From Ion‐Like Ethylzinc Aluminates to [EtZn(arene)2]+[Al(ORF)4]− Salts

Attempts to prepare previously unknown simple and very Lewis acidic [RZn]⁺[Al(OR^F)₄]^? salts from ZnR₂, AlR₃, and HO?R^F delivered the ion‐like RZn(Al(OR^F)₄) (R=Me, Et; R^F=C(CF₃)₃) with a coordinated counterion, but never the ionic compound. Increasing the steric bulk in RZn⁺ to R=CH₂CMe₃, CH₂SiMe₃, or Cp*, thus attempting to induce ionization, failed and led only to reaction mixtures including anion decomposition. However, ionization of the ion‐like EtZn(Al(OR^F)₄) compound with arenes yielded the [EtZn(arene)₂]⁺[Al(OR^F)₄]^? salts with arene=toluene, mesitylene, or o‐difluorobenzene (o‐DFB)/toluene. In contrast to the ion‐like EtZn(η³‐C₆H₆)(CHB₁₁Cl₁₁), which co‐crystallizes with one benzene molecule, the less coordinating nature of the [Al(OR^F)₄]^? anion allowed the ionization and preparation of the purely organometallic [EtZn(arene)₂]⁺ cation. These stable materials have further applications as, for example, initiators of isobutene polymerization. DFT calculations to compare the Lewis acidities of the zinc cations to those of a large number of organometallic cations were performed on the basis of fluoride ion affinity. The complexation energetics of EtZn⁺ with arenes and THF was assessed and related to the experiments.     

Rock porosity quantification by dual-energy X-ray computed microtomography

Porous media investigation by X-ray microtomography allows obtaining valuable quantitative and qualitative information, while preserving sample integrity. Modern X-ray nanotomography or Synchrotron radiation systems may distinguish structures sized only hundreds of nanometers. However, pores sized less than a few microns (microporosity) may be undetectable due to the system’s spatial resolution and noise in microfocus sources, compromising the quality of the measurement. In this study a dual-energy methodology was developed to generate density-based images from two scans made at two different voltages (80 kV and 130 KV) with a microfocus bench-top microtomography system. The images obtained were quantized in 256 gray levels, where the lowest value (zero) corresponded to voids and the highest value (255) corresponded to the densest regions mapped. From density images and single energy images, porosity was evaluated and compared. Results indicate that density images present better results than single energy images when both are compared with porosity obtained by the helium injection method. In addition, images acquired in dual-energy show good agreement with the sample’s real density values.     

From Binuclear Complexes to Molecular Necklaces: Incorporating Flexible Ligands into Rotaxanes

The conversion of binuclear complexes into larger molecular necklaces can be achieved through rigidifying flexible ligands by threading them through a crown ether to form either an interpenetrated [2]pseudorotaxane or a permanently interlocked [2]rotaxane. The resulting complexes and assemblies are characterized by ¹H and DOSY NMR in solution and single‐crystal X‐ray diffraction in the solid‐state.     

Thiadiazolo-Azaacenes

This work reports the synthesis and characterization of bis- and tetrakis(thiadiazolo)-appended di- and tetraazaacenes, displaying up to seven catenated benzene/pyrazine rings. The targets are obtained by condensation of benzo-bis(thiadiazole)-4,5-dione with aromatic di- and tetraamines. The condensation products—up to a heptacene-like species—are stable but can be insoluble. Soluble derivatives are readily processible, but do not show enhanced electron affinities, as the two or four attached benzothiadiazole units are effectively resonance-separated from the acene body, maximizing the number of Clar-sextets.     

Exactly solvable chain of interacting electrons with correlated hopping and pairing

A generalization of the Mattis-Nam model Mattis and Nam (1972) [7], which takes into account a correlated hopping and pairing of electrons, is proposed, its exact solution is obtained. In the framework of the model the stability of the zero energy Majorana fermions localized at the boundaries is studied in the chain in which electrons interact through both the on-site Hubbard interaction and the correlated hopping and pairing. The ground-state phase diagram of the model is calculated, the region of existence of topological states is determined. It is shown that low-energy excitations destroy bonds between electrons in the chain, leading to an insulator state.     

Mechanistic Insights into a Sustainable Mechanochemical Synthesis of Ettringite

Mechanochemistry offers an environmentally benign and facile synthesis method for a variety of cement paste constituents. In addition, these methods can be used to selectively tune the properties of cement components. The mineral ettringite is an important component of cementitious materials and has additional technological potential due to its ion exchange properties. Synthesis of ettringite via mechanochemistry is an environmentally friendly alternative to conventional wet-chemical synthesis established in industry. This contribution explores the mechanism of a two-step mechanochemical synthesis of ettringite, which was previously found to greatly improve the reaction conversion as compared with one-pot synthesis. The crystallinity of Al(OH)₃ was found to decrease during the first stage of this mechanochemical synthesis. This was correlated to a significant decrease in the particle size of Al(OH)₃ in this stage. No other significant changes were found for the other components, suggesting that mechanochemical activation of Al(OH)₃ is responsible for the enhanced formation of ettringite by the two-step approach. The environmentally friendly approach developed for ettringite synthesis offers a versatile synthetic strategy, which can be applied to synthesise further cementitious materials.     

Electrical Conduction Mechanisms of MxPS3, M1−xM'xPS3 and their Intercalation Compounds

Abstract

In the M_xPS₃ and M_1?xM'_xPS₃ systems, the P₂S₆ cluster contributes to the poor electrical conductivity for the compounds in which the energy level of the metal 3d orbital is deeper than those of the P, S 3p orbitals. For the compounds in which metal 3d orbital is closed to P and S 3p orbitals and has mixed valency, the induced mixed valency of P₂S₆, cluster and/or hopping mechanism contribute to the electrical conductivity. In the organic electron donor intercalation into M_xPS₃ and M_1?xM'_xPS₃ compounds, the new intercalation reaction is discovered, in which formation of tris-complexes of metal ions with guest molecules occurs in the host interlayer.     

Analysis of Carbamates as Fluorescent 1-Dimethylamino-naphthalene-5-sulfonate Esters

The fluorigenic labelling of several N-methyl carbamates is carried out using 1-dimethyl-aminonaphthalene-5-sulfonyl chloride (dansyl chloride). Prior to chromatography the carbamates are reacted in aqueous solution with the dansyl chloride. The derivative is extracted from the solution with n-hexane and subsequently spotted on a thin-layer plate for chromatography. For each N-methyl carbamate, two highly fluorescent spots are obtained. One is common to all N-methyl carbamates studied, whereas the other is characteristic of each individual carbamate. N.m.r. and infrared spectroscopic data indicate that the common spot is the methylamine derivative, and the second spot is the derivative from the phenyl moiety of each carbamate. The sensitivity of the method is less than one nanogram and has been successfully applied to the analysis of natural water samples.     

Chelating 2,2′-Diaminodiethylamine Cellulose Filters and X-ray Fluorescence for Preconcentration and Trace Analysis of Natural Waters

Abstract

The 2,2′-diaminodiethylamine (DEN) functional group can be expected to have ideal properties for the chelation of transition metals and their collection from aqueous solutions, independent of the alkali and alkaline earth ions concentration. Introducing DEN into cellulose filters allows straightforward preconcentration of trace cations by a simple filtration step, and the DEN-filter constitutes a suitable target for X-ray fluorescence (XRF) analysis. The linearity between the XRF-response on the loaded DEN-filter and the trace cation concentration in the solution appears excellent, up to a total filter capacity of ca. 3 μeq.cm^?2. The detection limits are around 0.5 μg. l^?1 in most practical cases. Accuracy and precision are around 10%. The applicability of the proposed procedure is illustrated on a comparative basis by XRF-analysis of drinking water and surface water, after preconcentration by DEN-filtration and by alternative procedures.