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Highly selective [4+4] cross-photodimerization of (4a-azonia)anthracenes driven by confinement of D-A hetero-guest pair in cucurbit[10]uril host
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Xianchen Hua, Junli Yanga, Fang Gaoa, Zhiyong Zhaoa, b, Simin Liua, b, *
Chinese Chemical Letters | 2025, 36(3) : 109967
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Chinese Chemical Letters | 2025, 36(3): 109967
• Communication •
Highly selective [4+4] cross-photodimerization of (4a-azonia)anthracenes driven by confinement of D-A hetero-guest pair in cucurbit[10]uril host
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Xianchen Hua, Junli Yanga, Fang Gaoa, Zhiyong Zhaoa, b, Simin Liua, b, *
Affiliations
  • a School of Chemistry and Chemical Engineering, Wuhan University of Science and Technology, Wuhan 430081, China
  • b The State Key Laboratory of Refractories and Metallurgy, Institute of Advanced Materials and Nanotechnology, Wuhan University of Science and Technology, Wuhan 430081, China
Published: 2025-03-15 doi: 10.1016/j.cclet.2024.109967
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The cross-photodimerization often comes with the formation of undesired and competitive homo-photodimer as side products. Herein, we report a series of highly selective [4 + 4] cross-photodimerization between anthracene and 4a-azoniaanthracene derivatives within a cucurbit[10]uril (CB[10]) host in water. Heteroternary inclusion complexes were formed through encapsulation of donor (D1-D2, anthracene derivative) and acceptor (A1-A3, 4a-azoniaanthracene derivatives) pairs in CB[10]. In the presence of CB[10] (1.0 equiv.), the [4 + 4] cross-photodimerization between D1 and A1/A2/A3 efficiently gave a single racemic cross-photodimer. Furthermore, the cross-photodimerization between 9-substituted anthracene D2 and A1/A3 was catalyzed by CB[10] (0.1 equiv.) to quantitatively yield a cross-photodimer with high regioselectivity. Efficient formation of selective cross-photodimers could be attributed to the exclusive encapsulation of D-A hetero-guest pairs in CB[10] and the confinement effect of the CB[10] host cavity. Our study further proves host–guest complexation as a powerful strategy for cross-cycloaddition reactions with high efficiency.

Supramolecular catalysis  /  Cross-photodimerization  /  Host-guest complexation  /  Charge-transfer interaction  /  Cucurbit[10]uril
Xianchen Hu, Junli Yang, Fang Gao, Zhiyong Zhao, Simin Liu. Highly selective [4+4] cross-photodimerization of (4a-azonia)anthracenes driven by confinement of D-A hetero-guest pair in cucurbit[10]uril host[J]. Chinese Chemical Letters, 2025 , 36 (3) : 109967 - . DOI: 10.1016/j.cclet.2024.109967
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Photochemical reactions involving anthracene and its derivatives, including photodimerization and other reactions, have been widely investigated over the past 100 years [1]. Furthermore, anthracene dimerization has been further used in the design of chiral ligand, carbon nanoring, molecular cage switch and optical materials/devices [2-4]. However, due to the poor reaction selectivity and homo-photodimerization as side reaction, till now only few intermolecular [4 + 4] cross-photodimerizations between anthracene and its derivatives have been reported [5-7]. Inspired by the natural features of enzymes, supramolecular nanoreactors/catalysts with confined cavities, often referred to as artificial enzymes, have been developed and made significant advancements in various types of organic reactions [8-14]. Supramolecular host working as nanoreactors/catalysts can profoundly govern reactivity and selectivity [15-17]. By introducing a host–guest complexation strategy, researchers have achieved enhanced efficiency and even stereoselectivity in the homo-photodimerization of anthracene derivatives [18]. However, to date, there is no efficient way to improve the cross-photodimerization between anthracene derivatives.
Cucurbit[n]uril (CB[n], n = 5–8, 10), a family of molecular containers known for their high binding affinity and selectivity toward cationic and neutral guests [19,20], have also been employed to promote various organic reactions [8,21-23]. CB[10] (Fig. 1A), which has the largest cavity among CB[n], has shown its remarkable capacity to accommodate large-sized molecules or donor-acceptor guest pair to form heteroternary complex by host-stabilized charge-transfer (HSCT) interaction (charge transfer interaction between a pyridinium and an aromatic ring is also defined as cation–π interaction [17]) [24-27]. Building upon our previous research involving CB[10]-catalyzed homo-photodimerization of anthracene or azaanthracene derivatives [28,29], we started to investigate the cross-photodimerization between anthracene and 4a-azoniaanthracene derivatives. We envisioned that by combining the selective encapsulation of the D-A pair with the pre-orientation of guests within CB[10], the intermolecular [4 + 4] cross-photodimerization between anthracene and 4a-azoniaanthracene derivatives could be accomplished with high efficiency (Fig. 1B).
The synthesis and characterization of donor molecules D1-D2 and acceptor molecules A1-A3 (Fig. 1A) were presented in the supplemental information (Scheme S1 and Figs. S1-S7 in Supporting information). In order to analyze the products after photoirradiation of D-A pairs, the homo-photodimerization reaction of each compound was investigated firstly. D1 did not undergo homo-photodimerization and the photoirradiation of D2 for 12 h afforded head-to-tail (HT) dimer HT-PD2-D2 (structural identification of HT-PD2-D2 was based on our previous report [28]) (Fig. S8 in Supporting information). A1 underwent homo-photodimerization to afford four regioisomeric photodimers (anti-HT, syn-HH, rac-anti-HH, rac-syn-HT) identified by 1H NMR spectra (Fig. S9 in Supporting information) [30-32]. Similar to A1, A2-A3 produced four regioisomeric photodimers upon photoirradiation (Figs. S10 and S11 in Supporting information). We also investigated the complexation of each guest with CB[10]. 1H NMR titration experiments revealed that the signals for the aromatic protons of D2 and A1-A3 underwent significant upfield shifts, suggesting that anthracene or 4a-azoniaanthracene units on guests were encapsulated by CB[10] to form inclusion complexes. ESI-MS analysis further confirmed that all guests (D2 and A1-A3) formed 1:2 host−guest homoternary complexes with CB[10] (Fig. S12-S19 in Supporting information).
The host–guest complexation between the hetero-guest pair D1-A1 and CB[10] was investigated by 1H NMR, fluorescence, and ESI-MS spectroscopies. 1H NMR spectra analysis showed that all proton signals of D1 and A1 in their equimolar mixture in the absence of CB[10] remained unchanged, implying no obvious interaction between D1 and A1 (Fig. 2a). However, the observation of shifted proton signals of D1 and A1 in the presence of CB[10] compared to CB[10]·D1 and CB[10]·A12 confirmed the formation of the heteroternary inclusion complex CB[10]·D1·A1 (Figs. 2b-d). Since the binding between CB[10] and D1 displayed slow exchange kinetics on the 1H NMR time scale [28], and no proton signals of D1 in CB[10]·D1 were found in the 1H NMR spectra of the mixture of D1, A1, and CB[10] (compare Fig. 2c with Fig. 2d), it was highly likely that CB[10]·D1·A1 exclusively formed. Multiple cross peaks in a ROESY spectrum of the hetero-guest pair and CB[10] mixture suggested that D1 and A1 were in close proximity (Fig. S20 in Supporting information). Additionally, the transparent solution of an equimolar mixture of D1 and A1, with a blue emission at 408 nm, turned yellow and displayed a red-shifted emission at 517 nm (yellow-green fluorescence) upon adding 1.0 equiv. of CB[10] (Fig. S21 in Supporting information). This change indicated the weak CT interaction between electron-rich guest D1 and electron-deficient guest A1 was significantly enhanced by the presence of CB[10] [27,33]. ESI-MS also confirmed the exclusive existence of the heteroternary inclusion complex CB[10]·D1·A1 (Fig. S22 in Supporting information): the ion peak at m/z 721.604 corresponded to the 1:1:1 complex CB[10]·D1·A1 ([CB[10]+ D1 + A1 – 2H+]3+= 721.601). The exclusive formation of the heteroternary complex CB[10]·D1·A1 implied the possibility of efficient cross-photodimerization of D1-A1 pair within the host.
Fig. 3A and Fig. S23A (Supporting information) presented a schematic of CB[10]-mediated intermolecular cross-photodimerization between D1 and A1. As depicted in Fig. S23B(b), after UV irradiation for 3 h, the 1H NMR spectrum of D1 and A1 showed complicated new peaks representing photoproducts, with much unreacted D1 and A1 remaining in the solution. Further analysis disclosed that only 41% of A1 was converted into four regioisomeric homo-photodimers (anti-HT-PA1-A1, syn-HH-PA1-A1, rac-anti-HH-PA1-A1, rac-syn-HT-PA1-A1; 36% relative yield). These products were identified by comparing Fig. S23B(b) to Fig. S9. Additionally, there was a cross-photodimer, rac-PD1-A1, formed in 64% relative yield. In contrast, in the presence of 1.0 equiv. of CB[10], the proton signals of bound D1 and A1 gradually diminished and completely disappeared after 50 min, with the appearance of new peaks representing photoproduct(s) (Figs. S23B(c) and (d), Fig. S24 in Supporting information). The photoproduct was identified as the pure cross-photodimer rac-PD1-A1 in nearly quantitative yield (characterization data for rac-PD1-A1 were showed in Figs. S25-S27 in Supporting information). Notably, the sample of rac-PD1-A1 used for 1H NMR (Fig. S23B (e)) was obtained by competitive guest displacement without further purification. This indicated the exclusive hetero-pairwise selectivity of CB[10] and highly efficient cross-photodimerization between D1 and A1 within CB[10]. Given that “the intra-complex photodimerization is unimolecular in nature” [34], an apparent rate constant (k1) of the cross-photodimerization reaction between D1 and A1 with 1.0 equiv. of CB[10] was calculated to be 0.04044 ± 0.00253 min−1 using pseudo-first-order kinetics (Fig. S28 in Supporting information). Clearly, all of these data proved that CB[10] functioned as a supramolecular nanoreactor in this case to accelerate the cross-photodimerization reaction and improve the reaction selectivity (avoiding homo-photodimerization).
Single crystals of the inclusion complex CB[10]·(±)PD1-A1 were obtained through the slow evaporation of an irradiated aqueous solution containing D1, A1, and CB[10], confirming the structure of the cross-photodimer rac-PD1-A1 (Fig. 3C). Surprisingly, a pair of racemic enantiomers, (±)PD1-A1, were co-encapsulated by a single CB[10] molecule to form a 1:2 racemic inclusion complex CB[10]·(±)PD1-A1. This differed from the observation of the co-existence of homo-chiral and hetero-chiral CB[10]-based ternary inclusion complexes [35]. Moreover, the 1:2 binding mode in crystal was different from a 1:1 binding mode between CB[10] and PD1-A1 in aqueous solution (Fig. S29 in Supporting information), which could be attributed to the crystal packing effect [36]. Crystallographic data, including CCDC number, were listed in Table S2 (Supporting information).
The exclusive formation of heteroternary complexes CB[10]·D1·A2 and CB[10]·D1·A3 was aslo verified by NMR, ESI-MS, and fluorence spectroscopies (Figs. S30-S33 in Supporting information). Similar to the cross-photodimerization between D1 and A1 in the presence of 1.0 equiv. of CB[10], the photoirradiation of D1 and A2/A3 exclusively yielded rac-PD1-A2/rac-PD1-A3 (Fig. 3A, Figs. S34-S45 in Supporting information). Single crystals of the inclusion complex CB[10]·(±)PD1-A3 were also obtained, confirming the structure of the cross-photodimer rac-PD1-A3 (Fig. S46 in Supporting information). In comparison, although having an extra methyl substituent at a different position, A2/A3 reacted with D1 similarly to A1 in the presence of CB[10]. Detailed cross-photodimerization data were provided in Table S1 (Supporting information).
The characterization of the heteroternary inclusion complex CB[10]·D2·A1 was illustrated in Fig. S47 (Supporting information). The typical chemical shift changes upon the addition of CB[10], the emission color change from blue (the solution of D2-A1) to vibrant yellow (the solution of D2-A1 with CB[10]), and ESI-MS confirmed the encapsulation of the D2-A1 pair in CB[10]. In a similar manner, we investigated the host–guest complexations of D2 and A2/A3 with CB[10] (Figs. S49-S52 in Supporting information). All of data verified that the D2-A pairs could be encapsulated by CB[10].
The cross-photodimerization between D2 and A1 with CB[10] was shown in Fig. 3B. Photoirradiation of the mixture of D2 and A1 for 6 h afforded seven photoproducts: the homo-photodimer HT-PD2-D2 in a relative yield of 31%, four homo-photodimers from A1 in 27%, the cross-photodimer rac-HH-PD2-A1 in 29%, and rac-HT-PD2-A1 in 13%, with a total conversion of 76% (Fig. S53, Table S1 in Supporting information). Relatively, in the presence of 0.1 equiv. of CB[10], the proton signals of D2 and A1 gradually disappeared under UV irradiation and eventually vanished after 2 h, with appearance of new and sharp proton signals representing the product(s) (Fig. S54 in Supporting information). After work-up, the photoproduct was identified to be the pure cross-photodimer rac-HH-PD2-A1 (Figs. S55-S57 in Supporting information). Single crystals of rac-HH-PD2-A1 unambiguously confirmed its HH configuration (Fig. 3D). An apparent rate constant (k1) for the cross-photodimerization of the D2 and A1 pair with 0.1 equiv. of CB[10] was then calculated to be 0.02852 ± 0.00093 min−1 with pseudo-first-order kinetics (Fig. S58a in Supporting information). To gain insight into why CB[10] can catalyze this cross-photodimerization reaction with high regioselectivity, we performed density functional theory (DFT) calculations. As depicted in Fig. 4, the energy of the heteroternay complex HH—CB[10]·D2·A1 was significant lower, by 84.1 kcal/mol, than that of HT-CB[10]·D2·A1, accounting for the exclusive formation of the cross-photodimer rac-HH-PD2-A1. The energy of CB[10]·rac-HH-PD2-A1 was 31.8 kcal/mol higher than that of HH—CB[10]·D2·A1, resulting in the occurrence of the catalytic cycle. Therefore, the cross-photodimerization between D2 and A1 catalyzed by CB[10] with high conversion and regio-selectivity, could be illustrated as in Fig. S58b (Supporting information).
Unexpectedly, while CB[10] could still catalyze the cross-photodimerization reaction between D2 and A2, two regioisomeric cross-photodimers rac-HH-PD2-A2 and rac-HT-PD2-A2 were obtained with relative yields of 65% and 35%, respectively (Figs. S59-S63, Table S1 in Supporting information). We speculated that the introduction of a 7-substituted methyl group on A2 led to the formation of both HH and HT arrangements, even though the heteroternary complex CB[10]·D2·A2 exclusively formed. Indeed, DFT calculations suggested that the energies of HH—CB[10]·D2·A2 and HT-CB[10]·D2·A2 were almost identical (Table S3 in Supporting information), explaining the low regioselectivity in this case. The cross-photodimerization between D2 and A3 was catalyzed by CB[10] to give a single cross-photodimer rac-HH-PD2-A3 (Figs. S64-S69 and Table S1 in Supporting information).
In summary, we have illustrated unreported examples of [4 + 4] cross-photodimerizations between anthracene and 4a-azoniaanthracene derivatives mediated by a host molecule. The CB[10] host demonstrated its remarkable ability to selectively encapsulate pairs of electron-donor (D) and electron-acceptor (A) molecules and significantly enhance the charge-transfer interaction between D and A molecules. The use of CB[10] as a host provided cross-photodimerization reactions between anthracene and 4a-azoniaanthracene derivatives with high reaction rate, yield, and selectivity. In the best example, only one single regioisomer as a cross-photodimer was yielded in the presence of a catalytic amount of CB[10]. This improvement can be attributed to the exclusive hetero-pairwise selectivity and nanoconfinement effect of CB[10]. These findings not only contribute to the understanding of supramolecular host–guest chemistry but also offer practical applications in the field of organic synthesis, particularly in cross-photocycloaddition reactions. Our work further paves the way for the exploration of supramolecular hosts and their potential in controlling and enhancing various chemical reactions. Given the significance of heteroternary complexes in the design of light-controlled supramolecular machines or fluorescence switches [37], we anticipate that our system could also make valuable contributions in this area.
Declaration of competing interest
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The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
CRediT authorship contribution statement
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Xianchen Hu: Writing – review & editing, Writing – original draft, Data curation, Conceptualization. Junli Yang: Writing – review & editing. Fang Gao: Writing – review & editing. Zhiyong Zhao: Writing – review & editing. Simin Liu: Writing – review & editing, Project administration, Conceptualization.
Acknowledgments
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This work was financially supported by the National Natural Science Foundation of China (No. 21871216). DFT calculations were supported by High-Performance Computing Center at Wuhan University of Science and Technology.
Supplementary materials
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Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.cclet.2024.109967.
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Year 2025 volume 36 Issue 3
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Article Info
doi: 10.1016/j.cclet.2024.109967
  • Receive Date：2024-02-23
  • Online Date：2025-11-07
  • Published：2025-03-15
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History
  • Received：2024-02-23
  • Revised：2024-04-19
  • Accepted：2024-05-05
Affiliations
    a School of Chemistry and Chemical Engineering, Wuhan University of Science and Technology, Wuhan 430081, China
    b The State Key Laboratory of Refractories and Metallurgy, Institute of Advanced Materials and Nanotechnology, Wuhan University of Science and Technology, Wuhan 430081, China
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表12种不同金属材料的力学参数
科
Family		 属数
Number of
genus		 种数
Number of
species		 占总种数比例
Percentage of
total species (%)		 属
Genus		 种数
Number of
species		 占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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