Abstract
Owing to their improved catalytic stability and ability to undergo repeated cycles, solid-supported catalysts show great potential for various catalytic reactions. In this study, we synthesized a catalyst comprising a palladium-2,2-bipyridine complex supported on TiO2 nanoparticles (TiO2@BDP-PdCl2) fully characterised and investigated its efficacy in Suzuki–Miyaura cross coupling reactions involving phenyl boronic acid with various aryl halides under mild reaction conditions. The 2,2′- bipyridine (bp) has shown excellent complexation properties for Pd (II) and it could be easily anchored onto functionalized TiO2 support by the bridging carboxylate ions. The composition and structure of the as-prepared catalyst was characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), Transmission Electron Microscope (TEM), X-ray photoelectron spectroscopy (XPS), and UV–Vis spectroscopy. The catalyst easily demonstrated separability, enhancing its practicality in catalytic processes. Subsequent utilization showed a consistent activity level, suggesting the stabilization of the aggregated catalyst species. This research sheds light on the importance of catalyst stability and maintenance during consecutive reaction cycles.
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Introduction
The design of robust catalysts is important for catalytic systems in the view of organic chemistry. Transitional metals and their complexes play a very important role during the formation of carbon–carbon bond. Among the transition metals, palladium-based Suzuki–Miyaura cross-coupling reaction of aryl halides with arylboronic acids has become a convenient synthetic method in organic chemistry1,2,3,4,5. Palladium (Pd) nanoparticle works well in catalytic coupling reactions to some extent, however catalysts suffer from obvious aggregation after several cycles and considerable metal leaching which is responsible for the decrease or loss of their intrinsic catalytic activities6,7,8,9,10,11. This is probably due to the lack of sufficient binding sites on the support materials, where only weak non-covalent interactions exist between the support materials and the metal nanoparticles12,13. Given the cost of palladium and its toxic nature, the separation, recovery, and reutilization of palladium catalysts are crucial. This underscores the heightened demand for non-aggregated metal nanoparticles in coupling reactions, aiming to improve the overall efficiency of the catalyst. The aggregation of Pd nanoparticles can be overcome or minimized by immobilizing them on some solid supports, such as carbon, metal oxides, and polymers which could generate strong covalent interaction with palladium species and stabilize the catalyst8,9,14,15,16,17,18,19. In this context, the distinctive features of heterogeneous palladium catalysts include their heightened catalytic sites, exceptional selectivity, ability to control catalyst chemo-, regio-, and enantioselectivities, ease of optimizing catalytic systems, and enhanced yields, making them widely employed in Suzuki coupling reactions16,20,21. The challenge at hand pertains to the design and synthesis of expensive ligands essential for constructing heterogeneous catalysts, particularly when anchoring them onto solid supports through covalent attachments22,23. As a result, many cost-effective materials such as silica, carbon, zeolite, cellulose, and chitosan were explored as alternative support options14,18,24,25,26,27,28,29. However, the exploration of a Pd catalyst supported by TiO2 nanoparticles in Suzuki reactions is limited in the current literature. Despite the numerous advantages it offers, including heightened catalytic activity, tailored reactivity, improved selectivity, as well as enhanced stability, durability, and recyclability, this approach remains relatively under explored22,30. Researchers has demonstrated that TiO2 significantly enhances catalyst performance, affording the ability to modulate catalytic activities for diverse reactions, spanning dehydrogenation31, hydrodesulphurization32, water gas shift33, and thermal catalytic decomposition34,35. The interactions between catalytic particles and mesoporous TiO2 play a pivotal role, profoundly influencing catalytic activity, stability, and selectivity in heterogeneous metal catalysts16. However, it's important to acknowledge that these electrostatic interactions may entail certain drawbacks, including weak bonding, limited stability under harsh conditions, diminishing catalytic activity over time, potential metal loss during catalyst preparation, and heightened sensitivity to reaction conditions, among others36. These considerations necessitate careful attention when designing and employing such catalyst systems. By keeping these limitations, we were interested to design chemical modification of TiO2 nanoparticles for stable supported heterogeneous catalytical applications, in particular under organic solution conditions, in which the surface of TiO2 nanoparticles needs the modification by organic modifiers. Carboxylic acids are often used as such modifiers, with a coordination of carboxylic groups (-COOH) to surface Ti atoms37. In this paper, for the first time we demonstrate a new and convenient solvothermal approach to chemically postmodify TiO2 nanoparticles with di-carboxylic acids derived from chelated Pd bipyridyl complexes. The resulting material demonstrates enhanced catalytic performance in Suzuki Coupling Reactions, showcasing its potential in various catalytic applications. This approach opens new avenues for the design and development of advanced heterogeneous catalysts for organic synthesis. To the best of knowledge, anchoring of palladium-2,2-bipyridine complex on TiO2 surface not reported yet in literature for catalytic applications.
Experimental
Materials & characterization
All commercially available solvents, unless otherwise mentioned, were used without any other purification. All chemicals were procured from Aldrich and Across chemical companies and used as-received without any further purification. Glassware was dried in an oven prior to use. Reactions were monitored by thin-layer chromatography (TLC) with Merck silica gel 60 F254 plates. Column chromatography was performed on silica gel 100–200 mesh from SDFCL. 1H and 13C NMR spectra were recorded on a Bruker DRX 500 MHz spectrometers using TMS (1H) as an external standard. Chemical shifts (δ) are reported in ppm. The coupling constants J are given in Hz. Fourier transform infrared (FTIR, VERTEX 70, Bruker) spectra were recorded to analyse the functional groups present in all the samples. X-ray diffraction measurements were performed on Rigaku Smart Lab II with Cu K_alpha (λ = 1.5405 Å) radiation source operating at 40 kV and 40 mA. Scanning electron microscopy (SEM, JEOL JSM-7610FFEG-SEM) were employed to observe the morphology. Thermogravimetric analysis (TGA, TA-Q50) was employed to determine the thermal stability of catalyst under N2 at a heating rate of 10 °C min−1 in a temperature range of 25–600 °C.
Preparation of TiO2 nanoparticles37:
The mixture of 2-propanol (2.5 mL, AR) and Titanium isopropoxide (6 mL) was added dropwise over 10 min into 0.1 M nitric acid solution (30 mL) under vigorous stirring at room temperature, and then the reaction mixture was heated to 80 °C and stirred vigorously for 10 h to achieve peptization. A Buchner funnel was used to remove the non-peptized agglomerates, and the filtrate was transferred into a Teflon-lined stainless-steel autoclave with a capacity of 100 mL. After heating at 200 °C for 12 h, the autoclave was allowed to cool to room temperature. The nanoparticles were isolated by centrifugation and washed with ethanol. The crude TiO2 NPs were then washed with ethanol three times to remove the unreacted precursor. The TiO2 NPs were dried in vacuo and stored in a sealed container at room temperature for further usage.
Synthesis of BDP-PdCl2 38:
In the dark and under nitrogen atmosphere, PdCl2 (80 mg, 0.45 mmol) and KCl (67 mg, 0.90 mmol) were dissolved in a 10 mL solution consisting of Methanol: Water in a 9:1 ratio and refluxed it for 3 h. To this reaction mixture, H2BDP (109 mg, 0.45 mmol) dissolved in 2 mL of ethanol was added. The reaction mixture was left to reflux for 12 h and filtered off. The moist product was subsequently suspended in water, which was prepared with 6–7 drops of 6 M HCl, and heated for an hour or more until it reduced to 1/3 of its initial volume. Afterward, the mixture was cooled in an ice bath and filtered once more. It was then washed with cold distilled water to retrieve light brownish coloured compound (80% yield). IR (KBr, cm−1): 3448 (s), 1677 (s), 1662 (w), 1607 (m), 1542(m), 1407(s), 1386(s), 1289(w), 1268(w), 1131(w), 786(m).
Synthesis of TiO2@BDP-PdCl2 39:
BDP-PdCl2 was dissolved into acetonitrile (CH3CN) solvent (3 mg/mL) to prepare a stock solution. Then, TiO2 NPs (1.5 mg/mL in acetonitrile) were mixed with the BDP-PdCl2 solution (3 mg/mL in acetonitrile) in a 1:1 volume ratio and stirred for 24 h. The mixture was then centrifuged to obtain TiO2@BDP-PdCl2 NPs. Product was purified by centrifugation and washed with methanol to remove unbound BDP-PdCl2. This step was repeated three times to obtain the final TiO2@BDP-PdCl2 product. The obtained TiO2@BDP-PdCl2 NPs were then dried in vacuo and stored at room temperature.
General reaction conditions for Suzuki coupling reactions
In a 25 mL reaction vial were placed aryl halide (1 mmol), phenylboronic acid (1.2 mmol), K2CO3 (1.2 mmol), and TiO2@BDP-PdCl2 (10 mg) in 1:1 ethanol/water (5 mL) and the resulting mixture was stirred at 80 ℃ for 3 h. The reaction was monitored by TLC and after the reaction, the mixture was extracted with ethyl acetate. The organic layer was dried with sodium sulphate, filtered, and concentrated in vacuo. The residue was then purified by column chromatography over silica gel (100 − 200 mesh size) with petroleum ether-ethyl acetate as the eluent. The products were confirmed with 1H and 13C NMR spectroscopic analysis.
General procedure for catalyst recovery
Iodobenzene (5.0 mmol), phenylboronic acid (6.0 mmol), K2CO3 (6.0 mmol), TiO2@BDP-PdCl2 (10 mg), and ethanol/H2O (25 mL) were placed in a 100 ml reaction flask and stirred at 80 ℃ for 6 h. After the reaction, ethyl acetate, ethanol, and deionized water were added successively for centrifugal cleaning, the catalyst and the product were separated by using centrifugation for 15 min at 10,000 rpm. The residual catalysts were then dried at room temperature under vacuum before being used again for the next reaction.
Results and discussions
In this study, H2BDP was employed for coordination with PdCl2, resulting in the formation of BDP-PdCl2. Subsequently, the BDP-PdCl2 complex was firmly attached to the TiO2 particle surface shown in Scheme 1. Analytical and spectroscopic assessments substantiated the successful synthesis and high purity of both the BDP-PdCl2 ligand and TiO2@BDP-PdCl2 composite.
FT-IR spectra of the TiO2 nanoparticles modified with BDP-PdCl2 are shown in Fig. 1a. In the spectrum of BDP-PdCl2 the bands are attributed to the stretching and bending coupled C–OH vibrations (νC-OH, at 1308–1275 cm−1), the in-plane bending of O–H (δO-H, at 1408 cm−1), and the stretching band of the carboxylic acid (νC=O, at 1677 cm−1), while the band at 1591 cm−1 is due to the C=C stretching vibration of phenyl ring (ν C = C). TiO2@BDP-PdCl2 showed the νC=C band at 1591 cm−1 as well as the carboxylate anion (COO−) asymmetric (νas, at 1512 cm−1) and symmetric (νs, at 1408 cm−1) stretching bands due to the splitting of carboxylate groups complexed with Ti surface centres. Notably, the absence of the νC=O stretching vibration of carboxylic acid at 1677 cm−1 in TiO2@BDP-PdCl2 further supports the formed complex.
Moreover, to delve into the intricacies of Pd complexation, encompassing the stages pre- and post-complexation, as well as the subsequent anchoring of BDP-PdCl2 onto the TiO2 surface, we executed an extensive array of UV–Vis studies (Fig. 1b). H2BDP exhibited a conspicuously robust absorption band peaking at 295 nm, attributed to the characteristic bipyridyl ligand-cantered n–π*-based transitions. In contrast, BDP-PdCl2 manifested a relatively subdued and broader band at 333 nm, correlated with a spin-allowed dπPd(II)-π*BDP-based metal-to-ligand charge transfer (IMLCT) transition along with intense absorption band at 280 nm, accompanied by a blue shift (Δλ = 10 nm), providing confirmation of the formation of the Pd complexation40,41,42. Furthermore, the absorption intensity of TiO2@BDP-PdCl2 was observed to be less pronounced and broader compared to BDP-PdCl2. The UV–Vis spectrum of TiO2@BDP-PdCl2 exhibited distinct broad absorption bands at 280 and 329 nm respectively, confirming the anchoring of BDP-PdCl2 onto the Ti surface. These absorption patterns align with the findings from the FT-IR.
In order to further characterize the crystalline composition, shape, and surface coverage after the solvothermal reaction, the samples were studied by XRD, SEM, XPS, and TGA measurements. The X-ray diffraction (XRD) pattern exhibits prominent and well-defined peaks, indicating the crystalline nature of the samples (Fig. 2a). Initially, the presence of characteristic peaks at 2θ values of 25.3°, 37.9°, 48.0°, 54.7°, 62.9°, 70.0°, and 75.3° confirms the anatase phase of TiO2, corresponding to the (101), (004), (200), (211), (204), (220), and (215) planes, respectively. Furthermore, in the XRD pattern of TiO2@BDP-PdCl2, we observed both newly emerging peaks and characteristic anatase peaks of TiO2, providing definitive evidence for the formation of TiO2@BDP-PdCl2. Post-modification of TiO2, as a result slight change in the morphology along with the porous surface was observed in the SEM micrographs (Fig. 2b, c). TG − differential TG (DTG) diagrams of TiO2@BDP-PdCl2 and TiO2 are shown in Figure S5. Both exhibit a nearly 7% weight loss at around 100 °C, attributed to the desorption of surface-adsorbed water molecules. Notably, TiO2 demonstrates superior thermal stability owing to its high degree of crystallinity. TiO2@BDP-PdCl2 exhibits a 60% thermal degradation at 400 °C, indicating commendable thermal stability of the catalyst below this temperature threshold. X-ray photoelectron spectroscopy (XPS) was employed to analyze the chemical and electronic states of carbon (C), palladium (Pd), and titanium (Ti) (Fig. 2d, e). Examination of the XPS spectrum of the 3p orbitals of the Ti core revealed two distinct peaks at binding energies (BE) of 458.41 eV and 464.32 eV. These peaks correspond to the Ti (2p3/2) and Ti (2p1/2) core levels of Ti4+ cations, indicating the absence of Ti3+. Moreover, the substantial energy gap of 5.91 eV between the Ti (2p3/2) and Ti (2p1/2) peaks, along with their area ratio of 3.45, signifies the robust bonding between titanium (Ti) and oxygen (O) atoms of anatase form of TiO2 nanoparticles (Fig. 2f)43. In the case of the Pd core, the XPS spectrum of the 3d orbitals exhibited peaks at approximately 338.01 eV and 343.17 eV for Pd 3d5/2 and Pd 3d3/2, respectively. Both Pd peaks are attributed to the Pd (II) state (Fig. 2g)44. The mass fraction of Ti on TiO2@BDP-PdCl2 reached 9.96%, which is similar to the amount of the metal precursor.
Application of TiO2@BDP-PdCl2 for the Suzuki- Miyaura cross coupling reaction
After characterizing the structure and properties of TiO2@BDP-PdCl2 catalyst was then examined for the carbon − carbon (C–C) bond formation reaction i.e., Suzuki–Miyaura cross coupling reaction. The C–C cross coupling of iodobenzene and phenylboronic acid were utilized as a model for the optimization of reaction conditions (Table 1). The effect of different reaction factors such as solvent, base, temperature, reaction time and catalyst amount were evaluated. In the initial phase of our investigation, we scrutinized the influence of various solvents (Table 1, entries 1 − 8). The use of water (H2O) led to the formation of the desired product, biphenyl, albeit with a lower yield of 34% after 6 h (Table 1, entry 1). In contrast, the use of a nonpolar solvent like toluene resulted in a substantial yield of biphenyl (Table 1, entry 2). Subsequently, a series of polar solvents including tetrahydrofuran (THF), dioxane, and acetonitrile were evaluated, and they exhibited efficiency by providing moderate to good yields (Table 1, entries 3 − 5). The utilization of a polar protic solvent such as ethanol was also explored, yielding a satisfactory product (Table 1, entry 6). Following this, we investigated the use of polar aprotic solvents such as DMF and propylene carbonate [7c], which produced biphenyl with yields of 74% and 45% respectively (Table 1, entry 7 & 8). Inspired by the previous reports11,25,45, the effect of a binary mixture of solvents containing ethanol/water (1:1) was investigated and delivers an excellent yield of biphenyl in 95% yield for 3 h (Table 1, entry 9). Next, we explored the impact of different bases on the reaction system. The employment of inorganic bases like Cs2CO3 and Na2CO3 yielded favourable biphenyl yields (Table 1, entries 9 − 11). Conversely, the utilization of organic bases like Et3N resulted in a 59% yield after 3 h (Table 1, entry 12). Following this, we assessed the influence of temperature on the reaction. It was observed that reducing the reaction temperature to 60 °C and 40 °C led to a decrease in biphenyl yield (Table 1, entries 14 − 16). Subsequently, we conducted the reaction while varying the catalyst quantity. It is noteworthy that augmenting the catalyst quantity from 10 to 20 mg yielded no discernible enhancements (Table 1, entry 15). Conversely, decreasing the catalyst amount from 10 to 5 mg resulted in a slight reduction in yield (Table 1, entry 16).
We have further expanded the catalytic potential of TiO2@BDP-PdCl2 to encompass a broader array of biaryl substrates (Table 2) using carefully optimized reaction conditions. The reaction of iodobenzene and bromobenzene with phenylboronic acid yielded biphenyl with exceptional efficiency (Table 2, entries 1–2), while chlorobenzene resulted in notably lower yields (Table 2, entry 3). Subsequently, we conducted reactions between phenylboronic acid and various aryl halides possessing both electron-donating (-OCH3) and electron-withdrawing (-COCH3 & -CHO) groups. It was observed that bromine derivatives (Table 2, Entries 5 & 8) and iodine derivatives (Table 2, Entries 4, 7 & 10) exhibited excellent reactivity with phenylboronic acid, furnishing the corresponding coupled products with yields ranging from 90 to 94%. Conversely, the yield was significantly reduced when chloride derivatives were utilized as substrates (Table 2, Entry 6 & 9).
In pursuit of discerning the influence of TiO2 as a solid support, we conducted the C–C cross coupling of iodobenzene and phenylboronic acid exclusively employing BDP-PdCl2, under uniform conditions. The utilization of BDP-PdCl2 led to a notably low conversion rate of 72% and a yield of 66%. The outcome is in concordance with earlier documented findings46. This data substantiates the pivotal role of solid support in mitigating aggregation-induced activity during C–C bond formation. It is known that TiO2 exhibits both photocatalytic and catalytic properties. In order to assess the impact of TiO2 on C–C cross coupling reactions, we conducted a Suzuki reaction under nearly identical conditions. The reaction occurred in the presence of TiO2 but yielded unsatisfactory results, while no reaction occurred in the absence of Pd.
Recyclability of the catalyst
The developed TiO2@BDP-PdCl2 catalyst was then investigated for the recyclability by using a standard reaction condition for the Suzuki-Mayura cross coupling reaction of iodobenzene and phenylboronic acid. Remarkably, the TiO2@BDP-PdCl2 catalyst showed excellent recyclability, although the yield of the reaction decreased slightly after each run, it remained at 85% after seven cycles (Fig. 3). TEM images revealed that both the freshly prepared catalyst and the reused catalyst maintained their structural integrity, as evidenced in Fig SI 6. Additionally, XPS analysis provided further confirmation of the stability of TiO2@BDP-PdCl2, even after five catalytic cycles (Fig SI 7).
Conclusions
In summary, TiO2 could be used as a solid support for Pd catalysis. TiO2 -supported Palladium-2,2-bipyridine complex was synthesized and fully characterized by various analytical techniques. The catalyst exhibits higher catalytic activity for the Suzuki–Miyaura coupling reaction. Moreover, TiO2@BDP-PdCl2 can be recycled and reused four times without a significant decrease in catalytic activity. The reactivity of the solid-supported catalyst remains high and enables the synthesis of various biphenyls from iodobenzene and phenylboronic acid derivatives. As of now, there is no existing documentation on the immobilization of the palladium-2,2-bipyridine complex on the TiO2 surface. We believe that a Pd catalyst supported by TiO2 has the potential to serve as a recyclable catalyst, demonstrating applicability in various C–C coupling reactions.
Data availability
All data generated or analysed during this study are included in this present article and available in supplementary information file.
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Acknowledgements
The URG & MIH acknowledges the financial support from the Khalifa University of Science and Technology faculty startup grant No FSU-2023-001.
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U.R., P.S.R., A.S.: Synthesis and characterization of materials, coupling reactions and analysis, methodology, writing draft, ESI & editing. S.P.: SEM analysis. Infas: conceptualization, supervision, project administration, data curation, writing – review & editing, and funding acquisition.
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Gandra, U.R., Reddy, P.S., Salam, A. et al. TiO2 supported pallidum-bipyridyl complex as an efficient catalyst for Suzuki–Miyaura reaction in aqueous-ethanol. Sci Rep 14, 7323 (2024). https://doi.org/10.1038/s41598-024-57534-9
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DOI: https://doi.org/10.1038/s41598-024-57534-9
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