Singlet Oxygen 1O2 Research Articles

Investigation into the Synergistic Effect of the Zinc Peroxide/Peroxymonosulfate Double-Oxidation System for the Efficient Degradation of Tetracycline.

The increasingly severe antibiotic pollution has become one of the most critical issues. In this study, a zinc peroxide/peroxymonosulfate (ZnO2/PMS) double-oxidation system was developed for tetracycline (TC) degradation. A small amount of ZnO2 (10 mg) and PMS (30 mg) could effectively degrade 82.8% of TC (100 mL, 50 mg/L), and the degradation process could be well described by the pseudo-second-order kinetic model. Meanwhile, the ZnO2/PMS double-oxidation system showed high adaptability in terms of reaction temperature (2-40 °C), initial pH value (4-12), common inorganic anions (Cl-, NO3-, SO42- and HCO3-), natural water source and organic pollutant type. The quenching experiment and electron paramagnetic resonance (EPR) characterization results confirmed that the main reactive oxygen species (ROS) was singlet oxygen (1O2). Moreover, three possible pathways of TC degradation were deduced according to the analyses of intermediates. On the basis of comparative characterization and experiment results, a synergistic activation mechanism was further proposed for the ZnO2/PMS double-oxidation system, accounting for the superior degradation performance. The released OH- and H2O2 from ZnO2 could activate PMS to produce major 1O2 and minor superoxide radicals (•O2-), respectively.

Porphyrin as Photosensitizers for Controlling Marine Biodegradation of Polymer Composites.

Biodegradable polymer-photosensitizer composites were developed, which is suppressed biodegradation due to bactericidal activity under light irradiation but proceeds under dark conditions. The composites exhibited antibacterial activity under light irradiation, which was attributed to the generation of singlet oxygen (1O2). Biodegradation was evaluated in seawater using the biochemical oxygen demand (BOD) method. In the dark, the composite and base polymer biodegraded to a similar degree. However, under light irradiation, the biodegradation of the composite was suppressed. In field tests, the rate of volume reduction of the composites decreased under illumination. The main cause of the suppression of biodegradation is suggested to be due to the decrease in the number of bacteria on the surface of the material and the inactivation of exoenzymes. The findings are expected to contribute to the development of biodegradable polymers that do not biodegrade during use but only when disposed of in the environment, thereby achieving on-demand degradation.

Functional biochar accelerates peroxymonosulfate activation for organic contaminant degradation via the specific B–C–N configuration

Functional biochar designed with heteroatom doping facilitates the activation of peroxymonosulfate (PMS), triggering both radical and non-radical systems and thus augmenting pollutant degradation efficiency. A sequence of functional biochar, derived from hyperaccumulator (Sedum alfredii) residues, was synthesized via sequential doping with boron and nitrogen. The SABC-B@N-2 exhibited outstanding catalytic effectiveness in activating PMS to degrade the model pollutant, acid orange 7 (Kobs = 0.0655 min−1), which was 6.75 times more active than the pristine biochar and achieved notable mineralization efficiency (71.98%) at reduced PMS concentration (0.1 mM). Relative contribution evaluations, using steady-state concentrations combined with electrochemical and in situ Raman analyses, reveal that co-doping with boron and nitrogen alters the reaction pathway, transitioning from PMS activation through multiple reactive oxygen species (ROSs) to a predominantly non-radical process facilitated by electron transfer. Moreover, the previously misunderstood concept that singlet oxygen (1O2) plays a central role in the degradation of AO7 has been clarified. Correlation analysis and density functional theory calculations indicate that the distinct BCN configuration, featuring the BC2O group and pyridinic-N, is fundamental to the active site. This research substantially advances the sustainability of phytoremediation by offering a viable methodology to synthesize highly catalytic functional biochar utilizing hyperaccumulator residues.

Near-infrared hemicyanine photosensitizer for targeted mitochondrial viscosity imaging and efficient photodynamic therapy

As a severe threat to human health, cancer has always been one of the most significant challenges facing the medical field. However, there is currently no effective technology or method to diagnose and treat cancer simultaneously. Therefore, developing a new approach that integrates diagnosis and treatment holds promise as a means of achieving personalized and precise cancer therapy. In this study, we developed a novel dual-functional near-infrared mitochondrial-targeted photosensitizer, Hcy-I, which is capable of simultaneously monitoring cellular viscosity and specifically targeting mitochondria for photodynamic therapy. Compared with traditional hemicyanine dyes, the introduction of iodine atoms in Hcy-I enhanced spin–orbit coupling (SOC) and promoted the intersystem crossing (ISC) rate, thereby increasing the efficiency of singlet oxygen (1O2) generation. In vitro experiments demonstrated that Hcy-I exhibited high sensitivity to viscosity variations and efficiently generated 1O2 under 638 nm laser irradiation, with an 1O2 quantum yield of up to 48.9 %. Cell experiments further revealed that this photosensitizer could effectively target mitochondria for photodynamic therapy, disrupting mitochondrial membrane potential and inducing cell death. When treated with Hcy-I at a concentration of 0.8 µM, the survival rate of HepG-2 cells was only 13 %. These results suggested that Hcy-I had the potential to integrate cancer diagnosis and treatment. The research not only promotes the development of photodynamic thereby technology, but also opens up new avenues for the diagnosis and treatment of cancer.

A novel visible light-driven oxygen doped C3N4/Bi12O17Cl2/ferrate(VI) system for Bisphenol A degradation: Radical and nonradical pathways

In this study, visible light-activated photocatalyst oxygen-doped C3N4@Bi12O17Cl2 (OCN@BOC) and Fe(VI) coupling system was proposed for the efficient degradation of bisphenol A (BPA). The comprehensive characterization of the OCN@BOC photocatalyst revealed its excellent photogenerated carrier separation rate in heterogeneous structures. The OCN@BOC/Fe(VI)/Vis system exhibited a remarkable BPA removal efficiency of over 84% within 5 min. Comparatively, only 37% and 59% of BPA were degraded by single OCN@BOC and Fe(VI) in 5 min, respectively. Reactive species scavenging experiments, phenyl sulfoxide transformation experiments, and electron paramagnetic resonance experiments confirmed the involvement of superoxide radicals (⋅O2−), singlet oxygen (1O2), as well as iron(V)/iron(IV) (Fe(V)/Fe(IV)) species in the degradation process of BPA. Furthermore, density functional theoretical calculations and identification of intermediates provided insights into the potential degradation mechanism of BPA during these reactions. Additionally, simulation evaluations using an ecological structure activity relationship model demonstrated that the toxicity of BPA to the ecological environment was mitigated during its degradation process. This study presented a novel strategy for removing BPA utilizing visible light photocatalysts, highlighting promising applications for practical water environment remediation with the OCN@BOC/Fe(VI)/Vis system.

Phenanthrene Appending Ruthenium Complexes: DNA Binding, Molecular Docking, TDDFT Calculation, and Photocytoxicity In Vitro

ABSTRACTPhotodynamic therapy (PDT) has been an effective tumor treatment to reduce the side effects of chemotherapy. Herein, we described the synthesis of two Ru (II) complexes by introducing a phenanthrene unit and their photocytotoxicity. Ru1 and Ru2 displayed high DNA affinities by intercalation. Under light, two complexes produced high singlet oxygen (1O2) quantum yields and cleaved DNA efficiently. Both high DNA affinities and 1O2 quantum yields of two complexes resulted in obvious photocytotoxicity towards Hela, A549, and A375 cells. Furthermore, low dark cytotoxicity was also observed for two complexes, which may promote them to act as potential PDT agents. TDDFT (Time‐dependent density functional theory) calculations also demonstrated two complexes that might display the PDT activities via 1O2 photogeneration.

A Highly Efficient Supramolecular Polymer-Based Singlet Oxygen Generator for Photocatalytic Minisci Alkylation.

Supramolecular polymers, with their specific functional units and structures, can effectively enhance the absorption and utilization of light energy, thereby facilitating more efficient photocatalytic organic reactions. In the present work, we constructed a supramolecular polymer consisting of benzothiazole derivatives (BTBP) and cucurbit[8]uril (CB[8]). The BTBP monomer, known for its unique chemical structure and properties, has been found to exhibit a remarkable capability in generating singlet oxygen (1O2). As a result of the constraining impact of the macrocyclic molecule, the inclusion of CB[8] resulted in an effective enhancement in the ability to generate 1O2 while forming supramolecular polymer BTBP-CB[8]. When evaluating the quantum yield of 1O2 using Rose Bengal (RB) as a reference photosensitizer (75% in water), BTBP-CB[8] demonstrated an enhanced 1O2 quantum yield compared to BTBP, with an impressive yield of 152.4%, demonstrating that the formation of supramolecular polymer contributes to its ability to generate 1O2. Subsequently, BTBP-CB[8], a highly efficient 1O2 generator, was employed for the photocatalytic Minisci alkylation reaction, resulting in an impressive reaction yield of up to 89%. The supramolecular polymer strategies employed in the construction of photocatalytic systems have exhibited remarkable efficacy in the production of 1O2, underscoring their immense prospects in photocatalysis.

Synergistic enhancement of singlet oxygen generation in Au and oxygen vacancy co-modified Bi2MoO6 ultrathin nanosheets for efficient ciprofloxacin degradation

Solar-driven molecular oxygen activation (MOA) is crucial for generating reactive oxygen species (ROS) for pollutant degradation, while the low activation efficiency greatly weakens the degradation efficiency. Herein, oxygen vacancies (OVs) and Au nanoparticles are co-introduced into Bi2MoO6 (ABMOH) to enhance the photocatalytic activity of Bi2MoO6 (BMO), thereby promoting MOA efficiency. Density functional theory demonstrates that the introduction of OVs not only improves the molecular oxygen adsorption on BMO, and but also strengthens the O-O bond dissociation of molecular oxygen, which is beneficial to MOA. Meanwhile, the unique localized surface plasmon resonance effect of Au nanoparticles immensely increases the photo-absorption capacity. Crucially, both OVs and Au nanoparticles work as “electron traps” to capture photogenerated electrons, thereby accelerating charge transfer. Based on the advantage of OVs and Au nanoparticles, ABMOH displays excellent MOA efficiency, and the degradation rate constant of ciprofloxacin (CIPF) by ABMOH-4 is 3.62-fold higher than BMO. Free radical trapping experiment and electron spin resonance suggest that singlet oxygen (1O2) can be selectively formed in the ABMOH system for CIPF degradation, and superoxide radical (•O2–) conversion and energy transfer are two pathways for 1O2 formation. This investigation serves as a beacon for the strategic design of high-performance and stable photocatalysts for MOA activation, paving the way for advancements in environmental remediation.

Nitrogen-doped iron-manganese porous carbon particle electrodes for electrocatalytic degradation of tetracycline: Interfacial reaction mechanisms

In this study, nitrogen-doped porous carbon-supported iron-manganese microspheres (FeMn@NC-700) were successfully synthesized and employed as three-dimensional particle electrodes (3DPE) for electro-oxidative of tetracycline (TCH) in water. FeMn@NC-700 exhibited stable catalytic activity and effective TCH removal capabilities under complex water quality conditions and varying pH levels. Under optimized conditions, the 3D/FeMn@NC-700 system reduced the TCH concentration from an initial 20 mg/L to 0.96 mg/L within 60 min, achieving a 95.23 %removal efficiency with an energy consumption of only 10.05 kWh/m3. The outstanding electrocatalytic activity of the 3D/FeMn@NC-700 system was attributed to the dynamic redox cycling between the Fe and Mn species on the 3DPE surface. Radical quenching experiments and electron paramagnetic resonance (EPR) analysis identified the predominant role of singlet oxygen (1O2), effectively removing TCH with the assistance of hydroxyl radicals (·OH) and superoxide anions (O2·-). The degradation pathways of major intermediate products of TCH were proposed, along with a toxicity assessment. In conclusion, the 3D/FeMn@NC-700 system represents a reliable and cost-effective technology for TCH wastewater treatment.

Carrier-Free Hybrid Nanoparticles for Enhanced Photodynamic Therapy in Oral Carcinoma via Reversal of Hypoxia and Oxidative Resistance.

In the present work, we pioneered a coordinated self-assembly approach aimed at fabricating carrier-free hybrid nanoparticles to address the inherent challenges of the anaerobic microenvironment and the oxidative resistance induced by reductive glutathione (GSH) in photodynamic therapy (PDT). In these nanoparticles, protoporphyrin IX (PP), HIF-1α inhibitor of N, N'-(2,5-Dichlorosulfonyl) cystamine KC7F2 (KC), and the cofactor Fe3+ present hydrogen bond and coordination interaction. The nanoparticles exhibited efficient cellular uptake by CAL-27 cells, facilitating their accumulation in tumors by enhanced permeability and retention (EPR) effect. Under irradiation at 650 nm, the formation of cytotoxic singlet oxygen (1O2) would be enhanced by the synergy effect on the Fenton reaction of Fe3+ ion and the downregulation of the HIF-1α, leading to the improved PDT efficacy both in vitro and in vivo biological studies. Our work opens a new supramolecular approach to prepare hybrid nanoparticles for effective synergy therapy with PDT against cancer cells.

Efficient elimination of organic contaminants via a non-radical pathway involving activation of sulfite by synergistic adsorption-catalysis bifunctional chitosan-modified MOF derivative

Usually, Metal-based sulfite activation systems follow a radical generation pathway but are rare in non-radical pathways. Singlet oxygen (1O2) generation-targeted catalyst was synthesized by introducing non-redox metal oxides ZnO into chitosan-modified cobalt-zinc bimetallic oxides (CZ1.0C) via template method. Compared with Co3O4, the catalyst CZ1.0C coupled to the sulfite system (CZ1.0C/SO32-) maintained good adaptability in a common water background and a wide pH range (7–11). In addition, the CZ1.0C/SO32- system showed high efficiency in the degradation of Congo red (kobs = 0.190 min−1) and 100 % sulfite utilization. EPR, probe experiments, and DFT calculations proved the dominant role of 1O2, with a concentration three orders of magnitude higher than that of radicals. The controlled generation of non-radicals was achieved owing to the doping of ZnO and the conversion of lattice oxygen and oxygen vacancies. The catalytic oxidation intermediate HSO5- has also been demonstrated in the system, which achieves non-radical pathway oxidation through electron-mediated interactions. This article aims to develop a new “waste control by waste” strategy, which combines high selective adsorption and catalysis to achieve sulfur resource recovery and water pollutants elimination.

In-situ encapsulation synthesis of Fe-SAPO-34 for efficient removal of tetracycline via peroxydisulfate activation: Highly dispersed active sites and ultra-low iron leaching

The agglomeration and leaching of metal species are critical issues for iron-based catalysts to remove tetracycline (TC) through peroxydisulfate (PDS) activation. In this work, iron-oxide species confined in cha cage of silicon aluminum phosphate zeolite (Fe-SAPO-34) was successfully synthesized by in-situ encapsulation method to address the above challenges. In Fe-SAPO-34/PDS system, approximately 92.6% TC was removed within 150 min at experimental conditions: [pH] = 3, [TC] = 20 mg/L, [Catalyst] = 0.10 g/L, [PDS] = 1 mM. Meanwhile, the biggest degradation rate constant is 0.03689 min−1, which surpasses the counterpart systems. This result originates from the well dispersion of Fe-oxide species in Fe-SAPO-34, providing more active sites for TC degradation. As expected, the Fe-oxide species leaching concentration is ultra-low (0.018 mg/L) in Fe-SAPO-34/PDS system, which is attributed that SAPO-34 has a confinement effect of cha cage and eight-ring pore openings to limit its leaching. The radical quenching tests and electron paramagnetic resonance (EPR) technology verify singlet oxygen (1O2) is the primary reactive oxygen species (ROS) in Fe-SAPO-34/PDS system. Furthermore, two possible pathways for TC degradation are proposed in line with the intermediate identified by liquid chromatography-mass spectrometry (LC-MS).

Removal of sulfadiazine from water by a three-dimensional electrochemical system coupled with persulfate: Enhancement effect of ball-milled CuO-Fe3O4@biochar

The CuO-Fe3O4@biochar (CFB) composite, synthesized via an eco-friendly mechanical ball milling, was employed as a particle electrode in a three-dimensional (3D) electrochemical reactor to investigate its efficiency in removing sulfadiazine (SD) from antibiotic wastewater. The study revealed that the addition of 5 g/L CFB into the 3D electrochemical system significantly enhanced SD removal, achieving a removal rate of 96.2 % compared to 33.5 % in a two-dimensional system, under optimal conditions of pH 7, persulfate concentration of 4 mM, and current density of 8 mA/cm2. The CFB particle electrode demonstrated superior catalytic activity compared to CuB, FeB, and CuFe particle electrodes. The ball milling process effectively reduced the agglomeration of CuO and Fe3O4, thereby increasing the active sites of the particle electrodes. The SD displayed remarkable removal efficiency across a broad pH spectrum ranging from 2 to 9. Scavenging experiments and electron paramagnetic resonance techniques suggested that SD removal primarily occurred via a non-radical pathway involving singlet oxygen (1O2). The synergistic effect between bimetallic ions and the reduction reaction at the cathode accelerated the cycling of Fe2⁺/Fe3⁺ and Cu⁺/Cu2⁺, thereby promoting PDS activation. Additionally, the positively charged surface of CFB facilitated contact with PDS through electrostatic attraction. The E-CFB-PDS system demonstrated excellent efficiency in removing antibiotics, and its stability and reusability make it a promising approach for treating organic pollutant wastewater.

Construction of N-Fe-S bridge in atomic iron catalyst for boosting Fenton-like reactions

Constructing the coordination environment of single-atom catalysts (SACs) can be an attractive technical strategy to regulate the generation of reactive oxygen species for Fenton-like reactions. Herein, we have constructed an asymmetric coordination of Fe single-atom catalyst (FeSA-NS-PCNS) with abundant N-Fe-S bridge (FeSA-N3S1) for robust Fenton-like reactions. 82.5 % of singlet oxygen (1O2) selectivity and high turnover frequency of bisphenol A degradation (0.568 min−1) were achieved at mild conditions. Experimental works and theoretical analyses illustrated that S doping breaks the inert environment of the original N-Fe-N symmetric coordination equilibrium and modulates the electron density of the atomic Fe center, which is beneficial for boosting PMS adsorption and reducing the energy barriers of vital *OH and *O intermediates. The coupling between the FeSA-N3S1 interface and peroxymonosulfate molecule boosts in-situ electron transfer through the N-Fe-S bridge, which induces more electron flow from the low valence Fe to OH* on the surface of Fe-*O-H, forming a high yield of 1O2. Moreover, we designed the Fenton-like reactions by FeSA-NS-PCNS membrane reactor for an efficient contaminant removal rate of over 90 % even after 11 cycles. This work provides a novel perspective on developing SACs with asymmetric coordination to regulate reactive oxygen species for the treatment of organic contaminants in water bodies.

Vacancy-strengthened Cu/Co composite oxides for efficient removal of methylene blue via peroxymonosulfate activation: Synergism of multiple Lewis acid sites

The development of suitable catalysts poses a challenge for the peroxymonosulfate (PMS) activation system used in decontamination process. Here we constructed a series of vacancy-strengthened Cu/Co composite oxides (CuCoO) composed of CuCo2O4 and CuO containing multiple Lewis acid sites. The results demonstrate that the as-prepared CuCoO-2 exhibited exceptional activation performance, broad-ranging degradation capacity, remarkable reusability and stability. The optimized CuCoO-2+PMS system achieved complete removal of methylene blue (MB) in 40 min, while maintaining a degradation efficiency of above 86 % even after 5 cycles. A comprehensive survey revealed that hydroxyl radical (·OH), sulfate radical (SO4.-) and singlet oxygen (1O2) collectively contribute to the degradation of MB in the CuCoO-2+PMS system. Especially, 1O2 was the dominant active species. The synergism of various Lewis acid sites (Cu+/2+, Co2+/3+ and VO/N) as unsaturated surface-bound centers played a pivotal role in promoting non-radical-driven activation of PMS. Meanwhile, the generated VO/N facilitated enhanced metallic valence circulation in CuCoO-2, strengthening electron mediation between PMS and MB. Additionally, possible degradation pathways and toxicity evaluations of MB and its intermediates were proposed. In conclusion, this work offers valuable insights into PMS activation by vacancy-strengthened CuCoO and is of great significance for water purification.

Pt/Pd dual-modified porphyrin metal-organic frameworks for NIR-II photothermal-enhanced photodynamic/catalytic therapy

Photodynamic therapy (PDT) and catalytic therapy were promising treatment modes, but tumor hypoxia and poor catalytic activity severely limited their efficacies. Herein, using a porphyrin metal–organic framework (PCN-224) as nanocarrier, a platinum/palladium (Pt/Pd) dual-modified PCN-224 nanoprobe (PCN-224-Pt@Pd) with strong peroxidase (POD)/catalase (CAT)-like activities was developed, achieving photothermal-promoted PDT/catalytic therapy. Compared with single ultrasmall Pt modifying, CAT-like activity of Pt/Pd dual-modifying increased oxygen concentration from 6.24 to 9.35 mg/L, which improved singlet oxygen (1O2) yield from 63.8 % to 82.9 %. Moreover, POD-like activity of Pt/Pd dual-modifying significantly accelerated hydroxyl radicals (·OH) generation. Importantly, PCN-224-Pt@Pd possessed near-infrared II (NIR-II) photothermal effect with a high efficiency (55.6 %), which further promoted ·OH production. Under combined therapy of PCN-224-Pt@Pd, the cell survival rate greatly reduced to 5.8 %, and the tumors were cured, suggesting NIR-II photothermal-enhanced PDT/catalytic therapy.

Photocatalytic degradation of toxic basic blue 41 and reactive orange M2R dyes using green synthesized zinc oxide nanoparticles

Zinc oxide nanoparticles (Cm-ZnO NPs) were synthesized to eliminate organic dye pollutants from textile dye effluents. The present study reports Cucumis maderaspatanus L. leaves utilized as a green reducing/stabilizing agent for Cm-ZnO NPs synthesis. The nanoparticles underwent thorough analysis using techniques such as XRD, UV–vis, TEM, and FT-IR. Photocatalytic degradation of toxic basic blue 41 (BB41) and reactive orange M2R (ROM2R) dyes using Cm-ZnO NPs, showed a degradation rate of 97.69 % and 94.30 % respectively under optimized conditions. The kinetics of photocatalytic degradation of BB41 and ROM2R dyes followed first-order kinetics. The scavenger studies were conducted to identify the photogenerated reactive species involved in dye degradation. The singlet oxygen (1O2) and hydroxyl radicals (●OH) are mainly responsible for the degradation of BB41 and ROM2R dye respectively. LC-MS analysis was used to identify the photocatalytic degraded products, and ECOSAR software assessed their toxicity. The recyclability was performed up to four cycles and the stability of Cm-ZnO NPs was confirmed by XRD analysis. Thus, the as-synthesized Cm-ZnO NPs are suitable for industrial textile wastewater treatment.

Peroxydisulfate activation by copper nanoparticles doped highly graphitized hollow carbon spheres for thiocyanate degradation

Thiocyanate (SCN-) is a toxic and refractory inorganic pollutant commonly found in industrial wastewater. This paper proposes an innovative solution to enhance the activation of peroxydisulfate (PDS) by designing a highly graphitized hollow carbon nanosphere structure catalyst doped with copper nanoparticles, thereby achieving efficient and complete degradation of SCN-. Specifically, the active sites and electron transfer ability of the catalyst were improved by controlling the pyrolysis temperature and acid etching time during the catalyst preparation process, thereby optimizing the PDS activation rate and SCN- degradation rate. In the optimized Cu-NPs@C/PDS system, a low dose of Cu-NPs@C-650–6 catalyst (0.2 g/L) and PDS ([PDS]0: [SCN-]0 = 3: 1) was sufficient to achieve 100 % degradation of 100 mg/L SCN- within 20 min. The non-radical oxidation pathway combined with singlet oxygen (1O2) and direct electron transfer process was identified as the main degradation mechanism of SCN-. The unique oxidation mechanism provided a higher SCN- degradation reaction rate constant (k1 = 0.39 min−1) and stronger environmental ion resistance. Density functional theory (DFT) calculations show that the CO bond is the primary PDS active site for the formation of inside-out electron delocalization, and the S atom in SCN- is a vulnerable site. This work offers technological support for the treatment of water bodies holding emerging electron-rich pollutants in addition to fresh insights into the creation of efficient catalysts for metal-carbon composites.

Near-Infrared Laser-Switching DNA Phase Separation Nanoinducer for Glioma Therapy.

DNA phase separation participates in chromatin packing for the modulation of gene transcription, but the induction of DNA phase separation in living cells for disease treatment faces huge challenges. Herein, we construct a Ru(II)-polypyridyl-loaded upconversion nanoplatform (denoted as UCSNs-R) to achieve the manipulation of DNA phase separation and production of abundant singlet oxygen (1O2) for efficient treatment of gliomas. The utilization of the UCSN not only facilitates high loading of Ru(II)-polypyridyl complexes (RuC) but also promotes the conversion of near-infrared (NIR) laser to ultraviolet light for efficient 1O2 generation. The released RuC exhibit DNA "light-switch" behavior and high DNA binding affinity that induce phase separation of DNA in living cells, thus resulting in DNA damage and suppressing tumor-cell growth. In vivo investigation demonstrates the high capability of UCSNs-R in inhibiting tumor proliferation under NIR laser illumination. This work represents a paradigm for designing a DNA phase separation nanoinducer through integration of the UCSN with Ru(II)-polypyridyl-based complexes for efficient therapy of gliomas.

A Hydrogen-Bonded Organic Framework Based on Triphenylamine for Photocatalytic Silane Hydroxylation.

Employing hydrogen-bonded organic frameworks (HOFs) as mild photocatalysts for organic conversions is still considerably challenging. In this work, we synthesized a hydrogen-bonded organic framework (HOF-16) and achieved the photocatalytic oxidation of silanes to generate silanols. Considering the constraints imposed by the framework structure, a significant improvement in the efficacy of singlet oxygen (1O2) generation is observed. HOF-16 exhibits remarkable photocatalytic performance when it comes to silane hydroxylation, displaying high efficiency, low catalyst loading, and good recyclability. This research highlights the immense potential of HOFs in the realm of organic photocatalysis.