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This research delves into the preparation of heteronuclear bimetallic catalysts and explores their catalytic properties in the thermal decomposition of ammonium perchlorate (AP). The study's central focus is on enhancing the thermal decomposition characteristics of AP and, consequently, the combustion performance of composite solid propellants. The synthesized materials underwent structural characterization by XRD, XPS, SEM, and FTIR. Catalytic properties were examined using DTA tests. Notably, catalysts derived from calcination at 500 °C exhibited heightened catalytic activity. They advanced the pyrolysis temperature by 135.4 °C and reduced the activation energy by 82.38 kJ/mol compared with pure AP. To further elucidate the decomposition mechanism of AP, the investigation also employed a combined approach involving DSC-TG-FTIR-MS analysis.
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Dimension and solvent molecules affect the performance of energetic metal-organic frameworks (EMOFs). High-dimensional EMOFs are usually characterized by high stability and low sensitivity due to their complex network structure. However, solvent molecules affect the detonation performance of EMOFs, and these molecules may be removed at low temperatures, resulting in structural collapse and affecting the stability of EMOFs. In this work, zero-dimensional (0D) Co(AFTO)2·(H2O)2 (EMOF 1) and Ni(AFTO)2·(H2O)2 (EMOF 2) with coordinated water molecules and [Co(AFTO)2]n·EtOH (EMOF 3) and [Ni(AFTO)2]n (EMOF 4) (AFTO = 5-(4-amino-furazan-3-yl)-1-hydroxytetrazole) with high-dimensional structure were synthesized using hydrothermal and self-assembly methods in ethanol, respectively. Structural and performance tests show that EMOF 3 and 4 exhibit remarkable thermal stability and low mechanical sensitivity. This method is a simple, effective, and green technique for synthesizing high-dimensional EMOFs with high stability through self-assembly in ethanol solution. In addition, EMOF 3 and 4 can be used as primary green laser explosives.
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Chitosan-lead (CS-Pb) carbon aerogels were prepared by ionic cross-linking and high-temperature carbonization using chitosan (CS) as the carbon precursor. The obtained carbon aerogels were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometry (XRD), and X-ray photoelectron spectroscopy (XPS). The obtained aerogels have a 3D structure and a large surface area, which can effectively prevent the agglomeration phenomenon of metals. Differential thermal analysis (DTA) was used to analyze the catalytic performance of a carbon aerogel for ammonium perchlorate (AP). The results showed that the CS-Pb carbon aerogel reduced the peak temperature of AP pyrolysis from 703.9 to 627.7 K. According to the Kissinger method calculations, the Ea of AP decomposition decreased about 27.2 kJ/mol. The TG data at different warming rates were analyzed by the Flynne-Walle-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS) methods, which are two of the isoconversion methods, and the activation energies of AP and AP+CS-Pb-3.5 were calculated. Between the conversion degrees (α) of 0.1 and 0.9, the Ea values obtained by the two isoconversion methods are similar and have a certain match. Also, the two isoconversion methods confirm Kissinger's calculation. Finally, thermogravimetry-mass spectrometry (TG-MS) was used to monitor the gases generated during the thermal decomposition of the AP+CS-Pb-3.5 system in real time.
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Two new three-dimensional (3D) energetic metal-organic frameworks (EMOFs), namely, [Cu(OBTT)(NC2H8)2]n (1) and [Cd3(OBTT)2(H2O)2]n·4H2O (2), where H3OBTT = 4,5-bis(1-hydroxytetrazol-5-yl)-1,2,3-triazole, were prepared, and their structures were characterized by single-crystal X-ray diffraction analysis, which revealed that the EMOFs feature a rigid 3D framework architecture. The possibility of these two EMOFs as potential catalysts for the thermal decomposition of ammonium perchlorate (AP) was investigated. The results show that they have significant catalytic activity, up to reducing the peak temperature of AP decomposition from 704.0 to 613.6 K and contracting the decomposition temperature range from 451 to 320 K, which is almost one-third less than the decomposition temperature range of pure AP. The Kissinger and Ozawa-Doyle methods were used to calculate the kinetic parameters of the thermal decomposition of pure and mixed AP samples. The experimental results suggest that compound 1 has potential applications in the field of explosives and propellants. All properties suggest that compound 1 can be used as a potential catalyst.
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Herein, we provide an efficient strategy for constructing three-dimensional (3D) energetic coordination polymers (ECPs), namely, metal-organic frameworks (EMOFs), avoiding solvent coordination without changing the organic ligands or metal nodes. Three ECPs with the same ligand and metal center, namely, two-dimensional (2D) layer ECP [Pb(HOBTT)(H2O)2]n (1), 3D solvent-free EMOFs [Pb(HOBTT)]n (2), and dense [Pb3(OBTT)2]n (3) (H3OBTT = 4,5-bis(1-hydroxytetrazol-5-yl)-2H-1,2,3-triazole), were rationally designed and synthesized via free protons. As expected, the theoretical density of 3 (4.080 g·cm-3) is greater than those of 2 (3.299 g·cm-3) and 1 (3.055 g·cm-3). Thermal stabilities indicate that their decomposition temperature exceeds 300 °C. Theoretical calculations show that the detonation performance of 3 is better than that of 1 and 2. The detonation performance of 1-3 was further proven by laser irradiation.
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The blood-brain barrier (BBB) permeability of molecules needs to meet stringent requirements of Lipinski's rule, which pose a difficulty for the rational design of efficient chelating agents for Parkinson's disease chelation therapy. Therefore, the iron chelators employed N-aliphatic alcohols modification of deferiprone were reasonably designed in this work. The chelators not only meet Lipinski's rule for BBB permeability, but also ensure the iron affinity. The results of solution thermodynamics demonstrated that the pFe3+ value of N-hydroxyalkyl substituted deferiprone is between 19.20 and 19.36, which is comparable to that of clinical deferiprone. The results of 2,2-diphenyl-1-picrylhydrazyl radical scavenging assays indicated that the N-hydroxyalkyl substituted deferiprone also possesses similar radical scavenging ability in comparison to deferiprone. Meanwhile, the Cell Counting Kit-8 assays of neuron-like rat pheochromocytoma cell-line demonstrated that the N-hydroxyalkyl substituted deferiprone exhibits extremely low cytotoxicity and excellent H2O2-induced oxidative stress protection effect. These results indicated that N-hydroxyalkyl substituted deferiprone has potential application prospects as chelating agents for Parkinson's disease chelation therapy strategy.
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Deferiprona/análogos & derivados , Deferiprona/síntese química , Quelantes de Ferro/síntese química , Quelantes de Ferro/farmacologia , Doença de Parkinson/tratamento farmacológico , Animais , Cálcio , Sobrevivência Celular/efeitos dos fármacos , Deferiprona/farmacologia , Desenho de Fármacos , Peróxido de Hidrogênio/toxicidade , Estresse Oxidativo/efeitos dos fármacos , Células PC12 , Ratos , ZincoRESUMO
π-Stacking is common in materials, but different π-π stacking modes remarkably affect the properties and performances of materials. In particular, weak interactions, π-stacking and hydrogen bonding, often have a great impact on the stability and sensitivity of high-energetic compounds. Therefore, several of energetic materials based on 1,1'-dihydroxyazotetrazole (1) with a nearly flat structure, such as the salts of aminoguanidine (2), 1,3-diaminoguanidine (3), imidazole (4), pyrazole (5) and triaminoguanidine (6), and a cocrystal of 2-methylimidazole (7), were designed and synthesized. Based on single-crystal diffraction data, thermal decomposition behaviors, and the mechanical sensitivity test, the compounds of 4, 5, and 7 with face-to-face π-π stacking display outstanding thermal stability and insensitivity.
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Graphitic carbon nitride quantum dots (CNQDs) with a high quantum yield (up to 43%) were synthesized by incorporating the unique organic functional group of barbituric acid into the framework of the carbon nitride structure by supramolecular pre-organization. The CNQDs were introduced onto the surface of basic zinc carbonate (BZC) by co-precipitation. The resulting CNQDs/BZC composite showed that the degradation efficiency of tetracycline was 2.4 times higher than that of ZnO. The Z-scheme mechanism for the as-prepared sample was proposed for the enhanced photocatalytic degradation rate. The ËO2- and ËOH radicals played major roles due to the suitable bandgap. Finally, the formation and possible photocatalytic mechanisms of the CNQDs/BZC composite are proposed.
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Nitroaromatic explosives in wastewater are hardly degraded, which seriously endangers the ecological environment and human safety. We report a core-shell structure hybrid material (IR-MOF3@COF-LZU1) with high crystallinity and graded porosity. It is an effective visible-light-driven photocatalyst that degrades p-nitrophenol (PNP). After 3.5 h, PNP was degraded well under visible light, and it is proven that the photocatalytic degradation is efficient. In addition, this photocatalytic activity adhered to pseudo-first-order kinetics, and a possible photocatalytic mechanism was discussed in detail.
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The special linear dioxo cation structure of the uranyl cation, which relegates ligand coordination to an equatorial plane perpendicular to the OâUâO vector, poses an unusual challenge for the rational design of efficient chelating agents. Therefore, the planar hexadentate ligand rational design employed in this work incorporates two bidentate catecholamine (CAM) chelating moieties and a flexible linker with a ß-dicarbonyl chelating moiety (ß-dicarbonyl(CAM)2 ligands). The solution thermodynamics of ß-dicarbonyl(CAM)2 with a uranyl cation was investigated by potentiometric and spectrophotometric titrations. The results demonstrated that the pUO22+ values are significantly higher than for the previously reported TMA(2Li-1,2-HOPO)2, and efficient chelation of the uranyl cation was realized by the planar hexadentate ß-dicarbonyl(CAM)2. The efficient chelating ability of ß-dicarbonyl(CAM)2 was attributed to the presence of the more flexible ß-dicarbonyl chelating linker and planar hexadentate structure, which favors the geometric arrangement between ligand and uranyl coordinative preference. Meanwhile, ß-dicarbonyl(CAM)2 also exhibits higher antiradical efficiency in comparison to butylated hydroxyanisole. These results indicated that ß-dicarbonyl(CAM)2 has potential application prospects as a chelating agent for efficient chelation of a uranyl cation.
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Antioxidantes/química , Catecolaminas/química , Quelantes/química , Termodinâmica , Urânio/química , Antioxidantes/síntese química , Antioxidantes/farmacologia , Compostos de Bifenilo/antagonistas & inibidores , Catecolaminas/síntese química , Catecolaminas/farmacologia , Cátions/química , Quelantes/síntese química , Quelantes/farmacologia , Ligantes , Estrutura Molecular , Picratos/antagonistas & inibidoresRESUMO
A convenient and highly efficient palladium-catalyzed reaction of [60]fullerene (C60) with aroyl compounds via enolate-mediated C-H activation and hydroxylation has been exploited for the first time to synthesize novel C60-fused dihydrofurans, and rare 1,4-fullerenols. Further functionalization including etherification, and esterification of synthesized 1,4-fullerenols provided efficient access to versatile fullerene derivatives. Moreover, a plausible reaction mechanism leading to the observed products is proposed.
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A convenient and efficient Pd(OAc)2-catalyzed N-heteroannulation reaction of [60]fullerene with benzoyl hydrazone esters was exploited to synthesize novel and scarce N-unsubstituted 2-fulleropyrrolines via the formation of C-C and C-N bonds. Besides, the self-sensitized photo-oxidation of 2-fulleropyrrolines was first discovered under very mild conditions to yield a ketoamide fullerene derivative in high yields. The reaction kinetics of this self-sensitized photo-oxidation has been explored, indicating that this photo-oxidation process is a first-order reaction possessing a low reaction activation energy (2.79 kJ mol-1). Moreover, a possible mechanism related to the observed products was proposed.
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This study explores the large-area synthesis of controllable morphology, uniform, and high-quality monolayer. MoSe2 is essential for its potential application in optoelectronics, photocatalysis, and renewable energy sources. In this study, we successfully synthesized snow-like MoSe2 monolayers using a simple chemical vapor deposition method. Results reveal that snow-like MoSe2 is a single crystal with a hexagonal structure, a thickness of â¼0.9 nm, and a lateral dimension of up to 20 µm. The peak position of the photoluminescence spectra is â¼1.52 eV corresponding to MoSe2 monolayer. The growth mechanism of the snow-like MoSe2 monolayer was investigated and comprised a four-step process during growth. Finally, we demonstrate that the snow-like MoSe2 monolayers are ideal electrocatalysts for hydrogen evolution reactions (HERs), reflected by a low Tafel slope of â¼68 mV/decade. Compared with the triangular-shaped MoSe2 monolayer, the hexangular snow-like shape with plentiful edges is superior for perfect electrocatalysts for HERs or transmission devices of optoelectronic signals.
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Five new bis(3-hydroxy-4-pyridinone) tetradentate chelators were synthesized in this study. The structures of these tetradentate chelators were characterized by ¹H-NMR, (13)C-NMR, FT-IR, UV-vis, and mass spectral analyses. The binding abilities of these tetradentate chelators for uranyl ion at pH 7.4 were also determined by UV spectrophotometry in aqueous media. Results showed that the efficiencies of these chelating agents are dependent on the linker length. Ligand 4b is the best chelator and suitable for further studies.
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Quelantes/síntese química , Piridonas/química , Urânio/química , Quelantes/química , Ligantes , Espectroscopia de Ressonância Magnética , Espectroscopia de Prótons por Ressonância Magnética , Espectroscopia de Infravermelho com Transformada de FourierRESUMO
Chlorination is an effective approach for understanding the feature of multiple additions on fullerene cages. The chlorofullerenes obtained are versatile synthons for further derivatization. However, chlorofullerenes used for chemical reaction studies are mainly based on the skew-pentagonal-pyramidal (SPP) C60Cl6. In this work, a new isomer of C60Cl10 that does not contain an SPP-C60Cl6 substructure was identified. Its electrochemical properties give it unexpected cyclic voltammetric behavior at more negative potentials relative to other chlorofullerenes. Friedel-Crafts arylation shows good reactivity of this compound. These new findings challenge opinions of fullerene addition patterns and will break the monopoly of C60Cl6 as a precursor for fullerene modifications.
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In this work, luminol functionalized gold nanoparticles (LuAuNPs) were used as colorimetric and chemiluminescent probes for visual, label free, sensitive and selective detection of minocycline (MC). The LuAuNPs were prepared by simple one-pot reduction of HAuCl4 with luminol, which exhibited a good chemiluminescence (CL) activity owing to the presence of luminol molecules on their surface and surface plasmon resonance absorption. In the absence of MC, the color of LuAuNPs was wine red and their size was relatively small (â¼25 nm), which could react with silver nitrate, producing a strong CL emission. Upon the addition of MC at acidic buffer solutions, the electrostatic interaction between positively charged MC and negatively charged LuAuNPs caused the aggregation of LuAuNPs, generating a purple or blue color. Simultaneously, the aggregated LuAuNPs did not effectively react with silver nitrate, producing a weak CL emission. The signal change was linearly dependent on the logarithm of MC concentration in the range from 30 ng to 1.0 µg for colorimetric detection and from 10 ng to 1.0 µg for CL detection. With colorimetry, a detection limit of 22 ng was achieved, while the detection limit for CL detection modality was 9.7 ng.
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Colorimetria/métodos , Ouro/química , Substâncias Luminescentes/química , Luminol/química , Nanopartículas Metálicas/química , Minociclina/análise , Adsorção , Limite de Detecção , Tamanho da Partícula , Nitrato de Prata/química , Eletricidade Estática , Ressonância de Plasmônio de Superfície/métodosRESUMO
A green-light-emitting diode device was fabricated based on a p-type Sb-doped ZnO segments/Cd-alloyed ZnO/n-type ZnO film/heteronanowires array structure. The structures and chemical components of the heteronanowire sample were studied by energy dispersive spectrometer, x-ray photoelectron spectrometer, etc, from which the statuses of Cd and Sb in the sample were confirmed. Spatially resolved photoluminescence measurement on a single heteronanowire revealed a large bandgap shift in the Cd(x)Zn(1 - x)O active region. In electroluminescence characterizations, the device showed that the green emission was centered at 550 nm, suggesting the successful formation and functioning of the double heterojunction nanowire light-emitting diodes.
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Although mechanochemistry is increasingly becoming an alternative to traditional chemical synthesis, highly efficient continuous mechanochemical synthesis techniques are still rare. In this work, a novel spiral gas-solid two-phase flow (S-GSF) synthesis technique for the mechanochemical synthesis of salophen complexes has been reported, which is an approach for continuous synthesis based solely on airflow impacting the reaction. The synthesis of salophen-Br-Cu was used as a model reaction to optimize the reaction conditions, and three other salophen complexes, namely, salophen-Br-Co, salophen-Br-Ni, and salophen-Br-Zn were synthesized on this basis. The structure and thermal stability of the obtained products were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, UV-vis spectroscopy, nuclear magnetic resonance spectroscopy, scanning electron microscopy, and differential thermal analysis (DTA). The results showed that these complexes can be obtained continuously at a rate close to 4 g min-1, and the corresponding space-time yield is close to 1.2 × 105 kg m-3 day-1. In addition, DTA was used to analyze the catalytic performance of the complex for ammonium perchlorate (AP). The results showed that compared to the conditions for pure AP, salophen-Br-Co and salophen-Br-Cu could significantly reduce the high-temperature decomposition of AP pyrolysis to 77.0 and 102.1 °C, respectively. According to the method of Kissinger calculations, the Ea of AP decomposition decreased from 217.3 kJ mol-1 to 131.0 and 118.5 kJ mol-1, respectively. The TG data at different heating rates were analyzed using two isoconversion methods, i.e. Flynne-Walle-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS). The activation energies of AP, AP + 10 wt% salophen-Br-Co, and AP + 10 wt% salophen-Br-Cu were calculated. When the conversion degree (α) is between 0.1 and 0.9, the Ea values obtained from the two isoconversion methods are similar and exhibit certain matching. These two isoconversion methods also confirm Kissinger's calculations.
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The assembly of 2D Ti3C2Tx nanosheets into 3D structures with orderable structure has great importance for their use as catalyst carriers. However, Ti3C2Tx nanosheets are prone to accumulate in aqueous solutions owing to the strong van der Waals forces between Ti3C2Tx nanosheet layers, degrading their chemical properties. Carbon aerogel (Ti3C2Tx/G/Co) with a 3D porous structure and cobalt as the active site was prepared by a simple co-assembly-freeze-drying-high-temperature carbonization method for application in catalysis of ammonium perchlorate.
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Due to its excellent charge extraction ability, fullerene derivative phenyl-C61-butyric acid methyl ester (PCBM) is widely used as electron transport materials (ETM) in invert perovskite solar cells. However, the complicated synthetic routes and low productivity of PCBM limiting its commercial application. Moreover, the insufficient defect passivation ability of PCBM is contributed to inferior device performance because it lacks hetero-atoms/groups with lone pair electrons, it is highly desirable for exploration of new fullerene-based ETM with excellent photoelectric properties. Therefore, three new fullerene malonate derivatives were synthesized by simple two-step reaction with a high yield, and then developed as electron transport materials in invert perovskite solar cells which fabricated in air condition. The constituent thiophene and pyridyl group of the fullerene-based ETM can heighten the chemical interaction between under-coordinated Pb2+ and lone pair electrons of N, S atom by electrostatic interaction. Hence, the air-processed unencapsulated device with new fullerene-based electron transport materials (C60-bis(pyridin-2-ylmethyl) malonate (C60-PMME)) can obtain a enhanced power conversion efficiency (PCE) of 18.38%, which is significantly higher than the PCBM-based devices (16.64%). Additionally, the C60-PMME-based devices exhibit significantly more outstanding long-term stability than PCBM-based devices, owing to the strong hydrophobic properties of these new fullerene-based ETM. This study shows the promising potentials of these new low-cost fullerene derivatives as ETM to replace commercially used fullerene derivatives PCBM.