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Differential associations with the created surroundings about fat gain simply by sexual intercourse as well as race/ethnicity but not grow older.
This suggests that the evaluation of the relevance of glucosinolates for AhR modulation in the gut cannot prescind from the way broccoli is processed, and that broccoli consumption does not necessarily produce substantial amounts of AhR ligands in the large intestine.As one of the most important subjects in chemistry, nitrogen activation and reduction to yield ammonia is still a big challenge. The lack of deep understanding of the nitrogen reduction reaction (NRR) impedes the development of high-performance catalysts. In the present study, we introduce a second transition metal (M = Mn, Fe, Co, Ni, Cu, Zn, and Mo) into the active site of a single-atom Fe-N-C catalyst to tune the electronic structure and study the activity of the as-designed neighboring bimetal Fe/M-N-C catalyst in the electrochemical NRR under acidic conditions, by performing first-principles calculations. By checking the stability of the catalysts, the adsorption ability for N2, the Gibbs free energy change for the potential-determining step in the NRR, and the hydrogen evolution reaction (HER) activity, only the Fe/Mn-N-C catalyst is predicted to be a promising candidate for the NRR as it shows significantly improved catalytic activity and strong selectivity against the HER. A mechanistic study reveals the synergistic effects of the bimetal active sites, and the introduced Mn atom generates a strong multi-reference effect on the electronic configuration to create more tunnels to transfer the d-orbital electrons to activate the inert N[triple bond, length as m-dash]N triple bond, inducing the "acceptance-donation" process to facilitate the activation and reduction of N2. The current results provide an effective strategy to design stable, active, and selective catalysts for the electrochemical NRR.During chronic inflammation, macrophage colony-stimulating factor (M-CSF) and receptor activator of nuclear factor-κB ligand (RANKL) have well established effects on gene networks that stimulate osteoclastogenesis, which is the culprit of several bone diseases. In this study, we investigated the anti-osteoclastogenic effects in vitro of oleuropein (OL) and its peracetylated derivative (Per-OL) by exploring the expression level of key hub genes involved in fate decision and lineage commitment, differentiation, and function of human blood monocyte-derived osteoclasts. Monocytes were purified from peripheral blood mononuclear cells of healthy individuals using commercial antibodies coated with magnetic beads and treated with M-CSF/RANKL in the presence or absence of OL or Per-OL (25 and 50 μM) for 6 days. We demonstrated that OL and especially Per-OL impair transcriptional gene circuits able to support osteoclastogenesis from human blood monocytes. Our results indicate that OL and notably Per-OL are promising candidates to control osteoclastogenesis.Correction for 'Synthetic-biology-based discovery of a fungal macrolide from Macrophomina phaseolina' by Yohei Morishita et al., Org. Biomol. Chem., 2020, DOI 10.1039/d0ob00519c.It is often desirable to enhance the motility of active nano- or microscale swimmers such as, e.g., self-propelled Janus particles as agents of chemical reactions or weak sperm cells for better chances of successful fertilization. Here we tackle this problem based on the idea that motility can be transferred from a more active guest species to a less active host species. We performed numerical simulations of motility transfer in two typical cases, namely for interacting particles with a weak inertia effect, by analyzing their velocity distributions, and for interacting overdamped particles, by studying their effusion rate. In both cases, we detected motility transfer with a motility enhancement of the host species of up to a factor of four. This technique of motility enhancement can find applications in chemistry, biology and medicine.Constructing a multi-bond network (MBN), which involves hierarchical dynamic bonds with different bond association energies, is an effective method for achieving super tough hydrogels. In this work, a small amount of poly(vinyl alcohol) (PVA) is introduced into a loosely chemically crosslinked poly(acrylic acid) (PAA) network. The hydrophilic PVA chains can physically interact and form hydrogen bonds with the PAA chains. After a freeze-thaw process, PVA could partially crystallize and the generated microcrystals could become new crosslinking points of the hydrogels. Meanwhile, the hydrogen bonds between PAA and PVA, which connect to the microcrystal "core" through PVA chains, could also become new crosslinking points of the hydrogels. The obtained ternary-crosslinked hydrogels (T-gel 10%) exhibit toughness as high as 8 times that in pure PAA hydrogels. When the PVA content exceeds 15 wt%, PVA chains will run through the whole PAA network. Thus the PVA chains will be crosslinked by microcrystals through freeze-thaw treatment, leading to a double network structure, resulting in a brittle hydrogel. The step-increased modulus of the hydrogels with different PVA contents clearly demonstrates the change in the network structure of the hydrogels. Successively, Fe3+ is introduced into the MBN hydrogels as a third cross-linking point. The obtained quaternary-crosslinked hydrogels (Q-gel 10%-Fe5) (50 wt% water content) exhibit significantly improved mechanical properties tensile strength as high as 6.83 MPa with a fracture energy of 29.9 MJ m-3. This work provides clear insight into the relationship between network structure and mechanical properties in super tough MBN hydrogels.Understanding the critical roles of ligands (e.g. thiolates, SR) in the formation of metal nanoclusters of specific sizes has long been an intriguing task since the report of ligand exchange-induced transformation of Au38(SR)24 into Au36(SR')24. Herein, we conduct a systematic study of ligand exchange on Au38(SC2H4Ph)24 with 21 incoming thiols and reveal that the size/structure preference is dependent on the substituent site. Specifically, ortho-substituted benzenethiols preserve the structure of Au38(SR)24, while para- or non-substituted benzenethiols cause its transformation into Au36(SR)24. Strong electron-donating or -withdrawing groups do not make a difference, but they will inhibit full ligand exchange. DHA Moreover, the crystal structure of Au38(SR)24 (SR = 2,4-dimethylbenzenethiolate) exhibits distinctive ππ stacking and "anagostic" interactions (indicated by substantially short AuH distances). Theoretical calculations reveal the increased energies of frontier orbitals for aromatic ligand-protected Au38, indicating decreased electronic stability.
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