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Article

Synthesis of Novel Tetra(µ3-Methoxo) Bridged with [Cu(II)-O-Cd(II)] Double-Open-Cubane Cluster: XRD/HSA-Interactions, Spectral and Oxidizing Properties

by
Abderrahim Titi
1,*,
Mouslim Messali
1,
Rachid Touzani
1,
Mohammed Fettouhi
2,
Abdelkader Zarrouk
3,
Nabil Al-Zaqri
4,
Ali Alsalme
4,
Fahad A. Alharthi
4,
Amjad Alsyahi
4 and
Ismail Warad
5,*
1
Laboratory of Applied and Environmental Chemistry (LCAE), Mohammed First University, 60000 Oujda, Morocco
2
Department of Chemistry, King Fahd University of Petroleum and Minerals, P.O. Box 5048, Dhahran 31261, Saudi Arabia
3
Laboratory of Materials, Nanotechnology and Environment, Faculty of Sciences, Mohammed V University, Av. I bn Battouta, Box 1014, 47963 Agdal-Rabat, Morocco
4
Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
5
Department of Chemistry, Science College, An-Najah National University, P.O. Box 7, Nablus 00970, Palestine
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2020, 21(22), 8787; https://doi.org/10.3390/ijms21228787
Submission received: 24 October 2020 / Revised: 15 November 2020 / Accepted: 18 November 2020 / Published: 20 November 2020
(This article belongs to the Special Issue Synthesis and Reactivity of Novel Aromatic Compounds)
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Abstract

:
A new double-open-cubane core Cd(II)-O-Cu(II) bimetallic ligand mixed cluster of type [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN was made available in EtOH/CH3CN solution. The 1-hydroxymethyl-3,5-dimethylpyrazole (NNOH) and 3,5-dimethylpyrazole (NNH) act as N,O-polydentate anion ligands in coordinating the Cu(II) and Cd(II) centers. The structure of the cluster in the solid state was proved by XRD study and confirmed in the liquid state by UV-vis analysis. The XRD result supported the construction of two octahedral and one square pyramid geometries types around the four Cu(II) centers and only octahedral geometry around Cd(II) two centers. Interestingly, NNOH ligand acts as a tetra-µ3-oxo and tri-µ2-oxo ligand; meanwhile, the N-N in NNH acts as classical bidentate anion/neutral ligands. The interactions in the lattice were detected experimentally by the XRD-packing result and computed via Hirschfeld surface analysis (HSA). The UV-vis., FT-IR and Energy Dispersive X-ray (EDX), supported the desired double-open cubane cluster composition. The oxidation potential of the desired cluster was evaluated using a 3,5-DTB-catechol 3,5-DTB-quinone as a catecholase model reaction.

Graphical Abstract

1. Introduction

Multinuclear cluster chemistry has gained high interest due to their biochemistry potential applications and structural diversity [1]. The synthesis of multinuclear Cu(II) complexes have been planned via various factors, for example, counter ions, ligands, reagents sequence, solvents, temperature and pH [2]. Cu(II) complexes with various ligands compositions and polynuclear structures are recorded in the literature with their molecular biology, magnetism applications and catalysis. Multi-copper clusters can enhance several oxidation reactions of amines and alcohols [3,4,5,6,7]. Copper (II) complexes clusters can also serve as metallo-pharmaceutical agents as antitumor, antimicrobials, antibacterial, antifungal, antipyretic, antidiabetic and antiviral agents [8,9,10,11,12]. The use of O, N, P-ligands as polydentate was been a good preference to build multilateral and multinuclear architectures cluster because of their electronic, steric effect and several coordination modes [13,14,15,16]. Tetra-nuclear Cu(II) clusters are existing as hot-urge points in bioinorganic modeling, magnetochemistry, multielectron transfer and catalysis. In the two last decades, plenty of cubane clusters were prepared by using alkoxo-bridged NOO or NNO types of donor ligands were prepared until now [17,18,19,20,21,22].
On the other hand, clusters with multiple spin molecular centers revealed a good catalytic aspect, especially in industrial oxidation processes [23,24,25,26,27,28,29]. Clusters with chelate mixed alcoholic pyrazole ligands and metal have recently received less interest due to their difficulty in preparation, low stability and rear in collecting suitable crystals to be judged by XRD single structure analysis [25,26,27,28].
We recently synthesized several novel tetra-nuclear metal cubane clusters; their structures were evaluated by XRD analysis, and their cluster catecholase catalytic activities were also evaluated by converting catechol to O-quinone as an oxidation model [21,22,30]. In this piece of work, the bimetallic Cd-O-Cu double-open cubane [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN cluster made available using chelate NNOH and NNH ligands, the structure of the cluster was proven by XRD, the tetrahedral-µ3-O and trigonal pyramidal-µ2-O bridges were detected. The octahedral and square pyramid geometries were resolved for both the metal centers. Moreover, physicochemical and HS analyses were determined to ensure the catecholase catalytic process of the desired cluster in mild or harsh conditions.

2. Results and Discussion

2.1. Cluster Preparation

The desired bimetallic cluster was prepared by stirring CuCl2.2H2O and Cd(NO3)2.4H2O metallic salts together with 1-hydroxymethyl-3,5-dimethylpyrazole (NNOH) and 3,5-dimethylpyrazole (NNH) at RT for 24 h using EtOH:CH3CN solution (Scheme 1). The desired reaction of clusterization was performed at RT in an open O2 atmosphere with equivalent amounts of each ligand and metal salt, and the final bimetallic [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN cluster was isolated in 78% yield. Moreover, the 3D structure was definite by XRD analysis (for the first time).

2.2. Single Crystal X-ray Diffraction (SC-XRD) Investigation

The 3D structure of the newly desired cluster is shown in Figure 1, whereas the selected atomic and angles distances are provided in Table 1. The cluster crystallized in the monoclinic/P21/c crystal system and space group, respectively. The cluster crystalized with 4Cu and 2Cd metal ion double open cubane core centers with [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN formula. All the organic NNOH and NNH and inorganic NO3 and Cl ligands acted as chelate or bridge anion donors, which stabilized the cluster as neutral with no, counter ions (Figure 1a). No solvents like MeOH or water molecules were detected, but only one uncoordinated CH3CN molecule was present in the crystal lattice (Figure 1b). The cationic units of the two Cd(II) and four Cu(II) centers were not directly bonded. On the other hand, all the centers had methoxo-bridge like 4μ3-O, 2μ2-O, 2μ2-NO3 or 2μ2-Cl- bridge functional groups. Furthermore, both NN− ligands, which acted as terminal bridge donors bidentate that coordinated to the Cu(II) centers only, supported the formation of two different Cu(II) geometrical centers: terminal 2Cu(II) centers with 6-coordinate [2N, 3O, 1Cl], constructing an octahedral center. Both centers were saturated with one OՈO-bidentate NO3 ligand (Figure 1c). Conversely, the other Cu(II) core centers were sterically forced to be with 5-coordinate [2N, 3O], constructing a square pyramid geometry center with τ[1O2O6N1N] = 3.12 °C (Figure 1d). Both core 2Cd(II) centers were constructed with distorted octahedral centers once the 6-coordinates [1N, 4O, 1Cl] were recorded (Figure 1e). It was delightful to observe that NNO− ligands coordinated with the both Cu and Cd centers via η3:η1-O,N-modes of coordination, hence the di-μ2-methoxo-trigonal pyramid-O center (Figure 1f), and two different tetra-μ3-methoxo-tetrahedral-O centers (Figure 1g,h).
Experimentally, several polar shorter interactions < 3 Å were detected in the crystal lattice since the cluster contains O, N and Cl heteroatoms together with polar H atoms. The non-bonded O atom of NO3 ligands played a critical role in the building of the net of H-bonds in cluster lattice. Therefore, 4 × 2 HCH….O-NO2 with 2.58 and 2.70 Å (Figure 2a) with full geometric parameters (Å, degree) are illustrated in Table 2 are recorded. The C-H…..πC=C ring of NN ligands as a short interaction with 2.80 Å distance played a critical role in stabilizing the crystal lattice since four bonds of such type were recorded (Figure 2b) and the interesting solvent interactions 2Cl…. Π CNCH3CN with 3.56 Å (Figure 2c) [31,32,33,34,35].

2.3. HS and 2D-FP Investigation

The surface was mapped to obtain more interaction information on the molecule and its surrounding molecules in the crystal lattice that played critical roles in stabilizing the structural formula via short intermolecular forces reflected by red spot sizes on the normalized dnorm [36,37,38,39,40,41]. The results illustrated in Figure 3 showed that the values of HS with three-dimensional shape and cave centers and shape ranged from 0.723 to 1.874 a.u. The red spots were behind the polar atoms such as oxygen, nitrogen, chlorine and hydrogen. Eleven red points were detected on the computed cluster surface, and they were attributed to the existence of 8 H-bond interactions. Two C-H…..O-NO2 (Figure 3a–c) formed H-bonds with a distance of 2.56 and 2.72 Å and two Cring-H….C=C with a length of 2.76 Å (Figure 3d). The computed HS and experimental XRD interactions were highly matched in their positions and structural parameter values.
The 2D-FP plots illustrated in Figure 4 were constructed from the 2D-HS by considering outside and inside closest-neighbor molecules. These integrated visions on contacts were helpful in the imagining of nonpolar and polar atoms interactions contributions in the cluster lattice. The other atom…atom contact rations were resolved as H…H (60.0%). Intermolecular contacts showed the larger contribution part and H…..M (Cu and Cd) (0.0%) interactions ratio. Early studies concerned H…H connections as steric repulsive interactions that disturb the molecular system [42]. Moreover, the understanding of H…H interactions was verified and changed in the 1990s since a new type of interaction named the dihydrogen bond (DHB) was recorded in crystal structures of different organometallic complexes [42,43,44,45]. The other atom…atom intermolecular forces are illustrated in the following importance order: H….H (60.0%) > H….C(10.0%) >H….N (5.6%) >H…..O (5.40%) > H…..Cl(1.0%) >H….M(0.0%).

2.4. FT-IR and EDX Investigations

For the preparation of [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2], the CH3CN cluster was followed up by FT-IR, as shown in Figure 5. The obtained bimetallic cluster reflected several IR bands matching with its continent functional groups. Several stretching vibrations were exposed in the cluster backbone like aliphatic and aromatic C-H, NO3, C=N, MeCN, C-O, C=C, Cu-O, Cd-O, Cu-N, Cd-N and M-Cl, which were cited to their expected wavenumbers (see experimental part). Kinetically, the important changes supporting the clusterization process were the vanishing of N-H (in NNH ligand) peak at 3170 cm−1 by the complexation NNH with metal centers and the appearing of new M-O/M-N bands at >400 cm−1 chemical shifts [21,22]. The broad peak at ~3400 cm−1 was mostly due to humidity on the crystal surface of the cluster. Peaks at ~2930–2820 cm−1 in both the ligand and the cluster were attributed to C-H stretching vibrations, the C=N stretching vibration in the free ligand shifted from 1610 cm−1 to 1560 cm−1 upon coordination to the metal center. The appearance of broad peaks at 265–2500 cm−1 in the cluster was only due to the presence of MeCN stretching vibration. The C=C and C-O stretching vibrations in both ligand and cluster were the same, with ~1480 and 1100 cm−1, respectively. The M-O and M-N bonds for the both metals (Cu and Cd) vibrations were in the low range ~400–450 cm−1.
The qualitative compositions of the cluster were confirmed by EDX analysis, as presented in Figure 6. The presence of Cu atoms was confirmed by energy signals at 1.2, 8.2 and 9.1 keV. Meanwhile, the Cd atoms peaks were cited to 3.3 and 3.5 keV positions, moreover, Cl to 2.4 keV position, respectively. Moreover, C, N and O atoms were cited to their expected atomic energy peaks as seen in Figure 6.

2.5. Electronic Transfer and Optical Energy Gap

The electronic absorption of the novel desired cluster and its free ligands in DMSO solvent were combined, as illustrated in Figure 7a. Peaks in the UV-region: the recorded λmax = 280 nm (ε = 1.0 × 103 L mol−1 cm−1) for the cluster, λmax = 282 nm (ε = 1.8 × 103 L mol−1 cm−1) for NNH ligand and λmax = 286 nm (ε = 1.6 × 103 L mol−1 cm−1) for NNOH ligand all can be assigned to π→π* ligands e-transition. The two broad and low-intensity peaks in the visible region at λmax = 605 nm (ε = 2.2 × 102 L mol−1 cm−1) and λmax = 685 nm (ε = 8.4 × 102 L mol−1 cm−1) cited to the Cu(II) d-d e-transfer in the cluster only confirmed the N-M and O-M bond coordination [46]. The experimental optical band gap energies (ΔEg) in DMSO were obtained by using the Tauc relation [40]. The organic ligands direct ΔEg was found to be 4.18 eV, as seen in Figure 7b. Meanwhile, the metallic direct ΔEg was found to be 1.73 eV, as seen in Figure 7c. The attained ΔEg results reflected the 4Cu(II) cluster centers complexes within the visible region; meanwhile, the NNO and NN ligands with invisible region electron transfer. Therefore, clusters with such optical performance properties are expected to be an important material for solar cells, optoelectronic devices and photonic devices [47].

2.6. Cluster Oxidation Potential toward Catecholase of Catechol

One of the goals of the present study is to evaluate the aerobic catecholase catalytic oxidation founding of the cluster. To accomplish this, 0.1 M of 3,5-di-tert-butylbenzene-1,2-diol (3,5-DBT) was mixed with 1 × 10−4 M of the desired cluster in DMF solvent under stirring an open RT system for around 1 h (Scheme 2). The formation of the 3,5-di-tert-butylcyclohexa-3,5-diene-1,2-dione (3,5-DTBQ) product was monitored by UV-vis analysis in 250–500 nm range [20,21,44], as seen in Figure 8.
In Figure 8a, the absorptions of 3,5-DTBQ product at λmax~400 nm were gradually raised by time only with the presence of the cluster catalyst. The result revealed without ambiguity that the cluster acts as an excellent oxidation catalyst since the reaction was completely finished within 1 h. Moreover, neither side products nor products were detected by the UV-vis absorption in the absence of the cluster Figure 8b.
The oxidation rates of the cluster using several concentrations of 3,5-DBT find to be suited to the Michaelis–Menten plot (Figure 9a), which was linearized to Lineweaver–Burk plot (Figure 9b), in order to figure out the Vmax, KM and Kcat kinetic parameters. The kinetic parameter values were compared to similar catalytic processes [48,49,50,51,52,53,54]. In general, the cluster catalyst results were excellent compared to other complexes, where many factors like solvents, substrate and complex nature control the ability of catalysts [2,20,51].

3. Materials and Methods

The commercially available CdCl2.4H2O and Cu(NO3)2.6H2O salts, solvents and chemicals, were served without purification. The NNOH and NNH were prepared in our lab [22]. EDX was performed using Brucker D/MAX 2500 X-ray diffractometer, with λ = 1.54 Å Cu K radiation, TU-1901 double-beam UV-visible spectrophotometer was used to measure the UV-vis. The TG was carried out using TGA SDT-Q600, FT-IR spectra were performed in the range of 4000–400 cm−1 of frequency using a PerkinElmer Spectrum, and HS calculation was performed using CRYSTAL EXPLORER 3.1 package [33].

3.1. Synthesis of [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN Bimetallic Cluster

0.16 mmol of each salt CdCl2.4H2O and Cu(NO3)2.6H2O were dissolved in 50 mL of ethanol solvent. After complete dissolving, 0.16 mmol of NNOH and NNH each (in 20 mL of CH3CN) were added to the reaction mixture, which was stirred for 24 h in an open condition. The reaction was then stopped and subjected to the solvent-evaporation process. After 3 weeks, light green plate crystals of [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN cluster had formed in 74% yield. Peaks of selected IR vibrations are listed as ν = 3018 (C-H), (1520–1380) (NO3), 2936 (C-H), 1622 (C=N), (2200–2550) (-CN), 1485 (C=C), 1020 (C-O), cm−1. The peak at 420–550 cm–1 belongs to M–O and M–N stretching vibrations [21,22]. UV-vis. (DMSO) at λmax = 280, 605 and 685 nm and m.p. > 340 °C.

3.2. Catechol Oxidation Reaction

The catalytic part was performed using the procedure described recently in the literature [22].

3.3. X-Ray

Single crystal X-ray data were collected on a Bruker D8 Quest diffractometer (MoKα radiation λ = 0.71073 Å) at 298 K. The structure was solved by direct methods and refined by full-matrix least-squares methods based on F2 using the SHELXL software [34]. Crystal data for the desired cluster is illustrated in Table 3.

4. Conclusions

A new [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN cluster of type double-open cubane core with Cd(II)-O-Cu(II) center was made available. The 3D structure of the newly synthesized cluster was proven by XRD crystal. The XRD showed the presence of both octahedral and square pyramid metal ions geometry centers. Moreover, the di-μ2-methoxo-trigonal pyramid-O center and tetra-μ3-methoxo-tetrahedral-O centers were recorded. Several shot interactions like HCH….O-NO2, C-H….π C=CNN and Cl…. Π CN were detected in the lattice by XRD and computed via HS-analysis. Furthermore, the cluster composition and structural behavior were proved spectrally furthermore via FT-IR, EDX and UV-vis. Finally, the cluster recorded an excellent catecholase potential when it was applied to the Catechol O-quinone room condition oxidation reaction.

Author Contributions

A.T. and M.M. carried out the experiments. I.W. wrote the manuscript, F.A.A., A.A. (Amjad Alsyahi) carried out the theoretical calculations. M.F. carried out XRD measurement. A.Z. and N.A.-Z. contributed to the final version of the manuscript. R.T., A.A. (Ali Alsalme) and N.A.-Z. supervised the project. All authors have read and agreed to the published version of the manuscript.

Funding

The authors extend their appreciation to the Deputyship for Research & Innovation, “Ministry of Education” in Saudi Arabia for funding this research work through the project number IFKSURG-1440-141.

Conflicts of Interest

The authors declare no competing interests.

References

  1. Paula, A.; Mistria, S.; Bertolasib, V.; Manna, S.C. DNA/protein binding and molecular docking studies of two tetranuclear Cu (II) complexes with double-open-cubane core like structure. Inorg. Chim. Acta 2019, 495, 119005. [Google Scholar] [CrossRef]
  2. Zheng, S.-R.; Pan, M.; Wu, K.; Chen, L.; Jiang, J.-J.; Wang, D.-W.; Shi, J.-Y.; Su, C.-Y. Assembly of Binuclear, Tetranuclear, and Multinuclear Complexes from Pincer-Like Mononuclear Metallotectons: Structural Diversity Dependent on Precursors. Cryst. Growth Des. 2015, 15, 625–634. [Google Scholar] [CrossRef]
  3. Aronica, C.; Chumakov, Y.; Jeanneau, E.; Luneau, D.; Neugebauer, P.; Barra, A.-L.; Gillon, B.; Goujon, A.; Cousson, A.; Tercero, J.; et al. Structure, Magnetic Properties, Polarized Neutron Diffraction, and Theoretical Study of a Copper(II) Cubane. Chem. Eur. J. 2008, 14, 9540. [Google Scholar] [CrossRef] [PubMed]
  4. Than, R.; Feldmann, A.A.; Krebs, B. Structural and functional studies on model compounds of purple acid phosphatases and catechol oxidases.Coord. Chem. Rev. 1999, 182, 211. [Google Scholar]
  5. Allen, S.E.; Walvoord, R.R.; Padilla-Salinas, R.; Kozlowski, M.C. Aerobic Copper-Catalyzed Organic Reactions. Chem. Rev. 2013, 113, 6234. [Google Scholar] [CrossRef] [Green Version]
  6. Bilyachenko, A.N.; Dronova, M.S.; Yalymov, A.I.; Lamaty, F.; Bantreil, X.; Martinez, J.; Bizet, C.; Shul’pina, L.S.; Korlyukov, A.A.; Arkhipov, D.E.; et al. Cage-like Copper(II) Silsesquioxanes: Transmetalation Reactions and Structural, Quantum Chemical, and Catalytic Studies. Chem. Eur. J. 2015, 21, 8758. [Google Scholar] [CrossRef]
  7. Dias, S.S.P.; Kirillova, M.V.; Andre, V.; Kłak, J.; Kirillov, A.M. New tricopper(II) cores self-assembled from aminoalcohol biobuffers and homophthalic acid: Synthesis, structural and topological features, magnetic properties and mild catalytic oxidation of cyclic and linear C5–C8 alkanes. Inorg. Chem. Front. 2015, 2, 525. [Google Scholar] [CrossRef]
  8. Fernandes, T.A.; Santos, C.I.M.; Andre, V.; Kłak, J.; Kirillova, M.V.; Kirillov, A.M. Copper(II) Coordination Polymers Self-Assembled from Aminoalcohols and Pyromellitic Acid: Highly Active Precatalysts for the Mild Water-Promoted Oxidation of Alkanes. Inorg. Chem. 2016, 55, 125. [Google Scholar] [CrossRef]
  9. Yoshikawa, Y.; Yasui, H. Zinc Complexes Developed as Metallopharmaceutics for Treating Diabetes Mellitus based on the Bio-Medicinal Inorganic Chemistry. Curr. Top. Med. Chem. 2012, 12, 210. [Google Scholar] [CrossRef]
  10. Muche, S.; Levacheva, I.; Samsonova, O.; Pham, L.; Christou, G.; Bakowsky, U.; Hołyńska, M. A Chiral, Low-Cytotoxic [Ni15]-Wheel Complex. Inorg. Chem. 2014, 53, 7642. [Google Scholar] [CrossRef]
  11. Vančo, J.; Marek, J.; Travniček, Z.; Račanska, E.; Muselik, J.; Švajlenova, O. Synthesis, structural characterization, antiradical and antidiabetic activities of copper(II) and zinc(II) Schiff base complexes derived from salicylaldehyde and β-alanine. J. Inorg. Biochem. 2008, 102, 595. [Google Scholar] [CrossRef] [PubMed]
  12. Yin, D.-D.; Jiang, Y.-L.; Shan, L. Synthesis, characterization of diorganotin (IV) schiff base complexes and their in vitro antitumor activity. Chin. J. Chem. 2001, 19, 1136. [Google Scholar] [CrossRef]
  13. Vanco, J.; Svajlenova, O.; Racanska, E.; Muselik, J.; Valentova, J.; Elem, J. Antiradical activity of different copper(II) Schiff base complexes and their effect on alloxan-induced diabetes. Med. Biol. 2004, 18, 155. [Google Scholar]
  14. Serna, Z.; De la Pinta, N.; Urtiaga, M.K.; Lezama, L.; Madariaga, G.; Juan, J.M.; Coronado, E.; Cortes, R. Defective Dicubane-like Tetranuclear Nickel(II) Cyanate and Azide Nanoscale Magnets. Inorg. Chem. 2010, 49, 11541. [Google Scholar] [CrossRef]
  15. Wang, H.; Wan, C.-Q.; Mak, T.C.W. High-nuclearity silver(I) cluster-based coordination polymers assembled with multidentate oligo-α-heteroarylsulfanyl ligands. Dalton Trans. 2014, 43, 7254. [Google Scholar] [CrossRef] [PubMed]
  16. Chen, C.; Zhang, J.; Li, G.; Shen, P.; Jin, H.; Zhang, N. Two coordination polymers constructed from a multidentate carboxylic acid ligand with a tertiary amine serve as acid–base catalysts for the synthesis of chloropropene carbonate from CO2 under atmospheric pressure. Dalton Trans. 2014, 43, 13965. [Google Scholar] [CrossRef] [PubMed]
  17. Penney, M.K.; Giang, R.; Burroughs, M.A., Jr.; Klausmeyer, K.K. Structure and luminescence of discrete and polymeric Ag(I) complexes formed by the multidentate pyridylphosphine (PPh2CH2)2N(3-CH2C5H4N). Polyhedron 2015, 87, 43. [Google Scholar] [CrossRef]
  18. Landers, A.E.; Phillips, D.J. Alkoxy-bridged complexes of copper(II) and nickel(II) with schiff bases of alcoholamines-including effects of structural distortion on the electronic spectra of Six-coordinate nickel(II) Complexes. Inorg. Chim. Acta 1979, 32, 53. [Google Scholar] [CrossRef]
  19. Si, S.-F.; Tang, J.-K.; Liao, D.-Z.; Jiang, Z.-H.; Yan, S.-P. Synthesis, structure, and characterization of dicopper(II) complex with a new amidate ligand. Inorg. Chem. Commun. 2002, 5, 76. [Google Scholar] [CrossRef]
  20. Xie, Y.; Jiang, H.; Chan, A.S.C.; Liu, Q.L.; Xu, X.L.; Du, C.X.; Zhu, Y. Structural and magnetic properties of O-bridged tetranuclear and binuclear Cu(II) complexes. Inorg. Chim. Acta 2002, 333, 138. [Google Scholar] [CrossRef]
  21. Koikawa, M.; Yamashita, H.; Tokii, T. Crystal structures and magnetic properties of tetranuclear copper(II) complexes of N-(2-hydroxymethylphenyl)salicylideneimine with a defective double-cubane core. Inorg. Chim. Acta 2004, 357, 2635. [Google Scholar] [CrossRef]
  22. Titi, A.; Shiga, T.; Oshio, H.; Touzani, R.; Hammouti, B.; Mouslim, M.; Warad, I. Synthesis of novel Cl2Co4L6 clusterusing 1-hydroxymethyl-3,5-dimethylpyrazole (LH) ligand: Crystal structure, spectral, thermal, Hirschfeld surface analysis and catalytic oxidation evaluation. J. Mol. Struct. 2020, 1199, 126995. [Google Scholar] [CrossRef]
  23. Titi, A.; Oshio, H.; Touzani, R.; Mouslim, M.; Zarrouk, A.; Hammouti, B.; Al-Zaqri, N.L.; Alsalme, A.; Warad, I. Synthesis and XRD of Novel Ni4(µ3-O)4 Twist Cubane Cluster Using Three NNO Mixed Ligands: Hirshfeld, Spectral, Thermal and Oxidation Properties. J. Clust. Sci. 2020, 26, 1. [Google Scholar] [CrossRef]
  24. Zienkiewicz, M.; Jabłonska-Wawrzycka, A.; Szlachetko, J.; Kayser, Y.; Stadnicka, K.; Sawka-Dobrowolska, W.; Jezierska, J.; Barszcz, B.; Sá, J. Effective catalytic disproportionation of aqueous H2O2 with di- and mono-nuclear manganese(ii) complexes containing pyridine alcohol ligands. Dalton Trans. 2014, 43, 8599. [Google Scholar] [CrossRef]
  25. Zienkiewicz, M.; Szlachetko, J.; Lothschütz, C.; Hodorowicz, M.; Wawrzycka, A.; Sá, J.; Barszcz, B. A novel single-site manganese(II) complex of a pyridine derivative as a catalase mimetic for disproportionation of H2O2 in water. Dalton Trans. 2013, 42, 7761. [Google Scholar] [CrossRef]
  26. El Kodadi, M.; Malek, F.; Touzani, R.; Ramdani, A. Synthesis of new tripodal ligand 5-(bis(3,5-dimethyl-1H-pyrazol-1-ylmethyl)amino)pentan-1-ol, catecholase activities studies of three functional tripodal pyrazolyl N-donor ligands, with different copper (II) salts. Catal. Commun. 2008, 9, 966. [Google Scholar] [CrossRef]
  27. Kim, E.; Woo, H.Y.; Kim, S.; Lee, H.; Kim, D.; Lee, H. Synthesis and X-ray crystal structure of derivatives from the N,N-bis(1H-pyrazolyl-1-methyl)aniline(dichloro)Zn(II) complex: Substituent effects on the phenyl ring versus the pyrazole ring. Polyhedron 2012, 42, 135. [Google Scholar] [CrossRef]
  28. Otero, A.; Fernández-Baeza, J.; Lara-Sánchez, A.; Sánchez-Barba, L.F. Metal complexes with heteroscorpionate ligands based on the bis(pyrazol-1-yl)methane moiety: Catalytic chemistry. Coord. Chem. Rev. 2013, 257, 1806. [Google Scholar] [CrossRef]
  29. Xue, F.; Zhao, J.; Hor, A.T.S. Cross-coupling of alkyl halides with aryl or alkyl Grignards catalyzed by dinuclear Ni(ii) complexes containing functionalized tripodal amine-pyrazolyl ligands. Dalton Trans. 2013, 42, 5150. [Google Scholar] [CrossRef]
  30. Han, X.-B.; Li, Y.-G.; Zhang, Z.-M.; Tan, H.-Q.; Lu, Y.; Wang, E.-B. Polyoxometalate-Based Nickel Clusters as Visible Light-Driven Water Oxidation Catalysts. J. Am. Chem. Soc. 2015, 137, 5486. [Google Scholar] [CrossRef]
  31. Asadi, Z.; Zarei, L.; Golchin, M.; Skorepova, E.; Eigner, V.; Amirghofran, Z. A novel Cu(II) distorted cubane complex containing Cu4O4 core as the first tetranuclear catalyst for temperature dependent oxidation of 3,5-di-tert-butyl catechol and in interaction with DNA & protein (BSA). Spectrochim. Acta A 2020, 227, 117593. [Google Scholar]
  32. Driessen, W.L. Synthesis of some new pyrazole-containing chelating agents. Recl. Trav. Chim. Pays-Bas 1982, 101, 441. [Google Scholar] [CrossRef]
  33. Wolff, S.K.; Grimwood, D.J.; McKinnon, J.J.; Jayatilaka, D.; Spackman, M.A. CrystalExplorer2. 1. University of Western Australia. In Crystal Explorer 2.1; University of Western Australia: Perth, Australia, 2007. [Google Scholar]
  34. Sheldrick, G.M. A magic triangle for experimental phasing of macromolecules. Acta Cryst. 2008, 64, 112. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Ng, C.K.; Tam, T.L.D.; Wei, F.; Lub, X.; Wu, J. Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts. Org. Chem. Front. 2019, 6, 110. [Google Scholar] [CrossRef]
  36. Dorn, T.; Janiak, C.; Abu-Shandi, K. Hydrogen-bonding, pi-stacking and Cl-anioninteractions of linear bipyridinium cations with phosphate, chloride and [CoCl4] 2-anions. CrystEngComm 2005, 7, 633–641. [Google Scholar] [CrossRef]
  37. Warad, I.; Awwadi, F.F.; Al-Ghani, B.A.; Sawafta, A.; Shivalingegowda, N.; Lokanath, N.K.; Mubarak, M.S.; Hadda, T.B.; Zarrouk, A.; Al-Rimawi, F.; et al. Ultrasound-assisted synthesis of two novel [CuBr(diamine)2·H2O]Br complexes: Solvatochromism, crystal structure, physicochemical, Hirshfeld surface thermal, DNA/binding, antitumor and antibacterial activities. Ultrason. Sonochem. 2018, 48, 1. [Google Scholar] [CrossRef]
  38. Warad, I.; Al-Demeri, Y.; Al-Nuri, M.; Shahwan, S.; Abdoh, M.; Naveen, S.; Lokanath, N.K.; Mubarak, M.S.; Hadda, T.B.; Mabkhot, Y.N. Crystal structure, Hirshfeld surface, physicochemical, thermal and DFT studies of (N1E, N2E)-N1,N2-bis((5-bromothiophen-2-yl)methylene)ethane-1,2-diamine N2S2 ligand and its [CuBr(N2S2)]Br complex. J. Mol. Struct. 2017, 1142, 217. [Google Scholar] [CrossRef]
  39. Saleem, F.A.; Musameh, S.; Sawafta, A.; Brandao, P.; Tavares, C.J.; Ferdov, S.; Barakat, A.; Al Ali, A.; Al-Noaimi, M.; Warad, I. Diethylenetriamine/diamines/copper (II) complexes [Cu(dien)(NN)]Br2: Synthesis, solvatochromism, thermal, electrochemistry, single crystal, Hirshfeld surface analysis and antibacterial activity. Arab. J. Chem. 2017, 10, 845. [Google Scholar] [CrossRef] [Green Version]
  40. Warad, I.; Khan, A.A.; Al-Resayes, S.I.; Haddad, S.F. Design and structural studies of diimine/CdX2 (X = Cl, I) complexes based on 2,2-dimethyl-1,3-diaminopropane ligand. J. Mol. Struct. 2014, 1062, 167. [Google Scholar] [CrossRef]
  41. Aouad, M.R.; Messali, M.; Rezki, N.; Al-Zaqri, N.; Warad, I. Single proton intramigration in novel 4-phenyl-3-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)-1H-1,2,4-triazole-5(4H)-thione: XRD-crystal interactions, physicochemical, thermal, Hirshfeld surface, DFT realization of thiol/thione tautomerism. J. Molec. Liq. 2018, 264, 621. [Google Scholar] [CrossRef]
  42. Warad, I.; Eftaiha, A.A.F.; Al-Nuri, M.A.; Husein, A.I.; Assal, M.; Abu-Obaid, A.; Al-Zaqri, N.; Hadda, T.B.; Hammouti, B. Metal ions as Antitumor Complexes-Review. J. Mater. Environ. Sci. 2013, 4, 542. [Google Scholar]
  43. Alkorta, I.; Elguero, J.; Grabowski, S.J. How To Determine Whether Intramolecular H···H Interactions Can Be Classified as Dihydrogen Bonds. J. Phys. Chem. A 2008, 112, 2721. [Google Scholar] [CrossRef] [PubMed]
  44. Richardson, B.; De Gala, S.; Crabtree, H.; Siegbahn, M. Unconventional Hydrogen Bonds: Intermolecular B-H···H-N Interactions. J. Am. Chem. Soc. 1995, 117, 12875. [Google Scholar] [CrossRef]
  45. Cramer, J.; Gladfelter, L. Ab Initio Characterization of [H3N·BH3]2, [H3N·AlH3]2, and [H3N·GaH3]2. Inorg. Chem. 1997, 36, 5358. [Google Scholar] [CrossRef]
  46. Warad, I.; Alkanad, K.; Suleiman, M.; Kumara, K.; Al-Ali, A.; Mohammed, Y.; Lokanath, N.K.; Zarrouk, A. Design, structural, C–H….H–C supramolecular interactions and computational investigations of Cd(N∩N″)X 2 complexes based on an asymmetrical 1,2-diamine ligand: Physicochemical and thermal analysis. J. Coord. Chem. 2019, 72, 12. [Google Scholar] [CrossRef]
  47. Thakurta, S.; Pilet, G.; Luneau, D.S. A novel tetra(μ3-phenoxo) bridged copper(II) Schiff base complex containing a Cu4O4 cubane core: Synthesis, structural aspects and magneto-structural correlations. Mitra Polyhedron 2009, 28, 819. [Google Scholar]
  48. Tauc, J.; Menth, A.; Optical processes in solids. Non-Cryst, J. Solids 1972, 8, 569. [Google Scholar]
  49. Aziz, B.; Abdullah, M. Crystalline and amorphous phase identification from the tanδ relaxation peaks and impedance plots in polymer blend electrolytes based on [CS:AgNt]x:PEO(x-1) (10 ≤ x ≤ 50). Electrochim. Acta 2018, 285, 30. [Google Scholar] [CrossRef]
  50. Kaddouri, Y.; Haddari, H.; Titi, A.; Yousfi, E.B.; Chetouani, A.; El Kodadi, M.; Touzani, R. Catecholase catalytic properties of copper (II) complexes prepared in-situ with heterocyclic ligands: Experimental and DFT study. Mor. J. Chem. 2020, 8, 184. [Google Scholar]
  51. Titi, A.; Al-Noaimi, M.; Kaddouri, Y.; El Ati, R.; Yousfi, E.B.; El Kodadi, M.; Touzani, R. Study of the catecholase catalytic properties of copper (II) complexes prepared in-situ with monodentate ligands. Mater. Today Proc. 2019, 13, 1134. [Google Scholar] [CrossRef]
  52. Modak, R.; Sikdar, Y.; Mandal, S.; Goswami, S. Synthesis, Crystal Structures, Magnetic Properties and Catecholase Activity of Double Phenoxido-Bridged Penta-Coordinated Dinuclear Nickel(II) Complexes Derived from Reduced Schiff-Base Ligands: Mechanistic Inference of Catecholase Activity. Inorg. Chem. Commun. 2013, 9, 26. [Google Scholar]
  53. Indira, S.; Vinoth, G.; Bharathi, M.; Bharathi, S.; Rahiman, A.K.; Bharathi, K.S. Catechol oxidase and phenoxazinone synthase mimicking activities of mononuclear Fe(III) and Co(III) complexes of amino-bis(phenolate)-based mixed ligands: Synthesis, spectral and electrochemical studies. Inorg. Chim. Acta 2019, 495, 118988. [Google Scholar] [CrossRef]
  54. Mandal, L.; Sasmal, S.; Sparkes, H.A.; Howard, J.A.K.; Mohanta, S. Crystal structure, catecholase activity and ESI-MS of a mixed valence cobalt(III)–cobalt(II) complex derived from a macrocyclic ligand: Identification/proposition of hydrogen bonded metal complex⋯solvent aggregates in ESI-MS. Inorg. Chim. Acta 2014, 412, 38. [Google Scholar] [CrossRef]
Ijms 21 08787 sch001 550
Scheme 1. Synthesis of the [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN bimetallic cluster.
Scheme 1. Synthesis of the [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN bimetallic cluster.
Ijms 21 08787 sch001
Ijms 21 08787 g001 550
Figure 1. (a) ORTEP structure (50% probability) of the bimetallic cluster, (b) molecular structure without protons showing no water in the crystal lattice, (c) octahedral geometry around Cu(II) centers, (d) pyramid geometry around the other Cu(II) centers, (e) distorted octahedral geometry around Cd(II) centers, (f) di-μ2-methoxo-trigonal pyramid-O centers, (g) and (h) two different tertra-μ3-methoxo-tetrahedral-O centers.
Figure 1. (a) ORTEP structure (50% probability) of the bimetallic cluster, (b) molecular structure without protons showing no water in the crystal lattice, (c) octahedral geometry around Cu(II) centers, (d) pyramid geometry around the other Cu(II) centers, (e) distorted octahedral geometry around Cd(II) centers, (f) di-μ2-methoxo-trigonal pyramid-O centers, (g) and (h) two different tertra-μ3-methoxo-tetrahedral-O centers.
Ijms 21 08787 g001
Ijms 21 08787 g002 550
Figure 2. (a) H….O-NO2 H-bonds, (b) H…Πc=C and (c) Cl…. ΠCNCH3CN interactions.
Figure 2. (a) H….O-NO2 H-bonds, (b) H…Πc=C and (c) Cl…. ΠCNCH3CN interactions.
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Ijms 21 08787 g003 550
Figure 3. HSA-mapped (a–c) dnorm and (d) shape index.
Figure 3. HSA-mapped (a–c) dnorm and (d) shape index.
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Ijms 21 08787 g004 550
Figure 4. HSA-computed cluster structure together with 2D-FP and H….X% interaction ratios.
Figure 4. HSA-computed cluster structure together with 2D-FP and H….X% interaction ratios.
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Ijms 21 08787 g005 550
Figure 5. FT-IR of (a) 3,5-dimethylpyrazole (NNH) ligand and (b) the desired cluster.
Figure 5. FT-IR of (a) 3,5-dimethylpyrazole (NNH) ligand and (b) the desired cluster.
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Ijms 21 08787 g006 550
Figure 6. EDX spectra of the desired cluster.
Figure 6. EDX spectra of the desired cluster.
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Ijms 21 08787 g007 550
Figure 7. (a) Electronic spectra of NNH, NNOH and cluster, (b) optical band gap of ligands, and (c) optical band gap of the metal center in the cluster dissolved in DMSO.
Figure 7. (a) Electronic spectra of NNH, NNOH and cluster, (b) optical band gap of ligands, and (c) optical band gap of the metal center in the cluster dissolved in DMSO.
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Ijms 21 08787 g008 550
Figure 8. Time-dependent 3.5-DBT oxidation process: (a) abs. vs. λ, and (b) abs. vs. t.
Figure 8. Time-dependent 3.5-DBT oxidation process: (a) abs. vs. λ, and (b) abs. vs. t.
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Ijms 21 08787 sch002 550
Scheme 2. Cluster catalytic oxidation of catechol to O-quinone.
Scheme 2. Cluster catalytic oxidation of catechol to O-quinone.
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Ijms 21 08787 g009 550
Figure 9. (a) Oxidation reaction initial rates vs. 3,5-DBT conc., and (b) the Lineweaver–Burk plots.
Figure 9. (a) Oxidation reaction initial rates vs. 3,5-DBT conc., and (b) the Lineweaver–Burk plots.
Ijms 21 08787 g009
Table
Table 1. Selected bond (Å) and angles lengths (°) of the desired cluster.
Table 1. Selected bond (Å) and angles lengths (°) of the desired cluster.
No.Bond TypeBond Length ÅNo.Angle TypeAngle Value (°)
1Cu2N11.972 (5)1N2Cu1N8170.5 (2)
2Cu1N21.951 (6)2N2Cu1O394.5 (2)
3Cu1O32.030 (4)3N2Cu1O493.7 (2)
4Cu1O42.041 (6)4N2Cu1O592.8 (2)
5Cu1O52.662 (8)5N2Cu1Cl196.3 (2)
6Cu1Cl12.712 (3)6N8Cu1O380.1 (2)
7Cu2O12.008 (4)7N8Cu1O489.3 (2)
8Cu2N62.010 (5)8N8Cu1O581.9 (2)
2Cu1N81.995 (6)9N8Cu1Cl191.5 (2)
10Cu2O21.927 (4)10O3Cu1O4161.0 (2)
11Cu2O32.279 (5)11O3Cu1O5110.5 (2)
12Cd1Cl12.542 (3)12O3Cu1Cl189.2 (1)
13Cd1N42.301 (5)13O4Cu1O551.9 (2)
14Cd1O12.472 (4)14O4Cu1Cl1106.9 (2)
15Cd1O22.235 (5)15O5Cu1Cl1157.5 (2)
16Cd1O12.299 (5)16N1Cu2N6101.6 (2)
17Cd1O32.362 (4)17N1Cu2O193.2 (2)
18Cl1Cu12.712 (3)18N1Cu2O2167.2 (2)
19N1N21.395 (9)19N1Cu2O390.6 (2)
Table
Table 2. Geometric parameters (Å, degree) for C-H…O interactions.
Table 2. Geometric parameters (Å, degree) for C-H…O interactions.
D-Hd(D-H)d(H..A)<DHAd(D..A)A
C6-H6A0.9702.620127.173.298O2 i
C18-H18A0.9702.578141.133.388O6 ii
Symmetry code: i: −x + 1, −y + 1, −z + 1; ii: −x + 1, −y + 1, −z + 1.
Table
Table 3. Crystal data and structure refinement of the desired cluster.
Table 3. Crystal data and structure refinement of the desired cluster.
Empirical FormulaC48 H71 Cd2 Cl2 Cu4 N19 O12
Formula weight1656.09
CCDC1956507
Temperature298(2) K
Wavelength0.71073 Å
Crystal systemMonoclinic
Space groupP 21/c
Unit cell dimensionsa = 10.860(9) Å
b = 20.665(19) Å
c = 17.212(16) Å
Β = 95.96(3)°
Volume3842(6) Å3
Z2
Density (calculated)1.432 g/cm3
Absorption coefficient1.759 mm−1
F(000)1668
Crystal size0.220 × 0.180 × 0.060 mm3
Theta range for data collection2.576 to 29.850°.
Index ranges−14 ≤ h ≤ 14, −27 ≤ k ≤ 27, −23 ≤ L ≤ 24
Reflections collected107,448
Independent reflections9719 [R(int) = 0.0711]
Refinement methodFull-matrix least-squares on F2
Data/restraints/parameters9719/2/401
Goodness-of-fit on F21.111
Final R indices [I>2sigma(I)]R1 = 0.0719, wR2 = 0.2085
R indices (all data)R1 = 0.1029, wR2 = 0.2370
Largest diff. peak and hole1.825 and −1.000 e.Å−3
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Titi, A.; Messali, M.; Touzani, R.; Fettouhi, M.; Zarrouk, A.; Al-Zaqri, N.; Alsalme, A.; Alharthi, F.A.; Alsyahi, A.; Warad, I. Synthesis of Novel Tetra(µ3-Methoxo) Bridged with [Cu(II)-O-Cd(II)] Double-Open-Cubane Cluster: XRD/HSA-Interactions, Spectral and Oxidizing Properties. Int. J. Mol. Sci. 2020, 21, 8787. https://doi.org/10.3390/ijms21228787

AMA Style

Titi A, Messali M, Touzani R, Fettouhi M, Zarrouk A, Al-Zaqri N, Alsalme A, Alharthi FA, Alsyahi A, Warad I. Synthesis of Novel Tetra(µ3-Methoxo) Bridged with [Cu(II)-O-Cd(II)] Double-Open-Cubane Cluster: XRD/HSA-Interactions, Spectral and Oxidizing Properties. International Journal of Molecular Sciences. 2020; 21(22):8787. https://doi.org/10.3390/ijms21228787

Chicago/Turabian Style

Titi, Abderrahim, Mouslim Messali, Rachid Touzani, Mohammed Fettouhi, Abdelkader Zarrouk, Nabil Al-Zaqri, Ali Alsalme, Fahad A. Alharthi, Amjad Alsyahi, and Ismail Warad. 2020. "Synthesis of Novel Tetra(µ3-Methoxo) Bridged with [Cu(II)-O-Cd(II)] Double-Open-Cubane Cluster: XRD/HSA-Interactions, Spectral and Oxidizing Properties" International Journal of Molecular Sciences 21, no. 22: 8787. https://doi.org/10.3390/ijms21228787

APA Style

Titi, A., Messali, M., Touzani, R., Fettouhi, M., Zarrouk, A., Al-Zaqri, N., Alsalme, A., Alharthi, F. A., Alsyahi, A., & Warad, I. (2020). Synthesis of Novel Tetra(µ3-Methoxo) Bridged with [Cu(II)-O-Cd(II)] Double-Open-Cubane Cluster: XRD/HSA-Interactions, Spectral and Oxidizing Properties. International Journal of Molecular Sciences, 21(22), 8787. https://doi.org/10.3390/ijms21228787

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