Structural study of Pt(II) and Pd(II) complexes with quinoline-2-carboxaldehyde thiosemicarbazone Scientific paper

Article Sidebar

Graphical Abstract
PDF (3,931 kB) Supplementary Material (2.6 MB)
Published: Apr 29, 2021
DOI: https://doi.org/10.2298/JSC201126079R
Keywords:
Single crystal X-ray diffraction non-covalent interactions N-heteroaromatic Schiff base chelate complexes.

Main Article Content

Predrag Ristić
University of Belgrade - Faculty of Chemistry, Studentski trg 12-16, 11000 Belgrade, Serbia
https://orcid.org/0000-0002-7489-6132
Marko Rodić
University of Belgrade – Faculty of Chemistry, Studentski trg 12-16, 11000 Belgrade, Serbia
https://orcid.org/0000-0002-4471-8001
Nenad Filipović
University of Belgrade – Faculty of Agriculture, Nemanjina 6, 11000 Belgrade, Serbia
https://orcid.org/0000-0003-2982-5324
Dragana Mitić
Innovation Centre of Faculty of Chemistry, University of Belgrade, Studentski trg 12-16, 11000 Belgrade, Serbia
Katarina Anđelković
University of Belgrade – Faculty of Chemistry, Studentski trg 12-16, 11000 Belgrade, Serbia
https://orcid.org/0000-0001-6335-0196
Tamara Todorović
University of Belgrade - Faculty of Chemistry, Studentski trg 12-16, 11000 Belgrade, Serbia
https://orcid.org/0000-0002-7740-3639

Abstract

Two square–planar complexes, [PtLCl] (1) and [PdLCl] (2), were synthesized with quinoline-2-carboxaldehyde thiosemicarbazone ligand (HL), and characterized by IR and NMR spectroscopy and single crystal X-ray dif­fract­ion analysis. In both complexes, L- is coordinated tridentately via the same donor atom set, while the fourth coordination site is occupied by a chloride ion. However, the complexes are not isostructural due to different types of non-cov­alent intermolecular interactions. These interactions were analyzed using Hirshfeld surfaces and two-dimensional fingerprint plots.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Article Details

How to Cite
[1]
P. Ristić, M. Rodić, N. Filipović, D. Mitić, K. Anđelković, and T. Todorović, “Structural study of Pt(II) and Pd(II) complexes with quinoline-2-carboxaldehyde thiosemicarbazone: Scientific paper”, J. Serb. Chem. Soc., vol. 86, no. 4, pp. 393–406, Apr. 2021.
Issue
Vol. 86 No. 4 (2021)
Section
Inorganic Chemistry
Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Creative Commons лиценца
Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution license 4.0 that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.

Read more....

Crossref
Scopus
Google Scholar
Europe PMC

References

P. Heffeter, V. F. S. Pape, É. A. Enyedy, B. K. Keppler, G. Szakacs, C. R. Kowol, Antioxidants Redox Signal. 30 (2019) 1062 (http://dx.doi.org/10.1089/ars.2017.7487)

J. Shim, N. R. Jyothi, N. A. M. Farook, Asian J. Chem. 25 (2013) 5838 (http://dx.doi.org/10.14233/ajchem.2013.oh105)

G. Pelosi, Open Crystallogr. J. 3 (2010) 16 (http://dx.doi.org/10.2174/1874846501003020016)

N. P. Prajapati, H. D. Patel, Synth. Commun. 49 (2019) 2767 (http://dx.doi.org/10.1080/00397911.2019.1649432)

T. S. Lobana, R. Sharma, G. Bawa, S. Khanna, Coord. Chem. Rev. 253 (2009) 977 (http://dx.doi.org/10.1016/j.ccr.2008.07.004)

E. J. Siddiqui, I. Azad, A R. Khan, T. Khan, J. Drug Deliv. Therapeut. 9 (2019) 689 (http://jddtonline.info/index.php/jddt/article/view/2888/2135)

T. R. Todorović, A. Bacchi, N. O. Juranić, D. M. Sladić, G. Pelizzi, T. T. Božić, N. R. Filipović, K. K. Andelković, Polyhedron 26 (2007) 3428 (http://dx.doi.org/10.1016/j.poly.2007.03.023)

N. Gligorijević, T. Todorović, S. Radulović, D. Sladić, N. Filipović, D. Gođevac, D. Jeremić, K. Anđelković, Eur. J. Med. Chem. 44 (2009) 1623 (http://dx.doi.org/10.1016/j.ejmech.2008.07.033)

T. R. Todorović, A. Bacchi, D. M. Sladić, N. M. Todorović, T. T. Božić, D. D. Radanović, N. R. Filipović, G. Pelizzi, K. K. Andelković, Inorg. Chim. Acta 362 (2009) 3813 (http://dx.doi.org/10.1016/j.ica.2009.04.047)

S. Bjelogrlic, T. Todorovic, A. Bacchi, M. Zec, D. Sladic, T. Srdic-Rajic, D. Radanovic, S. Radulovic, G. Pelizzi, K. Andelkovic, J. Inorg. Biochem. 104 (2010) 673 (http://dx.doi.org/10.1016/j.jinorgbio.2010.02.009)

T. Srdić-Rajić, M. Zec, T. Todorović, K. Anelković, S. Radulović, Eur. J. Med. Chem. 46 (2011) 3734 (http://dx.doi.org/10.1016/j.ejmech.2011.05.039)

N. Filipović, N. Polović, B. Rašković, S. Misirlić-Denčić, M. Dulović, M. Savić, M. Nikšić, D. Mitić, K. Anđelković, T. Todorović, Monatsheft. Chem.145 (2014) 1089 (http://dx.doi.org/10.1007/s00706-014-1197-6)

N. R. Filipović, S. Bjelogrlić, A. Marinković, T. Ž. Verbić, I. N. Cvijetić, M. Senćanski, M. Rodić, M. Vujčić, D. Sladić, Z. Striković, T. R. Todorović, C. D. Muller, RSC Adv. 5 (2015) 95191 (http://dx.doi.org/10.1039/C5RA19849F)

I. S. Djordjevic, J. Vukasinovic, T. R. Todorovic, N. R. Filipovic, M. V. Rodic, A. Lolic, G. Portalone, M. Zlatovic, S. Grubisic, J. Serb. Chem. Soc. 82 (2017) 825 (http://dx.doi.org/10.2298/JSC170412062D)

S. Poirier, H. Lynn, C. Reber, E. Tailleur, M. Marchivie, P. Guionneau, M. R. Probert, Inorg. Chem. 57 (2018) 7713 (http://dx.doi.org/10.1021/acs.inorgchem.8b00724)

L. M. Epstein, E. S. Shubina, Coord. Chem. Rev. 231 (2002) 165 (http://dx.doi.org/10.1016/S0010-8545(02)00118-2)

J. Kozelka, in Noncovalent Forces, S. Scheiner, Ed., Springer International Publishing, Cham, 2015, pp. 129 (http://dx.doi.org/10.1007/978-3-319-14163-3_6)

P. Ristić, V. Blagojević, G. Janjić, M. Rodić, P. Vulić, M. Donnard, M. Gulea, A. Chylewska, M. Makowski, T. Todorović, T. Todorović, N. Filipović, Cryst. Growth Des. 20 (2020) 3018 (http://dx.doi.org/10.1021/acs.cgd.9b01661)

P. N. Bourosh, M. D. Revenko, M. Gdaniec, E. F. Stratulat, Y. A. Simonov, J. Struct. Chem. 50 (2009) 510 (http://dx.doi.org/10.1007/s10947-009-0078-z)

CrysAlisPro Software system, Agilent Technologies UK Ltd., Cheadle

G. M. Sheldrick, Acta Crystallogr. Sect. A Found. Adv. 71 (2015) 3 (http://dx.doi.org/10.1107/S2053273314026370)

G. M. Sheldrick, Acta Crystallogr., C 71 (2015) 3 (http://dx.doi.org/10.1107/S2053229614024218)

C. B. Hübschle, G. M. Sheldrick, B. Dittrich, J. Appl. Crystallogr. 44 (2011) 1281 (http://dx.doi.org/10.1107/S0021889811043202)

A. L. Spek, Acta Crystallogr., D 65 (2009) 148 (http://dx.doi.org/10.1107/S090744490804362X)

C. F. Macrae, I. J. Bruno, J. A. Chisholm, P. R. Edgington, P. McCabe, E. Pidcock, L. Rodriguez-Monge, R. Taylor, J. van de Streek, P. A. Wood, J. Appl. Crystallogr. 41 (2008) 466 (http://dx.doi.org/10.1107/s0021889807067908)

C. F. MacRae, I. Sovago, S. J. Cottrell, P. T. A. Galek, P. McCabe, E. Pidcock, M. Platings, G. P. Shields, J. S. Stevens, M. Towler, P. A. Wood, J. Appl. Crystallogr. 53 (2020) 226 (http://dx.doi.org/10.1107/S1600576719014092)

C. R. Groom, I. J. Bruno, M. P. Lightfoot, S. C. Ward, Acta Crystallogr., B 72 (2016) 171 (http://dx.doi.org/10.1107/S2052520616003954)

J. J. McKinnon, D. Jayatilaka, M. A. Spackman, Chem. Commun. (2007) 3814 (http://dx.doi.org/10.1039/b704980c)

J. J. McKinnon, M. A. Spackman, A. S. Mitchell, Acta Crystallogr., B 60 (2004) 627 (http://dx.doi.org/10.1107/S0108768104020300)

M. Mohan, M. Manmohan, Synth. React. Inorg. Met. Chem. 12 (1982) 761 (http://dx.doi.org/10.1080/00945718208082693)

L. Yang, D. R. Powell, R. P. Houser, Dalton Trans. (2007) 955 (http://dx.doi.org/10.1039/b617136b)

R. Boese, M. T. Kirchner, J. D. Dunitz, G. Filippini, A. Gavezzotti, Helv. Chim. Acta 84 (2001) 1561 (http://dx.doi.org/10.1002/1522-2675(20010613)84:6<1561::AID-HLCA1561>3.0.CO;2-M)

I. Dance, New J. Chem. 27 (2003) 22 (http://dx.doi.org/10.1039/b206867b)

M. A. Spackman, J. J. McKinnon, CrystEngComm 4 (2002) 378 (http://dx.doi.org/10.1039/b203191b)

S. L. Tan, M. M. Jotani, E. R. T. Tiekink, Acta Crystallogr., E 75 (2019) 308 (http://dx.doi.org/10.1107/S2056989019001129).

Most read articles by the same author(s)

1 2 > >>