C-terminal processing of yeast Spt7 occurs in the absence of functional SAGA complex

Background  

Spt7 is an integral component of the multi-subunit SAGA complex that is required for the expression of ~10% of yeast genes. Two forms of Spt7 have been identified, the second of which is truncated at its C-terminus and found in the SAGA-like (SLIK) complex.     

Combined operando studies of new electrode materials for Li-ion batteries

The performances of Li-ion batteries depend on many factors amongst which the important ones are the electrode materials and their structural and electronic evolution upon cycling. For a better understanding of lithium reactivity mechanism of many materials the combination of X-Ray Powder Diffraction (XRPD) and Transmission Mössbauer Spectroscopy (TMS) providing both structural and electronic information during the electrochemical cycling has been carried out. Thanks to the design of a specific electrochemical cell, derived from a conventional Swagelock cell, such measurements have been realised in operando mode. Two examples illustrate the greatness of combining XRPD and TMS for the study of LiFe_0.75Mn_0.25PO₄ as positive electrode and TiSnSb as negative electrode. Different kinds of insertion or conversion reactions have been identified leading to a better optimization and design of performing electrodes.     

How M?ssbauer spectroscopy can improve Li-ion batteries

In the domain of Li-ion batteries, M?ssbauer spectroscopy is mainly used for the characterization of electrode materials and the analysis of electrochemical reactions. Depending on the properties under investigation, different approaches are often considered, which are based on ex situ, in situ and operando measurements. The specific electrochemical cells and sample preparations used for such measurements are described in this paper. Applications to selected examples of cathode and anode materials are presented in order to show how M?ssbauer spectroscopy, when associated with other techniques, provides essential information to understand the mechanisms and improves the performances of Li-ion batteries.     

Role of iron in Na <Subscript>1.5</Subscript>Fe <Subscript>0.5</Subscript>Ti <Subscript>1.5</Subscript>(PO <Subscript>4</Subscript>) <Subscript>3</Subscript>/C as electrode material for Na-ion batteries studied by operando Mössbauer spectroscopy

The role of iron in Na _1.5Fe _0.5Ti _1.5(PO ₄)₃/C electrode material for Na batteries has been studied by ⁵⁷Fe Mössbauer spectroscopy in operando mode. The potential profile obtained in the galvanostatic regime shows three plateaus at different voltages due to different reaction mechanisms. Two of them, at 2.2 and 0.3 V vs Na ⁺/Na ⁰, have been associated to redox processes involving iron and titanium in Na _1.5Fe _0.5Ti _1.5(PO ₄)₃. The role of titanium was previously elucidated for NaTi ₂(PO ₄)₃ and the effect of the substitution of Fe for Ti was investigated with ⁵⁷Fe Mössbauer spectroscopy. We show that iron is an electrochemically active center at 2.2 V with the reversible Fe ³⁺/Fe ²⁺ transformation and then remains at the oxidation state Fe ²⁺ along the sodiation until the end of discharge at 0 V.     

Quantum-Chemical Study of the FeNCN Conversion-Reaction Mechanism in Lithium- and Sodium-Ion Batteries

We report a computational study on 3d transition-metal (Cr, Mn, Fe, and Co) carbodiimides in Li- and Na-ion batteries. The obtained cell voltages semi-quantitatively fit the experiments, highlighting the practicality of PBE+U as an approach for modeling the conversion-reaction mechanism of the FeNCN archetype with lithium and sodium. Also, the calculated voltage profiles agree satisfactorily with experiment both for full (Li-ion battery) and partial (Na-ion battery) discharge, even though experimental atomistic knowledge is missing up to now. Moreover, we rationalize the structural preference of intermediate ternaries and their characteristic lowering in the voltage profile using chemical-bonding and Mulliken-charge analysis. The formation of such ternary intermediates for the lithiation of FeNCN and the contribution of at least one ternary intermediate is also confirmed experimentally. This theoretical approach, aided by experimental findings, supports the atomistic exploration of electrode materials governed by conversion reactions.     

Autocatalytic sonolysis of iron pentacarbonyl in room temperature ionic liquid [BuMeIm][Tf2N

The autocatalytic sonochemical reaction of Fe(CO)(5) decomposition in [BuMeIm][Tf(2)N] provides iron nanoparticles in higher yields than in tetralin. Such a difference is explained by the higher decomposition of the intermediate Fe(3)(CO)(12) according to the two-sites model of the sonochemical reactions and the specific properties of the ionic liquid.     

Structural and magnetic properties of Pr18Li8Fe5−xMxO39 (M=Ru, Mn, Co)

A polycrystalline sample of Pr₁₈Li₈Fe₄RuO₃₉ has been synthesized by a solid state method and characterized by neutron powder diffraction, magnetometry and Mössbauer spectroscopy; samples of Pr₁₈Li₈Fe_5−xMn_xO₃₉ and Pr₁₈Li₈Fe_5−xCo_xO₃₉ (x=1, 2) have been studied by magnetometry. All these compounds adopt a cubic structure (space group , a₀∼11.97 Å) based on intersecting 〈111〉 chains made up of alternating octahedral and trigonal-prismatic coordination sites. These chains occupy channels within a Pr-O framework. The trigonal-prismatic site in Pr₁₈Li₈Fe₄RuO₃₉ is occupied by Li⁺ and high-spin Fe³⁺. The remaining transition-metal cations occupy the two crystallographically-distinct octahedral sites in a disordered manner. All five compositions adopt a spin-glass-like state at 7 K (Pr₁₈Li₈Fe₄RuO₃₉) or below.