Early diagnosis of tumors is crucial in selecting appropriate treatment options to achieve the desired therapeutic effect, but it is difficult to accurately diagnose cancer by a single imaging modality due to technical constraints. Therefore, we synthesized a type of Fe3O4 nanoparticle with manganese dioxide grown on the surface and then prepared it by loading photosensitive drugs and traditional Chinese medicine monomers to create an integrated diagnosis/treatment multifunctional nanoplatform Fe3O4@MnO2-celastrol (CSL)/Ce6. This nanoplatform can have full advantage of the tumor microenvironment (TME) characteristics of hypoxia (hypoxia), acidic pH (acidosis), and increased levels of reactive oxygen species (e.g., H2O2), even outside the TME. Specific imaging and drug release can also enhance tumor therapy by adjusting the hypoxic state of the TME to achieve the combined effect of chemotherapy (CT) and photodynamic therapy (PDT). Moreover, the obtained Fe3O4@MnO2-CSL/Ce6 has H2O2- and pH-sensitive biodegradation and can release the anticancer drug celastrol (CSL) and photosensitizer Ce6 in TME and simultaneously generate O2 and Mn2+. Therefore, the "dual response" synergistic strategy also confers specific drug release on nanomaterials, relieves tumor hypoxia and antioxidant capacity, and achieves significant optimization of CT and PDT. Furthermore, the resulting Mn2+ ions and Fe3O4 nanoparticles can be used for T1/T2 magnetic resonance imaging on tumor-bearing mice, and the released Ce6 can simultaneously provide fluorescence imaging functions. Therefore, Fe3O4@MnO2-CSL/Ce6 realized the synergistic treatment of PDT and CT under multimodal near-infrared fluorescence/photoacoustic (photoacoustic) imaging monitoring, showing its great potential in the accurate medical treatment of tumors.A Pd(ii)-catalyzed three-component sp3 C-H alkoxycarbonylation of 8-methylquinonlines (8-MQs) with alcohols is accomplished using the colorless crystalline Mo(CO)6 as a CO source. The protocol is compatible with a wide range of 8-MQs and alcohols, furnishing the carbonylated adducts in moderate to good yields. The substrate scope, functional group tolerance and natural product mutation are the important practical features.A method consisting of solid-phase isotope dansylation (derivatization with dansyl chloride) and liquid chromatography-high resolution mass spectrometry (LC-HRMS) was developed for the quantitative analysis of phenolic compounds (phenols) in environmental samples. A magnetic-HLB (hydrophilic lipophilic balanced) material was synthesized and applied as an adsorbent in magnetic solid-phase extraction (MSPE) for the enrichment of the analytical targets. Furthermore, with the solid-phase isotope labeling, the desalting and removal of labeling residuals could be simplified over conventional in-solution labeling. In addition to overcoming the matrix effect by isotope dansylation, the sensitivity for the analysis of phenols by LC-HRMS was remarkably improved by over 100-fold. The method was systematically verified, and good accuracy (86.5-104.9%) and precision ( less then 8.6% and less then 11.4% for intra- and inter-day, respectively) were achieved for the tested 15 phenols. The limits of detection (LODs) of this method were estimated to be 0.2-5 ng L-1 and 5-100 ng kg-1 in estuary water and sediment samples, respectively. With this method, samples collected from the Daliao River estuary (Panjin, China) were analyzed. It was found that all of the targeted phenols were detected at concentrations ranging from unquantifiable to 485 ng L-1 (the total concentration of analytes found in each sample were in the range 822-957 ng L-1) and unquantifiable to 1368 ng kg-1 (the total concentration of analytes found in each sample were in the range 2251-2992 ng kg-1) in water and sediment, respectively.Aluminum ion aqueous batteries (AIBs) are among the most promising candidates for high energy density devices due to the multivalent redox processes associated with Al3+ ion intercalation. However, only a few stable AIB electrode materials have been reported so far. MoO3 is a very promising electrode material due to its octahedral layered crystal structure which can accommodate multivalent cation by intercalation. However, the poor electrochemical stability of MoO3 and the sluggish intercalation kinetics of Al3+ ion in Mo oxides electrodes limit its practical application. In this work, we propose a strategy to overcome such shortcomings of MoO3 by fabricating electrodes composed of self-ordered one-dimensional (1D) MoTaOx nanotubes synthesized via electrochemical anodization of Mo-Ta alloy substrates. We show that this approach allows for direct incorporation of Ta in the Mo oxide nanotubes. The resulting MoTaOx nanotubes, composed of octahedral MoO3 and rhombohedral Mo2Ta2O11 phases, exhibit remarkable electrochemical stability and Al-ion storage properties in aqueous electrolytes that are superior to that of pristine Mo oxide or other most efficient electrode materials reported to date. Such MoTaOx nanotube-based electrodes can achieve a specific capacity of 1180 mA h cm-3 (337 mA h g-1, 141 μA h cm-2) at 1.25 A cm-3 (∼0.35 A g-1, 0.15 mA cm-2). More importantly, the capacity retention of such nanotube array electrodes remains above 83% of the initial capacity after 3000 cycles.As a multifunctional platform, cyclodextrin capped gold nanoparticles (AuNP@CDs) have attracted extensive attention due to their advantages of high specific surface area and high loading capacity. AuNP@CDs have a core-shell structure, retaining the advantages of the two materials. AuNPs act as the support for the monolayer assembly of CDs. Some functional molecules can enter the hydrophobic cavity of CD through the host-guest interaction. In this brief review, we discuss the strategies for the synthesis of AuNP@CDs depending on the type and order of bonding. Their applications in drug delivery, catalysis, detection and bioimaging are highlighted. We hope to further stimulate AuNP@CD related research.The rational design of affordable, efficient and robust electrocatalysts towards the oxygen reduction reaction (ORR) is of vital importance for the future advancement of various renewable-energy technologies. https://www.selleckchem.com/products/iberdomide.html Herein, we develop a feasible and delicate synthesis of Fe/Fe3C/Fe2O3 hollow heterostructured nanoparticles in situ immobilized on highly graphitic nitrogen-doped carbon nanotubes (referred to as Fe/Fe3C/Fe2O3@N-CNTs hereafter) via a simple hydrogel-bridged pyrolysis strategy. The simultaneous consideration of interfacial manipulation and nanocarbon hybridization endows the formed Fe/Fe3C/Fe2O3@N-CNTs with sufficiently well-dispersed and firmly immobilized active components, regulated electronic configuration, enhanced electrical conductivity, multidimensional mass transport channels, and remarkable structural stability. Consequently, benefiting from the compositional synergy and architectural superiority, the as-obtained Fe/Fe3C/Fe2O3@N-CNTs exhibit excellent ORR catalytic activity, impressive durability and superior selectivity in an alkaline electrolyte, outperforming the commercial Pt/C catalyst and a majority of the previously reported Fe-based catalysts.