We prepare a totally nonflammable phosphate-based electrolyte composed of 5 mol L-1 (M) Li bis(fluorosulfonyl) imide (LiFSI) in a trimethyl phosphate (TMP) solvent. The concentrated 5 M LiFSI/TMP electrolyte shows good compatibility with graphite and no Al corrosion. More attractively, such a concentrated electrolyte can effectively suppress the growth of Li dendrites in Li metal batteries because of a stable LiF-rich SEI layer. Therefore, this highly concentrated electrolyte is promising for safe Li batteries.

Surfactant flooding as a potential enhanced oil recovery technology in depleted reservoirs after water flooding has attracted extensive attention. In this study, 12 surfactants belonging to five different types of surfactants and their compounded formulations were investigated for surfactant flooding under 90−120 °C and 20 × 10 4 mg/L salinity. Two surfactant formulations obtained a stable ultralow interfacial tension (IFT) level (≤10 −3 mN/m) with crude oil after aging for 125 days. The surfactant formulations were used to further investigate the effects of the initial IFT values, the dynamic reduction rate of IFT, and the surfactant concentration and emulsification on oil recovery through core flooding experiments. The results indicated that oil recovery increased with the decrease of the initial IFT values and the increase of the dynamic reduction rate of IFT. The 10 −3 mN/m IFT level yielded an additional oil recovery of approximately 7% compared with the 10 −1 mN/m IFT level. However, under the same IFT level (10 −4 mN/m), it was not the bigger the surfactant concentration that resulted in a higher additional oil recovery. In four surfactant concentrations (0.2%, 0.5%, 1%, and 3%), the 0.5% surfactant formulation obtained the highest oil recovery of 36.65%. Further study manifested that emulsification has important effects on oil recovery. When surfactant concentrations were increased to 1% and 3%, the emulsification was too strong, which makes it more difficult to displace oil. The two selected surfactant formulations could successfully yield additional oil recovery of 20−26%, which indicates these two formulations have great potential for improving oil recovery in high temperature and high salinity oil reservoirs.

DNA sequences with guanine repeats can form G-quartets that adopt G-quadruplex structures in the presence of specific metal ions. Using circular dichroism (CD) and ultraviolet-visible (UV–Vis) spectroscopy, we determined the spectral characteristics and the overall conformation of a G-quadruplex of PS2.M with an oligonucleotide sequence, d(GTG3TAG3CG3TTG2). UV-melting curves demonstrate that the Pb2+-induced G-quadruplex formed unimolecularly and the highest melting temperature (Tm) is 72°C. The analysis of the UV titration results reveals that the binding stoichiometry of Pb2+ ions to PS2.M is two, suggesting that the Pb2+ ions coordinate between adjacent G-quartets. Binding of ions to G-rich DNA is a complex multiple-pathway process, which is strongly affected by the type of the cations. Kinetic studies suggest that the Pb2+-induced folding of PS2.M to G-quadruplex probably proceeds through a three-step pathway involving two intermediates. Structural transition occurs after adding Pb(NO3)2 to the Na+- or K+-induced G-quadruplexes, which may be attributed to the replacement of Na+ or K+ by Pb2+ ions and the generation of a more compact Pb2+–PS2.M structure. Comparison of the relaxation times shows that the Na+→Pb2+ exchange is more facile than the K+→Pb2+ exchange process, and the mechanisms for these processes are proposed.

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Metal-free carbon monoxide-releasing polymers (CORPs) are synthesized via a direct polymerization approach, exhibiting not only improved stability but also accelerated wound healing performance as compared to CORM-3.

It has been shown that guanine-rich DNA can fold into a G-quadruplex with certain metal cations. The spectral characteristics, thermostability, and kinetics for the formation of a Pb(2+)-driven G-quadruplex of thrombin-binding aptamer (TBA) were measured in the current work using a combination of ultraviolet (UV) and circular dichroism (CD) spectroscopy along with stopped-flow technique. CD spectra demonstrated that TBA could fold into a unique G-quadruplex with a strong positive peak at 312 nm. Analysis of the titration data reveals that the binding stoichiometry is 1:1 for the titration of TBA with Pb(NO(3))(2), which is in accordance with the localization of the Pb(2+) ion between the adjacent G-quartets. Thermal denaturation profiles indicate that the Pb(2+)-induced intramolecular G-quadruplex is more stable than those driven by Na(+) or K(+) ions. Kinetic studies suggest that the Pb(2+)-induced folding G-quadruplex of TBA probably proceeds through the rapid formation of an intermediate Pb(2+)-TBA complex, which then isomerizes to the fully folded structure. Conformational changes transpire after the addition of Pb(NO(3))(2) to the Na(+)- or K(+)-induced G-quadruplexes, which may be attributed to the replacement of Na(+) or K(+) ions by Pb(2+) ions and the generation of a more compact structure of the Pb(2+)-TBA structure. The relaxation time, τ, of folding the G-quadruplex is reduced from 1.05 s in the presence of Pb(2+) ions alone to 0.34 s under the cooperation of initially added Na(+) ions, while τ is increased to 8.33 s under the competition of initially added K(+) ions.

Core−shell metal organic framework (MOF) crystals have attracted increasing attention due to their specific structure and remarkable properties. Herein, we demonstrate a facile approach for the synthesis of uniform multilayered core− shell MOF crystals

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