activity
VL  - 24
IS  - 29
SP  - 5194
EP  - 5214
DO  - 10.1039/d2ce00443g
ER  - 
@article{
author = "Araškov, Jovana B. and Višnjevac, Aleksandar and Popović, Jasminka and Blagojević, Vladimir and Fernandes, Henrique S. and Sousa, Sérgio F. and Novaković, Irena and Padrón, José M. and Holló, Berta Barta and Monge, Miguel and Rodríguez-Castillo, María and López-De-Luzuriaga, José M. and Filipović, Nenad and Todorović, Tamara",
year = "2022",
abstract = "Earth-abundant, cheap and non-toxic zinc-based coordination compounds are drawing research attention as promising candidates for various applications, such as photoluminescent materials and anticancer agents. In this paper we report six zinc complexes (1-3-NO3 and 1-3-Cl) with pyridyl-based thiazolyl-hydrazone ligands, which differ in the nature of substituents at the ligands' periphery, anion type, and geometry around the metal ion. The complexes were characterized by single-crystal and powder X-ray diffraction analysis, as well as IR and NMR spectroscopy. The symmetrical complexes 2-Cl and 3-Cl, where zinc atoms are located at a two-fold axis, do not exhibit photophysical properties, unlike their asymmetrical analogs 2-NO3 and 3-NO3 with the same complex cation. Asymmetrical pentacoordinated 1-Cl and hexacoordinated 1-NO3 complexes exhibit photophysical properties. An admixture of allowed intra-ligand (1IL) and chloro (X)-to-ligand charge-transfer (1XLCT) electronic transitions is responsible for the fluorescence of the 1-Cl complex. The origin of the emission of the 1-NO3 complex is ascribed to an admixture of 3IL and ligand-to-ligand charge-transfer (3LLCT) forbidden electronic transitions, while for 3-NO3 most electronic excitations are of LLCT character. The thermal stability of the complexes is in accord with the strength of respective intermolecular interactions. The antiproliferative activity of the complexes was in the nanomolar range on some of the investigated cancer cell lines. Contrary to the increase of antiproliferative activity of the complexes in comparison to the free ligands in cancer cell lines, an acute toxicity determined in the brine shrimp assay follows the opposite trend. The overall results suggest that Zn(ii) thiazoyl-hydrazone complexes have considerable potential as multifunctional materials.",
publisher = "Royal Society of Chemistry",
journal = "CrystEngComm",
title = "Zn(ii) complexes with thiazolyl-hydrazones: structure, intermolecular interactions, photophysical properties, computational study and anticancer activity",
volume = "24",
number = "29",
pages = "5194-5214",
doi = "10.1039/d2ce00443g"
}
Araškov, J. B., Višnjevac, A., Popović, J., Blagojević, V., Fernandes, H. S., Sousa, S. F., Novaković, I., Padrón, J. M., Holló, B. B., Monge, M., Rodríguez-Castillo, M., López-De-Luzuriaga, J. M., Filipović, N.,& Todorović, T.. (2022). Zn(ii) complexes with thiazolyl-hydrazones: structure, intermolecular interactions, photophysical properties, computational study and anticancer activity. in CrystEngComm
Royal Society of Chemistry., 24(29), 5194-5214.
https://doi.org/10.1039/d2ce00443g
Araškov JB, Višnjevac A, Popović J, Blagojević V, Fernandes HS, Sousa SF, Novaković I, Padrón JM, Holló BB, Monge M, Rodríguez-Castillo M, López-De-Luzuriaga JM, Filipović N, Todorović T. Zn(ii) complexes with thiazolyl-hydrazones: structure, intermolecular interactions, photophysical properties, computational study and anticancer activity. in CrystEngComm. 2022;24(29):5194-5214.
doi:10.1039/d2ce00443g .
Araškov, Jovana B., Višnjevac, Aleksandar, Popović, Jasminka, Blagojević, Vladimir, Fernandes, Henrique S., Sousa, Sérgio F., Novaković, Irena, Padrón, José M., Holló, Berta Barta, Monge, Miguel, Rodríguez-Castillo, María, López-De-Luzuriaga, José M., Filipović, Nenad, Todorović, Tamara, "Zn(ii) complexes with thiazolyl-hydrazones: structure, intermolecular interactions, photophysical properties, computational study and anticancer activity" in CrystEngComm, 24, no. 29 (2022):5194-5214,
https://doi.org/10.1039/d2ce00443g . .
6
8
7

Crystal chirality – cobalt complexes with thiazole based ligands

Šuljagić, Marija; Araškov, Jovana; Filipović, Nenad; Todorović, Tamara

(Belgrade: Serbian Chemical Society, 2016)

TY  - CONF
AU  - Šuljagić, Marija
AU  - Araškov, Jovana
AU  - Filipović, Nenad
AU  - Todorović, Tamara
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5953
AB  - Chirality is a striking property of the biological world. Many organic molecules, including the most biological amino acids are chiral and the DNA double helix in its standard form twists like a right-handed screw. The importance of chirality in biological systems was brought to light by the thalidomide tragedy [1]. On the other hand, there are many non-biological chiral crystals which have not been treated in terms of chirality, which include important enantioselective catalysts and sensing materials, as well as enenatioselective chromatographic materials. In dealing with chirality in relation to crystal structures it is essential to distinguish between three different objects that may be either chiral or achiral: 1) the molecular components of the crystal, 2) the crystal structure itself and 3) the symmetry group of the crystal structure. Chirality of crystals will be discussed taking cobalt complexes with thiazole based ligands as examples.
AB  - Hiralnost je izraženo svojstvo biološkog sveta. Mnogi organski molekuli su hiralni, uključujući 
većinu bioloških aminokiselina. Takođe, dvostruki heliks DNK u svom kanonskom obliku ima formu desnog zavrtnja. Međutim, značaj hiralnosti sagledan je tek nakon tragedije sa talidomidom [1]. S druge strane, postoje mnogi nebiološki hiralni kristali kojima nije razmatrana hiralnost, a oni uključuju važne enantioselektivne katalizatore i senzorske materijale, kao i enantioselektivne hromatografke materijale. Kada se radi o hiralnosti u kristalnim strukturama, važno je razlikovati tri različite grupe objekata koji mogu biti ili hiralni ili ahiralni: 1) molekulske komponente kristala, 2) same kristalne strukture, 3) simetrijske grupe kristalnih struktura. Hiralnost kristala će biti razmatrana na primerima kompleksa kobalta sa tiazolskim ligandima.
PB  - Belgrade: Serbian Chemical Society
C3  - Book of Abstracts - 4th Conference of Young Chemists of Serbia, November 5, 2016, Belgrade
T1  - Crystal chirality – cobalt complexes with thiazole based ligands
T1  - Hiralnost kristala – kompleksi kobalta sa derivatima tiazola
SP  - 44
EP  - 44
UR  - https://hdl.handle.net/21.15107/rcub_cer_5953
ER  - 
@conference{
author = "Šuljagić, Marija and Araškov, Jovana and Filipović, Nenad and Todorović, Tamara",
year = "2016",
abstract = "Chirality is a striking property of the biological world. Many organic molecules, including the most biological amino acids are chiral and the DNA double helix in its standard form twists like a right-handed screw. The importance of chirality in biological systems was brought to light by the thalidomide tragedy [1]. On the other hand, there are many non-biological chiral crystals which have not been treated in terms of chirality, which include important enantioselective catalysts and sensing materials, as well as enenatioselective chromatographic materials. In dealing with chirality in relation to crystal structures it is essential to distinguish between three different objects that may be either chiral or achiral: 1) the molecular components of the crystal, 2) the crystal structure itself and 3) the symmetry group of the crystal structure. Chirality of crystals will be discussed taking cobalt complexes with thiazole based ligands as examples., Hiralnost je izraženo svojstvo biološkog sveta. Mnogi organski molekuli su hiralni, uključujući 
većinu bioloških aminokiselina. Takođe, dvostruki heliks DNK u svom kanonskom obliku ima formu desnog zavrtnja. Međutim, značaj hiralnosti sagledan je tek nakon tragedije sa talidomidom [1]. S druge strane, postoje mnogi nebiološki hiralni kristali kojima nije razmatrana hiralnost, a oni uključuju važne enantioselektivne katalizatore i senzorske materijale, kao i enantioselektivne hromatografke materijale. Kada se radi o hiralnosti u kristalnim strukturama, važno je razlikovati tri različite grupe objekata koji mogu biti ili hiralni ili ahiralni: 1) molekulske komponente kristala, 2) same kristalne strukture, 3) simetrijske grupe kristalnih struktura. Hiralnost kristala će biti razmatrana na primerima kompleksa kobalta sa tiazolskim ligandima.",
publisher = "Belgrade: Serbian Chemical Society",
journal = "Book of Abstracts - 4th Conference of Young Chemists of Serbia, November 5, 2016, Belgrade",
title = "Crystal chirality – cobalt complexes with thiazole based ligands, Hiralnost kristala – kompleksi kobalta sa derivatima tiazola",
pages = "44-44",
url = "https://hdl.handle.net/21.15107/rcub_cer_5953"
}
Šuljagić, M., Araškov, J., Filipović, N.,& Todorović, T.. (2016). Crystal chirality – cobalt complexes with thiazole based ligands. in Book of Abstracts - 4th Conference of Young Chemists of Serbia, November 5, 2016, Belgrade
Belgrade: Serbian Chemical Society., 44-44.
https://hdl.handle.net/21.15107/rcub_cer_5953
Šuljagić M, Araškov J, Filipović N, Todorović T. Crystal chirality – cobalt complexes with thiazole based ligands. in Book of Abstracts - 4th Conference of Young Chemists of Serbia, November 5, 2016, Belgrade. 2016;:44-44.
https://hdl.handle.net/21.15107/rcub_cer_5953 .
Šuljagić, Marija, Araškov, Jovana, Filipović, Nenad, Todorović, Tamara, "Crystal chirality – cobalt complexes with thiazole based ligands" in Book of Abstracts - 4th Conference of Young Chemists of Serbia, November 5, 2016, Belgrade (2016):44-44,
https://hdl.handle.net/21.15107/rcub_cer_5953 .