Bowl-shaped Structure Research Articles

Subphthalocyanine metallo-organic cage as catalytic molecular photoreactor for the functionalization of fullerenes

ABSTRACT Subphthalocyanines (SubPcs) are aromatic chromophores with a bowlshaped structure and outstanding optoelectronic properties. The cavity formed by a C3-symmetry trispyridyl-SubPc, Pd(II)-metalloorganic capsule has proved an optimal, shape-complementary space for the complexation of C60. Taking advantage of the intense green light absorption of the SubPc components of the capsule, and their ability to transfer energy/electrons from the excited state, our group has recently described the unprecedented use of SubPc cages as molecular photoreactors to perform photoredox-triggered addition of diphenylamine radicals over encapsulated C60. Unfortunately, the reaction could only be performed using stoichiometric amounts of the cage due to inhibition of the SubPc cavity by the addition compound. Here, we describe the preparation of a more flexible SubPc cage built with a related C1-symmetry trispyridyl-SubPc (C1-SubPc-cage), which could facilitate the exchange between the complexed addition compound and pristine fullerene, thus allowing to use it in catalytic amounts. After assessing the ability of C1-SubPc-cage to host C60, the addition of α-aminoalkyl radicals in the presence of the cage under green light irradiation was tested. Curiously, optimisation of the reaction conditions (using catalytic amounts of C1-SubPc-cage in diluted solutions) rendered a different reaction outcome, that is, a cyclopropanated fullerene, in remarkably high yields.

Radical reactivity of antiaromatic Ni(II) norcorroles with azo radical initiators.

Norcorrole is a stable 16π-antiaromatic porphyrinoid that exhibits characteristic reactivities and physical properties. Here, we disclose the reaction of Ni(II) norcorroles with alkyl radicals derived from azo radical initiators. The radical selectively attacked the distal α-position relative to the meso-position to construct a nonaromatic bowl-shaped structure. The photophysical and electrochemical properties of the obtained radical adducts were compared to those of the parent Ni(II) norcorrole. The radical reactivity of Ni(II) norcorroles was investigated by density functional theory (DFT) calculations.

Construction of Polysiloxane Induced Multilevel Bowl-shaped Janus Particles for Fabrication of Photoluminescent, Enhanced, Heat-insulative Poly(styrene-co-butyl acrylate) Latex Coating

Silica-based nanoparticles (SNPs) are highly regarded as advantageous nanofillers for composite coating, owing to their high surface area, robust mechanical properties, chemical stability, and adaptability for surface modification. Recent studies have unveiled the potential photoluminescence of SNPs induced by intrinsic defect sites, eliminating the need for additional fluorescein molecules. However, the inadequate quantum yield and complex preparation processes for generating defect sites within SNPs have constrained their broader applications. Herein, we propose a facile method to prepare Janus silicon-based nanoparticles with a hierarchical bowl-shaped structure (JHSNPs) through the emulsification of methyltriethoxysilane hydrolysis and condensation products, coupled with the capillary force during nanoparticle formation. The distinctive structure enhances the formation of dioxasilyrane (=Si(O2)) and silylene (=Si:) defects, thereby exhibiting strong blue photoluminescence. The JHSNPs then serve as nanofillers for commonly used poly(styrene-co-butyl acrylate) (SA) waterborne coatings, significantly enhancing their mechanical properties, abrasion resistance, and UV radiation resistance compared to the original SA coatings. Moreover, with just a 1% addition of JHSNPs, the composite coating exhibits visible fluorescence intensity, conferring the self-detecting monitoring properties for external scratches. Due to the hierarchical air-entrapping void structure, JHSNPs composite coatings demonstrate excellent thermal isolation performance, with a 22% reduction in thermal conductivity. The design of JHSNPs opens new avenues to expand the versatility of silica-based nanoparticles in composite coatings, especially in the optical, safety, and energy-saving fields.

Bayesian Inference for Model Analyses of Supramolecular Complexes: A Case Study with Nanocarbon Hosts.

A 126 π-electron nanobowl molecule, phenine tridehydrosumanene, was synthesized in 12 steps through the development of a polygon cyclization strategy that assembled the polygonal precursors by Ni-mediated macrocyclization. The bowl-shaped structure accommodated C70 as a guest at the concave site, and the ball-in-bowl structure was determined by X-ray crystallography. The host-guest equilibrium in solution was studied with titration experiments using isothermal calorimetry, which provided an interesting test case for studying the host-guest stoichiometry. Bayesian inference was introduced for stoichiometric analyses of the equilibrium, and a procedure to estimate the volume of prior probability in the parameter space was developed. The Bayesian procedure functioned as Occam's razor and provided quantitative support for a specific stoichiometry. The method was examined with five host-guest examples comprising nanocarbon hosts, which suggested the versatility of Bayesian inference for studies of supramolecular complexes.

Formation of Nitrogen-Doped Positively Curved Molecules by π-Extension.

Two nitrogen-doped positively curved aromatic molecules bearing doubly fused pentagonal rings were synthesized and characterized. Crystallographic analysis confirms the formation of a bowl-shaped structure, which is induced by the fusion of adjacent pentagons to the rigid aromatic planes. Both compounds demonstrate good photoluminescence. These electron-rich bowl-shaped molecules can associate with C60 to form complexes in 2:1 ratio in toluene with different association constants depending on the molecular dimension of the hosts.

Improving Magnetic Resonance Imaging and Chemodynamic Therapy Properties via Tuning the Fe(II)/Fe(III) Ratio in Hydrophilic Single-Atom Nanobowls.

We developed an intrinsic hydrophilic single-atom iron nanobowl (Fe-SANB) for magnetic resonance imaging (MRI)-guided tumor microenvironment-triggered cancer therapy. Benefiting from the sufficient exposure of Fe single atoms and the intrinsic hydrophilicity of the bowl-shaped structure, the Fe-SANBs exhibited a superior performance for T1-weighted MRI with an r1 value of 11.48 mM-1 s-1, which is 3-fold higher than that of the commercial Gd-DTPA (r1 = 3.72 mM-1 s-1). After further coembedding Gd single atoms in the nanobowls, the r1 value can be greatly improved to 19.54 mM-1 s-1. In tumor microenvironment (TME), the Fe-SANBs can trigger pH-induced Fenton-like activity to generate highly toxic hydroxyl radicals for high-efficiency chemodynamic therapy (CDT). Both the MRI and CDT efficiency of these nanobowls can be optimized by tuning the ratio of Fe(II)/Fe(III) in the Fe-SANBs via controlling the calcination temperature. Furthermore, the generation of •OH at the tumor site can be accelerated via the photothermal effect of Fe-SANBs, thus promoting CDT efficacy. Both in vitro and in vivo results confirmed that our nanoplatform exhibited high T1-weighted MRI contrast, robust biocompatibility, and satisfactory tumor treatment, providing a potential nanoplatform for MRI-guided TME-triggered precise cancer therapy.

Density structure of Kīlauea volcano: implications for magma storage and transport

SUMMARY A Bayesian linear regression to determine the bias in the Nafe–Drake relationship between compressional velocity and density provides an improved model for the density structure of Kīlauea volcano, Hawaiʻi. In previous work, we combined the results of seismic tomography with the Nafe–Drake relationship between compressional velocity and density to explain the large values of gravity disturbances overlying the summits and rift zones of the island's volcanoes. These results were used to determine mechanisms for gravitational instability of the island flanks. Here, we use laboratory measurements of the relationship of velocity and density for a wide range of Hawaiʻi island rocks as a prior in a Bayesian regression, with seismic tomography, to refine the 3-D density structure for Kīlauea volcano. This refined structure shows dense bodies (3220 kg m−3) between 5 and 8 km below sea level that underly regions of magma storage, found from geodetic and geophysical studies, beneath the summit and East Rift Zone of Kīlauea volcano. Above these bodies, density isosurfaces surround and cradle sources of pressure change determined from geodetic models, both at the summit and along the East Rift Zone. Continued subsidence of the summit following the 2018 eruption is aligned with a bowl-shaped density structure, formed primarily by density isosurfaces between 2800 and 2900 kg m−3 at 4–6 km depth. These surfaces underly the ∼3 km depth at which dyke injection initiates, are largely aseismic, and from their density values are inferred to contain high concentrations of olivine. Taken together, these density structures are consistent with an olivine-rich mush with variable porosity that increases in density with depth and provides a mechanism to form olivine cumulates both at the summit and along the rift zones. This structural framework for Kīlauea volcano is consistent with melt and mush transport occurring over a large range of depths to accommodate the growth and spreading of the volcano.

Ultrasound Activated Nanobowls with Deep Penetration for Enhancing Sonodynamic Therapy of Orthotopic Liver Cancer.

Owing to the high penetration ability and the safety of ultrasound (US) of sonodynamic therapy (SDT), it has gained significant attention in tumor treatment. However, its therapeutic efficiency depends on the performance of the sonosensitizers. The hypoxic microenvironment and abnormal stromal matrix restrict the full potential of sonosensitizers. In this study, a US-activated bowl-shaped nanobomb (APBN) is designed as a novel sonosensitizer to enhance the SDT effect through various means. This enhancement strategy combines three major characteristics: relieving tumor hypoxia, amplifying bubble cavitation damage, and US-movement-enhanced permeation. The unique bowl-shaped structure of APBN provides more favorable attachment sites for the generated oxygen gas bubbles. Thus, when catalase-like APBN catalyzes endogenous hydrogen peroxide to produce oxygen, bubbles accumulate at the groove, preventing the dissipation of oxygen and increasing the number of cavitation nuclei to improve the acoustic cavitation effect. This approach differs from traditional SDT strategies because it couples the sonodynamic effect with reactive oxygen species generation and bubble cavitation damage rather than a single action. Additionally, the asymmetric bowl-shaped structure generates a driving force under the US field, improving the distribution of sonosensitizers in the tumors. Using US and photoacoustic imaging for dual localization, these sonosensitizers can improve the accuracy of orthotopic liver tumor treatment, which presents a promising avenue for the treatment of deep tumors.

Novel Pt/COF Janus micromotor with bowl-like structure as an effective catalyst in extremely acidic environments

To effectively enhance the catalytic activity and stability of the heterogeneous catalysts in extremely acidic environments, a novel Pt/COF Janus micromotor catalyst with bowl shape (BSJP) was prepared. The as-synthesized BSJP exhibited excellent catalytic degradation efficiency against methylene blue (MB) as the model substrate, owing to self-propelling motion caused by the unique bowl shape and the concentration effect of pollutants in the bowl-shaped structure. The catalyst has excellent catalytic efficiency. At circumneutral pH, the reaction rate constant of BSJP micromotor was 3.35 times of that of non-propellant particles. At pH = 2, Pt/COF-LZU1 BSJP exhibits the best activity with a maximum removal rate of 98.61 %. Moreover, even under extreme pH conditions (pH < 2), the catalytic degradation efficiency of MB remained high, and the structure and morphology of the catalyst remained unchanged. Importantly, the catalyst exhibited remarkable stability and recyclability. The degradation rate of MB and the removal rate of TOC remained above 90 % during the four cycles. This excellent catalytic performance under extremely acidic conditions was attributed to the physical confinement of Pt nanoparticles by stable COF-LZU1. This work confirms the broad application prospects of COF-carrier materials in water purification.

Is Enol Always the Culprit? The Curious Case of High Enantioselectivity in a Chiral Rh(II) Complex Catalyzed Carbene Insertion Reaction.

The mechanism of Rh2 (S-NTTL)4 catalyzed carbene insertion into C(3)-H of indole is investigated using DFT methods. Since the commonly accepted enol mechanism cannot account for enantioinduction, a concerted oxocarbenium pathway was proposed in an earlier work using a model catalyst. However, after considering the full catalytic system, this study finds that akin to other reactions, here, too, the enol pathway is of lower energy, which now naturally raises a conundrum regarding the mode of chiral induction. Herein, a new water promoted mechanistic pathway involving a metal-associated enol intermediate hydrogen bonding and stereochemical model are proposed to solve this puzzle. It is shown how the catalyst bowl-shaped structure along with substrate-catalyst binding is crucial for achieving high levels of enantioselectivity. A stereodetermining water-assisted proton transfer is proposed and confirmed through deuterium-labeling experiments. The water molecules are held together by H-bonding interactions with the carboxylate ligands that is reminiscent of enzyme catalysis. Although several previous studies have aimed at understanding the mechanism of metal catalyzed carbene insertion reactions, the origin of high stereoinduction especially with chiral metal complexes remains unclear, and till date there is no transition state model that can explain the high enantioselectivity with such chiral Rh complexes. The metal-associated enol pathway is currently underrepresented in catalytic cycles and may play a crucial role in catalyst design. Since the enol pathway is commonly adopted in other metal-catalyzed X-H insertion reactions involving a diazoester, the presented results are not specific to the current reaction. Therefore, this study could provide the direction for achieving high levels of enantioselectivity which is otherwise difficult to achieve with a single metal catalyst.

TARAGAI PERIDOTITE MASSIF AS AN EXPLOSIVE PIPE IN THE WESTERN BUREYA TERRANE (SOUTHERN RUSSIAN FAR EAST)

Taragai peridotite massif is interpreted as an explosive ultramafic pipe emplaced through the Neoproterozoic carbonate skarnoids and Early Paleozoic granites of the western Bureya terrane. Peridotites at the surface are represented by strongly eroded bowl-shaped structure filled with disintegrated explosive material containing abundant peridotite boulders and host rock xenoliths. Explosive character of the Taragai massif is further emphasized by the occurrence of magnetite, iron-carbonate-silicate (with magnetite) and Cu-Ag-Au microspherules characteristic of explosive eruptions. Formation of the Taragai ultramafic pipe is related to the assimilation of mantle wedge or lithospheric mantle material over the stagnant Izanagi slab by the ultra-hot and reduced upwelling fluid flow within the transform-type continental margin tectonic setting.

Dynamic and Persistent Cyclochirality in Hydrogen-Bonded Derivatives of Medium-Ring Triamines.

Cyclic triureas derived from 1,4,7-triazacyclononane (TACN) were synthesized; X-ray crystallography showed a chiral bowl-like conformation with each urea hydrogen-bonded to its neighbor with uniform directionality, forming a "cyclochiral" closed loop of hydrogen bonds. Variable-temperature 1H NMR, 1H-1H exchange spectroscopy, Eyring analysis, computational modeling, and studies in various solvents revealed that cyclochirality is dynamic (ΔG‡25°C = 63-71 kJ mol-1 in noncoordinating solvents), exchanging between enantiomers by two mechanisms: bowl inversion and directionality reversal, with the former subject to a slightly smaller enantiomerization barrier. The enantiomerization rate substantially increased in the presence of hydrogen-bonding solvents. Population of only one of the two cyclochiral hydrogen-bond directionalities could be induced by annulating one ethylene bridge with a trans-cyclohexane. Alternatively, enantiomerization could be inhibited by annulating one ethylene bridge with a cis-cyclohexane (preventing bowl inversion) and replacing one urea function with a formamide (preventing directionality reversal). Combining these structural modifications resulted in an enantiomerization barrier of ΔG‡25°C = 93 kJ mol-1, furnishing a planar-chiral, atropisomeric bowl-shaped structure whose stereochemical stability arises solely from its hydrogen-bonding network.

Diruthenium Tetracarboxylate-Catalyzed Enantioselective Cyclopropanation with Aryldiazoacetates.

A series of chiral bowl-shaped diruthenium(II,III) tetracarboxylate catalysts were prepared and evaluated in asymmetric cyclopropanations with donor/acceptor carbenes derived from aryldiazoacetates. The diruthenium catalysts self-assembled to generate C4-symmetric bowl-shaped structures in an analogous manner to their dirhodium counterparts. The optimum catalyst was found to be Ru2(S-TPPTTL)4·BArF [S-TPPTTL = (S)-2-(1,3-dioxo-4,5,6,7-tetraphenylisoindolin-2-yl)-3,3-dimethylbutanoate, BArF = tetrakis(3,5-bis(trifluoromethyl)phenyl)borate], which resulted in the cyclopropanation of a range of substrates in up to 94% ee. Synthesis and evaluation of first-row transition-metal congeners [Cu(II/II) and Co(II/II)] invariably resulted in catalysts that afforded little to no asymmetric induction. Computational studies indicate that the carbene complexes of these dicopper and dicobalt complexes, unlike the dirhodium and diruthenium systems, are prone to the loss of carboxylate ligands, which would destroy the bowl-shaped structure critical for asymmetric induction.

Anthropogenic problems threatening major cities: Largest surface deformations observed in Hatay, Turkey based on SBAS-InSAR

The surface deformation caused by tectonic activities and anthropogenic factors poses a great threat to cities worldwide. The investigation and monitoring of these deformations are crucial in order to create risk analysis for the future. The problem in this case is to investigate the surface deformations and their negative effects caused by groundwater use and to identify possible landslide areas. In this study, the surface deformations in Hatay province were analyzed using SBAS-InSAR. The results from these analyses were evaluated by field observations. Sentinel-1 descending (183 datasets) and ascending (147 datasets) track geometries were selected to determine the surface deformation and its temporal evolution. Both east-west and vertical surface deformations were calculated, and the surface deformation profiles, surface 3D models and time series were created. These time series were associated with monthly precipitation data. The deformation area was interpreted with regard to available well-log data and geological setting of the study area. As a result of the study, a surface deformation resembling a bowl like structure was observed in the industrial zone located in the city center of Hatay-Güzelburç. The deformation rates are approximately 22.3 cm/year in the form of subsidence, 3.6 cm/year in the form of eastern movement and 10.1 cm/year in the form of western movement. The deformation of this bowl-like structure decelerated in the winter and accelerated in the summer due to excessive water use. The average monthly precipitation dataset supports these results. The stratigraphic data from water wells and the presence of limestone outside the eastern boundary of the deformation area show a thick clay layer in the eastern block of the bowl-shaped deformation structure. The difference between these two units, which causes a sharp anomaly at the eastern border of the deformation area, is interpreted as a probable normal fault. The second study area where surface deformations are observed is the landslide zone. The deformation was found to be 7.5 cm/year in a westward direction and 1.5 cm/year as subsidence.

Activation-induced bowl-shaped nitrogen and oxygen dual-doped carbon material and its excellent supercapacitance

Porous heteroatom-doped carbon materials exhibit promising electrochemical applications because of tunable porous structure and doping heteroatom-induced charge redistribution. Nevertheless, it is still a great challenge to develop porous heteroatom-doped carbon materials with both high-content active heteroatom species and facilitated diffusion route. Herein, we report a bowl-shaped nitrogen and oxygen dual-doping carbon (N, O-doped carbon) material based on low-temperature defluorination pyrolysis and alkali-etched activation of 3-fluorophenol-3-amino-4-hydroxypyridine-formaldehyde co-condensed resin and its excellent supercapacitance. This low-temperature thermal treatment strategy ensures high-content pyrrolic nitrogen (4.6 at.%) and oxygen species (15.9 at.%) to avoid high-temperature treatment-induced heteroatom loss and undesired configuration conversion. In these processes, the defluorination pyrolysis promotes the transformation from the resin to carbon material to some extent, and KOH activation also promotes the ordered arrangement of 002 planes, which together assure the appropriate conductivity of the final microporous carbon material. More importantly, KOH-etched activation partially removes an unstable nano/microscale domain of the intermediate carbon microspheres to form a unique bowl-shaped structure extremely facilitating the diffusion of the substitutes and/or electrolyte ions. As expected, N, O-doped carbon material displays a remarkable specific capacitance of 486.4 F g−1 at 1 A g−1 with nitrogen/oxygen species-dependant pseudocapacitance and good electrochemical durability.

Anion photoelectron spectroscopy and quantum chemical calculations of bimetallic niobium-aluminum clusters NbAln-/0 (n = 3-12): identification of a half-encapsulated symmetric structure for NbAl12.

Bimetallic niobium-doped aluminum clusters, NbAln-/0 (n = 3-12), are investigated through a synergetic combination of size-selected anion photoelectron spectroscopy and theoretical calculations. It is found that the dominant structures of NbAln- anions with n = 3-8 can be described by gradually adding Al atoms to the NbAl3- core. Starting from n = 9, the lowest-energy geometric structures of NbAl9-12- transform into bilayer structures. In particular, NbAl12- has a C3v symmetric structure, which can be viewed as a NbAl6 regular hexagon over a bowl-shaped Al6 structure. More detailed analyses indicate that NbAl9 and NbAl12- possess unusual stability, which may be attributed to their closed-shell electron configurations with superatomic features.

The theoretical design of manganese catalysts with a Si-N-Si-C-Si-C six-membered ring core-based bowl-shaped quadridentate ligand for the hydrogenation of CO/CN bonds.

Herein, a new series of bowl-shaped quadridentate ligands with a Si-N-Si-C-Si-C six-membered ring core and their manganese catalysts were designed using the density functional theory (DFT) method for the hydrogenation of unsaturated CX (XN, O) bonds. The frameworks of these ligands named by LYG (LYG = P(R1)2CH2Si(CH2)(CH3)NSi(CH3)(CH2Si(CH3)CH2P(R3)2)CH2P(R2)2) have a Si-N-Si-C-Si-C six-membered ring core at the bottom of the bowl structure and each Si atom links with one phosphorus arm (-CH2PR2). The Mn catalyst Mn(CO)-LYG was constructed to catalyze the hydrogenation of CO/CN bonds. The calculated results indicate that due to the bowl-shaped structure of LYG quadridentate ligands, these Mn catalysts could be advantageous not only in the tuneup of catalytic activity and stereoselectivity by modifying three phosphorus arms but also in the homogeneous catalyst immobilization by linking with the Si-N-Si-C-Si-C six-membered ring core using different supports. This work might provide theoretical insights to design new framework transition-metal catalysts for the hydrogenation of CX bonds.

Acceleration Effect of Bowl-Shaped Structure in Aerobic Oxidation Reaction: Synthesis of Homosumanene ortho-Quinone and Azaacene-Fused Homosumanenes.

An oxidation reaction of hydroxyhomosumanene on silica gel providing homosumanene ortho-quinone and its synthetic application for azaacene-fused homosumanenes is described. Hydroxyhomosumanene is photochemically oxidized by air, when it is coated on silica gel; this aerobic oxidation proceeds faster than that of planar analogues. The difference of such reactivity was attributed to the unusual keto-enol tautomerization due to structural difference between planar and curved π-system. The homosumanene ortho-quinone was used in the synthesis of several azaacene-fused homosumanenes, azaacenohomosumanenes. X-ray diffraction analysis of the single crystals revealed their columnar stacking structures due to the interactions between each bowl. Azaacenohomosumanenes exhibited high electron affinity due to the combination of buckybowl and electron-deficient azaacene moieties.

Evaporation Caused Invaginations of Acoustically Levitated Colloidal Droplets.

Controlled buckling of colloidal droplets via acoustic levitation plays an important role in pharmaceutical, coating, and material self-assembly. In this study, the evaporation process of PTFE colloidal droplets with two particle concentrations (60 wt% and 20 wt%) was investigated under acoustic levitation. We report the occurrence of surface invagination caused by evaporation. For the high particle concentration droplet, the upper surface was invaginated, eventually forming a bowl-shaped structure. While for the low particle concentration droplet, both the upper and lower surfaces of the droplet were invaginated, resulting in a doughnut-like structure. For the acoustically levitated oblate spherical droplet, the dispersant loss at the equatorial area of the droplet is greater than that at the two poles. Therefore, the thickness of the solid shell on the surface of the droplet was not uniform, resulting in invagination at the weaker pole area. Moreover, once the droplet surface was buckling, the hollow cavity on the droplet surface would absorb the sound energy and results in strong positive acoustic radiation pressure at bottom of the invagination, thus further prompting the invagination process.

Smart transformation of bowl shape chitosan nanomotors to disc shape in simulated biological media and consequent controlled velocity

The design of nanomotors appropriate for targeted drug delivery to cancer cells have been extensively investigated in recent years. By Pickering emulsion method, nanomotors based on platinum nanoparticles and chitosan chains were synthesized and placed on a substrate of SiO2 nanoparticles using a crosslinking agent containing a disulfide bond. The SiO2 fraction was removed, and the final chitosan-platinum nanomotor was prepared with a bowl-shaped structure. Platinum is the motor of this particle and leads to the movement of nanoparticles in the presence of H2O2 fuel. Therefore, it predicts this nanomotor can move toward the media with higher concentration of peroxide, like cancerous tissues. This nanomotor is designed in such a way that by reaching the media with higher concentration of dithiothreitol (DTT), it stops. This controllability is derived from the change in the morphology of nanomotors from bowl-shape to disc-shape. The results showed that the synthesized nanomotor could act as a biosensor for detecting cancer cells because it is sensitive to specific factors such as pH, H2O2, and DTT. The minimum required values of H2O2 and DTT needed to move the nanomotors were determined by chronoamperometry and found to be 0.1 and 2%, respectively. The release of quercetin as an anti-cancer drug from the nanomotor showed that at acidic pH, the presence of H2O2 and DTT increases the drug release compared to normal conditions. The result of the MTT assay also confirmed that the nanomotors showed more toxicity in the presence of more H2O2 in cancer cells.