Alstrupgold7327

Constructing high-performance and cost-effective electrocatalysts for water oxidation, particularly for overall water splitting, is extremely needed, whereas still challenging. Herein, based on an economical and facile one-step surface sulfurization strategy, a three-dimensional nanostructure with uniform Fe-doped Ni3S2 nanoparticle arrays tightly implanted on nickel foam (Fe-doped Ni3S2-NF) has been fabricated for the extremely efficient electrochemical oxygen evolution reaction (OER). Owing to the unique electronic structure modulation between Ni and Fe sites, and high interfacial charge communication during the electrocatalytic process, the optimal Fe-doped Ni3S2-NF electrode shows an excellent OER activity with ultralow overpotentials of 166 and 235 mV at 10 and 100 mA cm-2 in alkaline solution, respectively, remarkably outcompeting the benchmark RuO2/NF and the overwhelming majority of the reported electrocatalysts. Furthermore, for overall water splitting, the Fe-doped Ni3S2-NF electrode as a bifunctional electrocatalyst assembled in a two-electrode device requires merely 1.56 V to gain a current density of 10 mA cm-2. This study presents a universal surface engineering strategy to conveniently and economically remould commercial metal materials into efficient electrocatalysts for various electrochemical reactions.In this work, we report a new type of reactivity of [(BDI*)Ti(Cl)η2-P(SiMe3)-PiPr2] (1) towards ketones (BDI* = 2,6-diisopropylphenyl-β-methyldiketiminate ligand). In the reaction of 1 with acetone, cyclopentanone or cyclohexanone, a ketone moiety is inserted into Ti-Pphosphanyl or Ti-Pphosphido bonds to form complexes with a new C-P-P moiety, providing [(BDI*)Ti(Cl)η2-P(SiMe3)-PiPr2-C(Me)2O] (2a), [(BDI*)Ti(Cl)η2-OC(Me)2P(SiMe3)-PiPr2] (2b), [(BDI*)Ti(Cl)η2-P(SiMe3)-P(iPr)2-C(CH2)4O] (3a), and [(BDI*)Ti(Cl)η2-P(SiMe3)-P(iPr)2-C(CH2)5O] (4a). Starting complex 1 reacts with cyclohexanone, yielding a monocrystalline complex [(ArN[double bond, length as m-dash]C(Me)CHC(Me)[double bond, length as m-dash]NAr)C(CH2)5OTi(Cl)PiPr2-P(SiMe3)C(CH2)5O] (4d) with the insertion of two ketone molecules. Interestingly, we found that monoinserted complexes 2a and 3a may be oxidized via a reaction with AgCl, leading to elimination of the -SiMe3 group and oxidation of the titanium atom. This reaction led us to isolate the Ti(iv) complex [(BDI*)Ti(Cl)η2-P-P(iPr)2-C(CH2)5O] (5) in crystalline form. To identify the kinds of products that may be formed and determine which products are the most energetically favoured ones, we conducted a thermodynamic DFT study of 1 towards acetone, cyclopentanone and cyclohexanone. Structures 2a, 2b, 3a, 3e, 4a, 4d, and 5 were characterized by X-ray crystallography, and complex 5 was also identified by NMR spectroscopy.Platinum-based anticancer drugs constitute the cornerstone of chemotherapy for various cancers. Although cytotoxic agents are considered to have immunosuppressive effects, increasing evidence suggests that some cytotoxic compounds can effectively stimulate the antitumor immune response by inducing a special type of apoptosis called immunogenic cell death (ICD). A platinum(iv) complex (DCP) modified with the derivative of synthetic capsaicin (nonivamide) was designed to elicit ICD. The complex exhibited high cytotoxicity against a panel of human cancer cell lines including pancreas (PANC-1), breast (MCF-7), and liver (HepG2) cancer cells, and osteosarcoma (MG-63) cells. In addition to causing DNA damage, DCP also triggered the translocation of calreticulin (CRT) as well as the release of ATP and HMGB1 protein in PANC-1 cells, thus manifesting an efficient ICD-inducing effect on cancer cells. Furthermore, the DCP-treated PANC-1 cell-conditioned culture medium promoted the release of IFN-γ and TNF-α to induce the immune response of human peripheral blood mononuclear cells, thereby increasing their cytotoxicity to cancer cells. Concurrently, the phagocytosis of PANC-1 cells by macrophages was also augmented by DCP. The results demonstrate that DCP is an effective inducer of ICD and a potential agent for chemoimmunotherapy of cancers.Adipose tissue-derived mesenchymal stem cell (ADSC)-based therapy is attractive for liver diseases, but the long-term therapeutic outcome is still far from satisfaction due to the low hepatic engraftment efficiency of ADSC transplantation. Herein, we propose a strategy based on liver sinusoidal endothelial cell (LSEC)-targeting peptide modification and near infrared (NIR) fluorescent probe labeling for enhancing LSEC-barrier-migration ability and in vivo tracking of ADSCs in a liver injury mouse model. RLTRKRGLK (RK), a LSEC-targeted peptide, and indocyanine green (ICG), a FDA approved infrared fluorescent dye, were simultaneously modified on the ADSC surface via a bioorthogonal click reaction. The equipped ADSCs not only exhibited significant binding ability towards LSEC both in vitro and in vivo, but could also be monitored by NIR imaging in vivo. In particular, the RK-modified ADSCs showed remarkable higher hepatic accumulation as compared to unmodified ADSCs, resulting in better therapeutic outcomes. Therefore, this study provides a simple and convenient method for enhancing the homing of transplanted ADSCs to injured liver accompanying with in vivo cell tracking ability, which may shed light on accelerating the clinical translation of the ADSC-based therapy for liver diseases.Bis-(diethyl-dithioxamidate)platinum(ii) is able to transport HCl from the donor aqueous phase to the receiving one over a mean distance of 12 cm in about 3 minutes across an organic membrane in the bulk, without stirring of the organic phase, i.e. at a rate far exceeding the unidirectional macroscopic diffusion coefficient. The way in which this surprising phenomenon can happen is linked to the behaviour of HCl which, because of dynamic interactions with [Pt(HEt2C2N2S2)2] (in which HCl is hosted as a tight ion pair [Pt(H2Et2C2N2S2)2][Cl]2) and chloroform molecules, gives rise to observable nanometric and micrometric domains, more dense than the surrounding bulk, whose formation and disaggregation processes accelerate the unidirectional macroscopic diffusion of HCl. TAK-981 Thermodynamic parameters obtained from the study of acid-base behaviour of the system Pt(ii) species/HCl/CHCl3 also agree with the proposed mechanism of HCl transport.