DOI QR코드

DOI QR Code

Magnetic CoFe2O4 Nanoparticles as an Efficient Catalyst for the Oxidation of Alcohols to Carbonyl Compounds in the Presence of Oxone as an Oxidant

  • Received : 2013.11.18
  • Accepted : 2014.03.16
  • Published : 2014.07.20

Abstract

Magnetically nano-$CoFe_2O_4$ efficiently catalyzes oxidation of primary and secondary benzylic and aliphatic alcohols to give the corresponding carbonyl products in good yields. The reactions were carried out in an aqueous medium at room temperature in the presence of oxone (potassium hydrogen monopersulfate) as an oxidant. In addition, the catalysts could be reused up to 6 runs without significant loss of activities. Catalyst was characterized by SEM, XRD and IR.

Keywords

Introduction

The synthesis and characterization of nanoparticles is of great interest in present study because of fundamental and technological benefits. A large number of applications such as catalysis entailing nanoparticles are now an industrial reality.1,2 Nanoparticles of metals and metal oxides have been widely used as catalysts in many organic reactions because of their high surface area and facile separation.3 Nanoparticles display high catalytic activity and chemical selectivity under mild circumstances.4 The extremely tinysize particles enlarge the surface area which, when exposed to the reactant, allow more reactions to take place simultaneously and hence accelerate the process.5 Magnetic NPs have a wide variety of distinctive magnetic properties such as super paramagnetic, high coercivity, low Curie temperature, high magnetic susceptibility, etc. Magnetic NPs are of paramount importance for researchers from a broad range of fields, including magnetic fluids, data storage, catalysis, and bio applications.6-10 Some defects have been found regarding homogeneous catalysts. For example, difficult workup of the perilous metal residues, and lack of recycling methods, which make them inconvenient for large-scale applications.11 In heterogeneous reaction, tedious methods like centrifugation and filtration are utilized to recover catalysts and end in loss of solid catalyst in the process of separation. Magnetic separation supplies a convenient method to remove and recycle magnetized species by utilizing an appropriate magnetic field.12-14 One of the significant transformations of organic synthesis is the oxidation of alcohols to carbonyl compounds and many methods have been probed in order to accomplish such a conversion and a variety of oxidants have been developed.15 Many highly efficient systems have been developed for catalytic alcohol oxidation. Traditional methods utilizing stoichiometric quantities of inorganic oxidants such as chromium (VI) reagents, permanganates, or N-chlorosuccinimide (NCS) are not environmentally friendly.16 Even grave environmental problems are created using hypervalent iodine reagents. Thus, the development of greener oxidation systems using less poisonous catalysts, oxidants, and solvents became a crucial aim for catalysis. Among the numerous methods, oxidation of organic compounds to corresponding carbonyl by O2 or TBHP required high temperatures and long times. Hence, mild, catalytic, economic and efficient alternative methods was needed.17-19 The search for catalytic oxidation of alcohols in an aqueous medium in the absence of an additional base is still a significant challenge.20 Oxone is a convenient, readily available, and relatively stable compound at room temperature, and therefore is utilized for various transformations in organic synthesis.21-29 In this paper, cobalt ferrite nanoparticles were synthesized by co-precipitation method.30 We have shown that CoFe2O4 MNPs are an active and reusable catalysts for oxidation of alcohols with oxone in the presence of water at room temperature (Scheme 1).

Scheme 1.Oxidation of alcohols with oxone in the presence of water at room temperature.

 

Experimental

Ferric chloride hexahydrate (FeCl3·6H2O), cobalt chloride hexahydrate (CoCl2·6H2O), sodium hydroxide (NaOH), aliphatic and benzylic alcohols were purchased from Merck (Darmstadt, Germany) and Fluka (Switzerland) and used without further purification. The IR spectra were measured on a Jasco 6300 FT-IR spectrometer (KBr disks). The structural properties of synthesized nanoparticles were analyzed by X-ray powder diffraction (XRD) with a X-Pert Philips advanced diffractometer using Cu (Kα) radiation (wavelength: 1.5406 Å), Pw3040/60, operated at 40 kV and 30 mA at room temperature in the range of 2θ from 4 to 120º. The particle size and morphology of the surfaces of sample were analyzed by a scanning electron microscopy) LEO Co., England, Model: 1455VP). The disc was coated with gold in an ionization chamber. TLC was used to follow the reactions. The aliphatic products detected by GC-FID (VARIAN C-P-3800 with FID detector, column CP-Sil 5 CB30 m × 0.32 mm).

Preparation of CoFe2O4 MNPs in Aqueous Solution. Cobalt ferrite nanoparticles were synthesized by the coprecipitation of Co2+ and Fe3+ ions (molar ratio 1:2) in sodium hydroxide solution30 FeCl3·6H2O (0.54 g) and CoCl2·6H2O (0.238 g) were dissolved in a 10 mL deionized water. NaOH (1.2 g) was dissolved in 10 mL water and this solution was added into the previously prepared solution while stirring at 80 ℃. The stirring was continued for 30 min and cooled to room temperature. The precipitate was isolated in a magnetic field, washed with deionized water three times, and finally dried.

General Procedure for the Oxidation of Alcohol. Alcohol (1 mmol), water (1 mL), and CoFe2O4 MNPs (11.8 mg, 5 mol %) were added to a round-bottomed flask. The reaction mixture was stirred for the two minutes, and then oxone (0.6 mmol) was added in three portions. The reaction mixture was placed at room temperature and stirred for the specified time (Table 5). The reaction was followed by TLC (EtOAc-cyclohexane, 2:10). After the completion of the reaction, the product was extracted in dichloromethane. The solvent was evaporated under reduced pressure to give the corresponding aromatic products. Purification of the residue using plate chromatography (silica gel) provided the pure carbonyl compounds. The aliphatic products in dichloromethane was dried with anhydrous MgSO4 and detected by GC-FID.

Table 5.Oxidation of various alcohols using CoFe2O4 MNPs catalyst (5 mol %) in water with Oxone at room temperature

 

Results and Discussion

Characterization of the Catalyst. Figure 1 shows the FTIR spectra of CoFe2O4 MNPs, where the peak at 580 cm−1 corresponds to the Fe–O bond. Generally, XRD can be used to characterize the crystallinity of nanoparticles, and it gives an average diameter of all the nanoparticles. The XRD pattern of the CoFe2O4 MNPs sample is shown in Figure 2. The position and relative intensity of all diffraction peaks matched well with standard CoFe2O4. The results indicate that the discernible peaks in Figure 2 can be indexed to (220), (311), (400), (511) and (440) planes of a cubic unit cell, which corresponds to cubic spinel structure of cobalt iron oxide (card no. 003-0864). The diameter of the CoFe2O4 determined by Debye-Scherre equation with XRD data (D = 0.94 χ/B Cos θ). The SEM analysis suggests that the CoFe2O4 MNPs are nanocrystalline and their shape is spherical (Figure 3). These results are in good harmony with the XRD analyses. The results show that the diameter of the CoFe2O4 MNPs, is about 60–90 nm.

Figure 1.FT-IR spectra of CoFe2O4 MNPs

Figure 2.XRD pattern of CoFe2O4 MNPs.

Figure 3.SEM image of CoFe2O4 MNPs

Optimization of Alcohol Oxidation Conditions. For optimizing the reaction conditions, we tried to convert 2-chlorobenzyl alcohol (1 mmol) to 2-chlorobenzaldehyde in the presence of CoFe2O4 as a nanomagnet catalyst (2.3 mg) and oxone (1 mmol was added in 3 stages in 30 minutes) in various solvents at room temperature. As shown in Table 1, 2-chlorobenzaldehyde was formed as the major product in all cases, and the highest yield for 2-chlorobenzaldehyde was achieved in water (Entry 3).

Table 1.Conversion of 2-chlorobenzyl alcohol to 2-chlorobenzaldehyde in different solvents with oxone and in the presence of CoFe2O4 MNPs catalyst at room temperature

Table 2 summarized the effect of different oxidants on the oxidation of 2-chlorobenzyl alcohol over nanomagnetic-CoFe2O4 catalyst at room temperature in water. These results showed that the higher yield was achieved with oxone as oxidant (Entry 3). We also observed that 2-chlorobenzyl alcohol was not oxidized with this system in the absence of oxidant under nitrogen atmosphere.

Table 2.Oxidation of 2-chlorobenzyl alcohol using various oxidizing reagents in water and in the presence of CoFe2O4 MNPs catalyst at room temperature

The amount of the catalyst and oxidant were also optimized. The results showed that 5 mol % of catalyst and 0.6 mmol of oxidant is the best choice for the oxidation of 1 mmol of alcohol (Tables 3 and 4). The competing reaction such as overoxidation of aldehydes to the corresponding carboxylic acids was not observed in any of the cases under the above conditions.

Table 3.Oxidation of 2-chlorobenzyl alcohol in water with Oxone (1 mmol) and different amounts of CoFe2O4 MNPs at room temperature

Table 4.Oxidation of 2-chlorobenzyl alcohol (1 mmol) in water with different amounts of oxone and in the presence of CoFe2O4 MNPs catalyst (5 mol %) at room temperature

Application Scope. The reaction condition, which was optimized for 2-chlorobenzyl alcohol, can be easily applied to various primary and secondary alcohols. The results for the oxidation of a variety of alcohols are summarized in Table 5. The oxidation of various benzylic alcohols gave the carbonyl compounds in high yields and short reaction times. The electron withdrawing groups reduced the reaction rate dramatically (Entry 11) and the electron donating groups on the benzene ring accelerate the reaction rate (Entry 14). The oxidation for aliphatic alcohols proceeded quite slowly (Entry 17-19). The competing reaction such as overoxidation of aldehydes to the corresponding carboxylic acids was not observed, either.

The catalyst was easily separated from the products by exposure of the reaction vessel to an external magnet and decantation of the reaction solution. The remaining catalyst was washed with acetone and water to remove residual product, and then dried. This catalyst could be subsequently reused in more than six iterative cycles without no obvious decrease in activity (Table 6).

Table 6.Recycling of the catalytic system for the oxidation of 2-chlorobenzyl alcohol to 2-chlorobenzaldehyde

 

Conclusion

We have introduced a straightforward and efficient method for oxidation of alcohols to their corresponding carbonyl compounds using oxone in the presence of nanomagnetic- CoFe2O4 catalyst in water at room temperature. The use of nontoxic and inexpensive materials, stability of the oxidation condition, simple procedure, short reaction times, good yields, and mild reaction conditions are the advantages of this method. In comparison with the other oxidants such as O2 or TBHP, oxidation by oxone accomplished at low temperatures and in short times.18,19 The catalyst could be subsequently reused in six iterative cycles, without no obvious decrease in activity. The application of this nanocatalyst to different oxidation reactions is currently under investigation in our laboratory.

References

  1. Conway, B.; Tilak, B. Advanced Catalysis; Academic Press: New York, 1992.
  2. Cao, H.; Suib, S. L. J. Am. Chem. Soc. 1994, 116, 5334. https://doi.org/10.1021/ja00091a044
  3. Arends, I. W. C. E. Angew. Chem. 2006, 118, 6398. https://doi.org/10.1002/ange.200602044
  4. Nasir Baig, R. B.; Rajender, S. V. Chem. Commun. 2013, 752.
  5. Montazeri, H.; Amani, A.; Shahverdi, H. R.; Haratifar, E.; Shahverdi, A. R. J. Nanostruct. Chem. 2013, 3, 25. https://doi.org/10.1186/2193-8865-3-25
  6. Patel, D.; Moon, J. Y.; Chang, Y.; Kim, T. J.; Lee, G. H. Colloid Surf. A 2008, 313-314, 91. https://doi.org/10.1016/j.colsurfa.2007.04.078
  7. Zhao, M.; Josephson, L.; Tang, Y.; Weissleder, R. Angew. Chem. Int. Ed. 2003, 42, 1375. https://doi.org/10.1002/anie.200390352
  8. Mornet, S.; Vasseur, S.; Grasset, F.; Veverka, P.; Goglio, G.; Demourgues, A. Prog. Solid State Chem. 2006, 34, 237. https://doi.org/10.1016/j.progsolidstchem.2005.11.010
  9. Stevens, P. D.; Fan, J.; Gardimalla, H. M. R.; Yen, M.; Gao, Y. Org. Lett. 2005, 7, 2085. https://doi.org/10.1021/ol050218w
  10. Jun, Y.; Choi, J.; Cheon, J. Chem. Commun. 2007, 1203.
  11. Chutia, P.; Kato, S.; Kojima, T.; Satokawa, S. Polyhedron 2009, 28, 370. https://doi.org/10.1016/j.poly.2008.10.063
  12. Melero, J. A.; Grieken, R. V.; Morales, G. Chem. Rev. 2006, 106, 3790. https://doi.org/10.1021/cr050994h
  13. Astruc, D.; Lu, F.; Aranzaes, J. R. Angew. Chem. Int. Ed. 2005, 44, 7852. https://doi.org/10.1002/anie.200500766
  14. Morent, S.; Vasseur, S.; Grasset, F.; Duguet, E. J. Mater. Chem. 2004, 14, 2161. https://doi.org/10.1039/b402025a
  15. Trost, B. M.; Fleming, I. Eds. Comprehensive Organic Synthesis (Oxidation); Pergamon Press: New York, 1991.
  16. Sheldon, R. A.; Kochi, J. K. Metal-catalyzed Oxidation of Organic Compounds; Academic: New York, 1981.
  17. Sheldon, R. A.; Arends, I. W. C. E.; Isabel, U. Green Chemistry and Catalysis; Wiley-VCH: Weinheim, Germany, 2007.
  18. Gawande, M. B.; Rathi, A.; Nogueira, I. D.; Ghumman, C. A. A.; Bundaleski, N.; Teodoro, O. M. N. D.; Branco, P. S. Chem. Plus Chem. 2012, 77, 865.
  19. Tonga, J.; Bo, L.; Li, Z.; Lei, Z.; Xia, C. J. Mol. Catal. A: Chem. 2009, 307, 58. https://doi.org/10.1016/j.molcata.2009.03.010
  20. Lu, T.; Du, Z.; Liu, J.; Ma, H.; Xu, J. Green Chem. 2013, 15, 2215. https://doi.org/10.1039/c3gc40730f
  21. Anipsitakis, G. P.; Dionysiou, D. D. Environ. Sci. Technol. 2003, 37, 4790. https://doi.org/10.1021/es0263792
  22. Cimen, Y.; Turk, H. Appl. Catal. A: Gen. 2008, 340, 52. https://doi.org/10.1016/j.apcata.2008.01.031
  23. Madhavan, J.; Maruthamuthu, P.; Murugesan, S.; Anandan, S. Appl. Catal. B: Environ. 2008, 83, 8. https://doi.org/10.1016/j.apcatb.2008.01.021
  24. Wozniak, L. A.; Stec, W. J. Tetrahedron Lett. 1999, 40, 2637. https://doi.org/10.1016/S0040-4039(99)00261-0
  25. Wozniak, L. A.; Koziolkiewicz, M.; Kobylanska, A.; Stec, W. J. Bioorg. Med. Chem. Lett. 1998, 8, 2641. https://doi.org/10.1016/S0960-894X(98)00492-2
  26. Webb, K. S.; Levy, D. Tetrahedron Lett. 1995, 36, 5117. https://doi.org/10.1016/0040-4039(95)00963-D
  27. Webb, K. S.; Ruszkay, S. J. Tetrahedron 1998, 54, 401. https://doi.org/10.1016/S0040-4020(97)10299-X
  28. Trost, B. M.; Curran, D. P. Tetrahedron Lett. 1981, 22, 1287. https://doi.org/10.1016/S0040-4039(01)90298-9
  29. Baumstark, A. L.; Beeson, M.; Vasquez, P. C. Tetrahedron Lett. 1989, 30, 5567. https://doi.org/10.1016/S0040-4039(01)93801-8
  30. Zhao, S. Y.; Lee, D. K.; Kim, C. W.; Cha, H. G.; Kim, Y. H.; Kang, Y. S. Bull. Korean Chem. Soc. 2006, 27, 237. https://doi.org/10.5012/bkcs.2006.27.2.237

Cited by

  1. Promotion effect of nickel for Cu–Ni/γ-Al2O3 catalysts in the transfer dehydrogenation of primary aliphatic alcohols vol.14, pp.1, 2017, https://doi.org/10.1007/s13738-016-0963-2
  2. Microwave-assisted pseudo four-component synthesis of trans,trans-2-amino-1,3,3-tricyano-5-nitro-4,6-bis(aryl)cyclohexenes using α-Fe2O3 nanoparticles vol.148, pp.6, 2017, https://doi.org/10.1007/s00706-016-1890-8
  3. Catalytic performance of graphene-bimetallic composite for heterogeneous oxidation of acid orange 7 from aqueous solution vol.24, pp.8, 2017, https://doi.org/10.1007/s11356-017-8379-9
  4. Nanoparticles as an Efficient and Reusable Catalyst for the Green Synthesis of 2,4,6,8,10,12-Hexabenzyl-2,4,6,8,10,12-hexaazaisowurtzitane as CL-20 Explosive Precursor vol.35, pp.3, 2017, https://doi.org/10.1080/07370652.2016.1190795
  5. Nanoparticles vol.38, pp.8, 2017, https://doi.org/10.1002/bkcs.11187
  6. Magnetic Fe–Co crystal doped hierarchical porous carbon fibers for removal of organic pollutants vol.5, pp.34, 2017, https://doi.org/10.1039/C7TA03990E
  7. Synthesis and Characterization of the First Generation of Polyamino-Ester Dendrimer-Grafted Magnetite Nanoparticles from 3-Aminopropyltriethoxysilane (APTES) via the Convergent Approach pp.1876-9918, 2018, https://doi.org/10.1007/s12633-016-9497-6
  8. vol.14, pp.4, 2018, https://doi.org/10.1108/MMMS-07-2017-0068
  9. Green Chemistry Approach for the Synthesis of Copper Oxide Nanoparticles Using Tragacanth Gel and Their Structural Characterization vol.59, pp.2, 2018, https://doi.org/10.1134/S0022476618020324
  10. Synthesis of 2-amino-4,6-diarylnicotinonitrile in the presence of CoFe2O4@SiO2-SO3H as a reusable solid acid nanocatalyst under microwave irradiation in solvent-freeconditions vol.11, pp.4, 2014, https://doi.org/10.1007/s12633-018-0034-7
  11. Sulfonic Acid-Functionalized Silica-Coated Magnetic Nanoparticles as a Reusable Catalyst for the Preparation of Pyrrolidinone Derivatives Under Eco-Friendly Conditions vol.11, pp.6, 2014, https://doi.org/10.1007/s12633-019-0087-2
  12. A novel CoFe2O4@Cr-MIL-101/Y zeolite ternary nanocomposite as a magnetically separable sonocatalyst for efficient sonodegradation of organic dye contaminants from water vol.10, pp.17, 2014, https://doi.org/10.1039/d0ra00877j
  13. Based on CuFe2O4 MNPs: Magnetically recoverable nanocatalysts in coupling reactions vol.50, pp.14, 2014, https://doi.org/10.1080/00397911.2020.1728335
  14. Greenness Assessment and Synthesis for the Bio-Based Production of the Solvent 2,2,5,5-Tetramethyloxolane (TMO) vol.2, pp.3, 2021, https://doi.org/10.3390/suschem2030023