Visible-light-active benzothiadiazole-based MOFs as efficient ROS generators for the synthesis of benzimidazoles and benzothiazoles

Abstract

The utilization of reactive oxygen species (ROS) in photochemical synthesis has garnered significant attention owing to their exceptional oxidative capacity under mild conditions. Recently, metal–organic frameworks (MOFs) have been employed to convert molecular oxygen (O₂) to ROS for photocatalysis. However, visible-light-active MOFs for effective oxygen activation remain scarce. Herein, a simple and effective strategy, linker functionalization, is utilized to immobilize the benzothiadiazole unit inside the UiO-68-type MOF (UiO-68-BTDB). The MOF was applied as the first example generating superoxide radical anions (O₂˙⁻) and singlet oxygen (¹O₂) for access to benzimidazoles and benzothiazoles in air at room temperature. Recycling experiments were performed to confirm the stability and reusability of UiO-68-BTDB as a robust heterogeneous catalyst.

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Introduction

Reactive oxygen species (ROS) represent highly active molecules that are typically generated during normal oxygen metabolism of aerobic life.^1–3 ROS, with exceptional oxidative capabilities, have presented tremendous potential in diverse applications, including photocatalytic organic transformation and photodynamic therapy.^4–6 Until now, efforts have been made to explore artificial chemical systems that produce ROS under environmentally friendly conditions. Among them, organic dyes and noble metal complexes have been widely utilized as photosensitizers to generate ROS for organic transformations.^7–9 However, most photosensitizers suffer from some restrictions of self-degradation, photobleaching and aggregation-caused quenching (ACQ), thus hindering their progress in photocatalytic reactions.^10–12

Metal–organic frameworks (MOFs) have garnered significant attention in the applications of photochemical synthesis for their highly crystalline porous structure and tunability in chemical functionality.^13–15 For visible-light-driven ROS generation, many predesigned organic and metal–organic chromophores are employed as linkers and integrated into MOFs, which is highly helpful to enhance the concentration of photocatalytic sites and avoid their self-quenching within the framework.^16–18 Furthermore, the porous nature of MOFs facilitates the transport and diffusion of ROS, thus enhancing their further interaction with incoming reactants.^19–21 On the other hand, the heterogeneous nature of MOF catalysts confers them with easy separation, enhanced stability, and reusability.

Among various photosensitive compounds, it is well known that benzothiadiazoles with bicyclic electron-deficient skeletons exhibit unique photoelectric properties.^22,23 Specifically, benzothiadiazoles have always served as highly efficient ROS photocatalysts because of their easily improved charge transfer efficiency by designing donor–acceptor–donor (D–A–D) type photosensitizers.^24–26 For example, a series of benzothiadiazole-containing linkers were introduced into the MOF frameworks by the Li group, and the obtained JNU series of MOFs showed photocatalytic activity for aerobic oxidation. Therefore, immobilizing benzothiadiazole units into MOFs may be an effective strategy to convert O₂ to ROS for photocatalytic reactions and is desirable.

Bearing these considerations in mind, 4,4′-(benzo[c][1,2,5]thiadiazole-4,7-diyl)dibenzoic acid (H₂BTDB) was selected as the light-harvester and organic ligand to build a visible-light-active MOF, UiO-68-BTDB. Due to the well-isolated benzothiadiazole chromophore in the framework, the MOF not only retained the visible light absorption of H₂BTDB, but also produced both singlet oxygen (¹O₂) and superoxide radical anions (O₂˙⁻). UiO-68-BTDB can also be used as a photocatalyst for the photochemical synthesis of benzimidazoles and benzothiazoles. By combining the generation of ¹O₂ and O₂˙⁻, UiO-68-BTDB exhibits excellent photocatalytic activity in the visible-light-induced condensation cyclization reaction to synthesize benzimidazoles and benzothiazoles.

Results and discussion

A Zr(IV)-based MOF, UiO-68-BTDB, with the underlying fcu topology, by immobilizing a π-conjugated, electron-deficient, benzothiadiazole-functionalized ligand 4,4′-(benzo[c][1,2,5]thiadiazole-4,7-diyl)dibenzoic acid (H₂BTDB) was synthesized (Fig. 1a).^27,28 Powder X-ray diffraction (PXRD) has been conducted to exhibit its isostructural framework with the parent MOF UiO-68 (Fig. 1b).²⁹ The existence of the incorporated H₂BTDB linker was further verified by ¹H-NMR spectroscopy and HRMS of the digested MOF samples (Fig. S1 and S2†). N₂ sorption measurement at 77 K of UiO-68-BTDB exhibited a type I reversible isotherm, and the Brunauer–Emmett–Teller (BET) surface area was calculated to be 2484 m² g⁻¹ (Fig. S3a†). Furthermore, the pore size was determined to be 1.34 nm (Fig. S3b†). Meanwhile, UiO-68-BTDB maintained its structural integrity after being soaked in different organic solvents for three days (Fig. S4†). Thermogravimetric (TG) analyses demonstrated that UiO-68-BTDB can retain its framework up to 450 °C (Fig. S5†).

Fig. 1 (a) Schematic representation of the synthesis of UiO-68-BTDB; (b) PXRD patterns of UiO-68-BTDB. (c) Solid state UV-vis diffuse reflectance spectra (red); inset: Tauc plot of the UiO-68-BTDB (blue); (d) Mott–Schottky plots of UiO-68-BTDB; (e) transient photocurrent responses of UiO-68-BTDB.

The optical and electrical properties were next investigated. As shown in Fig. S6,† UiO-68-BTDB gives emission at 510 nm, and this emission band was ascribed to the π–π* transition of the organic ligand in UiO-68-BTDB. To assess the visible light absorption capacity, the UV-visible diffuse reflectance spectrum was obtained. As shown in Fig. 1c, UiO-68-BTDB displayed a broad absorption ranging from 200 to 600 nm. The optical band gap (E_g) of UiO-68-BTDB was calculated to be about 2.55 eV by the Kubelka–Munk (KM) method from Tauc plots (Fig. 1c, inset). To evaluate the conduction band (CB) and the valence band (VB) levels, Mott–Schottky measurements were conducted at frequencies of 500, 750, and 1000 Hz. As shown in Fig. 1d, the CB position was determined to be −0.87 V vs. NHE for UiO-68-BTDB. The VB was thus estimated to be 1.68 V vs. NHE. Overall, UiO-68-BTDB has a more negative potential (−0.87 V vs. NHE) than that for the reduction of O₂ to the superoxide radical (−0.33 V vs. NHE), indicating that the MOF catalyst may initiate superoxide radical anion (O₂˙⁻) generation.

To further evaluate the photoelectric properties of the prepared MOF, we explored the charge separation capacity through photocurrent response analysis and electrochemical impedance spectroscopy (EIS). As shown in Fig. 1e, UiO-68-BTDB showed significantly higher photocurrent than the H₂BTDB linker, indicative of effective separation of photogenerated electron–hole pairs. Furthermore, this result was further proved by its relatively smaller radii and lower resistance for charge transfer (Fig. S7†), suggesting that introducing the benzothiadiazole photosensitizer into the MOF is beneficial for the charge separation efficiency. In addition, electron paramagnetic resonance (EPR) tests were performed to investigate its capacity to generate ROS upon visible-light irradiation. As shown in Fig. 2a, in the presence of 2,2,6,6-tetramethylpiperidinooxy (TEMP), the EPR signals observed confirmed the generation of singlet oxygen (¹O₂). Furthermore, the formation of superoxide radical anions (O₂˙⁻) was also indicated by adding 5,5-dimethyl-1-pyrroline N-oxide (DMPO) in the EPR experiments (Fig. 2b).

Fig. 2 (a) EPR detection of ¹O₂ generation with UiO-68-BTDB trapped by TEMP. (b) EPR detection of O₂˙⁻ generation with UiO-68-BTDB trapped by DMPO.

Among heteroaromatic compounds, benzimidazole and benzothiazole derivatives demonstrate potential applications in the pharmaceutical industry and materials science.^30–32 Various approaches have been devoted to synthesize benzimidazoles and benzothiazoles.^32–36 Among them, O₂-involved oxidation under visible light excitation is considered as a promising one owing to its effective and ecofriendly approach. In terms of the capability of generating ¹O₂ and O₂˙⁻ of UiO-68-BTDB, we envisioned that photocatalytic condensation cyclization to synthesize benzimidazole and benzothiazole would occur with UiO-68-BTDB as the photocatalyst. As shown in Table 1 (entry 1), the condensation cyclization of o-phenylenediamine with benzaldehyde can be achieved in 94% isolated yield with 1 mol% UiO-68-BTDB as the photocatalyst in EtOH and a 10 W blue LED as the light source. Control experiments demonstrated that no product was obtained in the absence of UiO-68-BTDB, a light source, or air (Fig. 3, and Table 1, entries 2–4), indicating the necessity of these reaction parameters. Solvent effects were examined, indicating that EtOH is beneficial for obtaining a high yield of the target product (entries 5–9). Finally, with 1 mol% of UiO-68-BTDB photocatalyst, the substrates could be efficiently converted to the target product with the highest yield (entries 10–12). Moreover, ligands without a benzothiadiazole unit were also chosen for comparison (Fig. S8†). The obtained UiO-68 was employed as a photocatalyst under similar conditions, and no product was observed (entry 13). A comparison of UiO-68-BTDB with common photocatalysts further demonstrates the superior photocatalytic performance of UiO-68-BTDB (Table S1†).

Fig. 3 Quenching experiments and control experiments.

Table 1 Control experiments of reaction conditions^a

Entry	Catalyst	Solvent	Amount (mol%)	Yield^b (%)
a o-Phenylenediamine (0.2 mmol), benzaldehyde (0.2 mmol), room temperature, a 10 W blue LED, open to air, 3 h. b Isolated yields. c Conditions in the absence of light. d Conditions in the absence of air.
1	UiO-68-BTDB	EtOH	1.0	94
2	—	EtOH	1.0	Trace
3^c	UiO-68-BTDB	EtOH	1.0	Trace
4^d	UiO-68-BTDB	EtOH	1.0	Trace
5	UiO-68-BTDB	DMF	1.0	26
6	UiO-68-BTDB	MeOH	1.0	88
7	UiO-68-BTDB	MeCN	1.0	45
8	UiO-68-BTDB	DCM	1.0	Trace
9	UiO-68-BTDB	THF	1.0	63
10	UiO-68-BTDB	EtOH	0.5	82
11	UiO-68-BTDB	EtOH	1.5	92
12	UiO-68-BTDB	EtOH	2.0	81
13	UiO-68	EtOH	1.0	Trace

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Under the standard reaction conditions, the substrate scope of aromatic aldehydes was studied to explore the general capability of UiO-68-BTDB as a photocatalyst for the above condensation cyclization reaction. As shown in Table 2, a variety of aromatic aldehydes (with either electron-withdrawing or electron-donating groups) with o-phenylenediamine proceeded and afforded the corresponding benzimidazoles with satisfactory yields. It was noted that higher yields of benzimidazole were observed with para-substituted benzaldehyde with electron-donating groups (–CH₃ and –OCH₃) compared to those with electron-withdrawing groups (–NO₂), demonstrating the significant electronic effect on the reaction.

Table 2 Photocatalytic condensation cyclization to prepare benzimidazole derivatives^a

Entry	Substrate	Product	Yield^b (%)
a Standard conditions: o-phenylenediamine (0.2 mmol), benzaldehyde (0.2 mmol), UiO-68-BTDB, 3 mL EtOH, a 10 W blue LED, room temperature, open to air, 3 h. b Isolated yields.
1			94
2			96
3			96
4			90
5			92
6			98
7			95

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To investigate the versatility of this method for access to 2-substituted benzothiazole, numerous para-substituted benzaldehydes were reacted with o-aminothiophenol under the standard conditions to obtain benzothiazoles. As can be seen from Table 3, most substrates gave excellent yields of the target products for only 1.5 h. Overall, the above results showed that UiO-68-BTDB is a general photocatalyst for the synthesis of benzimidazoles and benzothiazoles upon visible light irradiation.

Table 3 Photocatalytic condensation cyclization to prepare benzothiazole derivatives^a

Entry	Substrate	Product	Yield^b (%)
a Standard conditions: o-aminothiophenol (0.2 mmol), benzaldehyde (0.2 mmol), UiO-68-BTDB, 3 mL EtOH, a 10 W blue LED, room temperature, open to air, 1.5 h. b Isolated yields.
1			97
2			99
3			98
4			93
5			95
6			99
7			96

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To confirm the heterogeneous nature of UiO-68-BTDB, a series of related experiments were then carried out. As shown in Fig. S9,† the filter experiment showed that the yield of 3a is unchanged in the next 2 h after removing the catalyst and reacting for 1.5 h. No obvious BTDB²⁻ signal in the filtrate was observed in UV-vis spectra, indicating the stability and heterogeneity of UiO-68-BTDB. Additionally, the PXRD pattern of the recovered UiO-68-BTDB after five runs is well consistent with the fresh samples, indicating that it can be recycled for at least five runs without much loss of catalytic efficiency (Fig. S10†). These results commendably demonstrated the heterogeneous nature of UiO-68-BTDB in the photocatalytic condensation cyclization to prepare benzimidazoles and benzothiazoles.

The identification of ROS generated under photocatalytic conditions is essential for elucidating the reaction mechanism of the condensation cyclization. Thus, the ROS quenching tests were further conducted. As shown in Fig. 3 and Table S2,† when the radical scavenger 2,2,6,6-tetramethylpiperidinyl-1-oxide (TEMPO) was added to the reaction system, the yield of 3a decreased significantly to 16%, confirming the radical reaction process. The addition of isopropyl alcohol (IPA) had a very little effect on the yield, thus ruling out the presence of ˙OH. After adding NaN₃, a typical scavenger for ¹O₂, the reaction yield (26%) was dramatically decreased. The quenched yield (23%) was observed with the addition of the O₂˙⁻ scavenger p-benzoquinone (BQ). Furthermore, the reaction was greatly inhibited when the hole (h⁺) scavenger C₂O₄(NH₄)₂ or electron (e⁻) scavenger AgNO₃ was added. These results suggested that h⁺ and e⁻ both play a key role during the photocatalysis, and the major working oxygen species here might be ¹O₂ and O₂˙⁻. Overall, it can be deduced that the reaction involves two pathways of energy transfer and electron transfer.

According to the above pieces of evidence and literature reports,^32,33 a tentative reaction mechanism for the condensation cyclization to benzimidazole and benzothiazole was proposed. Initially, o-phenylenediamine/o-aminothiophenol and benzaldehyde are dehydrated to form intermediate I, electrons are excited, and charge carriers are separated on UiO-68-BTDB upon visible-light irradiation. Next, as shown in Fig. 4, the generated holes and electrons could initiate the following reactions: holes (E_v = 1.68 V) could capture an electron from intermediate I (E(I/II) = 0.45 V)³⁷ and afford II, which then dissociates a proton to give free radical intermediate III. The intermediate III undergoes cyclization and then reduced by photogenerated electrons to produce IV. At the same time, partial singlet electrons transformed into excited triplet electrons via intersystem crossing (ISC),³⁸ thus producing ¹O₂ through energy transfer (ET).³⁹ Aminal V, which has gained a proton from intermediate IV, further reacts with ¹O₂ to afford intermediate VI. After releasing hydrogen peroxide (H₂O₂), the target product is afforded. On the other hand, the photogenerated holes of UiO-68-BTDB oxidize intermediate I and further cyclize to intermediate II′. Meanwhile, the photogenerated electron converts O₂ into O₂˙⁻via a single electron transfer (SET) mechanism.⁴⁰ The target product is afforded by deprotonation of II′ by O₂˙⁻ and hydrogen abstraction by hydroperoxyl radicals from intermediate III′.

Fig. 4 Plausible mechanism of UiO-68-BTDB catalyzed the condensation cyclization reaction to synthesize benzimidazoles and benzothiazoles.

Conclusions

In conclusion, a benzothiadiazole-functionalized ligand (H₂BTDB) was rationally designed to construct one UiO-68-type MOF, UiO-68-BTDB. The MOF has a broad adsorption of visible light up to 600 nm and good charge separation efficiency. Merging these merits, UiO-68-BTDB can effectively activate O₂ to ¹O₂ and O₂˙⁻ under visible light irradiation. Meanwhile, UiO-68-BTDB is proved to be highly active in condensation cyclization to prepare benzimidazoles and benzothiazoles. Possible dual reaction pathways are proposed for the photocatalytic reaction, including ¹O₂ generation via energy transfer and O₂˙⁻ generation via photoinduced charge separation.

Data availability

Data are available from the authors on reasonable request.

Conflicts of interest

There are no conflicts to declare.

Acknowledgements

We gratefully acknowledge the financial support from the Applied Basic Research Programs of Science and Technology Department of Shanxi Province (202303021222245), the Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi (2023L309), the Yuncheng University Doctoral Research Launch Project (YQ-2023026), and the Taiyuan University of Science and Technology doctoral research start-up fund (no. 20232114).

Notes and references

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38. Intersystem Crossing (ISC) refers to a non-radiative leaping process in which the electrons of a molecule in an excited state undergo a spin reversal, resulting in a change in the multiplicity of the molecule. The process involves the crossing of a molecule from an excited singlet state to an excited triplet state.
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Footnote

† Electronic supplementary information (ESI) available: Experimental procedures, crystallographic data and other photocatalytic details. See DOI: https://doi.org/10.1039/d4qi01368a

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