Next Article in Journal
Drugs for COVID-19: An Update
Previous Article in Journal
Direct Correlation of Surface Tension and Surface Composition of Ionic Liquid Mixtures—A Combined Vacuum Pendant Drop and Angle-Resolved X-ray Photoelectron Spectroscopy Study
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 27
Issue 23
10.3390/molecules27238560
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Polyoxovanadate-Based Cyclomatrix Polyphosphazene Microspheres as Efficient Heterogeneous Catalysts for the Selective Oxidation and Desulfurization of Sulfides

by
Yinghui Hu
1,†,
Diping Huang
1,†,
Jing Yan
1,*,
Zhiliang Miao
1,
Lize Yu
2,
Ningjing Cai
2,
Quanhai Fang
1,
Qiuyu Zhang
1 and
Yi Yan
1,*
1
Department of Chemistry, School of Chemistry and Chemical Engineering, Key Laboratory of Special Functional and Smart Polymer Materials of Ministry of Industry and Information Technology, Northwestern Polytechnical University, Xi’an 710129, China
2
Queen Mary University of London Engineering School, Northwestern Polytechnical University, Xi’an 710129, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2022, 27(23), 8560; https://doi.org/10.3390/molecules27238560
Submission received: 1 November 2022 / Revised: 21 November 2022 / Accepted: 29 November 2022 / Published: 5 December 2022
Browse Figures
Review Reports Versions Notes

Abstract

:
The [V6O13]2− cluster is successfully immobilized to the polymeric framework of cyclomatrix polyphosphazene via the facile precipitation polymerization between the phenol group symmetrically modified [V6O13]2− and hexachlorocyclotriphosphazene. The structure of the as-prepared polyoxometalate-containing polyphosphazene (HCCP-V) was characterized by FT-IR, XPS, TGA, BET, as well as SEM and zeta potential. The presence of a rigid polyoxometalate cluster not only supports the porous structure of the polymeric framework but also provides an improved catalytic oxidation property. By using H2O2 as an oxidant, the as-prepared HCCP-V exhibited improved catalytic oxidation activity toward MPS, DBT, and CEES, which can achieve as high as 99% conversion. More importantly, the immobilization of POMs in the network of cyclomatrix polyphosphazene also provides better recyclability and stability of the heterogeneous catalyst.

1. Introduction

Metal-containing polymers (MCPs) receive broad attention due to the synergetic effect from the functionality of the metal unit and the processability of the polymeric framework [1,2,3,4,5]. As one of the potential candidates for the functional metal units [6], polyoxometalates (POMs) have been introduced to the polymeric framework via either covalent modification [7,8] or ionic interactions [9,10], due to their diverse applications in many fields, such as catalysis, energy conversion, memory storage, medicine, and so on [11,12,13]. The variety of POMs structures and components as well as the topology of polymers provide rational design of POMs-containing polymers for specific application [14], especially in the field of flexible electronics [15].
As a special class of POMs, vanadium-containing POMs have received extensive attention in recent years due to their unique properties [16]. The rich redox properties of vanadium enabled its application in the construction of a high-performance zinc-ion battery [17] as well as electrochemical capacitors [18]. Polyoxovanadates (POVs) also showed interesting biomedical applications, as antidiabetic, antibacterial, antiprotozoal, antiviral, and anticancer drugs [19]. For example, both decavanadate and metformin-decavanadate exert antiproliferative effects on melanoma cells at 10 times lower concentrations than monomeric vanadate [20].
More importantly, POVs have also been reported to be powerful catalysts for the catalytic oxidation of sulfides owing to their multiple redox state [21,22]. For example, isopolyoxovanadate [H3V10O28]3− showed high catalytic activity in oxidation of dibenzothiophene (DBT) to corresponding sulfone by using molecular oxygen as an oxidant under mild conditions [23]. Moreover, POVs also exhibited excellent catalytic properties in the decontamination of chemical warfare agents, such as sulfur mustard. For example, Hu and coworkers reported that H13[(CH3)4N]12[PNb12O40(VVO)2⋅(VIV4O12)2]⋅22 H2O can effectively catalyze both the hydrolysis of the nerve agent simulant diethyl cyanophosphonate (DECP) and selective oxidation of the mustard simulant 2-chloroethyl ethyl sulfide (CEES) [24]. To improve the recyclability and stability of POVs-based catalysts, different strategies have been developed to immobilize POVs: (i) Introduce POVs to the metal-organic framework (MOF) or other porous materials [25], such as zeolite, via non-covalent interaction. For example, several POVs-based MOFs, [Co(HDTBA)V2O6] [26], [Co2L0.5V4O12]⋅3DMF [27], and [Cu(mIM)4]V2O6 [28], were synthesized and can efficiently catalyze the H2O2- or tert-butyl hydroperoxide-based oxidation of sulfides and oxidative detoxification of the sulfur mustard simulant CEES. (ii) Immobilize POVs to the polymeric framework via covalent bonds [29]. For example, ring-opening metathesis polymerization of a POMs-based norbornene monomer was developed by Wang’s group [30]. Hill and coworkers reported the POMs-based gelating network via the polycondensation between [H3V10O28]3− and polyol precursors [31]. To extend the polymeric framework of POM-based MCPs, we developed a facile preparation method of POMs-containing cyclomatrix polyphosphazenes through the precipitation polymerization of hydroxyl-functional POMs and hexachlorocyclotriphosphazene [14]. It is hypothesized that if POVs can be introduced to such structure, the homogeneous distribution of POVs in the cyclomatrix framework and its porosity may provide multiple interaction sites between the catalyst and the substrate, which will enable better oxidation activity and recyclability for the selective oxidation of sulfides [32,33].
Herein, we report the immobilization of [V6O13]2− to the cyclomatrix polyphosphazene microspheres via the precipitation polymerization between phenyl symmetrically modified [V6O13]2− and hexachlorocyclotriphosphazene. The resulted HCCP-V displayed versatile properties in the selective oxidation of different sulfides, including methyl phenyl sulfide (MPS), DBT, and CEES. It is believed that the design of POMs-based cyclomatrix polyphosphazene microspheres may provide a new platform for the construction of POMs-based MCPs toward task-specific applications.

2. Results and Discussion

2.1. Structural and Morphological Characterization of HCCP-V

As shown in Scheme 1A, there are mainly two strategies to incorporate polyoxovanadates (POVs) into the polymeric framework: (i) poly-condensation between [H3V10O28]3− and polyol precursors [31], and (ii) free radical polymerization of vinyl groups symmetrically modified [V6O13]2− [34,35,36]. Owing to the multiple redox states of vanadium, the yield of such condensation is usually low, limiting the practical application of POV-based materials. To overcome such disadvantage, inspired by our previous study on the polyoxometalate-containing cyclomatrix polyphosphazene microspheres [14], precipitation polymerization was used to immobilize functional POV to the framework of cyclomatrix polyphosphazene. As shown in Scheme 1B, the synthetic methodology of target POV-containing cyclomatrix polyphosphazene HCCP-V is very straightforward. To improve the reactivity of the hydroxyl group of V6O13-OH toward P−Cl, phenol groups were introduced via the 1,1′-carbonyldiimidazole (CDI)-mediated condensation. Then, the target POV-containing cyclomatrix polyphosphazene microsphere can be facile-prepared via the precipitation polymerization between V6O13-PhOH and hexachlorocyclotriphosphazene (HCCP) with the aid of triethylamine as a base. As shown in Figure S2A, the peaks at 9.04, 8.19, 7.17, and 6.67 ppm can be assigned to the phenol groups, indicating the successful grafting of phenol groups to the [V6O13]2− cluster, which is in good accordance with the literature [14]. Meanwhile, the modification of phenol groups can also be demonstrated by the characteristic peaks of N–H at 3280 cm−1 and benzene ring at 1606 and 1553 cm−1 (Figure S2B). Moreover, the presence of characteristic peaks of V–O and V–O–V stretching at 951, 835, and 712 cm−1 indicated the structure integrity of the V6O13 cluster after CDI modification.
The phenol groups endowed V6O13-PhOH with improved reactivity towards HCCP, facilitating the preparation of HCCP-V. As shown in Figure 1A, the peaks at 1238 and 906 cm–1 can be assigned to P=N and P–O–Ph [37,38], indicating the successful precipitation polymerization. Furthermore, the characteristic peaks of V–O at 955 cm−1 and V–O–V at 805 and 706 cm−1 indicated that the vanadium clusters were introduced into the crosslink network. The characteristic peaks of the N–H bond and benzene ring were found at 3140, 1543 cm−1 and 1508, 1606 cm−1, indicating the existence of V6O13-PhOH. The introduction of the [V6O13]2− cluster to the framework of HCCP-V can be further proven by corresponding thermal gravimetric analysis (TGA). As shown in Figure 1B, the presence of [V6O13]2− not only improved the thermal stability of the cyclomatrix polyphosphazene but also increased the residual weight at a high temperature. According to the 42% residual of P2O5 and V2O5 at 900 °C, it can be calculated that there is ca. 18.85 wt.% of the [V6O13]2− cluster in the resulted HCCP-V (calculation is presented in the Supplementary Materials).
To further characterize the detailed structure of HCCP-V, X-ray photoelectron spectroscopy (XPS) was used. As shown in Figure 2A,B, the successful introduction of V6O13-PhOH to the polymeric framework can be proven by the presence of N1s signals from N–H of TBA+ at 401.1 eV and P=N at 398.8 eV, as well as the O1s signals from C–O–P at 533.8 eV and V–O at 531.6 eV. Moreover, the P2p signals at 135, 134, and 132.9 eV (Figure 2C) can be assigned to P–Cl (I), P=N (II), and C–O–P (III), respectively, indicating that most of the phosphazenes were involved in the cross-linked framework [14,39,40]. Furthermore, as shown in Figure 2D, the signals of V2p at 524 and 516.7 eV indicated that the valence state of V mostly retained +5, demonstrating that their redox properties were retained in the resulted HCCP-V, and enabled their potential application in the selective oxidation of sulfides.
As expected, the resulted HCCP-V displayed a spherical aggregated structure with a diameter of ca. 60 nm (Figure 3A and Figure S3). Due to the homogeneous distribution of the anionic [V6O13]2− cluster in the cyclomatrix structure, the resulted HCCP-V displayed a negative zeta potential of −32 mV (Figure 3B), which also indicated the relatively stable nature of such particles. In agreement with our previous study, the rigidity of the V6O13-PhOH cluster supported the porous structure of the resulted HCCP-V very well (typical IV-type isotherm), although the BET surface area was as low as 12.73 m2/g (Figure 3C) due to the possible occupation of the pores by the bulky TBA cations [34,41]. The pore size distribution calculated from the desorption curve mainly ranged from 30 to 65 nm (Figure 3D), revealing the nature of the mesoporous structure.

2.2. Catalytic Oxidation of MPS by HCCP-V

The [V6O13]2− clusters are known to be active towards the oxidation of sulfides [42]. To demonstrate the applicability of HCCP-V for H2O2-based oxidative removal reactions, different sulfides, including MPS, DBT, and CEES, were used as substrates in the catalytic oxidation [43] (as shown in Scheme 2).
Firstly, the catalytic oxidation of MPS was used as a model reaction to explore the heterogeneous catalytic activity of HCCP-V. Generally, the catalytic oxidation was carried out at different temperatures (25 °C, 40 °C, and 55 °C) with [MPS]:[H2O2]:[catalyst] = 1:1.2:1/400. As a control experiment, it can be found that no oxidation was observed when no catalyst was added or organic cyclomatrix phosphazenes HCCP-BPS was used (Figure S5). In contrast, the presence of V6O13-PhOH in HCCP-V enables the catalytic oxidation of MPS to methyl phenyl sulfoxide (MPSO). The reaction was monitored by HPLC (Figure 4), and it can be seen that with the prolongation of the reaction time, the peak of MPS at 7.6 min gradually decreased, and the peak of MPSO at 2.7 min increased, which is in good agreement with corresponding 1H NMR results (Figure S6). More importantly, the overoxidation was relatively suppressed, as less than 2% of methyl phenyl sulfone (MPSO2) was detected at a retention time of 3.3 min. The oxidation of MPS can be completed within 180 min with MPSO conversion as high as 99% at 25 °C. Moreover, the reaction rate can be promoted at high temperatures. For example, the reaction can be completed within 20 min at 55 °C (Table 1). The relationship between ln(Ct/C0) and the reaction time reveals that the kinetics of the catalytic oxidation of MPS by HCCP-V follows the second-order kinetics, with the highest reaction rate constant of 0.01189 min−1 at 55 °C.
By comparing the catalytic oxidation results at different temperatures (Figure 4 and Table 1) it can be found that the reaction rate was greatly improved with the increase of the reaction temperature. However, the conversion of MPS was reduced at high temperatures. Therefore, 40 °C was chosen as the optimized reaction temperature for catalytic oxidation of MPS.
To explore the effect of the oxidant dosage on the catalytic oxidation of MPS, the reaction was also investigated with [MPS]:[H2O2]:[catalyst] = 1:1:1/400 at different temperatures (25 °C, 40 °C, and 55 °C). As shown in Figure 5, the oxidation of MPS was completed in 120 min, and the conversion of MPS was 85.6% at 25 °C, which is lower than that of [MPS]:[H2O2]:[catalyst] = 1:1.2:1/400. Therefore, a slightly excess amount of the oxidant should be better for such kind of reaction. Similarly, increasing the reaction temperature can accelerate the oxidation by reducing the reaction time from 120 min at 25 °C to almost 12 min at 55 °C. However, the conversion of MPS was also decreased.
By comparing the catalytic results of MPS with different ratios of HCCP-V (Table 1), it can be concluded that (i) the reaction rate and TOF increased with the temperature, and (ii) under the same temperature, the excess amount of oxidant favored the catalytic oxidation reaction.

2.3. Catalytic Oxidation of DBT by HCCP-V

Besides MPS, dibenzothiophene (DBT) was also selected as the substrate to explore the potential application of HCCP-V in the oxidative desulfurization of diesel [44,45]. Generally, the oxidation of DBT was more challenging than MPS. Therefore, excess amounts of catalyst and high temperatures were usually used in the oxidation of DBT. The catalytic experiment was monitored by HPLC and performed at 70 °C (or 80 °C) in acetonitrile (solvent, 5 mL) with DBT (115.16 mg, 1 eq), catalyst (10 mg, 1/100 eq), H2O2 (313.4 μL, 5 eq or 0.5 mL, 8 eq), and naphthalene (internal standard). As shown in Figure 6A–C, in the case of 70 °C and 5 eq of H2O2, the peak of DBT with a retention time of 17.6 min gradually decreased, and the peaks of DBTSO at 3.7 min and DBTSO2 at 4.6 min gradually increased, indicating the successful catalytic oxidation of DBT. However, only 79.8% conversion of DBT and 52.5% conversion of DBTSO2 were achieved after 50 min, indicating that the amount of oxidant was insufficient to fully convert DBT. Moreover, the oxidative desulfurization catalyzed by HCCP-V followed the second-order kinetics with a reaction rate constant of 0.0007 min−1 (Figure 6C). By increasing the temperature to 80 °C, the reaction time was reduced from 50 min for 70 °C to 15 min, however, the conversion of both DBT and DBTSO2 was also decreased (Figure 6D–F).
Interestingly, by increasing the dosage of H2O2 from 5 to 8 eq and keeping the temperature at 70 °C, the oxidative desulfurization of DBT can be completed within 50 min. More importantly, the conversion curves of DBT and DBTSO2 were greatly improved to 92.2% and 98.9%, respectively (Figure 6G–I, Table 2).

2.4. Catalytic Oxidation of CEES by HCCP-V

To further explore the potential application of HCCP-V in the decontamination of chemical warfare agents, the catalytic oxidation of the mustard simulant 2-chloroethyl ethyl sulfide (CEES) [46,47] has been explored. As monitored by 1H NMR (Figure 7A), the proton b in CEES gradually disappeared and proton f in the oxidized product CEESO appeared in the down field [24], indicating that CEES is completely and rapidly oxidized in the presence of HCCP-V and H2O2 at room temperature, showing its promise as an effective catalyst for the removal of mustard under mild conditions. Moreover, this reaction selectively forms the less toxic 2-chloroethyl ethyl sulfoxide (CEESO) without overoxidation to the harmful 2-chloroethyl ethyl sulfone (CEESO2) product (Figure 7B).

2.5. Recyclability of HCCP-V

All the above results demonstrated the versatility of HCCP-V in the catalytic oxidation of sulfides. To investigate the stability of such heterogeneous catalyst, the recyclability of HCCP-V was studied. Generally, the model reaction of MPS catalytic oxidation was carried out with oxidant dosage of 1.2 eq and temperature of 40 °C. According to HPLC and the conversion curves (Figure S8), the reaction time for the complete oxidation of MPS was ca. 20 min, and the conversion of MPS was above 99% during 4 cycles, indicating the tight immobilization of V6O13-PhOH in the polymeric framework and the robustness of the catalyst. However, the conversion of MPSO in repeated experiments slightly decreased from 85.72% to 72.65% (Figure 8A). More importantly, the structure of the catalyst also remained intact, as shown in Figure 8B. It can be found that after 4 cycles of catalytic oxidation, the peaks of the V–O bond at 954 cm−1 and the V–O–V bond at 754 and 681 cm−1 did not change, indicating that the structures of V6O13-PhOH clusters were stable.

3. Materials and Methods

3.1. Materials

Hexachlorocyclotriphosphazene (HCCP) and sodium metavanadate were purchased from Aladdin Biochemical Technology Co., Ltd. (Shanghai, China). Pentaerythritol and p-aminophenol were supplied by Shanghai Macklin Biochemical Co., Ltd. (Shanghai, China). HCCP was purified by sublimation in vacuum at 60 °C, three times. Acetonitrile, dimethyl sulfoxide (DMSO), and N,N-dimethylformamide (DMF) were stirred overnight with CaH2 and distilled before use. Triethylamine (TEA) was dried with KOH and distilled before use. Other reagents and chemicals were analytical grade and used as received.

3.2. Synthetic Procedures of Polyoxovanadate-Based Cyclomatrix Polyphosphazene Microspheres

3.2.1. Synthesis of [N(C4H9)4]2[V6O13{(OCH2)3CCH2OH}2] (V6O13-OH)

The synthetic procedure of V6O13-OH has been reported already [48], and the modified method was as follows: NaVO3 (4 g, 2 eq) and pentaerythritol (2.23 g, 1 eq) were dissolved in 50 mL of deionized water at 60 °C. After cooling to room temperature, the pH of the solution was adjusted to 1.0 with 1.0 M HCl. The reaction mixture was heated at 80 °C for 6 h in the dark. Then, the dark green insoluble precipitate was removed by filtration to afford a deep red solution. To this solution, tetrabutylammonium bromide (TBABr) aqueous solution (4 g in 25 mL) was added dropwise and stirred for 1–2 h at room temperature. The resulted brick red precipitate was collected by filtration and washed with ethanol 3 times to afford the final product. Yield: 34%, based on V. FT-IR (KBr, cm−1): 3410 (−OH, m), 2961 (CH, s), 2923 (CH, s), 2853 (CH, m), 1637 (−OH, w), 1480 (CH, s), 1380 (s), 1126 (s), 1130 (m), 1067 (m), 1039 (C−O, m), 956 (V−O, s), 944 (vs), 811 (V−O−V, m), 720 (V−O−V, s), 582 (m). 1H NMR (400 MHz, DMSO-d6, δ): 5.74 (s, 2H, −OH), 4.87 (s, 12H, −CH2C−), 4.46 (s, 4H, −CCH2−), 3.15 (br, 16H, −NCH2−), 1.56 (br, 16H, −CH2−), 1.30 (br, 16H, −CH2−), 0.93 (br, 24H, −CH3).

3.2.2. Synthesis of [N(C4H9)4]2[V6O13{(OCH2)3CCH2OCONHC6H4OH}2] (V6O13-PhOH)

The solutions of p-aminophenol (523.8 mg, 1 eq) in 4 mL of DMSO and N,N’-carbonyldiimidazole (CDI, 934 mg, 1.2 eq) in 2 mL of DMSO were degassed by purging N2 for 30 min. The CDI solution was added dropwise to the Schlenk flask with p-aminophenol under N2 and stirred at room temperature in the dark for 5 h to obtain a 0.8 M stock solution. V6O13-OH (1.64 g, 1 eq) was dissolved in 7 mL of dry acetonitrile and purged N2 for 30 min in the dark. Then, 3.9 mL of the stock solution was added dropwise to the above solution. Dibutyltin dilaurate (0.92 mL, 1.2 eq) was used as a catalyst, and the reaction was stirred at 80 °C in the dark for 60 h. The reaction was monitored with FT-IR. After the reaction, precipitates were removed by centrifugation (9000 rpm, 5 min), and the supernatant was concentrated and added dropwise to TBABr aqueous solution (4 g in 25 mL). The resulted precipitate was collected and washed with dichloromethane and deionized water to afford the target compound. Yield: 44%, based on V. FT-IR (KBr, cm−1): 3280 (−NH, m), 2957 (CH, s), 2925 (CH, s), 2871 (CH, m), 1744 (w), 1693 (C=O, m), 1606 (Ph, s), 1553 (Ph, w), 1460 (CH, s), 1378 (s), 1220 (s), 1130 (m), 1068 (m), 1032 (C−O, m), 951 (V−O, s), 944 (vs), 835 (V−O−V, m), 712 (V−O−V, s), 579 (m) [49]. 1H NMR (DMSO-d6, 400 MHz, δ): 9.04 (s, 2H, −OH from phenol), 8.19 (s, 2H, −NH−), 7.17 (br, 4H, Ar−H), 6.67 (br, 4H, Ar−H), 4.87 (s, 6H, −CH2C−), 4.47(s, 4H, −CCH2−), 3.18 (br, 16H, −NCH2−), 1.57 (br, 16H, −CH2−), 1.23 (br, 16H, −CH2−), 0.93 (br, 24H, −CH3).

3.2.3. Precipitation Polymerization to Prepare Polyoxovanadate-Based Cyclomatrix Polyphosphazene Microspheres (HCCP-V)

The preparation was similar to our previous method [14,50], and the detailed procedure was as follows: V6O13-PhOH (0.8 g, 3 eq), TBABr (1.12 g, 20 eq), and HCCP (60.26 mg, 1 eq) were dissolved in a mixture solvent of 0.2 mL of DMF and 2.5 mL of acetonitrile. The reaction mixture was degassed with N2 for 30 min, followed by the addition of TEA (0.44 mL, 18 eq), then stirred at 90 °C in the dark for 72 h. The reaction was monitored with FT-IR. After the reaction, the resultant precipitate was collected by centrifugation (9000 rpm, 5 min), then washed with acetonitrile and ethanol to afford the target product. Yield: 71%. FT-IR (KBr, cm−1): 3140 (−NH, m), 2920 (CH, s), 2852 (CH, m), 1606 (Ph, s), 1543 (N−H, s), 1508 (Ph, m), 1238 (P=N, s), 955 (V−O, s), 906 (P−O−Ph, s), 805 (V−O−V, m), 706 (V−O−V, s), 650 (s).

3.3. Characterization

FT-IR spectra were recorded on a Bruker TENSOR27 with a resolution of 0.4 cm−1 over the range of 4000−400 cm−1. 1H NMR spectra were recorded with a Bruker Avance 400 spectrometer at 400 MHz in CDCl3 and DMSO-d6 using tetramethylsilane (TMS) as an internal standard. Thermal stability was investigated on a Mettler Toledo TGA 2 instrument with a heating rate of 10 °C/min in O2 atmosphere. X-ray photoelectron spectroscopy (XPS) spectra were recorded on a Kratos AXIS Ultra DLD spectrometer with a monochromatic Al Kα X-ray source. The nitrogen adsorption and desorption isotherm was measured at 77 K on an American Mike TriStar II 3020 analyzer. The morphology of the sample was observed on a FEI Verios G4 scanning electron microscope (SEM). The samples were coated with a thin sputtered Au before SEM characterization. High-performance liquid chromatography (HPLC) results were collected by the Shimadzu Essentia LC-16 with ultraviolet detector.

3.4. The Catalytic Oxidation Experiments

General procedure of the catalytic oxidation of methyl phenyl sulfide (MPS): MPS (78 mg, 1 eq) was dissolved in 5 mL of acetonitrile, and naphthalene (80.1 mg, 1 eq) was added as an internal standard. The mixture was stirred for 10 min (500 rpm) and an aliquot was taken as the t0 sample. Freshly ground HCCP-V (2.5 mg, 1/400 eq) was added as a catalyst, and after stirring for 10 min, 30 wt.% H2O2 (77 μL, 1.2 eq or 63 μL, 1 eq) was added as an oxidant. The reaction temperature was set at 25 °C, 40 °C, or 55 °C, respectively, and the whole process was monitored by HPLC (1 mL/min, acetonitrile:H2O = 7:3, injection volume: 10 μL, detector wavelength: 254 nm). After the reaction, the catalyst was collected by centrifugation, and the final product was characterized by 1H NMR.
General procedure of the catalytic oxidation of dibenzothiophene (DBT): DBT (115.16 mg, 1 eq) was dissolved in 5 mL of acetonitrile, and naphthalene (80.1 mg, 1 eq) was added as an internal standard. The mixture was stirred for 10 min (500 rpm) and an aliquot was taken as the t0 sample. Freshly ground HCCP-V (10 mg, 1/100 eq) was added as a catalyst, and after stirring for 10 min, 30 wt.% H2O2 (313.4 μL, 5 eq or 0.5 mL, 8 eq) was added as an oxidant. The reaction temperature was set at 70 °C or 80 °C, and the whole process was monitored by HPLC (the condition was the same as the one for MPS).
General procedure of the catalytic oxidation of 2-chloroethyl ethyl sulfide (CEES): CEES (75 μL, 1 eq) was dissolved in 5 mL of acetonitrile. After stirring for 10 min (500 rpm), an aliquot was taken as the t0 sample. Freshly ground HCCP-V (2.5 mg, 1/400 eq) was added as a catalyst, and after stirring for 10 min, 30 wt.% H2O2 (77 μL, 1.2 eq) was added as an oxidant. The whole process was monitored by 1H NMR.

4. Conclusions

Functional polyoxovanadate [V6O13]2− were successfully immobilized to cyclomatrix polyphosphazene microspheres via precipitation polymerization. The rigidity and anionic nature of [V6O13]2− endowed the resulted HCCP-V with porosity and a negative charged surface. Owing to the homogeneous distribution of the [V6O13]2− cluster in the network and the high stability of the P=N framework, HCCP-V exhibited versatility in the catalytic oxidation of sulfides. By using H2O2 as an oxidant, the conversion of MPS, DBT, and CEES could be achieved as high as 99.6%, 92.2%, and 100% within 60 min, respectively. Moreover, the selectivity of MPSO, DBTSO2, and CEESO could be as high as 99%. Furthermore, the conversion of MPS was above 99% during 4 cycles, demonstrating the high stability and recyclability of such heterogeneous catalyst. This work provides facile methodology for the preparation of POMs-based MCPs for selective oxidation of sulfides. Moreover, the catalytic oxidation activity may be further improved by introducing other functional groups to the cyclomatrix polyphosphazene structure via synergetic interaction.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules27238560/s1, Figure S1: FT-IR spectrum (A) and 1H NMR spectrum (B) of V6O13-OH in DMSO-d6; Figure S2: 1H NMR spectrum (A) in DMSO-d6 and FT-IR spectrum (B) of V6O13-PhOH; Figure S3: SEM image of HCCP-V dispersed in EtOH; Figure S4: HPLC and standard curve of MPSO; Figure S5: Catalytic oxidation of MPS with H2O2 as oxidant: (A) no catalyst; (B) HCCP-BPS; Figure S6: 1H NMR spectra in CDCl3 for the product of the catalytic oxidation of MPS with different ratio of HCCP-V at different temperature (25 °C, 40 °C, and 55 °C): (A) 1.2 eq, (B) 1 eq; Figure S7: HPLC and standard curve of DBTSO2; Figure S8: HPLC traces and conversion curve of MPS oxidation during recycle experiment; Table S1: Comparison with other POM-based catalysts for catalytic oxidation of different sulfides. [51,52,53,54,55,56,57,58,59].

Author Contributions

Y.H., investigation and writing—original draft; D.H. and L.Y., investigation of the catalytic oxidation; Z.M., N.C. and Q.F., investigation on the preparation of the catalyst; J.Y., Q.Z. and Y.Y., project administration, funding acquisition, and writing—review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by NSFC (Nos. 21975205, 21504068), the Natural Science Foundation of Chongqing (cstc2020jcyj-msxmX1078), the Shaanxi National Science Foundation (2020JM-138), and the Open Project of the State Key Laboratory of Supramolecular Structure and Materials (sklssm2022022).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We would like to acknowledge the support by the NSFC (Nos. 21975205, 21504068), the Natural Science Foundation of Chongqing (cstc2020jcyj-msxmX1078), the Shaanxi National Science Foundation (2020JM-138), and the Open Project of the State Key Laboratory of Supramolecular Structure and Materials (sklssm2022022). N.C. and Q.F. are thankful for the support from the College Students’ Innovative Entrepreneurial Training Plan Program (S202210699412, S202210699433). The authors also thank the Analytical and Testing Center of Northwestern Polytechnical University for SEM testing.

Conflicts of Interest

There are no conflict to declare.

Sample Availability

Samples of the compounds are not available from the authors.

References

  1. Ho, C.L.; Wong, W.Y. Metal-containing polymers: Facile tuning of photophysical traits and emerging applications in organic electronics and photonics. Coord. Chem. Rev. 2011, 255, 2469–2502. [Google Scholar] [CrossRef]
  2. Yan, Y.; Zhang, J.Y.; Ren, L.X.; Tang, C.B. Metal-containing and related polymers for biomedical applications. Chem. Soc. Rev. 2016, 45, 5232–5263. [Google Scholar] [CrossRef] [Green Version]
  3. Friebe, C.; Hager, M.D.; Winter, A.; Schubert, U.S. Metal-containing Polymers via Electropolymerization. Adv. Mater. 2012, 24, 332–345. [Google Scholar] [CrossRef]
  4. Hailes, R.L.N.; Oliver, A.M.; Gwyther, J.; Whittell, G.R.; Manners, I. Polyferrocenylsilanes: Synthesis, properties, and applications. Chem. Soc. Rev. 2016, 45, 5358–5407. [Google Scholar] [CrossRef] [Green Version]
  5. Hardy, C.G.; Zhang, J.Y.; Yan, Y.; Ren, L.X.; Tang, C.B. Metallopolymers with transition metals in the side-chain by living and controlled polymerization techniques. Prog. Polym. Sci. 2014, 39, 1742–1796. [Google Scholar] [CrossRef]
  6. Yan, J.; Zheng, X.W.; Yao, J.H.; Xu, P.; Miao, Z.L.; Li, J.L.; Lv, Z.D.; Zhang, Q.Y.; Yan, Y. Metallopolymers from organically modified polyoxometalates (MOMPs): A review. J. Organomet. Chem. 2019, 884, 1–16. [Google Scholar] [CrossRef]
  7. Thorimbert, S.; Hasenknopf, B.; Lacote, E. Cross-Linking Organic and Polyoxometalate Chemistries. Isr. J. Chem. 2011, 51, 275–280. [Google Scholar] [CrossRef]
  8. Proust, A.; Matt, B.; Villanneau, R.; Guillemot, G.; Gouzerh, P.; Izzet, G. Functionalization and post-functionalization: A step towards polyoxometalate-based materials. Chem. Soc. Rev. 2012, 41, 7605–7622. [Google Scholar] [CrossRef]
  9. Yan, Y.; Wu, L.X. Polyoxometalate-Incorporated Supramolecular Self-Assemblies: Structures and Functional Properties. Isr. J. Chem. 2011, 51, 181–190. [Google Scholar] [CrossRef]
  10. Li, B.; Li, W.; Li, H.L.; Wu, L.X. Ionic Complexes of Metal Oxide Clusters for Versatile Self Assemblies. Acc. Chem. Res. 2017, 50, 1391–1399. [Google Scholar] [CrossRef]
  11. Long, D.L.; Burkholder, E.; Cronin, L. Polyoxometalate clusters, nanostructures and materials: From self assembly to designer materials and devices. Chem. Soc. Rev. 2007, 36, 105–121. [Google Scholar] [CrossRef]
  12. Long, D.L.; Tsunashima, R.; Cronin, L. Polyoxometalates: Building Blocks for Functional Nanoscale Systems. Angew. Chem. Int. Ed. 2010, 49, 1736–1758. [Google Scholar] [CrossRef]
  13. Li, C.Z.; Zhao, X.C.; Wang, A.Q.; Huber, G.W.; Zhang, T. Catalytic Transformation of Lignin for the Production of Chemicals and Fuels. Chem. Rev. 2015, 115, 11559–11624. [Google Scholar] [CrossRef]
  14. Zhang, J.P.; Miao, Z.L.; Yan, J.; Zhang, X.; Li, X.Z.; Zhang, Q.Y.; Yan, Y. Synthesis of Negative-Charged Metal-Containing Cyclomatrix Polyphosphazene Microspheres Based on Polyoxometalates and Application in Charge-Selective Dye Adsorption. Macromol. Rapid Commun. 2019, 40, e1800730. [Google Scholar] [CrossRef]
  15. Dubal, D.P.; Chodankar, N.R.; Kim, D.H.; Gomez-Romero, P. Towards flexible solid-state supercapacitors for smart and wearable electronics. Chem. Soc. Rev. 2018, 47, 2065–2129. [Google Scholar]
  16. Streb, C. Structure and Bonding in Molecular Vanadium Oxides: From Templates via Host-Guest Chemistry to Applications. In Polyoxometalate-Based Assemblies and Functional Materials; Song, Y.F., Ed.; Springer, Berlin, Germany, 2018; Volume 176, pp. 31–47.
  17. Zhou, T.; Xiao, H.R.; Xie, L.L.; Han, Q.; Qiu, X.J.; Xiao, Y.M.; Yang, X.L.; Zhu, L.M.; Cao, X.Y. Research on the electrochemical performance of polyoxovanadate material K4Na2V10O28 as a novel aqueous zinc-ion batteries cathode. Electrochim. Acta 2022, 424, 140621. [Google Scholar] [CrossRef]
  18. Vannathan, A.A.; Chandewar, P.R.; Shee, D.; Mal, S.S. Polyoxovanadate-Activated Carbon-Based Hybrid Materials for High-Performance Electrochemical Capacitors. J. Electrochem. Soc. 2022, 169, 050538. [Google Scholar] [CrossRef]
  19. Aureliano, M.; Gumerova, N.I.; Sciortino, G.; Garribba, E.; McLauchlan, C.C.; Rompel, A.; Crans, D.C. Polyoxidovanadates’ interactions with proteins: An overview. Coord. Chem. Rev. 2022, 454, 214344. [Google Scholar] [CrossRef]
  20. De Sousa-Coelho, A.L.; Aureliano, M.; Fraqueza, G.; Serrao, G.; Goncalves, J.; Sanchez-Lombardo, I.; Link, W.; Ferreira, B.I. Decavanadate and metformin-decavanadate effects in human melanoma cells. J. Inorg. Biochem. 2022, 235, 111915. [Google Scholar] [CrossRef]
  21. Wang, J.L.; Liu, X.M.; Du, Z.Y.; Xu, Y. Organo-functionalized polyoxovanadates: Crystal architecture and property aspects. Dalton Trans. 2021, 50, 7871–7886. [Google Scholar] [CrossRef]
  22. Anjass, M.; Lowe, G.A.; Streb, C. Molecular Vanadium Oxides for Energy Conversion and Energy Storage: Current Trends and Emerging Opportunities. Angew. Chem. Int. Ed. 2021, 60, 7522–7532. [Google Scholar] [CrossRef] [PubMed]
  23. Tang, N.F.; Zhang, Y.N.; Lin, F.; Lu, H.Y.; Jiang, Z.X.; Li, C. Oxidation of dibenzothiophene catalyzed by C8H17N(CH3)(3) (3)H3V10O28 using molecular oxygen as oxidant. Chem. Commun. 2012, 48, 11647–11649. [Google Scholar] [CrossRef] [PubMed]
  24. Dong, J.; Hu, J.F.; Chi, Y.N.; Lin, Z.G.; Zou, B.; Yang, S.; Hill, C.L.; Hu, C.W. A Polyoxoniobate-Polyoxovanadate Double-Anion Catalyst for Simultaneous Oxidative and Hydrolytic Decontamination of Chemical Warfare Agent Simulants. Angew. Chem. Int. Ed. 2017, 56, 4473–4477. [Google Scholar] [CrossRef] [PubMed]
  25. Nohra, B.; El Moll, H.; Albelo, L.M.R.; Mialane, P.; Marrot, J.; Mellot-Draznieks, C.; O’Keeffe, M.; Biboum, R.N.; Lemaire, J.; Keita, B.; et al. Polyoxometalate-Based Metal Organic Frameworks (POMOFs): Structural Trends, Energetics, and High Electrocatalytic Efficiency for Hydrogen Evolution Reaction. J. Am. Chem. Soc. 2011, 133, 13363–13374. [Google Scholar] [CrossRef] [PubMed]
  26. Wang, X.; Zhang, T.; Li, Y.H.; Lin, J.F.; Li, H.; Wang, X.L. In Situ Ligand-Transformation-Involved Synthesis of Inorganic-Organic Hybrid Polyoxovanadates as Efficient Heterogeneous Catalysts for the Selective Oxidation of Sulfides. Inorg. Chem. 2020, 59, 17583–17590. [Google Scholar] [CrossRef]
  27. Lu, B.B.; Yang, J.; Liu, Y.Y.; Ma, J.F. A Polyoxovanadate Resorcin 4 arene-Based Porous Metal Organic Framework as an Efficient Multifunctional Catalyst for the Cycloaddition of CO2 with Epoxides and the Selective Oxidation of Sulfides. Inorg. Chem. 2017, 56, 11710–11720. [Google Scholar] [CrossRef]
  28. Li, J.K.; Huang, X.Q.; Yang, S.; Xu, Y.Q.; Hu, C.W. Controllable Synthesis, Characterization, and Catalytic Properties of Three Inorganic-Organic Hybrid Copper Vanadates in the Highly Selective Oxidation of Sulfides and Alcohols. Cryst. Growth Des. 2015, 15, 1907–1914. [Google Scholar] [CrossRef]
  29. Monakhov, K.Y.; Bensch, W.; Kogerler, P. Semimetal-functionalised polyoxovanadates. Chem. Soc. Rev. 2015, 44, 8443–8483. [Google Scholar] [CrossRef] [Green Version]
  30. Miao, W.K.; Yan, Y.K.; Wang, X.L.; Xiao, Y.; Ren, L.J.; Zheng, P.; Wang, C.H.; Ren, L.X.; Wang, W. Incorporation of Polyoxometalates into Polymers to Create Linear Poly(polyoxometalate)s with Catalytic Function. Acs Macro Lett. 2014, 3, 211–215. [Google Scholar] [CrossRef]
  31. Sullivan, K.P.; Neiwert, W.A.; Zeng, H.D.; Mehta, A.K.; Yin, Q.S.; Hillesheim, D.A.; Vivek, S.; Yin, P.C.; Collins-Wildman, D.L.; Weeks, E.R.; et al. Polyoxometalate-based gelating networks for entrapment and catalytic decontamination. Chem. Commun. 2017, 53, 11480–11483. [Google Scholar] [CrossRef]
  32. Kickelbick, G. Concepts for the incorporation of inorganic building blocks into organic polymers on a nanoscale. Prog. Polym. Sci. 2003, 28, 83–114. [Google Scholar] [CrossRef]
  33. Zhou, Y.T.; Wemyss, A.M.; Brown, O.B.; Huang, Q.Y.; Wan, C.Y. Structure and electrochemical properties of hierarchically porous carbon nanomaterials derived from hybrid ZIF-8/ZIF-67 bi-MOF coated cyclomatrix poly(organophosphazene) nanospheres. New J. Chem. 2020, 44, 4353–4362. [Google Scholar] [CrossRef]
  34. Chen, K.; Liu, S.Q.; Zhu, W.; Yin, P.C. Surface Engineering Promoted Insulin-Sensitizing Activities of Sub-Nanoscale Vanadate Clusters through Regulated Pharmacokinetics and Bioavailability. Small 2022, 18, 2203957. [Google Scholar] [CrossRef] [PubMed]
  35. Ma, L.T.; Xu, Z.W.; Chen, Y.D.; Zhang, M.X.; Yin, J.F.; Li, M.; Chen, K.; Yin, P.C. Sub-nanoscaled Metal Oxide Cluster-Integrated Polymer Network for Quasi-Homogeneous Catalysis. Acs Appl. Mater. Interfaces 2020, 12, 38655–38661. [Google Scholar] [CrossRef]
  36. Huang, B.; Xiao, Z.C.; Wu, P.F. A New Scheme to Prepare Polyoxovanadate-Polymer Hybrid Materials. J. Clust. Sci. 2021, 32, 1739–1745. [Google Scholar] [CrossRef]
  37. Ahmad, M.; Nawaz, T.; Hussain, I.; Chen, X.; Imran, M.; Hussain, R.; Assiri, M.A.; Ali, S.; Wu, Z.P. Phosphazene Cyclomatrix Network-Based Polymer: Chemistry, Synthesis, and Applications. Acs Omega 2022, 7, 28694–28707. [Google Scholar] [CrossRef]
  38. Fu, J.W.; Huang, X.B.; Zhu, L.; Tang, X.Z. One-pot synthesis of porous cyclomatrix-type polyphosphazene nanotubes with closed ends via an in situ template approach. Scr. Mater. 2008, 58, 1047–1049. [Google Scholar] [CrossRef]
  39. Maaskant, E.; Gojzewski, H.; Hempenius, M.A.; Vancso, G.J.; Benes, N.E. Thin cyclomatrix polyphosphazene films: Interfacial polymerization of hexachlorocyclotriphosphazene with aromatic biphenols. Polym. Chem. 2018, 9, 3169–3180. [Google Scholar] [CrossRef] [Green Version]
  40. Wang, Y.; Yu, Y.W.; Li, L.; Zhang, H.B.; Chen, Z.; Yang, Y.C.; Jiang, Z.H.; Mu, J.X. Preparation and Properties of Novel Crosslinked Polyphosphazene-Aromatic Ethers Organic-Inorganic Hybrid Microspheres. Polymers 2022, 14, 2411. [Google Scholar] [CrossRef]
  41. Orum, S.M. Novel cyclomatrix polyphosphazene nanospheres: Preparation, characterization and dual anticancer drug release application. Polym. Bull. 2022, 79, 2851–2869. [Google Scholar] [CrossRef]
  42. Han, J.W.; Hill, C.L. A coordination network that catalyzes O-2-based oxidations. J. Am. Chem. Soc. 2007, 129, 15094–15095. [Google Scholar] [CrossRef] [PubMed]
  43. Akopyan, A.; Eseva, E.; Polikarpova, P.; Kedalo, A.; Vutolkina, A.; Glotov, A. Deep Oxidative Desulfurization of Fuels in the Presence of Brönsted Acidic Polyoxometalate-Based Ionic Liquids. Molecules 2020, 25, 536. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Zhang, M.; Zhu, W.S.; Xun, S.H.; Li, H.M.; Gu, Q.Q.; Zhao, Z.; Wang, Q. Deep oxidative desulfurization of dibenzothiophene with POM-based hybrid materials in ionic liquids. Chem. Eng. J. 2013, 220, 328–336. [Google Scholar] [CrossRef]
  45. Hao, L.W.; Sun, L.L.; Su, T.; Hao, D.M.; Liao, W.P.; Deng, C.L.; Ren, W.Z.; Zhang, Y.M.; Lu, H.Y. Polyoxometalate-based ionic liquid catalyst with unprecedented activity and selectivity for oxidative desulfurization of diesel in Omin BF4. Chem. Eng. J. 2019, 358, 419–426. [Google Scholar] [CrossRef]
  46. Hou, Y.J.; An, H.Y.; Zhang, Y.M.; Hu, T.; Yang, W.; Chang, S.Z. Rapid Destruction of Two Types of Chemical Warfare Agent Simulants by Hybrid Polyoxomolybdates Modified by Carboxylic Acid Ligands. Acs Catal. 2018, 8, 6062–6069. [Google Scholar] [CrossRef]
  47. Tian, H.R.; Zhang, Z.; Liu, S.M.; Dang, T.Y.; Li, X.H.; Lu, Y.; Liu, S.X. A novel polyoxovanadate-based Co-MOF: Highly efficient and selective oxidation of a mustard gas simulant by two-site synergetic catalysis. J. Mater. Chem. A 2020, 8, 12398–12405. [Google Scholar] [CrossRef]
  48. Achim Miiller, J.M. Hartmut Bogge, Anja Stammler, Alexandru Botar, Cis-/trans-isomerism of bis-(trisalkoxy)-hexavanadates: Cis-Na-2[V(IV)6O7(OH)6{(OCH2)3CCH2OH}2]•8H–O, cis-(CN3H6)3[(V(IV)V(V)5O13){(OCH2)3CCH2OH}2]•4,5H2O and trans-(CN3H6)2[(V(V)6O13){(OCH2)3CCH2OH}2] •H2O. Z. Anorg. Allg. Chem. 1995, 621, 1818–1831. [Google Scholar] [CrossRef]
  49. Yalcin, G.; Kayan, A. Synthesis and characterization of Zr, Ti, Al-phthalate and pyridine-2-carboxylate compounds and their use in ring opening polymerization. Appl. Catal. A Gen. 2012, 433–434, 223–228. [Google Scholar] [CrossRef]
  50. Huang, Z.; Chen, S.; Lu, X.; Lu, Q. Water-triggered self-assembly polycondensation for the one-pot synthesis of cyclomatrix polyphosphazene nanoparticles from amino acid ester. Chem. Commun. 2015, 51, 8373–8376. [Google Scholar] [CrossRef]
  51. Tian, H.; Zhang, Z.; Dang, T.; Liu, S.; Lu, Y.; Liu, S. Hollow lindqvist-like-shaped {V6} cluster-based metal-organic framework for the highly efficient detoxification of mustard gas simulant. Inorg. Chem. 2021, 60, 840–845. [Google Scholar] [CrossRef]
  52. Hou, Y.; An, H.; Chang, S.; Zhang, J. Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants. Catal. Sci. Technol. 2019, 9, 2445–2455. [Google Scholar] [CrossRef]
  53. An, H.; Hou, Y.; Wang, L.; Zhang, Y.; Yang, W.; Chang, S. Evans-showell-type polyoxometalates constructing high-dimensional inorganic-organic hybrid compounds with copper-organic coordination complexes: Synthesis and oxidation catalysis. Inorg. Chem. 2017, 56, 11619–11632. [Google Scholar] [CrossRef] [PubMed]
  54. Li, J.; Wei, C.; Guo, D.; Wang, C.; Han, Y.; He, G.; Zhang, J.; Huang, X.; Hu, C. Inorganic-organic hybrid polyoxovanadates based on [V4O12]4- or [VO3]22- clusters: Controllable synthesis, crystal structures and catalytic properties in selective oxidation of sulfides. Dalton Trans. 2020, 49, 14148–14157. [Google Scholar] [CrossRef]
  55. An, H.; Hou, Y.; Chang, S.; Zhang, J.; Zhu, Q. Highly efficient oxidation of various thioethers catalyzed by organic ligand-modified polyoxomolybdates. Inorg. Chem. Front. 2020, 7, 169–176. [Google Scholar] [CrossRef]
  56. Li, Q.; Wang, G.; Qiu, J.; Wang, N.; Zhang, Q.; Lei, Q.; Hu, Y.L.; Zhang, Y. Catalytic oxidative desulfurization of model fuel using [HPMo][HTAC]2/SiO2 as a amphiphilic catalyst. Adv. Mater. Res. 2011, 396–398, 827–832. [Google Scholar]
  57. Ding, Y.; Wang, J.; Liao, M.; Li, J.; Zhang, L.; Guo, J.; Wu, H. Deep oxidative desulfurization of dibenzothiophene by novel POM-based IL immobilized on well-ordered KIT-6. Chem. Eng. J. 2021, 418, 129470. [Google Scholar] [CrossRef]
  58. Gao, Y.; Cheng, L.; Gao, R.; Hu, G.; Zhao, J. Deep desulfurization of fuels using supported ionic liquid-polyoxometalate hybrid as catalyst: A comparison of different types of ionic liquids. J. Hazard Mater. 2021, 401, 123267. [Google Scholar] [CrossRef]
  59. Cedeño, L.; Gomez, H.; Fraustro, A.; Guerra, H.; Cuevas, R. Oxidative desulfurization of synthetic diesel using supported catalysts. Catal. Today 2008, 133, 244–254. [Google Scholar] [CrossRef]
Molecules 27 08560 sch001 550
Scheme 1. (A) Some typical reported methods for the preparation of polyoxovanadate-containing polymers. (B) Synthetic route of polyoxovanadate-based cyclomatrix polyphosphazene microspheres, inset is an image of the resulted HCCP-V. (C) Typical oxidation reaction of sulfur-containing compounds.
Scheme 1. (A) Some typical reported methods for the preparation of polyoxovanadate-containing polymers. (B) Synthetic route of polyoxovanadate-based cyclomatrix polyphosphazene microspheres, inset is an image of the resulted HCCP-V. (C) Typical oxidation reaction of sulfur-containing compounds.
Molecules 27 08560 sch001
Molecules 27 08560 g001 550
Figure 1. The FT-IR spectra (A) and TGA curve in O2 (B) of HCCP-V.
Figure 1. The FT-IR spectra (A) and TGA curve in O2 (B) of HCCP-V.
Molecules 27 08560 g001
Molecules 27 08560 g002a 550Molecules 27 08560 g002b 550
Figure 2. Curve-fitted XPS high-resolution spectra of HCCP-V: (A) N1s, (B) O1s, (C) P2p, and (D) V2p.
Figure 2. Curve-fitted XPS high-resolution spectra of HCCP-V: (A) N1s, (B) O1s, (C) P2p, and (D) V2p.
Molecules 27 08560 g002aMolecules 27 08560 g002b
Molecules 27 08560 g003 550
Figure 3. (A) SEM image of HCCP-V dispersed in EtOH, inset is a size distribution based on the SEM image. (B) Zeta potential result for the dispersion of HCCP-V in H2O. (C) N2 isotherm adsorption and desorption curve (C) and pore size distribution (D) of HCCP-V.
Figure 3. (A) SEM image of HCCP-V dispersed in EtOH, inset is a size distribution based on the SEM image. (B) Zeta potential result for the dispersion of HCCP-V in H2O. (C) N2 isotherm adsorption and desorption curve (C) and pore size distribution (D) of HCCP-V.
Molecules 27 08560 g003
Molecules 27 08560 sch002 550
Scheme 2. Schematic illustration for the selective oxidation of sulfides by HCCP-V.
Scheme 2. Schematic illustration for the selective oxidation of sulfides by HCCP-V.
Molecules 27 08560 sch002
Molecules 27 08560 g004 550
Figure 4. HPLC, conversion, and kinetics curves during the catalytic oxidation of MPS by 1/400 eq of HCCP-V and 1.2 eq of H2O2 at different temperatures: (A–C) 25 °C, (D–F) 40 °C, and (G–I) 55 °C. Naphthalene with a retention time of 10.2 min was used as an internal standard.
Figure 4. HPLC, conversion, and kinetics curves during the catalytic oxidation of MPS by 1/400 eq of HCCP-V and 1.2 eq of H2O2 at different temperatures: (A–C) 25 °C, (D–F) 40 °C, and (G–I) 55 °C. Naphthalene with a retention time of 10.2 min was used as an internal standard.
Molecules 27 08560 g004
Molecules 27 08560 g005 550
Figure 5. HPLC, conversion, and kinetics curves during the catalytic oxidation of MPS by 1/400 eq of HCCP-V and 1.0 eq of H2O2 at different temperatures: (A–C) 25 °C, (D–F) 40 °C, and (G–I) 55 °C. Naphthalene with a retention time of 10.2 min was used as an internal standard.
Figure 5. HPLC, conversion, and kinetics curves during the catalytic oxidation of MPS by 1/400 eq of HCCP-V and 1.0 eq of H2O2 at different temperatures: (A–C) 25 °C, (D–F) 40 °C, and (G–I) 55 °C. Naphthalene with a retention time of 10.2 min was used as an internal standard.
Molecules 27 08560 g005
Molecules 27 08560 g006 550
Figure 6. HPLC spectra, conversion curves, and kinetics curves during the catalytic oxidation of DBT by HCCP-V under different conditions: (A–C) 70 °C, 5 eq of H2O2, (D–F) 80 °C, 5 eq of H2O2, and (G–I) 70 °C, 8 eq of H2O2. Naphthalene with a retention time of 10.2 min was used as an internal standard.
Figure 6. HPLC spectra, conversion curves, and kinetics curves during the catalytic oxidation of DBT by HCCP-V under different conditions: (A–C) 70 °C, 5 eq of H2O2, (D–F) 80 °C, 5 eq of H2O2, and (G–I) 70 °C, 8 eq of H2O2. Naphthalene with a retention time of 10.2 min was used as an internal standard.
Molecules 27 08560 g006
Molecules 27 08560 g007 550
Figure 7. Catalytic oxidation of CEES by HCCP-V:H2O2 = 1:1.2 at room temperature: (A) 1H NMR spectra of the catalytic oxidation process (CDCl3). (B) The conversion curves of CEES and CEESO.
Figure 7. Catalytic oxidation of CEES by HCCP-V:H2O2 = 1:1.2 at room temperature: (A) 1H NMR spectra of the catalytic oxidation process (CDCl3). (B) The conversion curves of CEES and CEESO.
Molecules 27 08560 g007
Molecules 27 08560 g008 550
Figure 8. (A) The conversion of MPS and MPSO during 4 cycles of reuse of HCCP-V. (B) FT-IR spectra for the catalyst HCCP-V during 4 cycles of reuse.
Figure 8. (A) The conversion of MPS and MPSO during 4 cycles of reuse of HCCP-V. (B) FT-IR spectra for the catalyst HCCP-V during 4 cycles of reuse.
Molecules 27 08560 g008
Table
Table 1. The catalytic oxidation results of MPS by HCCP-V in CH3CN.
Table 1. The catalytic oxidation results of MPS by HCCP-V in CH3CN.
CatalystT/°C[MPS]:[H2O2]:[Catalyst]t/mink/min−1TOF/min−1Conversion/%
HCCP-BPS401:1.2:1/400180---
HCCP-V251:1.2:1/4001800.000132.2099.0
HCCP-V401:1.2:1/400500.001397.9899.6
HCCP-V551:1.2:1/400200.0118918.7193.4
HCCP-V251:1:1/4001200.000132.8685.6
HCCP-V401:1:1/400500.00086.5882.1
HCCP-V551:1:1/400120.012825.2175.5
Table
Table 2. The catalytic oxidation results of DBT by HCCP-V in CH3CN.
Table 2. The catalytic oxidation results of DBT by HCCP-V in CH3CN.
CatalystT/°C[DBT]:[H2O2]:[Catalyst]t/mink/min−1TOF/min−1Conversion/%
HCCP-V701:5:1/100500.00071.6079.8
HCCP-V701:8:1/100500.000991.8492.2
HCCP-V801:5:1/100150.0064.7070.5
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Hu, Y.; Huang, D.; Yan, J.; Miao, Z.; Yu, L.; Cai, N.; Fang, Q.; Zhang, Q.; Yan, Y. Polyoxovanadate-Based Cyclomatrix Polyphosphazene Microspheres as Efficient Heterogeneous Catalysts for the Selective Oxidation and Desulfurization of Sulfides. Molecules 2022, 27, 8560. https://doi.org/10.3390/molecules27238560

AMA Style

Hu Y, Huang D, Yan J, Miao Z, Yu L, Cai N, Fang Q, Zhang Q, Yan Y. Polyoxovanadate-Based Cyclomatrix Polyphosphazene Microspheres as Efficient Heterogeneous Catalysts for the Selective Oxidation and Desulfurization of Sulfides. Molecules. 2022; 27(23):8560. https://doi.org/10.3390/molecules27238560

Chicago/Turabian Style

Hu, Yinghui, Diping Huang, Jing Yan, Zhiliang Miao, Lize Yu, Ningjing Cai, Quanhai Fang, Qiuyu Zhang, and Yi Yan. 2022. "Polyoxovanadate-Based Cyclomatrix Polyphosphazene Microspheres as Efficient Heterogeneous Catalysts for the Selective Oxidation and Desulfurization of Sulfides" Molecules 27, no. 23: 8560. https://doi.org/10.3390/molecules27238560

APA Style

Hu, Y., Huang, D., Yan, J., Miao, Z., Yu, L., Cai, N., Fang, Q., Zhang, Q., & Yan, Y. (2022). Polyoxovanadate-Based Cyclomatrix Polyphosphazene Microspheres as Efficient Heterogeneous Catalysts for the Selective Oxidation and Desulfurization of Sulfides. Molecules, 27(23), 8560. https://doi.org/10.3390/molecules27238560

Article Metrics

Back to TopTop