Nickel substituted polyoxometalates in layered double hydroxides as metal

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May 17, 2023

Nickel substituted polyoxometalates in layered double hydroxides as metal

Scientific Reports volume 13,

Scientific Reports volume 13, Article number: 4114 (2023) Cite this article

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Three nickel substituted Keggin-type polyoxometalates, α-[SiW9O37{Ni(H2O)}3]−10 (denoted as SiW9Ni3), was intercalated into Zn3Al based Layered Double Hydroxide (Zn3Al-LDH) by the selective ion-exchange technique. The as-synthesized nanocomposite, SiW9Ni3@Zn3Al, was used as heterogeneous nanoreactor to promote the synthesis of drug-like aminoimidazopyridine small molecule skeletons via the well-known Ugi-type Groebke–Blackburn–Bienaymé reaction (GBB 3-CRs) in the absence of any acid/additive and under mild and solvent-free conditions. A synergistic catalytic effect between SiW9Ni3 polyoxometalate and Zn3Al-LDH precursors is evidenced by a higher catalytic property of the SiW9Ni3@Zn3Al composite compared to the individual constituents separately. Lewis/Bronsted acidity of the SiW9Ni3 polyoxometalate and Zn3Al-LDH precursors appear to be essential for the catalytic performance of the composite. Furthermore, the catalytic performance of SiW9Ni3@Zn3Al was also tested in GBB 3-CRs synthesis of amino imidazothiazole under mild and solvent-free conditions.

The ‘greening’ of the global chemical processes has become an important challenge in chemical industry1. Green chemistry provides "Green" paths for reactions not only via reducing of byproducts, produced waste, energy costs and materials consumption but also by well advised in the selection of nonhazardous solvents and green catalysts2. Furthermore, in development of efficient green synthesis procedures, Solvent-free (S-F) approach has become a major focus of researchers due to advantages over the classical method of synthesis. The S-F procedure decreases the use of organic toxic solvents and Volatile Organic Compounds (VOCs) and minimizes the formation of other wastes3,4. On the other hand, development of various approaches for heterogenizing of homogeneous catalysts, which minimizes consumption of materials like solvents, energy and time, can result in significant economic and environmental benefits. Therefore, from both environmental and economic viewpoints, organic reactions under solvent-free and recoverable catalyst conditions have gained considerable interest in recent years5.

Multicomponent reactions (MCRs) with combinatorial methods have been used as a convenient approach toward the synthesis of various classes of compounds6,7,8,9. The isocyanide-based multicomponent reactions (IMCRs), such as the versatile well-known Ugi, Passerini and Oakes-Yavari-Nair (OYN) reactions10, is one of the pivotal reactions in this area11. Due to antifungal and antibacterial activities of some aminoimidazo[1,2-a]pyridines, these small drug-like molecules are important class of pharmaceutical compounds11. To date, a number of Lewis and Bronsted acids such as acetic acid, TsOH, Cell-SO3H, RuCl3, MOFs12, MgCl2, SnCl2, ZrCl4, and ZnCl2 have been applied for the synthesis of aminoimidazopyridines via GBB 3-CRs13. Given that some of these catalytic systems suffer from low yields, harsh reactions conditions, long reaction times, tiresome work-up which lead to the generation of large amounts of toxic waste and co-occurrence of several side reactions14,15,16,17,18,19,20,21,22. Afterwards, some of them are impossible to use because of the economy/environmental considerations. Correspondingly, there is enough space for the development of new synthetic methods as an attractive goal.

Polyoxometalates (POMs) are a large group of inorganic anionic clusters, which mostly composed of oxo-bridged early transition metals (TMs) such as tungsten, molybdenum, vanadium, etc., in their highest oxidation states23. Owing to their structural versatilities and tunable chemical and physical properties such as redox behavior, Lewis/Bronsted acidity, molecular structure diversities and high negative charges, they have been applied in a wide range of fields including catalysis, medicine, materials and environment24,25,26,27. To date, a wide variety of POMs have generally been applied as acid and oxidation catalysts, especially Bronsted acids. Albeit, their use as Lewis acid catalysts is limited due to occupation of d orbitals of high-valent metal centers with the surface oxo ligands28,29. In this case, to develop the POMs as catalysts, the physical and chemical properties of them can be adjusted by incorporation of transition-metals into their framework, which can create catalytically active sites in the structure of POMs30,31. However, a problem in POMs applications lies in the necessity of converting soluble POMs to solid materials due to their relatively low surface area (< 10 m2 g−1) and high solubility in polar solvents32. Thus, heterogenizing of POMs makes them encouraging candidates as nanocatalysts for various kinds of chemical reactions and green chemistry33,34. On the basis of previous reports, intercalation of POMs into Layered Double Hydroxides (LDH) is a way to develop the heterogenized POMs-based catalysts heterogeneous catalysts with unique properties. LDHs with general formula [M2+1−xM3+x(OH)2]x+(An−)x/n·yH2O, are a large class of positively charged brucite-like layers with building blocks of divalent and trivalent metal cations as well as exchangeable anions such as Cl−, CO32−, NO3− between the layers.

In this work, the nanoreactor of a Zn3Al–NO3 LDH pillared with the Keggin-type three-nickel-substituted of α-[SiW9O37{Ni(H2O)}3]−10 anions as a atomically thin-type materials were synthesized and confirmed structurally with various techniques including TGA, FT-IR, SEM, X-ray diffraction (XRD), energy dispersive X-ray (EDX), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET) and zeta potential. Here we focus on catalytic application of nickel substituted polyoxometalate intercalated Zn3Al–NO3 layered double hydroxide as a heterogeneous catalyst for the acid-catalyzed synthesis of small molecule of aminoimidazopyridine via the GBB 3-CRs under mild and S-F conditions without the necessity of any Bronsted acid or additives (Fig. 1).

Illustration of the procedure for the SiW9Ni3@Zn3Al nanocomposite and the synthesis route of amino imidazothiazole over the POM–LDH catalyst.

All the chemicals were purchased from commercial companies and used without further purification. Powder X-ray diffraction (XRD) patterns were recorded on a Philips XʼPert MPD diffractometer equipped with Cu Kα radiation (λ = 1.54056 Å) and operated at 40 kV 30 mA. FT-IR spectra were recorded on a Bruker model vector 22 Fourier transform spectrophotometer, using KBr Pellet. Surface areas and pore size distributions were investigated using nitrogen physisorption at 77 K on a Micromeritics Tristar II Plus surface area analyzer. The SEM images and corresponding energy dispersive X-ray (EDX) analytical data were determined by using FESEM-TESCAN MIRA3 scanning electron microscope equipped with an EDX detector. TEM was carried out with a Zeiss-EM10C microscope operating at 80 kV. Thermogravimetric analyses (TGA) were performed by a STA PT-1000 LINSEIS apparatus.

The preparation of SiW9Ni3@Zn3Al nanocomposite was performed through a three-step procedure: (1) synthesis of α-[SiW9O37{Ni(H2O)}3]−10, (2) hydrothermal synthesis of the Zn3Al–NO3 layered double hydroxide and finally (3) intercalation of the [SiW9O37{Ni(H2O)}3]−10 anions into the Zn3Al–NO3 via anion exchange process under N2 atmosphere. Decarbonated-deionized water is used in experiments. It is prepared by boiling and bubbling nitrogen gas into the deionized water to remove the dissolved CO2.

Firstly, 91 g of Sodium tungstate was dissolved in 100 mL of water. After clarifying, 5.5 g of sodium silicate was magnetically dissolved in the above solution. Then 65 mL of HCl acid (6 M) was added to the stirring solution. Next, the mixture was boiled to concentrate it to half of its volume. After cooling down, the solution was filtered, then 20 g of anhydrous sodium carbonate was added to the filtrate. Then, the solution was magnetically stirred for 20 min. Finally, the sodium salt of the a-9-tungstosilicate precipitated. The FT‐IR spectrum matched the literature data35.

Firstly, 3.4 g (12 mmol) NiSO4·7H2O was dissolved in 150 mL of sodium acetate (0.5 M). In the next step, 11.2 g (4 mmol) SiW9 was added to the solution at 70 ºC. After cooling to room temperature, a solution of 4.2 g KCl in 12 mL distilled water was added to yield an iridescent green product. The obtained precipitate was recrystallized from hot water. The FT-IR spectrum matched the literature data36.

In a typical experiment, a solution of 3.8 g Al(NO3)3·9H2O (0.01 mol) and 7.8 g Zn(NO3)2·4H2O (0.03 mol) in 100 ml decarbonated H2O was mixed with a solution of 3.2 g NaOH (0.08 mol) in 100 ml of decarbonated H2O. In two minutes, the obtained slurry was transferred to autoclave, aged for 12 h at 100 ºC. It was washed with decarbonated H2O and ethanol for several times upon cooling to room temperature37.

In a typical procedure, a solution of 3.2 g SiW9Ni3 (1.14 mmol) in a 40 mL of decarbonated water was taken dropwise to the slurry of Zn3Al–NO3 under N2 atmosphere while vigorously stirring. Then the resulted green slurry was stirred for 5 h at 60 °C. Finally, the green precipitate of SiW9Ni3@Zn3Al was filtered, washed with decarbonated water and ethanol for several times to remove the unreacted reagents and dried overnight at 60 °C under a vacuum.

In a typical procedure, to a mixture of aldehyde (1 mmol) and 2-aminopyridines (1 mmol) the SiW9Ni3@Zn3Al catalyst (1 mol%) was added under S-F condition at room temperature. The resulting solution was then stirred well for 5 min. Afterwards, 1.2 mmol of alkyl isocyanide was taken to the reaction media and stirred well at 35 °C for proper time. Progress of the reaction was checked by TLC. At the end of the reaction, after cooling the reaction mixture, CH2Cl2 (4 mL) was added. The catalyst was readily recovered (after the adding of CH2Cl2) from the reaction media using centrifuge (3000 rpm for 10 min) separation. Afterwards, it was washed with diethyl ether and dichloromethane solvents and dried under vacuum to reuse in the next run (ESI).

Zn3Al–NO3 LDH was synthesized successfully via hydrothermally treating of an aqueous solution including Zn(NO3)2·4H2O, Al(NO3)3·9H2O and NaOH. Intercalating POM anions of α-[SiW9O37{Ni(H2O)}3]10− into the Zn3Al–NO3 interlayers under N2 atmosphere leads to the construction of novel intercalated assembly of SiW9Ni3@Zn3Al nanocomposite (Fig. 2).

Schematic illustration of the preparation route for the intercalation of SiW9Ni3 anions into Zn3Al-LDH.

Successful intercalation of SiW9Ni3 anions into the Zn3Al–NO3 is proved by comparison of FT-IR spectra of the Zn3Al–NO3, SiW9Ni3 and SiW9Ni3@Zn3Al nanocomposite (Fig. 3a,b). The FT-IR spectrum of Zn3Al–NO3 precursor shows a sharp peak at ca. 1379 cm−1 which is related to the ν3 stretching vibration of nitrate in the interlayer galleries38. The intensity of the corresponding band in the spectrum of SiW9Ni3@Zn3Al extremely decreases which indicates the large amount of nitrate anions were exchanged with the guest anions. The FT-IR spectrum of SiW9Ni3 indicates characteristic peaks at 987, 939, 889 and 810 cm−1 attributing to the stretching vibrations of Si–O, W–Od, W–Ob and W–Oc, in which d, b, and c represents terminal, corner sharing, and edge sharing oxygen, respectively36. These stretching peaks can be clearly observed in the FT-IR spectrum of SiW9Ni3@Zn3Al. The slight shift of the corresponding bands of SiW9Ni3 in SiW9Ni3@Zn3Al to 973, 946, 898 and 778 respectively can be referred to the hydrogen bonding interactions between LDH layers and POMs anions38,39. All these data demonstrate the successful intercalation of guest anions SiW9Ni3 into the LDH host layers. The XRD patterns of Zn3Al–NO3 and its intercalated product of SiW9Ni3@Zn3Al are shown in Fig. 3c. For Zn3Al–NO3, two sharp basal reflections at 2θ = 10° and 2θ = 20° are indexed to (003) and (006) planes respectively40. According to the XRD spectroscopy of SiW9Ni3@Zn3Al, when the small nitrate anions are exchanged by large SiW9Ni3 anions, the space between the layers of lamellar expand and the basal (003) and (006) reflections of SiW9Ni3@Zn3Al shifts to lower position. For SiW9Ni3@Zn3Al composite, the obvious shift of the characteristic diffraction peak (003) to the left compared to the Zn3Al–NO3 confirms the successful intercalation of POMs. The gallery height value of around 0.98 nm is obtained by subtracting the thickness of the Zn3Al–NO3 layer (0.48 nm) from the value of d(003) spacing of the SiW9Ni3@Zn3Al, which is in accordance with the diameter of Keggin-type POMs41. Furthermore, the diffraction peaks in the XRD pattern of the SiW9Ni3@Zn3Al are obviously broadened due to overlapping of them with the strong characteristics of the polyoxometalates38. Besides, all the diffraction peaks related to pristine ZnAl-NO3 remain unchanged after the intercalation of SiW9Ni3 anions, indicating that the crystal structure of layered double hydroxide is retained (Fig. 3c).

(a, b) FT-IR spectra of Zn3Al–NO3, SiW9Ni3@Zn3Al and SiW9Ni3; (c) XRD pattern of Zn3Al–NO3 and SiW9Ni3@Zn3Al; (d) TGA curves of Zn3Al–NO3 and SiW9Ni3@Zn3Al.

The thermal properties of Zn3Al–NO3 and SiW9Ni3@Zn3Al composite were investigated with TGA thermogram. As can be observed in Fig. 3d, the TGA curves of Zn3Al–NO3 and SiW9Ni3@Zn3Al, have three weight loss levels. The first lost weight of 7.27% and 1.12% for Zn3Al–NO3 and SiW9Ni3@Zn3Al is occurred between 50 and 150 °C respectively. This is ascribed to the evaporation of surface moisture and the structurally bonded intercalated water molecules. The second and the largest weight loss of 25% and 15.3% for Zn3Al–NO3 and SiW9Ni3@Zn3Al at 150 to 500 °C is related to two processes of dehydroxylation and removal of interlayer anions. The second and the largest weight loss of 25% and 15.3% for Zn3Al–NO3 and SiW9Ni3@Zn3Al at 150 to 500 °C is related to the destruction of the layered structure. The last stage of weight loss for Zn3Al–NO3 and SiW9Ni3@Zn3Al can be ascribed to the formation of a spinel phase due to the decay of the mixed metal oxide and decomposition of the POM anions on Zn3Al LDH during the temperature range of 500–80042,43,44. Furthermore, SiW9Ni3@Zn3Al reveals its superior thermal resistance compared to the Zn3Al–NO3 at higher temperatures, by increasing residues from 64% of Zn3Al LDH to 84% of SiW9Ni3@Zn3Al (Fig. 3d).

As represented in Fig. 4, the morphological characteristics of Zn3Al–NO3 and SiW9Ni3@Zn3Al were investigated by SEM and TEM analyses. The pure Zn3Al–NO3 consists of the irregular hexagonal stacks and plates of LDHs crystallites with the thickness of about 26 nm (Fig. 4a,b). As shown in Fig. 4c,d, after intercalation of SiW9Ni3 anions, the lamellar structure of Zn3Al–NO3 plates has not significantly changed, however an obvious separation between the layers can be attributed the effectively hosting of the large polyoxometalates anions. Furthermore, TEM analysis of the SiW9Ni3@Zn3Al represent the Pseudo-hexagonal LDHs lamellae with irregular edges, confirming the results reported from the SEM analysis (Fig. 4e,f). The average size of the Nano sheets is about 300 nm. Moreover, the homogenous distributed dark small dots (yellow arrows) are ascribed to the intercalated SiW9Ni3 anions (Fig. 4h). The LDH platelets are shown by red arrow (Fig. 4h). The size distribution histogram for POM particles (Fig. 4h, inset) shows a mean diameter of 6.5–7 nm, confirming that POM preserves its monodispersity after immobilization on the LDH support.

FE-SEM images of (a, b) Zn3Al–NO3; (c, d) SiW9Ni3@Zn3Al; TEM images of (e–h) SiW9Ni3@Zn3Al. POM particle size histogram for SiW9Ni3@Zn3Al (h, inset).

The EDX results of Zn3Al–NO3 and Zn3Al–SiW9Ni3 revealed the presence of all the elements of the Zn3Al LDH and SiW9Ni3 anions (Zn, Al, O, W and Ni) in the samples which support this assumption that the SiW9Ni3 anions have been exchanged successfully with the interlayer NO3− anions of Zn3Al LDH (Fig. 5a,b). Zeta potential as a standard characterization technique, was used to evaluate and SiW9Ni3@Zn3Al surface charge. According to current study, the interlayer nitrate anions are likely to be exchanged with SiW9Ni3 anions with high negative charge, leading to increase the surface charge of the nanocomposite. It can be seen in Fig. 5c the zeta potential of the Zn3Al–NO3 shifted from a positive value (37.3) to a negative value (− 20.9) in SiW9Ni3@Zn3Al nanocomposite. As a result, the increase of the charge density in SiW9Ni3@Zn3Al nanocomposite can be ascribed to the successful intercalation of POM anions into Zn3Al-LDH (Fig. 5c). As shown in Fig. 5d the adsorption isotherm of the SiW9Ni3@Zn3Al illustrate a type IV isotherm at lower pressure (P/P0 < 0.1) with H3 type hysteresis loops. According to the Brunauer, Deming, Deming and Teller (BDDT) classification the adsorption isotherm confirm the presence of39,45,46. Furthemore, BET data revealed that the specific surface area of SiW9Ni3@Zn3Al (46 m2/g) is significantly increased in comparison with the reported data of Zn3Al–NO3 (9 m2/g) in other works40. This finding probably caused by the interlayer opening due to the existence of POM anion.

EDX patterns of (a) Zn3Al–NO3 and (b) SiW9Ni3@Zn3Al; zeta-potentials of (c) Zn3Al–NO3 and SiW9Ni3@Zn3Al; (d) Adsorption–desorption isotherm of SiW9Ni3@Zn3Al.

After careful characterization of the composite, the catalytic activity of SiW9Ni3@Zn3Al was investigated for the Ugi-like three-component synthesis of imidazopyridines as small biologically interest molecules11,47,48. In this study, the reaction between 1 mmol of 2-aminopyridine, 1 mmol of benzaldehyde, and 1.2 mmol of cyclohexyl isocyanide was selected as benchmark model reaction (Table 1S). Due to the important role of solvents in this reaction, the influence of the various solvents as well as solvent-free (S-F) condition were evaluated. Solvents such as toluene, H2O, EtOH, MeOH and CH2Cl2 were used with different times and reaction temperature in the model reaction (Table 1S, entries 1–8). However, the obtained data in Table 1S explains high yield of 3-aminoimidazo[1,2-a]pyridine (94%) synthesized under S-F condition, in 1 h and 35 °C (Table 1S, entry 16). Therefore, the influence of the catalyst dosage, temperature and reaction time was investigated to define the optimum conditions for the three-component synthesis of imidazopyridines, in S-F condition. The results indicate that under the constant amount of catalyst and reaction time, an increase of temperature from 25 to 35 °C resulted in the sharp increase of the yield of the reaction in S-F condition (Table 1S, entries 8, 9). Furthermore, experimental data indicate that increase in temperature results in higher yields in the other solvents as well [50 °C in water (Table 1S, entries 1, 2) and 30 °C in ethanol (Table 1S, entries 4, 5)]. Additionally, the results were clearly demonstrated that by increasing the catalyst dosage in a constant temperature, the yield of the product increased (entries 13 and 16). Moreover, the yield of the product raised by increasing the reaction time from 0.5 to 1 h (ESI).

To investigate the role of both SiW9Ni3 and Zn3Al–NO3 components in the progress of model reaction under optimized reaction conditions, a series of control experiments was performed (Table 1). It can be inferred from the results that the homogeneous form of SiW9Ni3 (Table 1, entry 1) exhibited a higher activity in comparison with the host Zn3Al-LDH (Table 1, entry 2) under identical conditions. The above results indicate that the inserted POM anions in the SiW9Ni3@Zn3Al composite are probably the main catalytic active sites. Due to the higher catalytic performance of SiW9Ni3@Zn3Al composite (Table 1, entry 3) than either of the individual constituents alone, it can be say that intercalating of SiW9Ni3 anions into the Zn3Al–NO3 interlayers can combine both Bronsted/Lewis acid sites of POM anions and Lewis acid effect of Zn2+ of Zn3Al–NO3 layered double hydroxide37,49,50. The cooperative effect of this catalytic system was demonstrated by the synthesis of aminoimidazopyridines with a good yield.

According to Table 2S, to expand the generality of this process, a series of substrates 1, 2 and 3 were examined with SiW9Ni3@Zn3Al as the catalyst under the optimized conditions. The results show that all the aldehyde derivatives of the isocyanides and aminopyridines offered good to excellent yields. A closely look to the data displayed in the Table 2S, it is observed that Aryl aldehydes with electron-deficient groups (entries 2, 3, 4) accelerate the reaction compared to benzene (entry 1) while the electron-donating groups (entries 6–12) bound to the 2-aminopyridine ring required longer reaction times albeit with lower yields (ESI).

In order to ascertain the heterogeneity of the SiW9Ni3@Zn3Al catalyst, hot filtration experiment was carried out. The catalyst was filtered from the reaction media after short reaction time. Then the reaction was checked if it proceeds in the absence of the catalyst under the same reaction conditions or not. However, it was observed that upon removal of catalyst no progress has been occurred even after carrying out the reaction mixture for longer duration confirming that the catalysis was true heterogeneous.

To investigate the recycling of the SiW9Ni3@Zn3Al, six reaction cycles have been tested. In each cycle, the solid catalyst was centrifuged and readily filtered from the reaction medium and then used in the next cycle. As illustrated in Fig. 1S, the catalyst shows high catalytic performance at least in 5 consecutive runs. However, the reaction time increased after fifth run (100 min). The FT-IR spectrum of the used catalyst revealed that the structure of the SiW9Ni3@Zn3Al catalyst almost retained its structural composition, even after six consecutive runs (Fig. 1Sb). Also, XRD spectra of the fresh and reused catalyst confirm the retention of SiW9Ni3@Zn3Al structural integrity (ESI).

In summary, the POM anions of SiW9Ni3 has been confirmed to intercalated into the interlayers of Zn3Al-LDH, leading to the formation of the SiW9Ni3@Zn3Al via the selective ion-exchange synthetic approach. In the synthesis of amino imidazopyridines via three-component Ugi-like reaction (isocyanide-based), SiW9Ni3@Zn3Al illustrates better catalytic performance (yield: ~ 98%) than those of SiW9Ni3 and Zn3Al–NO3, both individual constituents. Moreover, the SiW9Ni3@Zn3Al composite showed remarkable catalytic activity for the synthesis of amino imidazothiazole with high yields under mild and S-F conditions as well. In particular, Zn3Al–NO3 not only shows excellent capacity to act as a support for highly dispersed and firmly immobilized SiW9Ni3 guests but also contributes to improve the catalytic activity of composite via the synergic effect of Lewis acid effect of Zn2+ of Zn3Al–NO3 layered double hydroxide and Bronsted/Lewis acid sites of POM anions. Additionally, according to SEM and BET results, the separation of the LDH layers by the uniform dispersion of POM entities in the LDH gallery and significant increase in specific surface area is not negligible in the catalytic performance of SiW9Ni3@Zn3Al. Furthermore, recovery experiments exhibit that the catalyst can be easily separated from the reaction media and be reused for more than 5 cycles without obvious decrease in catalytic performance.

All data generated or analysed during this study are included in this published article (and its Supplementary Information files).

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Organic and Nano Group (ONG), Department of Chemistry, Iran University of Science and Technology (IUST), P.O. Box 16846-13114, Tehran, Iran

Azra Ghiasi Moaser & Sadegh Rostamnia

Department of Chemistry, University of Kurdistan, P.O. Box 66135-416, Sanandaj, Iran

Ahmad Gholami Afkham & Roushan Khoshnavazi

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Dr A.G.M. wrote the main manuscript text and did perform the experimental tests. A.G.A. did perform the experimental tests. Prof. S.R., and Prof. R.K., are supervisors and reviewed the manuscript.

Correspondence to Roushan Khoshnavazi or Sadegh Rostamnia.

The authors declare no competing interests.

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Ghiasi Moaser, A., Afkham, A.G., Khoshnavazi, R. et al. Nickel substituted polyoxometalates in layered double hydroxides as metal-based nanomaterial of POM–LDH for green catalysis effects. Sci Rep 13, 4114 (2023). https://doi.org/10.1038/s41598-023-31356-7

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Received: 13 October 2022

Accepted: 10 March 2023

Published: 13 March 2023

DOI: https://doi.org/10.1038/s41598-023-31356-7

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