Enabling the Li-ion conductivity of Li-metal fluorosulphates by ionic liquid grafting

Recently unveiled ‘alkali metal fluorosulphate (AMSO₄F)’ class of compounds offers promising electrochemical and transport properties. Registering conductivity value as high as 10⁻⁷ S cm⁻¹ in NaMSO₄F phases, we explored the fluorosulphate group to design novel compounds with high Li-ion conductivity suitable for solid electrolyte applications. In the process, we produced sillimanite-structured LiZnSO₄F by low temperature synthesis (T ≤ 300 °C). Examining this phase, we accidentally discovered the possibility of improving the ionic conductivity of poor conductors by forming a monolayer of ionic liquid at their particle surface. This phenomenon was studied by solid-state NMR, XPS and AC impedance spectroscopy techniques. Further, similar trends were noticed in other fluorosulphate materials like tavorite LiCoSO₄F and triplite LiMnSO₄F. With this study, we propose ‘ionic liquid grafting’ as an interfacial route to enable good Li-ion conductivity in otherwise poor conducting ceramics.     

Determination of the absolute structure of (+)-akaterpin

We describe the total synthesis and structural determination of (+)-akaterpin (1), an inhibitor of phosphatidylinositol-specific phospholipase C (PI-PLC). The key features of the synthetic strategy include the resolution of β,γ-unsaturated ketone (±)-2a with chiral sulfoximine 6. The absolute stereochemistry was determined by comparison of the specific optical rotation data of (+)-1 and (-)-1 with that of natural akaterpin.     

Total Synthesis of (−)‐Norzoanthamine

No bones about it : (?)‐Norzoanthamine, a promising candidate for an anti‐osteoporotic drug, was the target of a total synthesis (see scheme). The final bisaminal formation with AcOH/H₂O gave the DEFG ring, while the cyclization precursor was prepared by installing the remaining bisaminal unit after oxidative cleavage of the cyclopentanol moiety.

     

Yrare bands of 121Xe

High-spin states in ¹²¹Xe have been studied via the ¹⁰⁹Ag (16O, p3n) ¹²¹Xe reaction at a beam energy of 80 MeV. Several rotational bands based on one- and three-quasiparticle excitations have been established. Among them, an unfavoured yrare rotational band with unfavoured signature has been newly identified. Received: 19 November 1998     

Long-Range Electron Transfer in Rigid 310-Helical Oligopeptides Containing Redox Cyclic a-Amino Acids

Intrahelical photoinduced electron transfer processes (ET) in conformationally restricted oligopeptides have been studied by nanosecond time-resolved transient spectroscopy. The helical peptides were constructed from sterically hindered alpha-aminoisobutyric acid (Aib) and two cyclic alpha-amino acids (Aib class) bearing electron acceptor and donor side chains (DkNap, ThQx). This helical backbone design provides high conformation stability, as previously demonstrated, and yields reliable 3(10)-helical architectures in solution. The forward ET between ThQx and 3DkNap is followed by a slow back ET thus giving rise to an accumulation of the charge-separated ion pairs for hundreds of nanoseconds. We demonstrate the modulation of electronic interactions by the number of intervening Aib residues separating acceptor-donor side chains and propose modifications of the peptide framework by inclusion of a non-Aib amino acid residue. These well-defined and sterically stable frameworks are suited for the precise evaluation of intrahelical electron transfer processes mediated by peptides.