Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/102903
Title: Solvent-induced formation of novel ni(Ii) complexes derived from bis-thiosemicarbazone ligand: An insight from experimental and theoretical investigations
Authors: Mahmoudi, G.
Babashkina, M. G.
Maniukiewicz, W.
Afkhami, F. A.
Nunna, B. B.
Zubkov, F. I.
Ptaszek, A. L.
Szczepanik, D. W.
Mitoraj, M. P.
Safin, D. A.
Issue Date: 2021
Publisher: MDPI AG
Citation: Solvent-induced formation of novel ni(Ii) complexes derived from bis-thiosemicarbazone ligand: An insight from experimental and theoretical investigations / G. Mahmoudi, M. G. Babashkina, W. Maniukiewicz, et al. — DOI 10.3390/ijms22105337 // International Journal of Molecular Sciences. — 2021. — Vol. 22. — Iss. 10. — 5337.
Abstract: In this work, we report solvent-induced complexation properties of a new N2S2 tetradentate bis-thiosemicarbazone ligand (H2LI), prepared by the condensation of 4-phenylthiosemicarbazide with bis-aldehyde, namely 2,2’-(ethane-1,2-diylbis(oxy)dibenzaldehyde, towards nickel(II). Using ethanol as a reaction medium allowed the isolation of a discrete mononuclear homoleptic complex [NiLI ] (1), for which its crystal structure contains three independent molecules, namely 1-I, 1-II, and 1-III, in the asymmetric unit. The doubly deprotonated ligand LI in the structure of 1 is coordinated in a cis-manner through the azomethine nitrogen atoms and the thiocarbonyl sulfur atoms. The coordination geometry around metal centers in all the three crystallographically independent molecules of 1 is best described as the seesaw structure. Interestingly, using methanol as a reaction medium in the same synthesis allowed for the isolation of a discrete mononuclear homoleptic complex [Ni(LII)2 ] (2), where LII is a monodeprotonated ligand 2-(2-(2-(2-(dimethoxymethyl)phenoxy)ethoxy)benzylidene)-N-phenylhydrazine-1-carbothioamide (HLII). The ligand LII was formed in situ from the reaction of LI with methanol upon coordination to the metal center under synthetic conditions. In the structure of 2, two ligands LII are coordinated in a trans-manner through the azomethine nitrogen atom and the thiocarbonyl sulfur atom, also yielding a seesaw coordination geometry around the metal center. The charge and energy decomposition scheme ETS-NOCV allows for the conclusion that both structures are stabilized by a bunch of London dispersion-driven intermolecular interactions, including predominantly N–H···S and N–H···O hydrogen bonds in 1 and 2, respectively; they are further augmented by less typical C–H···X (where X = S, N, O, π), CH···HC, π···π stacking and the most striking, attractive long-range intermolecular C–H···Ni preagostic interactions. The latter are found to be determined by both stabilizing Coulomb forces and an exchange-correlation contribution as revealed by the IQA energy decomposition scheme. Interestingly, the analogous long-range C–H···S interactions are characterized by a repulsive Coulomb contribution and the prevailing attractive exchange-correlation constituent. The electron density of the delocalized bonds (EDDB) method shows that the nickel(II) atom shares only ~0.8|e| due to the σ-conjugation with the adjacent in-plane atoms, demonstrating a very weak σ-metalloaromatic character. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Keywords: NI INTERACTIONS
Σ-METALLOAROMATICITY
NI(II) COMPLEXES
INTERMOLECULAR C–H
URI: http://hdl.handle.net/10995/102903
Access: info:eu-repo/semantics/openAccess
SCOPUS ID: 85106181964
PURE ID: 22112113
605350c5-2e60-486b-a801-e8ad7fd24127
ISSN: 16616596
DOI: 10.3390/ijms22105337
metadata.dc.description.sponsorship: This paper has been supported by the RUDN University Strategic Academic Leadership Program (Fedor I. Zubkov, synthesis of the ligands). DFT calculations were partially performed using the PL-Grid Infrastructure and resources provided by the ACC Cyfronet AGH (Cracow, Poland). M. P. Mitoraj acknowledges the financial support of the Polish National Science Center within the Sonata Bis Project 2017/26/E/ST4/00104.
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