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Article

Synthesis, Characterization, Computational and Biological Activity of Some Schiff Bases and Their Fe, Cu and Zn Complexes

by
Tareq M. A. Al-Shboul
1,
Mohammad El-khateeb
2,
Zaid H. Obeidat
3,
Taher S. Ababneh
3,
Suha S. Al-Tarawneh
1,
Mazhar S. Al Zoubi
4,
Walhan Alshaer
5,
Anas Abu Seni
3,
Taqwa Qasem
4,
Hayato Moriyama
6,
Yukihiro Yoshida
6,
Hiroshi Kitagawa
6 and
Taghreed M. A. Jazzazi
3,*
1
Department of Chemistry and Chemical Technology, Tafila Technical University, Tafila 66110, Jordan
2
Chemistry Department, Jordan University of Science and Technology, Irbid 22110, Jordan
3
Department of Chemistry, Yarmouk University, Irbid 21163, Jordan
4
Department of Basic Medical Sciences, Yarmouk University, Irbid 21163, Jordan
5
Cell Therapy Center, The University of Jordan, Amman 11942, Jordan
6
Division of Chemistry, Graduate School of Science, Kyoto University, Kitashirakawa-Oiwakecho, Sakyo-ku, Kyoto 606-8502, Japan
*
Author to whom correspondence should be addressed.
Inorganics 2022, 10(8), 112; https://doi.org/10.3390/inorganics10080112
Submission received: 1 July 2022 / Revised: 16 July 2022 / Accepted: 20 July 2022 / Published: 2 August 2022
(This article belongs to the Special Issue Synthesis, Structure and Properties of Schiff Base Metal Complexes)
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Abstract

:
Four new symmetrical Schiff bases derived from 2,2′-diamino-6,6′-dibromo-4,4′-dimethyl-1,1′-biphenyl or 2,2′-diamino-4,4′-dimethyl-1,1′-biphenyl, and 3,5-dichloro- or 5-nitro-salicylaldehyde, were synthesized and reacted with copper-, iron- and zinc-acetate, producing the corresponding complexes. The Schiff bases and their metal complexes were characterized by 1H-, 13C-NMR, IR and UV-Vis spectroscopy and elemental analysis. The structures of one Schiff base and the two zinc complexes were resolved by X-ray structure determination. Density functional theory (DFT) calculations at the B3LYP/6-31G(d) level of the latter compounds were carried out to optimize and examine their molecular geometries. The biomedical applications of the Schiff bases and their complexes were investigated as anticancer or antimicrobial agents.

Graphical Abstract

1. Introduction

Schiff bases are a well-documented class of ligands that are capable of bonding to almost all metals of the periodic table [1]. They are generally formed through a condensation reaction of carbonyl compounds with primary amines, in which mono-, di- or tri-functional amines lead to bi-, tri-, tetra- or poly-dentate Schiff bases. Symmetrical Schiff bases are formed when diamines are reacted with the same aldehydes or ketones in a 1:2 molar ratio. On the other hand, unsymmetrical Schiff bases may be obtained when two different aldehydes or ketones are reacted with diamines.
Due to the presence of N/O donor atoms in any Schiff base, they can coordinate to metals, leading to new metal complexes. Two main methods are used to synthesize Schiff base complexes. The first involves basic conditions, in which the Schiff base reacts with the metal ion in alcoholic or aqueous solutions [2]. The second methodology depends on a template reaction of primary amines, aldehydes or ketones to react simultaneously with metal ions [3]. This method is used to synthesize Schiff base complexes derived from macrocyclic and cyclic ligands.
Schiff bases and their complexes have versatile applications [4]. For instance, they are used in medicinal and pharmaceutical chemistry. In the medical sector, they are used as anticancer, antitubercular, anti-inflammatory, antipyretic and analgesic agents [5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22]. Moreover, Schiff bases are used in dye synthesis [23], for antioxidative activity [24], immobilization of enzymes [25], cation carriers in potentiometric sensors [8,26] and as effective corrosion inhibitors [27]. Schiff bases and their metal complexes are also used in electrochemical sensors and chromatographic methods for detection with high selectivity and sensitivity [28,29]. The biological and medicinal activities of Schiff base metal complexes are greater than those of free Schiff bases [30,31,32,33]. Furthermore, divalent metal Schiff base complexes, especially those involving Fe(II), Ru(II) and Cu(II), have been widely used in catalysis for the oxidation of alcohols, cyclopropanation reactions and base hydrolysis of amino acid esters [34,35,36,37,38,39,40,41,42].
Motivated by all of the aforementioned applications, we are interested in the synthesis of new Schiff base ligands and their metal complexes. The reaction of M(OAc)2 (M = Cu(II), Co(II) or Ni(II) with 2,2′-bis(2-hydroxybenzylideneamino)-4,4′-dimethyl-1,1′-biphenyl allowed the synthesis of their complexes. The ligands are in tetradentate binding mode via ONNO motif of the two phenolic oxygen atoms and two azomethine nitrogen atoms [43].
In our previous studies, new Schiff base ligands derived from 2,2′-diamino-4,4′-dimethyl-1,1′-biphenyl-salicylaldehyde were prepared and characterized. These ligands were then reacted with Cu(II), Mn(II) or Zn(II) acetate, forming tetra-coordinate metal complexes. The anticancerous and antiproliferative activities of one representative ligand and its metal complexes were reported [22]. Additionally, 4-thiazolidinone derivatives were prepared, and their biological activity, along with their metal complexes, was tested as a fungicide and found to have good activities against fungi [44]. The preparation and characterization of substituted 2,2′-bis(2-oxidobenzylideneamino)-4,4′-dimethyl-1,1′-biphenyl complexes of zinc, potassium and titanium were studied [45,46,47]. Recently, we undertook the evaluation and molecular modelling of bis-Schiff base derivatives as potential leads for the management of diabetes mellitus [48].
As an extension of our research in the area of Schiff base complexes, we report herein the synthesis of two new symmetrical Schiff bases by the condensation reactions of 2,2′-diamino-6,6′-dibromo-4,4′-dimethyl-1,1′-biphenyl and 2,2′-diamino-4,4′-dimethyl-1,1′-biphenyl with salicylaldehyde derivatives to produce the desired tetradentate Schiff base ligands. The copper, zinc and iron complexes of these new Schiff bases were obtained. To obtain a qualitative understanding of the structural characteristics and relative energies of the prepared Schiff bases and metal complexes, a density functional theory (DFT) computational analysis was carried out. Moreover, by certain biological testing, these Schiff bases and their complexes were demonstrated to be antimicrobial and anticancer agents.

2. Results and Discussion

2.1. Synthesis

Symmetrical Schiff bases were prepared via the condensation reaction of 2,2′-diamino-4,4′-dimethyl-1,1′-biphenyl or 2,2′-diamino-6,6′-dibromo-4,4′-dimethyl-1,1′-biphenyl with 3,5-dichloro- or 5-nitro-salicylaldehyde, as shown in Scheme 1. Copper(II), iron(II) and zinc(II) complexes of these Schiff bases were prepared by their reactions with metal acetate in a 1:1 ligand-to-metal molar ratio. A base (sodium methoxide or triethylamine) was added to subtract the acidic proton.
The metal complexes Z1M–Z4M were colored complexes and characterized by molar conductivity, UV-Vis, IR, 1H- and 13C-NMR spectra where applicable. The complexes had non-electrolytic behavior, evident by the very low (~0) molar conductivity, suggesting that the complexes were indeed neutral. The UV-Vis absorption spectra of the Schiff bases and their metal complexes were measured in DMSO solutions. The spectra of the Schiff bases displayed two bands (310–359 and 451–452 nm), which may be attributed to intraligand absorptions (π-π* and n-π) of the conjugated system and the azomethine group [49]. However, the metal complexes showed only one band in the range of 361–412 nm, which may be attributed to a metal-to-ligand charge transfer band.
The 1H-NMR spectra of the free Schiff bases presented the phenolic signal (12.61–13.63 ppm). This peak disappeared in the spectra of the Zn(II) complexes. This proves that the two hydroxyl groups in the free Schiff base ligands lost their protons, and new bonds between the metal and the two oxygen atoms were formed. Moreover, the signal in the range of 8.04–8.58 ppm of the free Schiff bases that was attributed to the azomethine proton (CH=N) was shifted upfield in the zinc complexes’ spectra, thereby supporting its bond formation with the Zn center. These 1H-NMR values for both the free ligands and zinc complexes were consistent with those published for similar compounds [22,45,46,47,50,51]. The 13C-NMR spectra of the free Schiff bases displayed peaks in the ranges of 21.23–21.39 ppm and 161.04–166.32 ppm, corresponding to the methyl and azomethine carbons, respectively. These peaks were shifted to 20.99–21.03 ppm and 168.72–175.62 ppm upon complexation to zinc. Although a small shift was observed for the methyl peak, a big shift was observed for the azomethine carbon, another indication of the N-bonding to zinc.
In the IR spectra of the Schiff bases, the characteristic bands in regions 3467–3450, 2900–3100, 1627–1613, 1476–1413 and 1356–1323 cm−1 may be attributed to the absorption of ν(O-H), ν(C-H), ν(C=N), ν(C=C) and ν(C-O), respectively. The ν(C=N) band was shifted to a lower wavenumber in the corresponding spectra of the complexes. This indicated that this group was coordinated to the metal center. In addition, the disappearance of the weak and broad band of the hydroxyl group gave important evidence of the complexation of the phenolic groups. Moreover, two new bands, in the ranges of 400–450 and 500–550 cm−1 due to M-N and M-O stretching, appeared in the metal complexes’ spectra and represented another proof of O/N coordination to metals. These results are in good agreement with those previously published for similar complexes [22,52,53,54,55,56].

2.2. X-ray Structural Analysis

The single crystals of ZH4 suitable for X-ray structure determination were grown from an EtOH solution. The structure is displayed in Figure 1, in which the C1–C15 length of the biphenyl moiety is 1.498(4) Å. The imine moieties had a C=N bond (C22-N3: 1.275(5) Å; C8-N1: 1.265(5) Å) slightly shorter than those of the unsubstituted analogue (1.283(1) Å) [47] and the analogous 3-methoxy substituted ligand (1.285(2) and 1.280(2) Å) [47]. This might be due to the presence of the electron-withdrawing nitro group. The C-N(nitro) bond lengths of 1.451(5) and 1.423(5) Å were within a normal C-N single bond. The C-O distances (1.325(5) and 1.320(5) Å) were similar to those of the unsubstituted analogue (1.354(2) Å) and the analogous 3-methoxy substituted ligand (1.353(7) Å). However, the C-Br bond distances (1.896(3) and 1.893(3) Å) were within the same range observed for both the unsubstituted and MeO-substituted analogues [46,47].
Samples of complexes Z1Zn and Z2Zn were recrystallized from the THF/pentane and CH2Cl2/MeOH solvent mixtures, respectively. Z1Zn was in a monoclinic system and contained THF as a solvent molecule. Z2Zn was in a triclinic system, where the contribution of highly disordered solvent molecules (42 e– in a unit cell) was removed using the PLATON/SQUEEZE [57]. The structures of these two complexes, with the atomic numbering schemes, are presented in Figure 2 and Figure 3, respectively. The unit cell had two molecules, which were crystallographically independent. Because the molecular structures were quite similar to each other, only one molecule is discussed hereafter. The Zn atom, in each molecule, was penta-coordinated with two oxygen atoms from the deprotonated hydroxyl groups, as well as two nitrogen atoms from the azomethine groups, in addition to a water molecule occupying the apical position. The Zn-O bond lengths (Z1Zn: 2.027(3) and 1.966(3) Å; Z2Zn: 1.9496(18) and 1.9740(18) Å) were comparable to each other and to those found for bis(2-oxidobenzylideneamino)-4,4′-dimethyl-1,1′-biphenylzinc [46]. The Zn-N bond distances (Z1Zn: 2.048(3) and 2.107(3) Å; Z2Zn: 2.140(2) and 2.039(2) Å) were slightly longer than the Zn-O bonds within the same molecules. The Zn-O (of H2O molecules) bond distances (Z1Zn: 2.082(3) Å; Z2Zn: 2.1966(18) Å) were longer than the other Zn-O bond lengths within these molecules. These bond distances were very comparable to those reported for similar Zn complexes [46]. The geometry around the Zn center of Z1Zn was a distorted trigonal bipyramid (index of the degree of trigonality τ = 0.78 [58]), with the O1 and N2 in the axial positions (O1-Zn-N2 = 172.81(13)°), while N1, O2 and O3 occupied the equatorial places (O2-Zn-N1= 125.96(14)°; O2-Zn-O3 = 109.26(13)°; O3-Zn-N1= 124.75(13)°). This geometry was similar to that reported for bis(2-oxidobenzylideneamino)-4,4′-dimethyl-1,1′-biphenylzinc; however, in this case, one of the N atoms and the O of the coordinated methanol occupy the axial position [46]. The deviation of Z2Zn from the trigonal bipyramid was higher than that of Z1Zn (τ = 0.16). Two bond angles (O1-Zn-N2 = 159.44(8)°; O7-Zn-N1 = 146.80(8)°) were much higher than the equatorial angle of 120 degrees, while the other two angles (O2-Zn-N1 = 114.63(8)°; O1-Zn-O2 = 109.04(7)°) were slightly less than 120 degrees. This implied that both O2 and N1 were within the equatorial position in addition to O1, with greater deviation. This left O7 and N2 to most probably have axial positions.

2.3. Computational Study

The optimized geometry of ZH4 is depicted in Figure 4. The selected structural parameters for the optimized ligand, along with those determined experimentally, are listed in Table 1.
The calculated C1–C15 bond length (1.492 Å) between the aryl units of the biphenyl backbone, which was estimated to be 1.498(4) Å by the crystallographic study, featured a typical single-bond value, thus ruling out interactions between the π-systems of these moieties.
This value was close to the calculated average value of 1.494 Å, for a series of twelve comparable complexes bearing the biphenyl backbone around the coordination sphere [18].
The aryl moieties of the biphenyl backbone were twisted with angles between the planes by 87.31° (exp. 83.89°). The large torsion angle was attributed to the steric requirements enforced by bromine substituents. This was consistent with the experimentally reported aryl–aryl dihedral angle of 80° for a similar dibromo-substituted biphenyl ligand [59]. Smaller torsion angles (between 21° and 68°) for the halide-free analogues, where there was flexible twisting between the two biphenyl planes, were observed [46]. The optimized geometries of Z1Zn and Z2Zn are elucidated in Figure 5. The results indicated that the monoligated complexes exhibited a penta-coordinated zinc ion with distorted trigonal bipyramidal geometry. The computed H2O···M bond was 2.247 Å (exp. 2.082(3) Å) and 2.238 Å (exp. 2.1966(18) Å) for the Z1Zn and Z2Zn complexes, respectively. Additionally, the calculated Zn-O bond lengths around the Zn ion were [Z1Zn: 1.970, 1.947 Å (exp. 2.027(3) and 1.966(3) Å); Z2Zn: 1.949, 1.983 Å (exp. 1.9496(18) and 1.9740(18) Å)], while the calculated Zn-N bond lengths were [Z1Zn: 2.048, 2.102 Å, (exp. 2.048(3) and 2.107(3) Å); Z2Zn: 2.087, 2.057, Å (exp. 2.140(2) and 2.039(2) Å)].
Such slight structural variations between the experimental and calculated values were attributed to the experimental data being acquired for crystalline materials with lattice interactions, such as packing effects and intermolecular van der Waals forces, whereas the calculated values corresponded to an isolated molecule in the gas phase.
The calculated bond length between the aryl units of the biphenyl backbone was 1.489 Å (exp. 1.489 Å) and 1.488 Å (exp. 1.491 Å) for the Z1Zn and Z2Zn complexes, respectively, alluding to a typical single bond and excluding π-interactions between the aryl units. The calculated twist angle between the planes of the aryl moieties of the biphenyl backbone was 59.39° (exp. 60.61°) and 59.19° (exp. 55.81°) for the Z1Zn and Z2Zn complexes, respectively. Such large torsion angles were attributed to the steric and electronic requirements enforced within the coordination sphere.

2.4. Antimicrobial and Anticancer Assays

The results showed significant antimicrobial activity for both the Schiff bases and their metal complexes against Gram-positive bacterial strains (Micrococcus luteus and Staphylococcus aureus), which were demonstrated as a zone of inhibition (Table 2, Figure 6). These compounds showed different activity towards the two bacteria types. For instance, ZH2, ZH3, ZH4 and their zinc complexes showed antimicrobial activity against Micrococcus luteus and Staphylococcus aureus, while Z2Fe, Z4Fe and Z4Cu showed antimicrobial activity against Staphylococcus aureus only. The selectivity of these compounds raises an interesting concern about the exact mechanism of these compounds as antimicrobial agents. The Schiff bases and certain complexes showed limited antimicrobial activity on Gram-negative bacteria (Escherichia coli).
The IC50 of the Schiff bases and their metal complexes showed a variable reduction in viability of the tested cancer cell lines compared to the normal fibroblasts. For instance, the IC50 of ZH1 showed significant inhibition of cancer cell line growth compared to the HDF cell line. In addition, the IC50 of the tested compounds showed a selective anticancer effect against MCF7 compared to the A549 and HDF cell lines, as shown in Table 3. ZH1, its zinc complexes and Z2Fe showed selective anticancer effects against the MCF7 cell line. Interestingly, Z2Cu showed the lowest IC50 values against all cell lines.

3. Experiment

3.1. Materials and Methods

Elemental analyses (C, H and N) were measured at the Institute of Organic and Macromolecular Chemistry of the Friedrich Schiller University in Jena, Germany. Infrared spectra were recorded with a Bruker FT-IR-4100 spectrometer (Bremen, Germany). 1H- and 13C-NMR spectra were recorded on a Bruker AC 400 MHz spectrometer. Chemical shifts were reported in ppm relative to TMS as internal standards. Melting points were recorded on a melting point apparatus, SMP3. Electronic absorption spectra were measured on a PS-2600 Pasco spectrophotometer (Saarbrucken, Germany) in DMSO solvent using 8 × 10–5 M solutions. All reagents were obtained from Merck, Acros or Sigma Aldrich (Taufkirchen, Germany) and used without further purification. The starting amines, 2,2′-diamino-4,4′-dimethyl-6,6′-dibromobiphenyl [29] and halide-free analogue [47], were prepared according to literature procedures. The theoretical modelling of Schiff base ligands was performed using Wave function Spartan’18 Parallel Suite on a desktop computer with core i725.

3.2. General Procedure for the Preparation of Ligands (ZH1–ZH4)

2,2′-Diamino-4,4′-dimethyl-6,6′-dibromobiphenyl or 2,2′-diamino-4,4′-dimethyl-1,1′-biphenyl (2.35 mmol) and salicylaldehyde derivatives (4.7 mmol) in 10 mL of absolute ethanol was refluxed for 5 h. During this time, the corresponding Schiff base was precipitated, collected, washed with ethanol and stripped to dryness. The solid was recrystallized from a CH2Cl2/methanol mixture to give pure crystalline compounds.
2,2′-Bis(3,5-dichlorosalicylideneamino)-4,4′-dimethyl-1,1′-biphenyl (ZH1):
Yellow (55%). M.P. = 233–235 °C. 1H-NMR (400 MHz, CDCl3): 13.19 (2 H, s, OH); 8.18 (2 H, s, CH꞊N); 6.76–7.28 (10 H, m, Ar-H); 2.37 (6 H, s, CH3). 13C-NMR (400 MHz, CDCl3): 161.04 (C꞊N); 119.17–155.22 (Ar); 21.30 (CH3). Anal. Calc. for C28H20Cl4N2O2: C, 60.24; H, 3.61; N, 5.02%. Found: C, 60.13; H, 3.59; N, 5.00%. (IR, cm−1, KBr): υ(O-H) = 3467 (br,w); υ(C-H) = 2921 (w); υ(C꞊N) = 1619 (s); υ(C꞊C) = 1448 (m); υ(C-O) = 1352 (s); υ(C-Cl) = 775. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 359 (2.37 × 103), 452 (3.75 × 101).
2,2′-Bis(5-nitrosalicylideneamino)-4,4′-dimethyl-1,1′-biphenyl (ZH2):
Orange (63%). M.P. = 197–199 °C. 1H-NMR (400 MHz, CDCl3): 13.62 (2 H, s, OH); 8.50 (2 H, s, CH꞊N); 6.83–8.10 (12 H, m, Ar-H); 2.42 (6 H, s, CH3). 13C-NMR (400 MHz, CDCl3): 166.37 (C꞊N); 118.15–160.33 (Ar); 21.39 (CH3). Anal. Calc. for C28H22N4O6: C, 65.88; H, 4.34; N, 10.97%. Found: C, 65.86; H, 4.22; N, 10.87%. (IR, cm−1, KBr): υ(O-H) = 3461 (br,w); υ(C-H) = 2923 (w); υ(C꞊N) = 1917 (s); υ(C꞊C) = 1476 (m); υ(C-O) = 1340 (s); υ(NO2) = 1385, 1574. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 351 (2.31 × 103), 452 (1.76 × 102).
3,5-Dichlorosalicylideneamino-6,6′-dibromo-4,4′-dimethyl-1,1′-biphenyl (ZH3):
Orange (79%). M.P. = 249–250 °C. 1H-NMR (400 MHz, CDCl3): 12.61 (2 H, s, OH); 8.36 (2H, s, CH꞊N); 6.92–7.41 (8 H, m, Ar-H); 2.38 (6 H, s, CH3). 13C-NMR (400 MHz, CDCl3): 161.58 (C꞊N); 118.28–155.51 (Ar); 21.23 (CH3). Anal. Calc. for C28H18Cl4Br2N2O2: C, 46.96; H, 2.53; N, 3.91%. Found: C, 46.92; H, 2.50; N, 3.89%. (IR, cm−1, KBr): υ(O-H) = 3465 (br,w); υ(C-H) = 2923 (w); υ(C꞊N) = 1613 (s); υ(C꞊C) = 1452 (m); υ(C-O) = 1354 (s); υ(C-Br) = 669; υ(C-Cl) = 742. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 357 (5.85 × 103), 459 (7.62 × 101).
5-Nitrosalicylideneamino-6,6′-dibromo-4,4′-dimethyl-1,1′-biphenyl (ZH4):
Yellow (82%). M.P. = 244–245 °C. 1H-NMR (400 MHz, CDCl3): 13.13 (2 H, s, OH); 8.58 (2 H, s, CH꞊N); 6.83–8.25 (10 H, m, Ar-H); 2.41 (6 H, s, CH3). 13C-NMR (400 MHz, CDCl3): 166.32 (C꞊N), 117.76–161.11 (Ar); 21.31 (CH3). Anal. Calc. for C28H20Br2N4O6: C, 50.32; H, 3.02; N, 8.38%. Found: C, 50.32; H, 2.99; N, 8.37%. (IR, cm−1, KBr): υ(O-H) = 3450 (br,w); υ(C-H) = 2940 (w); υ(C꞊N) = 1619 (s); υ(C꞊C) = 1413 (m); υ(C-O) = 1338 (s); υ(C-Br) = 646; υ(NO2) = 1393, 1578. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 310 (5.45 × 103), 451 (1.85 × 102).

3.3. General Procedure for the Synthesis of Cu, Fe and Zn Complexes

To a solution of 1.30 mmol Schiff base in 10 mL of absolute ethanol, 1.30 mmol of metal(II) acetate hydrate dissolved in 3 mL of absolute ethanol was added dropwise at room temperature under inert atmosphere. The reaction mixture was refluxed for 6 h. During this time, the corresponding complex was precipitated, collected by filtration, washed with cold ethanol and dried under a vacuum.
Z1Zn: Yellow (60%). M.P. = 270–272 °C. 1H-NMR (400 MHz, CDCl3): 8.16 (2 H, s, CH꞊N); 6.91–7.49 (10 H, m, Ar-H); 2.42 (6 H, s, CH3). 13C-NMR (400 MHz, CDCl3): 170.32 (C꞊N), 118.41–164.08 (Ar); 21.01 (CH3). Anal. Calc. for ZnC28H18Cl4N2O2: C, 54.10; H, 2.92; N, 4.51%. Found: C, 54.08; H, 2.90; N, 4.49%. (IR, cm−1, KBr): υ(C-H) = 2923 (w); υ(C꞊N) = 1605 (s); υ(C꞊C) = 1438 (m); υ(C-O) = 1317 (s); υ(Zn-N) = 430 (w); υ(Zn-O) = 542 (w); υ(C-Cl) = 764. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 396 (2.21 × 103).
Z2Zn: Yellow (72%). M.P. = 250–253 °C. 1H-NMR (400 MHz, CDCl3): 8.28 (2 H, s, CH꞊N); 6.78–8.18 (12 H, m, Ar-H); 2.35 (6 H, s, CH3). 13C-NMR (400 MHz, CDCl3): 175.39 (C꞊N), 116.92–170.82 (Ar); 21.03 (CH3). Anal. Calc. for ZnC28H20N4O6: C, 58.60; H, 5.51; N, 9.76%. Found: C, 58.57; H, 5.48; N, 9.73%. (IR, cm−1, KBr): υ(C-H) = 2923 (w); υ(C꞊N) = 1605 (s); υ(C꞊C) = 1472 (m); υ(C-O) = 1313 (s); υ(Zn-N) = 416 (w); υ(Zn-O) = 507 (w); υ(NO2) = 1391, 1550. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 384 (5.80 × 103).
Z3Zn: Yellow (49%). M.P. > 293 °C. 1H-NMR (400 MHz, CDCl3): 8.10 (2 H, s, CH꞊N); 6.76–7.34 (8 H, m, Ar-H); 2.30 (6 H, s, CH3). 13C-NMR (400 MHz, CDCl3): 168.72 (C꞊N), 118.16–163.89 (Ar); 20.99 (CH3). Anal. Calc. for ZnC28H16Cl4Br2N2O2: C, 43.14; H, 2.07; N, 3.59%. Found: C, 42.99; H, 1.98; N, 3.54%. (IR, cm−1, KBr): υ(C-H) = 2921 (w); υ(C꞊N) = 1611 (s); υ(C꞊C) = 1440 (m); υ(C-O) = 1315 (s); υ(Zn-N) = 428 (w); υ(Zn-O) = 550 (w); υ(C-Br) = 673; υ(C-Cl) = 758. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 400 (2.95 × 103).
Z4Zn: Yellow (74%). M.P. = 270–273 °C. 1H-NMR (400 MHz, CDCl3): 8.35 (2 H, s, CH꞊N); 6.74–8.19 (10 H, m, Ar-H); 2.34 (6 H, s, CH3). 13C-NMR (400 MHz, CDCl3): 175.62 (C꞊N), 116.69–169.62 (Ar); 21.03 (CH3). Anal. Calc. for ZnC28H18Br2N4O6: C, 45.96; H, 2.48; N, 7.66%. Found: C, 45.93; H, 2.44; N, 7.62%. (IR, cm−1, KBr): υ(C-H) = 2921 (w); υ(C꞊N) = 1609 (s); υ(C꞊C) = 1385 (m); υ(C-O) = 1315 (s); υ(Zn-N) = 416 (w); υ(Zn-O) = 491 (w); υ(C-Br) = 650; υ(NO2) = 1385, 1546. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 382 (2.24 × 103).
Z1Fe: Red (63%). M.P. = 260–261 °C. Anal. Calc. for FeC28H18Cl4N2O2: C, 54.94; H, 4.34; N, 4.58%. Found: C, 51.92; H, 4.33; N, 4.54%. (IR, cm−1, KBr): υ(C-H) = 2923 (w); υ(C꞊N) = 1605 (s); υ(C꞊C) = 1436(m); υ(C-O) = 1317 (s); υ(Fe-N) = 442 (w); υ(Fe-O) = 491 (w); υ(C-Cl) = 771. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 363 (2.31 × 103).
Z2Fe: Red (66%). M.P. > 290 °C. Anal. Calc. for FeC28H20N4O6: C, 59.59; H, 3.57; N, 9.95%. Found: C, 59.53; H, 3.53; N, 9.95%. (IR, cm-1, KBr): υ(C-H) = 2921 (w); υ(C꞊N) = 1607 (s); υ(C꞊C) = 1468 (m); υ(C-O) = 1315 (s); υ(Fe-N) = 416 (w); υ(Fe-O) = 504 (w); υ(NO2) = 1376, 1552. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 361 (6.70 × 103).
Z3Fe: Red (60%). M.P. > 320 °C. Anal. Calc. for FeC28H16Cl4Br2N2O2: C, 43.68; H, 2.09; N, 3.64%. Found: C, 43.63; H, 1.97; N, 3.62%. (IR, cm−1, KBr): υ(C-H) = 2921 (w); υ(C꞊N) = 1611 (s); υ(C꞊C) = 1439 (m); υ(C-O) = 1317 (s); υ(Fe-N) = 450 (w); υ(Fe-O) = 497 (w); υ(C-Br) = 673; υ(C-Cl) = 762. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 368 (2.24 × 103).
Z4Fe: Red (72%). M.P. > 289 °C Anal. Calc. for FeC28H18Br2N4O6: C, 46.57; H, 2.51; N, 7.76%. Found: C, 46.55; H, 2.49; N, 7.74%. (IR, cm-1, KBr): υ(C-H) = 2923 (w); υ(C꞊N) = 1609 (s); υ(C꞊C) = 1384 (m); υ(C-O) = 1315 (s); υ(Fe-N) = 407 (w); υ(Fe-O) = 485 (w); υ(C-Br) = 652; υ(NO2) = 1399, 1552. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 359 (5.64 × 103).
Z1Cu: Green (71%). M.P. > 250 °C. Anal. Calc. for CuC28H18Cl4N2O2: C, 54.26; H, 2.93; N, 4.52%. Found: C, 54.18; H, 2.87; N, 4.47%. (IR, cm−1, KBr): υ(C-H) = 2914 (w); υ(C꞊N) = 1601 (s); υ(C꞊C) = 1434(m); υ(C-O) = 1323 (s); υ(Cu-N) = 416 (w); υ(Cu-O) = 538 (w); υ(C-Cl) = 764. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 403 (2.32 × 103).
Z2Cu: Green (69%). M.P. > 270 °C. Anal. Calc. for CuC28H20N4O6: C, 58.79; H, 3.52; N, 9.79%. Found: C, 58.78; H, 3.49; N, 9.68%. (IR, cm−1, KBr): υ(C-H) = 2925 (w); υ(C꞊N) = 1605 (s); υ(C꞊C) = 1466 (m); υ(C-O) = 1315 (s); υ(Cu-N) = 430 (w); υ(Cu-O) = 518 (w); υ(NO2) = 1383, 1546. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 389 (4.45 × 103).
Z3Cu: Green (67%). M.P. > 282 °C. Anal. Calc. for CuC28H16Cl4Br2N2O2: C, 43.25; H, 2.07; N, 3.60%. Found: C, 43.19; H, 2.02; N, 3.61%. (IR, cm−1, KBr): υ(C-H) = 2916 (w); υ(C꞊N) = 1605 (s); υ(C꞊C) = 1434 (m); υ(C-O) = 1317 (s); υ(Cu-N) = 416 (w); υ(Cu-O) = 548 (w); υ(C-Br) = 677; υ(C-Cl) = 756. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 412 (3.38 × 103).
Z4Cu: Green (74%). M.P. >303 °C Anal. Calc. for CuC28H18Br2N4O6: C, 46.08; H, 2.49; N, 7.68%. Found: C, 46.05; H, 2.46; N, 7.66%. (IR, cm−1, KBr): υ(C-H) = 2927 (w); υ(C꞊N) = 1607 (s); υ(C꞊C) = 1378 (m); υ(C-O) = 1317 (s); υ(Cu-N) = 516 (w); υ(Cu-O) = 548 (w); υ(C-Br) = 652; υ(NO2) = 1378, 1546. UV-Vis in CH2Cl2: λmax(nm) (εmax, M−1cm−1): 388 (4.10 × 103).

3.4. Computational Study

The ground-state molecular geometries of ZH4, Z1Zn and Z2Zn were fully optimized in the gas phase, without any constraints at the B3LYP/6-31G(d) level of theory [60,61,62]. The initial geometries were extracted from the experimentally determined crystal structure. All electronic structure calculations were performed using the Spartan’18 package [63].

3.5. Antimicrobial Assay

For the evaluation of the antibacterial activity of all synthesized compounds, two Gram-positive bacteria and Gram-negative bacteria were used in the current study: Micrococcus luteus and Staphylococcus aureus, and Escherichia coli, respectively. The antimicrobial assay procedures were performed according to the recommendation of the National Committee for Clinical Laboratory Standards (NCCLS) [64,65,66]. Briefly, the synthesized compounds were dissolved in DMSO at a concentration of 10 mg/mL. After the inoculation of the bacterial strains in the culture media, 50 μL sized wells were generated in the agar media, followed by the addition of 50 μL of the tested compounds. After 24–48 h of incubation, the diameter of the inhibition zone was measured.

3.6. Anticancer Assay

3.6.1. Cell Culture

The parental breast cancer cell line (MCF7), non-small-cell lung cancer cell line (A549) and human dermal fibroblasts cell line (HDF) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). MCF7 and A549 cells were cultured as an attached monolayer and maintained in RPMI 1640 medium (EuroClone, Milan, Italy) supplemented with 10% (v/v) heat-inactivated fetal bovine serum (FBS) (EuroClone), 1% penicillin-streptomycin (EuroClone) and 2 mM L-glutamine. MDA-MB-231 cells were cultured as an attached monolayer and maintained in MEM (EuroClone) supplemented with 10% (v/v) heat-inactivated fetal bovine serum (FBS) (EuroClone), 1% penicillin-streptomycin (EuroClone) and 2 mM L-glutamine. The HDF were cultured as an attached monolayer and maintained in DMEM (EuroClone) supplemented with 10% (v/v) heat-inactivated fetal bovine serum (FBS) (EuroClone), 1% penicillin-streptomycin (EuroClone) and 2 mM L-glutamine. All cells were incubated at 37 °C in a 5% CO2 tissue culture incubator (Memmert, Schwabach, Germany).

3.6.2. Cell Viability Assay (MTT)

To determine the IC50 of the ZH1–ZH4 and Z1Zn–Z4Cu compounds on the selected cell lines, an MTT assay was performed. Approximately (8 × 103 cells/well) of MDA-MB-231, MCF7 and HDF cell lines were seeded into a 96-well plate (Corning, Burlington, VT, USA). All cell lines were treated with different concentrations of the ZH1–ZH4 and Z1Zn–Z4Cu compounds, ranging from 0.5 to 500 μg/mL. Then, the cells were incubated at 37 °C in a 5% CO2 incubator for 72 h, after which the old media was aspirated, and the MTT assay salt (Bioworld, Visalia, CA, USA) in 100 μL of fresh media was added to each well. Following that, the plates were incubated at 37 °C for 3 h, and then 50 μL of solubilization solution (DMSO) was added to each well to determine viability. The absorbance of the solution was measured at 560 nm using a Glomax plate reader (Promega, Madison, WI, USA).

3.7. X-ray Structure Determination of ZH4, Z1Zn and Z2Zn

The intensity data of the X-ray diffraction peaks were collected on a Rigaku XtaLAB (Japan) P200 diffractometer, using Mo Kα radiation (λ = 0.71073 Å) fitted with SHELXTL for structure determination [67]. A direct method using SHELXS-2014 was employed to solve the structure, and Fourier transformation was carried out using SHELXL-2014, employing full-matrix least-square refinement calculations [67].

3.7.1. Crystallographic Data for ZH4

C28H20Br2N4O6, Mr = 668.30 g mol−1, yellow block, triclinic, space group P-1 (#2), a = 8.76912(19) Å, b = 9.1844(2) Å, c = 16.8884(4) Å, α = 86.163(2)°, β = 79.388(2)°, γ = 82.3382(16)°, V = 1323.72(6) Å3, T = −173(2) °C, Z = 2, ρcalcd. = 1.677 g cm−3, µ(Mo Kα) = 3.123 mm−1, F(000) = 668, 6740 independent reflections, 5844 refined parameters, R1 = 0.0485 [for I > 2σ(I)], wR2 = 0.1071 (for all data), GOF = 1.186, and largest difference peak and hole: 0.59/−0.53 e Å−3.

3.7.2. Crystallographic Data for Z1Zn

2(C28H20Cl4N2O3Zn)∙3(C4H8O), Mr = 1495.66 g mol−1, yellow block, monoclinic, space group Cc (#9), a = 16.6298(3) Å, b = 23.0060(4) Å, c = 17.5585(3) Å, β = 97.7800(15)°. V = 6655.79(15) Å3, T = −173(2) ˚C, Z = 4, ρcalcd. = 1.492 g cm−3, µ(Mo Kα) = 1.102 mm−1, F(000) = 3072, 14627 independent reflections, 836 refined parameters, R1 = 0.0385 [for I > 2σ(I)], wR2 = 0.1037 (for all data), GOF = 1.019, and largest difference peak and hole: 1.40/−0.89 e Å−3. Flack parameter: 0.073(3).

3.7.3. Crystallographic Data for Z2Zn

C28H22N4O7Zn, Mr = 591.88 g mol−1, yellow block, triclinic, space group P-1 (#2), a = 11.6582(3) Å, b = 11.7904(2) Å, c = 20.2835(4) Å, α = 94.4710(16)°, β = 102.436(2)°, γ = 90.9990(18)°, V = 2712.69(11) Å3, T = −173(2) ˚C, Z = 4, ρcalcd. = 1.449 g cm−3, µ(Mo Kα) = 0.959 mm−1, F(000) = 1216, 11549 independent reflections, 737 refined parameters, R1 = 0.0543 [for I > 2σ(I)], wR2 = 0.1230 (for all data), GOF = 1.078, and largest difference peak and hole: 1.20/−0.47 e Å−3.

4. Conclusions

New Schiff bases and their Fe, Cu and Zn complexes were synthesized and characterized by various spectroscopic methods. The structure of the ZH4, Z1Zn and Z2Zn were determined by DFT calculations and X-ray diffraction measurements. The crystallographically determined geometry of the ligands, as well as the measured vibrational spectra of ZH4, Z1Zn and Z2Zn, are in good agreement with the theoretical results. The antimicrobial and anticancer activities of the Schiff bases and their metal complexes were evaluated. The compounds ZH2–ZH4 and their zinc complexes showed antimicrobial activity against Micrococcus luteus, while ZH2, ZH3, Z2Zn, Z3Zn and Z2Fe showed antimicrobial activity against Staphylococcus aureus. An anticancer assay showed that most of our tested compounds had variable reduction in viability of the tested cancer cell lines compared to the normal fibroblasts. Moreover, ZH1, Z2Fe and all zinc complexes showed selective anticancer effects against the MCF7 cell line, and Z2Cu showed the lowest IC50 values against all cell lines.

Author Contributions

Conceptualization, M.E.-k., T.M.A.A.-S. and H.K.; methodology, S.S.A.-T.; software, T.S.A.; validation, T.M.A.J., A.A.S. and Z.H.O.; formal analysis, M.S.A.Z. and W.A.; investigation, T.Q.; resources, T.M.A.J.; data curation, T.M.A.A.-S.; writing—original draft preparation, Y.Y., H.M. and M.E.-k.; writing—review and editing, H.M., H.K., Y.Y. and M.E.-k.; visualization, S.S.A.-T.; supervision, T.M.A.J.; project administration, T.M.A.A.-S. and T.S.A.; funding acquisition, T.M.A.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Scientific Research Deanship at Yarmouk University (Irbid, Jordan), grant number 86/2021.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The crystallographic data reported in this manuscript have been deposited with the Cambridge Crystallographic Data Centre under deposition no. CCDC-2141222, 2173302 and 2173303 for ZH4, Z1Zn and Z2Zn, respectively. This data can be obtained free of charge via http://www.ccdc.cam.ac.uk/data_request/cif (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge, CB2 1EZ, UK).

Acknowledgments

We highly appreciate the generous financial support of project 86/2021 by the Scientific Research Deanship at Yarmouk University (Irbid, Jordan).

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript or in the decision to publish the results.

Sample Availability

Samples of the compounds are available from the authors.

References

  1. Vigato, P.A.; Tamburini, S. The challenge of cyclic and acyclic schiff bases and related derivatives. Coord. Chem. Rev. 2004, 248, 1717–2128. [Google Scholar] [CrossRef]
  2. Salmon, L.; Bousseksou, A.; Donnadieu, B.; Tuchagues, J.P. Two novel iron (II) materials based on dianionic N4O2 Schiff bases: Structural properties and spin-crossover characteristics in the series [Fe (3-X, 5-NO2-sal-N(1,4,7,10)](X = H, 3-MeO, 3-EtO). Inorg. Chem. 2005, 44, 1763–1773. [Google Scholar] [CrossRef] [PubMed]
  3. Keypour, H.; Goudarziafshar, H.; Brisdon, A.K.; Pritchard, R.G.; Rezaeivala, M. New macrocyclic Schiff-base complexes incorporating a phenanthroline unit. Part 2: Template synthesis of some manganese (II) complexes and crystal structure studies. Inorg. Chim. Acta 2008, 361, 1415–1420. [Google Scholar] [CrossRef]
  4. Abu-Diefa, A.M.; Mohameda, I.M.A. A review on versatile applications of transition metal complexes incorporating Schiff bases. Beni-Seuf Univ. J. Appl. Sci. 2015, 4, 119–133. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Murphy, E.F.; Ferri, D.; Baiker, A.; Van Doorslaer, S.; Schweiger, A. Novel routes to Cu (salicylaldimine) covalently bound to silica: Combined pulse EPR and in situ attenuated total reflection-IR studies of the immobilization. Inorg. Chem. 2003, 42, 2559–2571. [Google Scholar] [CrossRef] [PubMed]
  6. Fahmi, N.; Masih, I.; Soni, K. Template synthesis, characterization, electrochemical behavior, antimicrobial, nematicidal and pesticidal activities of palladium (II) macrocyclic complexes. J. Macromol. Sci. Pure Appl. Chem. 2015, 52, 548–560. [Google Scholar] [CrossRef]
  7. Pingaew, R.; Prachayasittikul, S.; Ruchirawat, S. Synthesis, cytotoxic and antimalarial activities of benzoyl thiosemicarbazone analogs of isoquinoline and related compounds. Molecules 2010, 15, 988–996. [Google Scholar] [CrossRef]
  8. Pavan, F.R.; Maia, P.I.D.S.; Leite, S.R.; Deflon, V.M.; Batista, A.A.; Sato, D.N.; Franzblau, S.G.; Leite, C.Q. Thiosemicarbazones, semicarbazones, dithiocarbazates and hydrazide/hydrazones: Anti–Mycobacterium tuberculosis activity and cytotoxicity. Eur. J. Med. Chem. 2010, 45, 1898–1905. [Google Scholar] [CrossRef]
  9. Farooqi, S.I.; Arshad, N.; Channar, P.A.; Perveen, F.; Saeed, A.; Larik, F.A.; Javed, A.; Yamin, M. New aryl Schiff bases of thiadiazole derivative of ibuprofen as DNA binders and potential anti-cancer drug candidates. J. Biomol. Struct. Dyn. 2020, 39, 3548–3564. [Google Scholar] [CrossRef]
  10. Chinnasamy, R.P.; Sundararajan, R.; Govindaraj, S. Synthesis, characterization, and analgesic activity of novel Schiff base of isatin derivatives. J. Adv. Pharm. Technol. Res. 2010, 1, 342. [Google Scholar] [CrossRef] [Green Version]
  11. Chaubey, A.K.; Pandeya, S.N. Synthesis & anticonvulsant activity (Chemo Shock) of Schiff and Mannich bases of Isatin derivatives with 2-Amino pyridine (mechanism of action). Int. J. Pharmtech Res. 2012, 4, 590–598. [Google Scholar]
  12. Aboul-Fadl, T.; Mohammed, F.A.H.; Hassan, E.A.S. Synthesis, antitubercular activity and pharmacokinetic studies of some Schiff bases derived from 1-alkylisatin and isonicotinic acid hydrazide (INH). Arch. Pharm. Res. 2003, 26, 778–784. [Google Scholar] [CrossRef] [PubMed]
  13. Avaji, P.G.; Kumar, C.V.; Patil, S.A.; Shivananda, K.N.; Nagaraju, C. Synthesis, spectral characterization, in-vitro microbiological evaluation and cytotoxic activities of novel macrocyclic bis hydrazone. Eur. J. Med. Chem. 2009, 44, 3552–3559. [Google Scholar] [CrossRef] [PubMed]
  14. Ali, S.; Singh, V.; Jain, P.; Tripathi, V. Synthesis, antibacterial, anticancer and molecular docking studies of macrocyclic metal complexes of dihydrazide and diketone. J. Saudi Chem. Soc. 2019, 23, 52–60. [Google Scholar] [CrossRef]
  15. Liu, J.; Lin, Y.; Liu, M.; Wang, S.; Li, Y.; Liu, X.; Tian, L. Synthesis, structural characterization and cytotoxic activity of triorganotin 5-(salicylideneamino) salicylates. Appl. Organomet. Chem. 2019, 33, e4715. [Google Scholar] [CrossRef]
  16. Avaji, P.G.; Patil, S.A. Synthesis, spectral characterization and microbiological studies of Co (II), Ni (II) and Cu (II) complexes with some novel 20-membered macrocyclic hydrazino-1,2,4-triazole Schiff bases. J. Enzyme Inhib. Med. Chem. 2009, 24, 140–150. [Google Scholar] [CrossRef]
  17. Bagihalli, G.B.; Patil, S.A. Synthesis, spectral characterization, in vitro biological and DNA cleavage studies of Co (II), Ni (II), Cu (II), and Zn (II) complexes with 1, 2, 4-triazole Schiff bases. J. Coord. Chem. 2009, 62, 1690–1700. [Google Scholar] [CrossRef]
  18. Zafar, H.; Kareem, A.; Sherwani, A.; Mohammad, O.; Ansari, M.A.; Khan, H.M.; Khan, T.A. Synthesis and characterization of Schiff base octaazamacrocyclic complexes and their biological studies. J. Photochem. Photobio. B Biol. 2015, 142, 8–19. [Google Scholar] [CrossRef]
  19. Abd El-Halim, H.F.; Mohamed, G.G.; Anwar, M.N. Antimicrobial and anticancer activities of Schiff base ligand and its transition metal mixed ligand complexes with heterocyclic base. Appl. Organomet. Chem. 2018, 32, e3899. [Google Scholar] [CrossRef]
  20. Kumar, K.S.; Ganguly, S.; Veerasamy, R.; De Clercq, E. Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4 (3) H-ones. Eur. J. Med. Chem. 2010, 45, 5474–5479. [Google Scholar] [CrossRef]
  21. Nirmal, R.; Meenakshi, K.; Shanmugapandiyan, P.; Prakash, C.R. Synthesis Pharmacological Evaluation of Novel Schiff Base Analogues of 3-(4-amino) Phenylimino) 5-fluoroindolin-2-one. J. Young Pharm. 2010, 2, 162–168. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Ababneh, T.S.; El-khateeb, M.; Tanash, A.K.; AL-Shboul, T.M.; Shammout, M.J.A.; Jazzazi, T.M.; Safa, D.; Samar, T. Synthesis, computational, anticancerous and antiproliferative effects of some copper, manganese and zinc complexes with ligands derived from symmetrical 2,2’-diamino-4,4’-dimethyl-1,1’-biphenyl-salicylaldehyde. Pol. J. Chem. Technol. 2021, 23, 7–15. [Google Scholar] [CrossRef]
  23. Carter, M.J.; Rillema, D.P.; Basolo, F. Oxygen carrier and redox properties of some neutral cobalt chelates. Axial and in-plane ligand effects. J. Am. Chem. Soc. 1974, 96, 392–400. [Google Scholar] [CrossRef]
  24. Issa, Y.M.; Sherif, O.E.; Abbas, S.M. Chelation behaviour of Ce (III), Th (IV), and UO2 (VI) with 5,7-dihydroxy-6-formyl-2-methylbenzopyran-4-one Schiff bases. Monatsh. Chem. 1998, 129, 985–998. [Google Scholar] [CrossRef]
  25. Pandeya, S.N.; Sriram, D.; Nath, G.; De Clercq, E. Synthesis, antibacterial, antifungal and anti-HIV evaluation of Schiff and Mannich bases of isatin derivatives with 3-amino-2-methylmercapto quinazolin-4(3H)-one. Pharm. Acta Helv. 1999, 47, 7–11. [Google Scholar] [CrossRef]
  26. Upadhyay, K.K.; Kumar, A.; Upadhyay, S.; Mishra, P.C. Synthesis, characterization, structural optimization using density functional theory and superoxide ion scavenging activity of some Schiff bases. J. Mol. Struct. 2008, 873, 5–16. [Google Scholar] [CrossRef]
  27. Dutta, B.; Some, S.; Ray, J.K. Thermal cyclization of 3-arylamino-3-(2-nitrophenyl)-propenal Schiff base hydrochlorides followed by triethyl phosphite mediated deoxygenation: A facile synthesis of quindolines. Tetrahedron Lett. 2006, 47, 377–379. [Google Scholar] [CrossRef]
  28. Nishinaga, A.; Yamada, T.; Fujisawa, H.; Ishizaki, K.; Ihara, H.; Matsuura, T. Catalysis of cobalt-Schiff base complexes in oxygenation of alkenes: On the mechanism of ketonization. J. Mol. Cat. 1988, 48, 249–264. [Google Scholar] [CrossRef]
  29. Petzold, H.; Alrawashdeh, A.I.; Heider, S.; Haufe, L.; Rüffer, T. Synthesis of 6,6′-Bis (dimethylamino)-and 6,6′-Dibromo-Substituted 2,2′-Diphosphanylbiphenyls and Their Palladium Complexes. Eur. J. Inorg. Chem. 2013, 27, 4858–4866. [Google Scholar] [CrossRef]
  30. Rulev, Y.A.; Gugkaeva, Z.; Maleev, V.I.; North, M.; Belokon, Y.N. Robust bifunctional aluminium–salen catalysts for the preparation of cyclic carbonates from carbon dioxide and epoxides. Beilstien. J. Org. Chem. 2015, 11, 1614–1623. [Google Scholar] [CrossRef] [Green Version]
  31. Bïlïcï, A.; Kaya, İ.; Doğan, F. Monomer/polymer Schiff base copper (II) complexes for catalytic oxidative polymerization of 2,2′-dihydroxybiphenyl. J. Polym. Sci. Part A Polym. Chem. 2009, 47, 2977–2984. [Google Scholar] [CrossRef]
  32. Rayati, S.; Rafiee, N.; Wojtczak, A. cis-Dioxo-molybdenum (VI) Schiff base complexes: Synthesis, crystal structure and catalytic performance for homogeneous oxidation of olefins. Inorg. Chim. Acta. 2012, 386, 27–35. [Google Scholar] [CrossRef]
  33. Reddy, P.M.; Shanker, K.; Srinivas, V.; Krishna, E.R.; Rohini, R.; Srikanth, G.; Ravinder, V. Hydrolysis of Letrozole catalyzed by macrocyclic Rhodium (I) Schiff-base complexes. Spectrochim. Acta Part A Mol. Biomol. Spect. 2015, 139, 43–48. [Google Scholar] [CrossRef] [PubMed]
  34. Tunçel, M.; Serin, S. Synthesis and characterization of new azo-linked Schiff bases and their cobalt (II), copper (II) and nickel (II) complexes. Trans. Met. Chem. 2006, 31, 805–812. [Google Scholar] [CrossRef]
  35. Rathi, P.; Singh, D.P. Synthesis, antimicrobial, antioxidant, and molecular docking studies of thiophene based macrocyclic Schiff base complexes. J. Mol. Struct. 2015, 1100, 208–214. [Google Scholar] [CrossRef]
  36. Boghaei, D.M.; Askarizadeh, E.; Bezaatpour, A. Molecular and biomolecular spectroscopy. Spectrochim. Acta Part A 2008, 69, 624–628. [Google Scholar] [CrossRef]
  37. Abbaspour, A.; Esmaeilbeig, A.R.; Jarrahpour, A.A.; Khajeh, B.; Kia, R. Aluminium (III)-selective electrode based on a newly synthesized tetradentate Schiff base. Talanta 2002, 58, 397–403. [Google Scholar] [CrossRef]
  38. Mahajan, R.K.; Kaur, I.; Kumar, M. Silver ion-selective electrodes employing Schiff base p-tert-butyl calix [4] arene derivatives as neutral carriers. Sens. Actuators B Chem. 2003, 91, 26–31. [Google Scholar] [CrossRef]
  39. Ashraf, M.A.; Mahmood, K.; Wajid, A.; Maah, M.J.; Yusoff, I. Synthesis, characterization, and biological activity of Schiff bases. In Proceedings of the 2011 International Conference on Chemistry and Chemical Process, Bangkok, Thailand, 7–9 May 2011; IACSIT Press: Singapore, 2011; Volume 10, p. 185. [Google Scholar]
  40. Deivanayagam, P.; Bhoopathy, R.P.; Thanikaikarasan, S. Synthesis, characterization, antimicrobial, analgesic and CNS studies of Schiff base Cu(II) complex derived from 4-choro-o-phenylene diamine. Int. J. Adv. Chem. 2014, 2, 166–170. [Google Scholar] [CrossRef] [Green Version]
  41. Chakraborty, H.; Paul, N.; Rahman, M.L. Catalytic activities of Schiff base aquocomplexes of copper (II) towards hydrolysis of amino acid esters. Trans. Met. Chem. 1994, 19, 524–526. [Google Scholar] [CrossRef]
  42. El-Hendawy, A.M.; Alkubaisi, A.H.; El-Kourashy, A.E.G.; Shanab, M.M. Ruthenium (II) Complexes of O, N-donor Schiff base ligands and their use as catalytic organic oxidants. Polyhedron 1993, 12, 2343–2350. [Google Scholar] [CrossRef]
  43. Ababneh, T.S.; Al-Shboul, T.M.; Jazzazi, T.M.; Alomari, M.I.; Görls, H.; Westerhausen, M. Crystallographic and computational study of the structure of copper(II) 2,2′-bis(2-oxidobenzylideneamino)-4,4′-dimethyl-1,1′-biphenyl. Trans. Met. Chem. 2020, 45, 435–442. [Google Scholar] [CrossRef]
  44. Al-Ebaisat, H.S.; Ababneh, T.S.; Al-Shboul, T.M.; Jazzazi, T.M. Synthesis, characterization and antifungal activity of some substituted 4-thiazolidinone derivatives. J. Pure App. Chem. Res. 2015, 5, 125–130. [Google Scholar] [CrossRef] [Green Version]
  45. Jazzazi, T.M.A.; Ababneh, T.S.; Abboushi, E.K. Zinc(II) complexes of symmetrical tetradentate Schiff base ligands derived from 2,2’-diamino-6,6’-dibromo-4,4’-dimethyl-1,1’-biphenyl-salicylaldehyde: Synthesis, characterization and computational study. Jord. J. Chem. 2019, 14, 81–87. [Google Scholar]
  46. Al-Shboul, T.M.; Ziemann, S.; Görls, H.; Krieck, S.; Westerhausen, M. Substituted 2,2′-Bis (2-oxidobenzylideneamino)-4,4′-dimethyl-1,1′-biphenyl Complexes of Zinc. Z. Anorg. Allg. Chem. 2019, 645, 292–300. [Google Scholar] [CrossRef]
  47. Al-Shboul, T.M.; Ziemann, S.; Görls, H.; Jazzazi, T.M.; Krieck, S.; Westerhausen, M. Synthesis of dipotassium 2,2′-Bis (2-oxidobenzylideneamino)-4,4′-dimethyl-1,1′-biphenyl drivatives and use as ligand transfer reagent. Eur. J. Inorg. Chem. 2018, 14, 1563–1570. [Google Scholar] [CrossRef]
  48. Daoud, S.; Thiab, S.; Jazzazi, T.M.A.; Alshboul, T.M.A.; Ullah, S. Evaluation and molecular modelling of bis-Schiff base derivatives as potential leads for management of diabetes mellitus. Acta Pharm. 2022, 72, 449–458. [Google Scholar] [CrossRef]
  49. Thaker, B.; Surati, K.; Oswal, S.; Jadeja, R.; Gupta, V. Synthesis, spectral, thermal and crystallographic investigations on oxovanadium(IV) and manganese(III) complexes derived from heterocyclic β-diketone and 2-amino ethanol. Struct. Chem. 2007, 18, 295–310. [Google Scholar] [CrossRef]
  50. Miessler, G.; Tarr, D. Inorganic Chemistry, 3rd ed.; Pearson Prentice-Hall: Northfield, MN, USA, 2005. [Google Scholar]
  51. Agarwal, U.; Singh, N.P.; Kumar, A.; Kumar, K. Synthesis, Spectral Study and Antibacterial Activity of Asymmetrical Tetradentate Schiff Base Complexes. Rasayan J. Chem. 2020, 13, 1685–1691. [Google Scholar] [CrossRef]
  52. Ejidike, I.P.; Ajibade, P.A. Synthesis, characterization, antioxidant, and antibacterial studies of some metal (II) complexes of tetradentate schiff base ligand:(4E)-4-[(2-(E)-[1-(2, 4-dihydroxyphenyl) ethylidene] aminoethyl) imino] pentan-2-one. Bioinorg. Chem. Appl. 2015, 2015, 1–9. [Google Scholar] [CrossRef] [Green Version]
  53. Ran, X.; Wang, L.; Lin, Y.; Hao, J.; Cao, D. Syntheses, characterization and biological studies of zinc (II), copper (II) and cobalt (II) complexes with Schiff base ligand derived from 2-hydroxy-1-naphthaldehyde and selenomethionine. Appl. Organomet. Chem. 2010, 24, 741–747. [Google Scholar] [CrossRef]
  54. Iftikhar, B.; Javed, K.; Khan, M.S.U.; Akhter, Z.; Mirza, B.; Mckee, V. Synthesis, characterization and biological assay of Salicylaldehyde Schiff base Cu (II) complexes and their precursors. J. Mol. Struct. 2018, 1155, 337–348. [Google Scholar] [CrossRef]
  55. Reshma, R.; Selwin Joseyphus, R.; Arish, D.; Reshmi Jaya, R.J.; Johnson, J. Tridentate imidazole-based Schiff base metal complexes: Molecular docking, structural and biological studies. J. Biomol. Struct. 2021, 40, 1–13. [Google Scholar] [CrossRef] [PubMed]
  56. Osowole, A.A.; Ott, I.; Ogunlana, O.M. Synthesis, spectroscopic, anticancer, and antimicrobial properties of some metal (II) complexes of (substituted) nitrophenol Schiff base. Int. J. Inorg. Chem. 2012, 2012, 1–6. [Google Scholar] [CrossRef]
  57. Sheldrick, G.M. Crystal structure refinement with SHELXL. Acta Cryst. 2015, C71, 9–18. [Google Scholar]
  58. Addison, A.W.; Rao, T.N.; Reedijk, J.; van Rijn, J.; Verschoor, G.C. Synthesis, structure, and spectroscopic properties of copper(II) compounds containing nitrogen and sulphur donor ligands; the crystal and molecular structure of aqua[1,7-bis(N-methylbenzimidazol-2’-yl)-2,6-dithiaheptane]copper(II) perchlorate. J. Chem. Soc. Dalton Trans. 1984, 7, 1349–1356. [Google Scholar] [CrossRef]
  59. Al-Shboul, T.M.A.; Görls, H.; Westerhausen, M. Calcium-mediated hydrophosphination of diphenylethyne and diphenylbutadiyne as well as crystal structure of 1,4-diphenyl-1,4-bis(diphenylphosphanyl)buta-1,3-diene. Inorg. Chem. Commun. 2008, 11, 1419–1421. [Google Scholar] [CrossRef]
  60. Becke, A.D. Density-functional thermochemistry. IV. A new dynamical correlation functional and implications for exact-exchange mixing. J. Chem. Phys. 1996, 104, 1040–1046. [Google Scholar] [CrossRef]
  61. Becke, A.D. Density-functional thermochemistry. III. The role of exact exchange. J. Chem. Phys. 1993, 98, 5648–5652. [Google Scholar] [CrossRef] [Green Version]
  62. Lee, C.; Yang, W.; Parr, R.G. Development of the Colic-Salvetti correlation-energy formula into a functional of the electron density. Phys. Rev. 1988, B 37, 785–789. [Google Scholar] [CrossRef] [Green Version]
  63. Spartan, version 18; Software for Computational Chemistry; Wavefunction. Inc.: Irvine, CA, USA, 2018.
  64. Kassim, A.; Omuse, G.; Premji, Z.; Revathi, G. Comparison of Clinical Laboratory Standards Institute and European Committee on Antimicrobial Susceptibility Testing guidelines for the interpretation of antibiotic susceptibility at a university teaching hospital in Nairobi, Kenya: A cross-sectional study. Ann. Clin. Microbiol. 2016, 15, 21. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. MacLowry, J.D.; Jaqua, M.J.; Selepak, S.T. Detailed methodology and implementation of a semiautomated serial dilution microtechnique for antimicrobial susceptibility testing. Appl. Microbio. 1970, 20, 46–53. [Google Scholar] [CrossRef] [PubMed]
  66. Sheldrick, G.M. SHELXS-2014, Program for Structure Solution; University of Göttingen: Göttingen, Germany, 2014. [Google Scholar]
  67. Sheldrick, G.M. SHELXL-2014, Program for Structure Refinement; University of Göttingen: Göttingen, Germany, 2014. [Google Scholar]
Inorganics 10 00112 sch001 550
Scheme 1. Synthesis of symmetrical Schiff bases ZH1–ZH4 and their Cu, Fe and Zn complexes.
Scheme 1. Synthesis of symmetrical Schiff bases ZH1–ZH4 and their Cu, Fe and Zn complexes.
Inorganics 10 00112 sch001
Inorganics 10 00112 g001 550
Figure 1. Molecular structure of ZH4 determined by X-ray diffraction at 100 K. White: H, gray: C, blue: N, red: O, and orange: Br.
Figure 1. Molecular structure of ZH4 determined by X-ray diffraction at 100 K. White: H, gray: C, blue: N, red: O, and orange: Br.
Inorganics 10 00112 g001
Inorganics 10 00112 g002 550
Figure 2. Molecular structure of Z1Zn determined by X-ray diffraction at 100 K. The ellipsoids are drawn with a 50% probability. White: H, gray: C, blue: N, red: O, light green: Cl, and blue-gray: Zn.
Figure 2. Molecular structure of Z1Zn determined by X-ray diffraction at 100 K. The ellipsoids are drawn with a 50% probability. White: H, gray: C, blue: N, red: O, light green: Cl, and blue-gray: Zn.
Inorganics 10 00112 g002
Inorganics 10 00112 g003 550
Figure 3. Molecular structure of Z2Zn determined by X-ray diffraction at 100 K. The ellipsoids are drawn with a 50% probability. White: H, gray: C, blue: N, red: O, and blue-gray: Zn.
Figure 3. Molecular structure of Z2Zn determined by X-ray diffraction at 100 K. The ellipsoids are drawn with a 50% probability. White: H, gray: C, blue: N, red: O, and blue-gray: Zn.
Inorganics 10 00112 g003
Inorganics 10 00112 g004 550
Figure 4. Different views of the optimized ground-state geometry for the ZH4 ligand at the B3LYP/6-31G(d) level of theory. (O: red, N: blue, C: gray, and Br: brick). Dotted line for O–H···N hydrogen bonding.
Figure 4. Different views of the optimized ground-state geometry for the ZH4 ligand at the B3LYP/6-31G(d) level of theory. (O: red, N: blue, C: gray, and Br: brick). Dotted line for O–H···N hydrogen bonding.
Inorganics 10 00112 g004
Inorganics 10 00112 g005 550
Figure 5. The optimized ground-state geometries of Z1Zn (A) and Z2Zn (B) complexes at the B3LYP/6-31G(d) level of theory. (O: red, N: blue, C: gray, and Cl: green). Dotted line for O–H···O hydrogen bonding.
Figure 5. The optimized ground-state geometries of Z1Zn (A) and Z2Zn (B) complexes at the B3LYP/6-31G(d) level of theory. (O: red, N: blue, C: gray, and Cl: green). Dotted line for O–H···O hydrogen bonding.
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Inorganics 10 00112 g006 550
Figure 6. A representative bacterial culture showing the inhibition zone in Gram-positive (Staphylococcus aureus and Micrococcus luteus) bacteria by compounds ZH1, ZH2, ZH3 and ZH4 ((left) and (middle)) compared to lack of antimicrobial activity against Gram-negative bacteria (Escherichia coli) (right).
Figure 6. A representative bacterial culture showing the inhibition zone in Gram-positive (Staphylococcus aureus and Micrococcus luteus) bacteria by compounds ZH1, ZH2, ZH3 and ZH4 ((left) and (middle)) compared to lack of antimicrobial activity against Gram-negative bacteria (Escherichia coli) (right).
Inorganics 10 00112 g006
Table
Table 1. Selected calculated and experimental bond lengths (Å) and angles (°) of ZH4.
Table 1. Selected calculated and experimental bond lengths (Å) and angles (°) of ZH4.
Bond (Å)Calc.Exp. Angle (°)Calc.Exp.
C1–C151.4921.498O-N-O124.53, 124.53122.95, 123.04
C=N1.290, 1.2901.265, 1.275C-O-H107.92, 107.92100.31, 106.76
C-O1.332, 1.3321.325, 1.320C-N=C121.04, 121.03121.20, 120.86
C-Br1.918, 1.9181.896, 1.893C-C=N121.89, 121.90120.41, 120.38
C-N(imine)1.408, 1.4081.424, 1.427Br-C-CH117.56, 117.56118.09, 118.30
C-N(nitro)1.461, 1.4611.453, 1.451Br-C-C120.05, 120.05119.28, 119.05
C-CH31.510, 1.5101.515, 1.509
N···H1.742, 1.7421.804, 1.896
Table
Table 2. The antimicrobial activity as shown by the inhibition area in the tested compounds.
Table 2. The antimicrobial activity as shown by the inhibition area in the tested compounds.
Tested Compounds (10 mg mL−1) Inhibition Zone (mm)Micrococcus luteus (ATCC 934)Staphylococcus aureus (ATCC 29213)Escherichia coli (ATCC 25922)
ZH1---
ZH21012-
ZH3148-
ZH43622-
[Z1Zn]---
[Z2Zn]1521-
[Z3Zn]2518-
[Z4Zn]1525-
[Z1Fe]---
[Z2Fe]-14-
[Z3Fe]---
[Z4Fe]-20-
[Z1Cu]--10
[Z2Cu]---
[Z3Cu]--20
[Z4Cu]-11-
Amoxicillin253510
Table
Table 3. IC50 values (μg/mL) of the tested compounds after the cell viability assay (MTT), showing variable responses of the treated cell lines with different specificity.
Table 3. IC50 values (μg/mL) of the tested compounds after the cell viability assay (MTT), showing variable responses of the treated cell lines with different specificity.
Cell LinesZH1ZH2ZH3ZH4Z1ZnZ1CuZ2ZnZ2FeZ2CuZ3ZnZ3CuZ4ZnZ4FeZ4CuDoxorubicin
A54925.2320.341.062.17224.943.781.2118.14.0199.4130.025.268.634.70.15
MCF720.5231.777.5Not covered17.310.425.241.41.917.7172.014.136.519.20.03
Fibroblasts46.8291.871.169.268.28.568.7134.11.527.629.228.316.710.40.37
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Al-Shboul, T.M.A.; El-khateeb, M.; Obeidat, Z.H.; Ababneh, T.S.; Al-Tarawneh, S.S.; Al Zoubi, M.S.; Alshaer, W.; Abu Seni, A.; Qasem, T.; Moriyama, H.; et al. Synthesis, Characterization, Computational and Biological Activity of Some Schiff Bases and Their Fe, Cu and Zn Complexes. Inorganics 2022, 10, 112. https://doi.org/10.3390/inorganics10080112

AMA Style

Al-Shboul TMA, El-khateeb M, Obeidat ZH, Ababneh TS, Al-Tarawneh SS, Al Zoubi MS, Alshaer W, Abu Seni A, Qasem T, Moriyama H, et al. Synthesis, Characterization, Computational and Biological Activity of Some Schiff Bases and Their Fe, Cu and Zn Complexes. Inorganics. 2022; 10(8):112. https://doi.org/10.3390/inorganics10080112

Chicago/Turabian Style

Al-Shboul, Tareq M. A., Mohammad El-khateeb, Zaid H. Obeidat, Taher S. Ababneh, Suha S. Al-Tarawneh, Mazhar S. Al Zoubi, Walhan Alshaer, Anas Abu Seni, Taqwa Qasem, Hayato Moriyama, and et al. 2022. "Synthesis, Characterization, Computational and Biological Activity of Some Schiff Bases and Their Fe, Cu and Zn Complexes" Inorganics 10, no. 8: 112. https://doi.org/10.3390/inorganics10080112

APA Style

Al-Shboul, T. M. A., El-khateeb, M., Obeidat, Z. H., Ababneh, T. S., Al-Tarawneh, S. S., Al Zoubi, M. S., Alshaer, W., Abu Seni, A., Qasem, T., Moriyama, H., Yoshida, Y., Kitagawa, H., & Jazzazi, T. M. A. (2022). Synthesis, Characterization, Computational and Biological Activity of Some Schiff Bases and Their Fe, Cu and Zn Complexes. Inorganics, 10(8), 112. https://doi.org/10.3390/inorganics10080112

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