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. 2022 Aug 11;7(33):29356–29368. doi: 10.1021/acsomega.2c03603

Palladium-Supported Polydopamine-Coated NiFe2O4@TiO2: A Sole Photocatalyst for Suzuki and Sonogashira Coupling Reactions under Sunlight Irradiation

Prashanth Goud Banda 1, Raghasudha Mucherla 1,*
PMCID: PMC9404510  PMID: 36033688

Abstract

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The effective utilization of solar energy in synthetic organic chemistry has gained extensive attention owing to its enormous energy and environmentally benign nature. In this context, we designed and synthesized a magnetically retrievable, sole palladium (Pd)-supported polydopamine-coated core@shell (NiFe2O4@TiO2) heterogeneous nanophotocatalyst for Suzuki and Sonogashira coupling reactions under sunlight irradiation. The synthesized catalyst was characterized by powder X-ray diffraction (PXRD), Fourier-transform infrared, UV–vis, scanning electron microscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and vibrating sample magnetometer analysis. The photocatalytic activity of the synthesized nanocatalyst under sunlight irradiation was assessed for both Suzuki and Sonogashira coupling reactions, where it worked excellently well with a high yield of the product up to 98 and 96%, respectively. Its efficacy was also investigated in the conversion of substituted substrates in both the coupling reactions into desired biaryls and diarylacetylenes. Unique features of the synthesized catalyst are (i) its effective performance for both the aforesaid coupling reactions under ambient reaction conditions for a short reaction time in polar protic solvents (ethanolic water/EtOH) with good yield without any byproduct, (ii) magnetic retrieval of the catalyst from the reaction mixture employing an external magnet is an added advantage, and (iii) the retrieved catalyst could potentially be reutilized for up to five consecutive runs without appreciable diminution of catalytic efficacy, and its stability was confirmed by inductively coupled plasma optical emission spectroscopy analysis and XRD.

1. Introduction

Solar energy has considerable potential as a green energy resource owing to its superabundance, cost efficiency, and non-polluting nature. The use of sunlight to carry out chemical reactions, frequently named photo-catalysis, is a significant method to harness solar energy.1−3 It shows good potency in a number of chemical processes such as photocatalytic degradation of pollutants, photocatalyzed organic reactions in the presence of various nanostructures, and so forth.4−6 Two important phenomena in the photocatalysis process are efficient photogeneration of the electron–hole (e––h+) pair and their separation.7,8 The use of photo-generated holes or electrons for oxidation or reduction of organic molecules is an important aspect in light-driven chemical reactions. Regardless, the simultaneous application of both the photo-generated e––h+ pairs for organic chemical reactions provides an outstanding catalytic perspective for cost-efficient and environmentally benign synthesis. Very limited reports are available on this aspect, and it has grabbed the attention of researchers to take it as a challenge in synthetic organic chemistry.9−11

Organic reactions involving C–C bond coupling (Suzuki and Sonogashira) are extremely significant with convenient approaches in synthetic organic chemistry in the preparation of natural products, pharmaceutical drugs, functional conjugated organic molecular materials, and so forth.12−15 The traditional way of carrying out coupling reactions is the homogeneous catalysis using Pd/Pd complexes.16 The notable limitations associated with the homogeneous Pd/Pd complex catalyst are its non-reusability, air and water sensitivity, and product contamination by residual Pd/ligands, thus making it inseparable.17 These limitations accompanying the homogeneous catalysis motivated the scientific community to develop novel approaches in the form of heterogeneous catalysis with a focus on catalyst recovery and reuse.18−21 Thus, development of eco-friendly heterogeneous photocatalysts for various organic coupling reactions with excellent stability, reusability, separability, and activity under ambient reaction conditions is crucial for synthetic organic applications.22,23

For the efficacious harvest of solar energy, several photocatalysts have been developed. TiO2 is a well-known photocatalyst, but its usage is restricted due to a wide band gap (3.2 eV) that falls in the UV region. Due to environmental concerns, there is an urgency to perform the photocatalytic activity under visible light irradiation.24−26 Consequently, the photocatalyst that absorbs visible light and that can be easily separable from the reaction mixture is the pressing priority. Incorporating magnetic materials into solid matrices is the best choice that enables the integration of prominent methods for both photo-catalysis and magnetic separation.27 Among the magnetic materials, spinel ferrites have extraordinary properties such as a low band gap, good stability against photo-corrosion, unique superparamagnetic nature, easy preparation, low cost, high adsorption capacity, and so forth.28 Among the magnetic spinel ferrites, NiFe2O4, as an n-type semiconductor with a low band gap (∼1.63 eV), has attracted much attention due to its effective light absorption capacity and stable physical and chemical properties. In accordance with the aforesaid facts, it is expected and reported that the integration of TiO2 (high band gap) with NiFe2O4 (low band gap) leads to a core–shell material with a tuned band gap for visible light absorption. The resulting material thus possesses better magnetic separation for use as a good photocatalyst.29,30

To make this photocatalyst suitable for Suzuki and Sonogashira coupling reactions, we propose incorporating Pd nanoparticles (NPs) onto the NiFe2O4@TiO2 core@shell material owing to the effectiveness of Pd in catalyzing the coupling reactions. For the past few years, it has been reported that the supported Pd NPs have been explored to be a substitute for Pd complexes as a catalyst to overcome its limitations.31−34 For good binding of Pd particles on the surface of the catalyst, it is an established fact that polydopamine (PDA) could be used as a universal surface modifying agent. It is because of the fact that PDA can form coordinate bonds with transition metal ions via its N- and O-binding sites, which can easily be reduced to metal NPs. Thus, it results in the formation of metal-supported PDA that could be used as an effective catalyst.35−37

Reports on the availability of a sunlight-driven sole magnetic photocatalyst under ambient conditions for both Suzuki and Sonogashira coupling reactions are scarce. Hence, in the present work, we propose to synthesize Pd(0) NPs supported on PDA-coated NiFe2O4@TiO2 (NiFe2O4@TiO2@PDA-Pd) as a nanophotocatalyst for C–C coupling reactions. Pd(0) NPs can be supported on the NiFe2O4@TiO2@PDA material via a simple method involving immersion of Pd(II) ions in NiFe2O4@TiO2@PDA followed by their reduction with sodium borohydride. In Suzuki and Sonogashira coupling reactions, this catalyst is expected to exhibit effective photo-catalytic activity under sunlight absorption and is validated in the present work. Furthermore, the NiFe2O4@TiO2@PDA-Pd can be easily separated with an external magnet for its reusability, without appreciable loss in catalytic efficacy.

2. Experimental Section

2.1. Materials

Ferric nitrate (Finar, 99%); nickel nitrate (Finar, 99%); titanium(IV) isopropoxide (Sigma-Aldrich, 99%); dopamine hydrochloride (98%); PdCl2 (Sigma-Aldrich, 99%); NaBH4 (Finar, 99%); NaOH (Finar, 96%); HNO3 (Finar, 69%); methanol (MeOH, Finar, 99%); ethanol (EtOH, Finar, 99%); ethyl acetate (EtAC, Finar, 99%); and n-hexane (Finar, 98%) were used as starting materials, and double distilled (DD) water was used all through the experiments.

2.2. Synthesis of NiFe2O4 NPs

Nickel ferrite (NiFe2O4) NPs were synthesized using the hydrothermal method. In this method, Ni(NO3)2·6H2O and Fe(NO3)3·9H2O were taken in a 1:2 ratio and dissolved in 40 mL of DD water. A clear solution was obtained after 15 min of stirring at room temperature (RT). The pH of the solution was adjusted to 12 using 2 M NaOH solution with continuous stirring for 30 min. The resulting solution was placed in a stainless-steel autoclave and was heated at 180 °C for 12 h. Then, it was allowed to cool to RT. The attained product was washed three times with DD water and ethanol, followed by drying in an oven at 60 °C. Finally, it was subjected to calcination at 800 °C for 2 h. Thus, NiFe2O4 NPs were prepared.

2.3. Synthesis of NiFe2O4@TiO2 (core@shell) NPs

Initially, 1 g of synthesized nickel ferrite (NiFe2O4) was dispersed in 50 ml of methanol. The mixture was magnetically stirred for 15 min. 2.5 g of titanium tetraisopropoxide [yield of TiO2 (anatase): 1 g] was then introduced into the mixture and stirred for 10 min, followed by the addition of 10 mL of DD water. After 10 min, HNO3 was added slowly to maintain the pH of the solution at 2. The resulting solution was continuously stirred for 90 min, turning into a gel-like material. The gel was dried in an oven at 60 °C for 1 h and calcined at 500 °C for 2 h. NiFe2O4@TiO2 NPs were thus prepared.

2.4. Surface Modification of NiFe2O4@TiO2 with PDA

1 g of synthesized NiFe2O4@TiO2 NPs was added to 500 mL of Tris buffer (10 mM, pH 8.5). 1 g of dopamine was then introduced into the resulting solution. The resulting mix was mechanically stirred at RT for 24 h. During the process, dopamine was polymerized to PDA and got coated over NiFe2O4@TiO2, resulting in the formation of NiFe2O4@TiO2@PDA NPs. PDA-coated NiFe2O4@TiO2 was separated employing an external magnet at the end of the reaction and was washed with DD water and ethanol, followed by drying in an oven at 40 °C to form the surface-modified NiFe2O4@TiO2 with PDA.

2.5. Synthesis of the NiFe2O4@TiO2@PDA-Pd Catalyst

1 g of synthesized NiFe2O4@TiO2@PDA was dispersed in 200 mL of DD water for 20 min. Subsequently, 0.05 g of PdCl2 in 20 mL of water was introduced into the reaction mixture with stirring for 24 h. Consequently, with vigorous stirring, 0.05 g of NaBH4 was added to the reaction mixture. During the process, Pd(II) got reduced to Pd(0) and deposited on NiFe2O4@TiO2@PDA. After 1 h of stirring, the resulting Pd-supported NiFe2O4@TiO2@PDA (NiFe2O4@TiO2@PDA-Pd) was isolated with the aid of an external magnet, washed thoroughly with DD water, and then dried at 60 °C under vacuum for 12 h.

2.6. Photocatalytic Suzuki Coupling Reaction

The photocatalytic activity of the prepared catalyst for a typical Suzuki coupling reaction (SCR) between aryl halides and arylboronic acid was investigated. In this process, aryl halides (1 mmol), arylboronic acid (1.5 mmol), K2CO3 (2.5 mmol), and the NiFe2O4@TiO2@PDA-Pd catalyst (5 mg) were mixed in a round-bottom (RB) flask with 3 mL of EtOH and H2O as a solvent in a 1:1 volume ratio. The reaction mixture was continuously stirred under direct sunlight from 11.00 am to 3.00 pm. The average intensity of the sunlight was measured to be 50–60 mW/cm2 using a Newport Optical Power Meter (model 842.PE) with an average outdoor temperature of 30 °C. On completion of the reaction [as confirmed by thin-layer chromatography (TLC)], the catalyst was isolated by simple means with the aid of a magnet. After being extracted twice with ethyl acetate, the products were purified using column chromatography. 1H and 13C NMR spectral analysis was performed to analyze the products. The separated catalyst was thoroughly washed with DD water and ethanol (three times) for recycling applications, and the dried catalyst (at 60 °C overnight) was used in the next run.

2.7. Photocatalytic Sonogashira Coupling Reaction

The photocatalytic performance of the prepared catalyst for a typical Sonogashira coupling reaction between aryl halides and arylacetylene to yield diarylacetylene was investigated. In this experiment, aryl halides (1 mmol), arylacetylene (1.3 mmol), K2CO3 (2 mmol), and the NiFe2O4@TiO2@PDA-Pd catalyst (10 mg) were mixed in an RB flask with 3 mL of the EtOH solvent. The reaction was continuously stirred under the irradiation of sunlight at an average outdoor temperature of 30 °C. On completion of the reaction (as confirmed by TLC), the catalyst was set apart with the aid of a magnet. After being extracted twice with ethyl acetate, the products were purified using column chromatography. 1H and 13C NMR spectral analysis was performed to analyze the products. The separated catalyst was washed with DD water and ethanol for recycling applications, and the dried catalyst (at 60 °C overnight) was used in the next run.

2.8. Characterization of the Catalyst

Powder X-ray diffraction (PXRD) analysis of the synthesized materials (NiFe2O4, NiFe2O4@TiO2, and NiFe2O4@TiO2@PDA-Pd) was carried out on a PAN Analytical Advance X-ray diffractometer with Ni-filtered Cu Kα (λ = 1.5406 Å) radiation in a 2θ scan range between 10 and 60° to assess the crystalline nature of the catalyst. The Fourier-transform infrared (FT-IR) spectrum for all the materials was recorded in the range of 4000–400 cm–1 using the PerkinElmer Spectrum using the KBr pellet technique. The surface morphology of the synthesized photocatalyst was examined using scanning electron microscopy (SEM, Carl Zeiss SMT Ltd., Zeiss EVO 18), transmission electron microscopy (TEM), and selected area electron diffraction (SAED) (TEM, Jeol/JEM 2100 at 200 kV). X-ray photoelectron spectroscopy (Kratos/Shimadzu Amicus, Model: ESCA 3400) was used to determine the binding energies of elements in the catalyst. UV–vis diffuse reflectance spectra of all the materials was recorded on Analytik Jena, SPECORD 210 PLUS at RT. The magnetic hysteresis curves of the catalyst were recorded using a vibrating sample magnetometer (VSM, Lake Shore, Model: 8600 Series). Inductively coupled plasma optical emission spectroscopy (ICP-OES) analysis was aimed to ascertain the quantity of Pd in the synthesized nanocatalyst (PerkinElmer Optima 5300 DV). 1H NMR and 13C NMR spectra were recorded on an ADVANCED-III Bruker 400 MHz NMR spectrometer using CDCl3 as the solvent and tetramethylsilane as an internal standard where chemical shifts are mentioned as parts per million (ppm).

3. Results and Discussion

3.1. Preparation of the NiFe2O4@TiO2@PDA-Pd Catalyst

The NiFe2O4@TiO2@PDA-Pd catalyst was synthesized by a multistep procedure (Scheme 1). In step I, the NiFe2O4 NPs were prepared by the hydrothermal method. In step II, the in situ NiFe2O4@TiO2 core@shell structure was prepared via the sol–gel method. In step III, NiFe2O4@TiO2 NPs were surface-modified by PDA where dopamine was polymerized in Tris buffer solution (10 mM, pH 8.5) under continuous stirring. Finally, in step IV, palladium(0) NPs were supported on NiFe2O4@TiO2@PDA by impregnation of Pd(II) ions over the surface of the polymer (PDA) layer followed by its subsequent reduction with sodium borohydride. This led to the synthesis of the palladium-supported PDA-coated core@shell nanophotocatalyst (NiFe2O4@TiO2@PDA-Pd). An external magnet was used to isolate the synthesized photocatalyst, which was then dried under vacuum conditions for further use. The overall synthesis of the nanophotocatalyst is depicted in Scheme 1.

Scheme 1. Preparation Path of the NiFe2O4@TiO2@PDA-Pd Nanophotocatalyst.

Scheme 1

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3.2. Characterization of the NiFe2O4@TiO2@PDA-Pd Catalyst

The indexed XRD patterns of the synthesized NiFe2O4, NiFe2O4@TiO2, and the NiFe2O4@TiO2@PDA-Pd catalyst are shown in Figure 1. The broad peaks observed in the figure reveal the nanoscale range of the particles possessing a small crystallite size. The observed peaks in Figure 1a(I) at 2θ values of 18.5, 30.4, 35.8, 37.3, 43.4, 53.8, 57.4, and 63.0° are attributed to (111), (220), (311), (222), (422), (511), and (440) diffractions, respectively, signifying the formation of single-phase pure crystalline spinel NiFe2O4 (ICDD card no. 10–0325). A small peak was detected in the figure at 2θ of 33.2° for the NiFe2O4 sample calcined at 800 °C, which corresponds to a small quantity of the impure phase of α-Fe2O3 that occurs naturally as hematite (ICDD card 33-0664).38 The additional peaks appeared at 2θ of 25.3 and 48.1° along with the diffraction peaks of NiFe2O4 in Figure 1a(II) attributed to (101), (200) diffractions of anatase (JCPDS card no. 78-2486), thus signifying the formation of NiFe2O4@TiO2 NPs.39 The diffraction patterns of the catalyst in Figure 1a(III) depict that the crystallinity of NiFe2O4@TiO2 NPs was intact and not altered despite the PDA coating and Pd loading as well. Also, Figure 1a(III) has no noticeable peak related to Pd NPs owing to the low palladium content on the PDA surface.

Figure 1.

Figure 1

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(a) XRD spectra and (b) FTIR spectra of samples.

FT-IR spectra of the prepared samples are shown in Figure 1b. Two significant peaks were noticed in the range of 600–400 cm–1 for all the samples characteristic of the spinel structure. The peaks detected at 406 and 596 cm–1 correspond to the intrinsic vibrations of metal ion–oxygen complexes in octahedral and tetrahedral sites in the spinel structure, respectively, and the peaks around ∼1600 and ∼3400 cm–1 represent the bending and stretching mode of surface-adsorbed H2O and also the stretching mode of OH groups [Figure 1b(I)]. The peaks that appeared at 1505 and 1280 cm–1 in Figure 1b(III), which are not seen in Figure 1b(I,III), were attributed to C=C stretching and C–N stretching modes, respectively, that indicated the presence of −C=C–NH functional groups of PDA. The observed peak at around ∼3390 cm–1 indicates the presence of −OH of phenol in NiFe2O4@TiO2@PDA. These outcomes infer that PDA has been successfully deposited on the surface of NiFe2O4@TiO2 NPs by its adsorption. In the FTIR spectrum of the NiFe2O4@TiO2@PDA-Pd nanocatalyst, no dramatic changes were observed as evident from Figure 1b(IV). Meanwhile, the peak intensity observed at 1505 and 1280 cm–1 has shifted to a low frequency owing to the bonding interactions between the PDA functional groups and the Pd NPs.40,41

The surface morphology of the synthesized nanocatalyst NiFe2O4@TiO2@PDA-Pd was observed by SEM images shown in Figure 2a,b that represents a near spherical cluster-like structure of the catalyst. Keen examination of the image depicts the presence of small particles supported on a continuous layer over a core–shell justifying the immobilization of Pd NPs on the PDA layer over the NiFe2O4@TiO2 core–shell structure as NiFe2O4@TiO2@PDA-Pd. Furthermore, the energy-dispersive X-ray spectroscopy (EDX) detector attached to SEM was used to establish the existence of Pd particles over PDA on NiFe2O4@TiO2 NPs. The SEM–EDX spectrum shown in Figure 2c describes the presence of Pd, N, Ti, Fe, Ni, C, and O elements in the catalyst. Thus, the SEM–EDX images portray the successful coating of PDA on NiFe2O4@TiO2 and also effective loading of Pd over the surface of NiFe2O4@TiO2@PDA. Accumulation of Pd NPs on the surface of PDA in the catalyst was also confirmed by TEM analysis. TEM images portray a spherical shape of the NPs in the catalyst, thus further confirming the morphology observed by SEM. The TEM image in Figure 2d reveals the presence of a thin continuous PDA layer around NiFe2O4@TiO2 with a thickness of about 15.24 nm. The two TEM images shown in Figure 2e,f noticeably represent the thick and uniform distribution of small Pd NPs throughout the PDA surface. They depict the magnified images at 100 and 200 nm where Pd NPs are homogeneously decorated on the peripheral surface of NiFe2O4@TiO2@PDA without large agglomeration, inferring that Pd NPs are effectively immobilized on the surface of PDA.

Figure 2.

Figure 2

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(a,b) SEM images, (c) EDX, (d) PDA layer, (e,f) TEM images with a particle size histogram, (g) HRTEM image, and (h) SAED pattern of NiFe2O4@TiO2@PDA-Pd.

The particle size distribution histogram of the catalyst which is embedded in Figure 2e,f estimated the average size of the Pd NPs to be around 28.6 nm. It was found that the dark Pd NPs were coated over the gray PDA layer on the dark core–shell of NiFe2O4@TiO2. These TEM images are in accordance with SEM information with respect to the morphology. The high-resolution TEM (HRTEM) image shown in Figure 2g is indicative of the number of grains with different orientation of the planes, thus confirming the polycrystalline nature of the material. The lattice fringe spaces of 0.30 nm shown in the figure could possibly be ascribed to the (111) crystal plane of Pd NPs. The SAED pattern of NiFe2O4@TiO2@PDA-Pd is depicted in Figure 3h. It shows diffraction rings composed of a bright spot possessing sixfold symmetry that manifests the polycrystalline nature of the material.

Figure 3.

Figure 3

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(a) Ti 2p peaks, (b) N 1s peak, (c) Pd 3d peaks, and (d) magnetization curve of NiFe2O4@TiO2@PDA-Pd; inset: zoomed-in region of the area under the curve.

X-ray photoelectron spectroscopy (XPS) was employed to confirm the effective coordination of Pd on the PDA layer. It is a powerful tool to understand the electronic properties of the coordinated particles on the surface such as the electron environment, binding energy, and chemical valence states of the metals. The XPS spectra of the NiFe2O4@TiO2@PDA-Pd nanophotocatalyst are shown in Figure 3 where the chemical valence states of Ti, N, and Pd in the catalyst were analyzed.

The two noticeable bands at binding energies 458.4 and 464.9 eV were ascribed to the Ti 2p3/2 and Ti 2p1/2 photoelectrons in the Ti4+ chemical state, respectively, whereas the two peaks at 455.4 and 463.4 eV were attributed to the Ti 2p3/2 and Ti 2p1/2 photoelectrons in the Ti3+ state in the TiO2 chemical state, respectively (Figure 3a).42 The peak at 399.7 eV in Figure 3b represents the N1s photoelectrons of the NH group. It is evident from the N1s spectrum of Figure 3b that the NiFe2O4@TiO2 core@shell NPs were successfully coated with PDA. Furthermore, the two observed bands at binding energies 335.3 and 340.6 eV in Figure 3c can be indexed as Pd(0) 3d5/2 and Pd(0) 3d3/2, respectively. These values confirm the presence of Pd(0) in the prepared catalyst which was not noticeable in XRD. These results were in accordance with the values of metallic Pd.43 The magnetic performance of the synthesized nanocatalyst was investigated with the VSM at RT. Figure 3d demonstrates the magnetization curve of the NiFe2O4@TiO2@PDA-Pd catalyst. From the figure, the saturation magnetization (Ms), coercivity (Hc), and remanence magnetization (Mr) are found to be 31.9 emu/g, 0.146 kOe, and 7.57 emu/g, respectively. The magnetization data reveals the good magnetic behavior of the synthesized catalyst, thus becoming evidential of the magnetic recovery and reusability of the catalyst.

The UV–vis diffuse reflectance spectra of the synthesized NiFe2O4, NiFe2O4@TiO2, NiFe2O4@TiO2@PDA, NiFe2O4@TiO2@PDA-Pd, and pure TiO2 were recorded, and the results are depicted in Figure 4a. It is obvious from the figure that pure TiO2 and NiFe2O4 show absorption bands with absorption edges at 400 and 700 nm, respectively, as illustrated in Figure 4a(I,II), indicating the absorption of TiO2 in the UV region and that of NiFe2O4 in the visible region. However, after the surface modification of NiFe2O4 with TiO2, the obtained core@shell (NiFe2O4@TiO2) material also exhibited the band with the absorption edge in the visible region as seen in Figure 4a(III), confirming the ability of NiFe2O4@TiO2 to absorb visible light. Even after coating NiFe2O4@TiO2 with PDA and also supported by the metal (Pd) on its surface, the resulting NiFe2O4@TiO2@PDA-Pd magnetic photocatalyst still exhibits absorption in the visible region as evident from Figure 4a(IV,V). The band gap energy (Eg) of all the samples was estimated from the Tauc plot of (αhυ)2 versus hυ as presented in Figure 4b. Extrapolation of the hυ value to α = 0 results in absorption band gap energy (Eg). As seen from Figure 4b, Eg for pure NiFe2O4 and TiO2 was found to be 1.67 and 3.29 eV, respectively, which is in accord with the reported values.44,45 In contrast, the band gap energy of NiFe2O4@TiO2 was observed to be 1.63 eV which indicates the absorption in the visible region. Furthermore, the decrease in energy gap (Eg) upon core@shell formation confirms the electronic coupling between NiFe2O4 and TiO2. After surface modification with PDA supported by the Pd metal, an even stronger visible-region band gap energy of 1.22 eV was observed for the NiFe2O4@TiO2@PDA-Pd nanocatalyst.

Figure 4.

Figure 4

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(a) UV–vis absorption spectra and (b) band gap energies of the samples.

3.3. Application of the NiFe2O4@TiO2@PDA-Pd Catalyst in Suzuki and Sonogashira Coupling Reactions under Sunlight

In the past few decades, Pd has been employed as an active catalyst for C–C coupling reactions. Nevertheless, most of the times, the coupling reactions with Pd as a catalyst take place under heating conditions, which consumes lot of energy. Therefore, it would be a significant improvement if we could improve the catalytic activity of Pd as a catalyst at ambient temperatures using the visible region of the sunlight which is an abundant and environmentally sustainable energy source. As our synthesized catalyst shows absorption in the visible region, we tried to test the validity of our catalyst for the Suzuki and Sonogashira coupling reactions under natural sunlight under ambient conditions (photocatalytic coupling reactions).

3.3.1. Suzuki Coupling Reaction

A simple SCR involving aryl halides and arylboronic acid was performed using the synthesized NiFe2O4@TiO2@PDA-Pd nanophotocatalyst under sunlight, at an average outdoor temperature of 30 °C. Optimization of various vital reaction conditions for the SCR, viz., nature of the solvent, base, light source, and Wt % of Pd, was performed. The effect of various solvents in the presence of K2CO3 as a base with 5% of Pd by weight on the photocatalytic SCR was observed. The obtained yield of the product was low in the presence of polar aprotic solvents, namely, dimethyl sulfoxide and dimethylformamide, and also in the presence of nonpolar solvents such as toluene (Table S1, entries 1–3). However, observed yield of the product was high in the presence of polar protic solvents such as ethanol and methanol (Table S1, entries 4,5). Furthermore, the reaction in pure H2O resulted in moderate yield (Table S1, entry 6) of the product. It was observed that 98% yield of the product was obtained in the presence of a mixture of EtOH and H2O as a solvent in a 1:1 ratio, indicating the significant enhancement in the photocatalytic activity (Table S1, entry 7). These results infer that photocatalyzed Suzuki reactions in the presence of the NiFe2O4@TiO2@PDA-Pd nanophotocatalyst require protic solvents. Furthermore, the influence of other bases (Cs2CO3, NaOH, Et3N) (Table S1, entries 12–14) in the solvent EtOH·H2O (1:1) was also explored, but good yield was observed in the presence of only K2CO3 as a base among all (Table S1, entry 7).

To study the influence of light on the SCR, the reaction was performed in dark at RT and also at 60 °C. It was found that moderate yields (30 and 64%) (Table S1, entries 15,16) were obtained in dark at RT and at 60 oC, respectively. While performing the reaction under visible light (Hg lamp 250W), the product yield was improved (85%) (Table S1, entry 17). To test the feasibility of environmental concerns, the reaction was initiated in natural sunlight, and an excellent yield (98%) of the product was observed. Furthermore, no product was observed in the presence of NiFe2O4, NiFe2O4@TiO2, and NiFe2O4@TiO2@PDA separately. Thus, this study indicates the significance of Pd presence in the synthesized nanocatalyst (NiFe2O4@TiO2@PDA-Pd) in carrying out the SCR.

The choice of Pd loading as 5% by weight in all the aforementioned optimization experiments was made based on the previously reported values in different catalysts.40,41 Even though we got good yield (98%) with 5% loading of Pd, to test the effect of Pd loading, we performed the reaction, and the yield was monitored with different Pd loadings such as 1, 2.5% (<5%), and with 7.5% (>5%) for the same reaction time as that of 5% Pd loading (Table 1). Low yield was observed with 1 and 2.5% (30% and 65%, respectively), whereas the same yield (98%) was observed with 7.5%. Thus, the efficacy of the catalyst in the coupling reaction was proved to be good with a Pd loading of 5% by weight (Table 1, entry 3).

Table 1. Influence of Catalyst Loading on the Suzuki Coupling Reactiona.
S. No. catalyst loading (wt %) yield (%)b
1 1 30
2 2.5 65
3 5 98
4 7.5 98
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a

Reaction conditions: iodo benzene (1.0 mmol), phenyl boronic acid (1.5 mmol), NiFe2O4@TiO2@PDA-Pd catalyst (5 mg), and K2CO3 (2.5 mmol) in EtOH·H2O (3 mL) under sunlight at 30 °C for 0.5 h.

b

Isolated yields.

The reaction generality was further investigated by NiFe2O4@TiO2@PDA-Pd under the sunlight using several aryl halides and substituted arylboronic acids to validate the scope of the synthesized catalyst (Table 2). It is observed that the presence of electron-withdrawing groups (EWGs) and electron-donating groups (EDGs) produces outstanding yields for para-substituted aryl halides. The reaction progressed effectively regardless of substrates with the EWG and EDG yielding more than 85% in most of the cases, except in case of aryl bromides and chlorides due to the stronger C–halogen bond than the C–I bond (Table 2, entries 10–12). Furthermore, it was observed that the reaction progressed faster on substrates with EDGs than on substrates with EWGs. This fact could be addressed by the inductive effects of the substituent groups on the substrates.46

Table 2. Substrate Scope of the SCR Catalyzed by NiFe2O4@TiO2@PDA-Pd under Sunlight Irradiationa.

3.3.1.

3.3.1.

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a

Reaction conditions: aryl halide (1.0 mmol), phenyl boronic acid (1.5 mmol), NiFe2O4@TiO2@PDA-Pd catalyst (5 mg), and K2CO3 (2.5 mmol) in EtOH·H2O (3 mL) under sunlight at 30 °C.

b

Isolated yields.

3.3.2. Sonogashira Coupling Reaction

The catalytic potential of the synthesized NiFe2O4@TiO2@PDA-Pd catalyst with 5% by weight of Pd loading was further extended to test the feasibility of the Sonogashira coupling reaction involving aryl halides and arylacetylenes under sunlight, at an average outdoor temperature of 30 °C. Optimization of various vital reaction conditions, viz., nature of the solvent, base, and light source for the Sonogashira reaction, was performed. In this reaction, the solvent played a significant role. EtOH was found to be an excellent solvent for this reaction out of a variety of solvents tested (Table S2, entries 1–5). High yield of the product was obtained in the presence of K2CO3 as the base when compared to other bases (Cs2CO3, NaOH, and Et3N) (Table S2, entries 6–8).

Influence of the light source on the Sonogashira reaction was also established in the presence of the synthesized catalyst. The product yield was very low in dark at RT and moderate (59%) at 60 °C. Under vis light (Hg lamp 250W), the yield was 81%, and under sunlight, higher yield (96%) was obtained (Table S2, entries 9–11). Thus, the fact of using sunlight in getting high yield was established. The feasibility of the Sonogashira reaction was verified with NiFe2O4, NiFe2O4@TiO2, and NiFe2O4@TiO2@PDA separately, and no products were observed.

The substrate scope of the Sonogashira coupling reaction over the NiFe2O4@TiO2@PDA-Pd nanophotocatalyst was also investigated using the optimized conditions. The aryl halides with EWGs or EDGs have resulted in a higher yield of the product (Table 3).

Table 3. Substrate Scope of the Sonogashira Coupling Reaction Catalyzed by NiFe2O4@TiO2@PDA-Pd under Sunlight Irradiationa.

3.3.2.

3.3.2.

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a

Reaction conditions: aryl halide (1.0 mmol), phenyl acetylene (1.3 mmol), NiFe2O4@TiO2@PDA-Pd catalyst (10 mg), and K2CO3 (2 mmol) in EtOH (3 mL) under sunlight at 30 °C.

b

Isolated yields.

The efficacy of the catalyst was compared with that of already reported catalysts for Suzuki and Sonogashira coupling reactions (Table S3). It is evident from Table S3 that our proposed NiFe2O4@TiO2@PDA-Pd nanophotocatalyst acts efficiently in producing the desired products in both Suzuki and Sonogashira coupling reactions with an excellently good yield (98 and 96%) in short reaction time (0.5 and 2.5 h) under natural sunlight. Thus, our catalyst shows its supremacy in its activity among other reported systems.

3.4. Stability and Recyclability of the Catalyst

Two significant parameters to be examined while evaluating a photocatalytic reaction are photo-stability and recyclability. The photo-stability and recyclability of our NiFe2O4@TiO2@PDA-Pd catalyst in photocatalytic Suzuki and Sonogashira coupling reactions were investigated in this study. Owing to the magnetic nature of the photocatalyst, it was retrieved from the reaction mixture in a simple manner with the aid of an external magnet after each cycle. The magnetically retrieved catalyst was washed with EtOH and dried, and its catalytic performance was assessed in the next run. Figure 5 shows the reuse of the recovered catalyst five times without any substantial loss of its photocatalytic activity, indicating the good stability of the catalyst.

Figure 5.

Figure 5

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Recyclability of NiFe2O4@TiO2@PDA-Pd for photocatalytic activity. (a) Suzuki and (b) Sonogashira reactions.

Many heterogeneous catalysts have leaching issues, and the leached Pd NPs into the solution lead to the decrease in the Pd content in the catalyst which was mainly responsible for its activity. To test the Pd leaching, ICP-OES analysis of the recovered catalyst was performed. It was observed that the Pd content of the nanocatalyst had decreased from (3.61) wt % to (2.26) wt % in the Suzuki reaction and to (2.45) wt % in the Sonogashira reaction after five time use. To further confirm the recyclable nature of the magnetic reusable catalyst, XRD analysis and FT-IR analysis on the recovered photocatalyst were performed. Figure S1 shows the XRD spectra of the NiFe2O4@TiO2@PDA-Pd photocatalyst after five times of reused experiments. No impurity peaks were detected in the XRD spectra of the reused photocatalyst, thus confirming the stability and recyclability of the catalyst. Furthermore, FT-IR analysis of the photocatalyst after five cycles of reuse was performed where it confirmed the fact that absorption peaks of the reused catalyst are intact like those of the fresh catalyst (Figure S2).

3.5. Heterogeneity of the Catalyst

Heterogeneity of the designed catalyst was tested via the hot filtration method and leaching test. In this method, Suzuki and Sonogashira coupling reactions were carried out separately in the presence of the synthesized photocatalyst NiFe2O4@TiO2@PDA-Pd in direct sunlight under optimum reaction conditions. The SCR was carried out for 15 min (half the reaction time) under the reaction conditions, and subsequently, the reaction mixture was separated into two equal halves. From one half of the reaction mixture, the catalyst was separated and retrieved employing an external magnet, and the reaction was allowed to continue in both portions for an extra 15 min. In the same way, the Sonogashira coupling reaction was also performed using the prepared catalyst under optimal conditions for 90 min in sunlight, followed by the separation of the reaction mixture into two equal halves. By following the aforementioned procedure, the catalyst in one part is magnetically separated, and the reaction in both halves was allowed to progress for extra 60 min. From both the coupling reactions, it is evident that in the absence of the catalyst, no further progress in the reaction was observed, whereas the other half portion of the reaction mixture, in the absence of the catalyst, has progressed to the complete conversion of the substrates into desired products, as mentioned in the Figure S3. This infers the fact that there is trivial leaching of Pd into the reaction mixture, confirming the heterogeneity of the developed catalyst. Furthermore, Pd leaching from the catalyst was also assessed by ICP-OES analysis which confirmed the Pd leaching to be <0.2% (nominal).

3.6. Active Species Trapping Experiment

Active species trapping experiments were performed using scavengers to understand the role of photogenerated active species (e––h+ pair) in the photocatalytic mechanism of the NiFe2O4@TiO2@PDA-Pd photocatalyst. In this experiment, K2S2O8 was used as an e– scavenger, and ammonium oxalate (AO) was used as a h+ scavenger. In the presence of K2S2O8, poor yield (38%) of the product was observed (Table S1, entry 18), whereas in the presence of AO, 51% yield of the product was observed (Table S1, entry 19). Thus, the trapping experiments indicate that both the photogenerated active species play a significant role in the C–C coupling reaction with a major contribution from photogenerated electrons.

3.7. Photocatalytic Mechanism of Suzuki and Sonogashira Coupling Reactions

A plausible photocatalytic mechanism for the Suzuki and Sonogashira coupling reactions in the presence of the NiFe2O4@TiO2@PDA-Pd photocatalyst was proposed based on the performed experimental observations and previously reported data.47−49 Simulated visible light irradiation of the catalyst led to the simultaneous formation of photogenerated electrons (e–) and holes (h+) in NiFe2O4 and TiO2, as illustrated in Figure 6. It is because light irradiation led to the promotion of an e– from the valence band (VB) to the conduction band (CB) leaving a h+ in the VB. Thus, photogenerated e––h+ pairs are formed simultaneously in NiFe2O4 and TiO2. The photogenerated e– from the CB of NiFe2O4 can be easily transferred to the CB of TiO2 by the simultaneous transfer of photogenerated h+ from the VB of TiO2 to the VB of NiFe2O4. This is ascribed to the more negative CB potential of NiFe2O4 than that of TiO2 and more positive VB potential of TiO2 than that of NiFe2O4. Furthermore, it is also evident by the fact that the combination of NiFe2O4 and TiO2 develops interfacial contact between them, thus creating a pathway for easy transfer of e– from the CB of NiFe2O4 to the CB of TiO2 and therefore hinders the e––h+ pair recombination. The photogenerated e– available in the CB of TiO2 will be transported through the PDA layer to the Pd surface. Active Pd NPs act as electron reservoirs and thus trap the electrons reaching their surface. These photogenerated electrons and Pd NPs act as active sites and attack the C–X bond of the adsorbed aryl halides forming the aryl–Pd complex via oxidative addition. On the other hand, arylboronic acid combines with OH– in a basic reaction medium to produce aryl-B(OH)3–. Furthermore, C–B bond cleavage occurs to generate the biaryl–Pd complex in the presence of h+ (transmetalation). In the final step, a biaryl product is obtained via reductive elimination.50,51

Figure 6.

Figure 6

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Plausible photocatalytic mechanism over the NiFe2O4@TiO2@PDA-Pd nanophotocatalyst of Suzuki and Sonogashira coupling reactions.

For the Sonogashira coupling reaction also, the photogenerated electrons and Pd NPs act as active sites attacking the C–X bond of the adsorbed aryl halide and resulting in the aryl–Pd complex. Simultaneously, photogenerated holes attract the electronic clouds of the alkyne units in phenyl acetylene, making the terminal spC–H more acidic. Then, K2CO3 deprotonates terminal H of the alkyne unit, and the resulting species combines with the aryl–Pd complex to form an alkynated Pd complex. In the final reductive elimination step, diarylacetylene is formed.52,53

The proposed mechanism reveals the uniqueness of the synthesized photocatalyst as a sole catalyst for both Suzuki and Sonogashira coupling reactions under sunlight irradiation.

4. Conclusions

In summary, we have designed and developed a magnetically recyclable Pd-supported PDA-coated core@shell NiFe2O4@TiO2 nanocatalyst, with good photocatalytic activity for both Suzuki and Sonogashira coupling reactions under sunlight irradiation under ambient conditions. The activity of the catalyst was validated for both coupling reactions, and its effectiveness for reactions involving a variety of substrates under sunlight irradiation to yield biaryls and diarylacetylenes was tested. The reactions were facilitated by low Pd loading in the presence of eco-friendly polar protic solvents (ethanolic water/ethanol) in a very short reaction duration with an excellent yield (96–98%). The catalyst is validated for substituted substrates in both Suzuki and Sonogashira reactions to give a good yield of the product, indicating its efficacy. The plausible mechanism has been proposed for the coupling reactions where the simultaneous utilization of both the photogenerated e––h+ pairs in various steps of the coupling reactions denotes an exceptional catalytic view point of the catalyst. The catalyst was retrieved with the aid of an external magnet and was reutilized for five cycles. ICP-OES analysis indicated the stability of the catalyst without considerable loss after reusing five times which was further confirmed by FTIR and XRD analysis. It was found that the NiFe2O4@TiO2@PDA-Pd nanophotocatalyst exhibits greater activity with high yield in comparison to a number of reported catalysts.

Acknowledgments

Author M.R. is grateful to the National Institute of Technology Warangal (NITW) for the Research Seed Money (P1082 Plan Gen.-RSM), the DST-FIST grant, and SR/FST/CSII/2018/65 awarded to Department of Chemistry, NITW, for the financial support of this work. B.P.G. is grateful to NITW for the Senior Research Fellowship.

Supporting Information Available

The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acsomega.2c03603.

  • Screening of reaction conditions for Suzuki and Sonogashira coupling reactions; XRD and FTIR spectra of reused catalysts; hot filtration and the leaching test of the NiFe2O4@TiO2@PDA-Pd catalyst for Suzuki and Sonogashira coupling reactions; comparison of the NiFe2O4@TiO2@PDA-Pd catalyst with other previously reported catalysts; and characterization data of products along with copies of 1H and 13C NMR spectra (PDF)

Author Contributions

M.R. and B.P.G. designed and developed the photocatalyst and validated its activity for coupling reactions. The manuscript was written through contributions of all the authors. All the authors have given approval for the final version.

The authors declare no competing financial interest.

Supplementary Material

ao2c03603_si_001.pdf (1.2MB, pdf)

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