RESUMO
A new class of electrolyte based on TFSI- and triphenolate-borohydride anions was designed and produced which fulfill all requirements of easy synthesis, high ionic conductivity, wide potential window, and noncorrosion of Al current collector. The electrolyte composed of magnesium triphenolate borohydride and Mg(TFSI)2 in glyme simultaneously displays a high conductivity of 5.5 mS cm-1 at 25 °C and a reversible Mg plating/stripping with high current density and Coulombic efficiency at room temperature. By addition of a slight amount of MgCl2 to this electrolyte, a Coulombic efficiency of 90% in an SS/Mg cell, stable cycling performance, and a wide anodic potential of 3.4 V vs Mg2+/Mg on Al current collector can be reached. Reversible and efficient Mg insertion/deinsertion with a high capacity of 94 mAh g-1 and 96% Coulombic efficiency was obtained in a Mo6S8 Chevrel cathode phase.
RESUMO
The solubilities of C1C4im(+) and Tf2N(-) in nitric aqueous phases have been measured for several ligand types and concentrations (0.04 M tributylphosphine oxide, 0.05 M N,N'-dimethyl-N,N'-dibutylmalonamide, 0.10 M 1-methyl-3-[4-(dibutylphosphinoyl)butyl]-3H-imidazol-1-ium bis(trifluoromethylsulphonyl)imidate, and 1.1 M N,N-dihexyloctanamide). The data evidence a significant difference between the solubilities of the cations and anions of the ionic liquid as a consequence of several ion-exchange and/or ion-pairing mechanisms involving all ions present in the system as well as the protonation/nitric-extraction ability of the ligand.
RESUMO
The preparation of a series of N-hydroxy peptides is described, along with their acylation on the oxygen of the pseudopeptide bond. Nineteen N-acyloxy peptides, first examples of this new class of pseudopeptides, were thus synthesized; they present a range of acyl groups, including N-protected amino acyl groups. Possibilities of elongation for these pseudopeptides were also investigated.
Assuntos
Peptídeos/síntese química , Peptídeos/química , Conformação ProteicaRESUMO
2-Methoxyprop-2-yl peroxides were synthesized and evaluated in vitro against Plasmodium falciparum. These acyclic artemisinin-related peroxides revealed moderate to good activity but were devoid of alkylating property towards the synthetic model of heme Mn(II)-TPP.