Erratum: μ-Oxalato-bis-[bis-(triphenyl-phosphine)copper(I)] dichloro-methane disolvate. Corrigendum.

An erroneous claim in the paper by Royappa et al. [Acta Cryst. (2013), E69, m126] is corrected and a reference added for a previously published report of a closely related structure.[This corrects the article DOI: 10.1107/S1600536813002080.]

Distribution of Non-uniform Demagnetization Fields in Paramagnetic Bulk Solids

A general calculation for the distribution of non-uniform demagnetization fields in paramagnetic bulk solids is described and the fields for various sample geometries are calculated. Cones, ellipsoids, paraboloids and hyperboloids with similar sample aspect ratios are considered. Significant differences in their demagnetization fields are observed. The calculation shows that the demagnetization field magnitudes decrease along the axis of symmetry (along $z$) where an externally applied magnetic field is aligned, and increase in the vicinity of the lateral surfaces with the largest field values found in the cone and the narrowest field distributions found in the hyperboloid. Application is made to the theoretical modeling of the $^{1}$H-NMR spectra of a single crystal of field-induced superconductor $\lambda$-(BETS)$_{2}$FeCl$_{4}$ with a rectangular sample geometry, providing a good fit to the measured NMR spectra. This calculation is also applicable to diamagnetic or ferromagnetic materials in general.Comment: 7 pages, 7 figures, submitted to Physical Review B (Corresponding author: [email protected]

μ-Oxalato-bis[bis(triphenylphosphine)copper(I)] dichloromethane disolvate. Corrigendum

An erroneous claim in the paper by Royappa et al. [Acta Cryst. (2013), E69, m126] is corrected and a reference added for a previously published report of a closely related structure

Erratum: μ-Oxalato-bis-[bis-(triphenyl-phosphine)copper(I)] dichloro-methane disolvate. Corrigendum.

An erroneous claim in the paper by Royappa et al. [Acta Cryst. (2013), E69, m126] is corrected and a reference added for a previously published report of a closely related structure.[This corrects the article DOI: 10.1107/S1600536813002080.]

Statistical modeling and sizing determination guides for dispersed rosin sizes

Four cationic dispersed rosin sizes were studied in terms of their performance when pH, temperature, and water hardness were varied. Three of the sizes were based on fortified rosin with different concentrations of fumaric acid, and the fourth size was based on esterified rosin. Statistical tools are used to refine and simplify an earlier model proposed by Nitzman and Royappa, who first examined the relationship between sizing and the factors of pH, temperature, water hardness, and fortification. The simplified models provide some insight into the differences between esterified sizes and fortified sizes in terms of paper sizing, Based on the algorithmic modeling approach, guidelines are proposed for choosing different levels of pH, temperature, and water hardness for use with different rosin sizes

Tetrakis(acetonitrile)copper(I) hydrogen oxalate–oxalic acid–acetonitrile (1/0.5/0.5)

In the title compound, [Cu(CH3CN)4](C2HO4)·0.5C2H2O4·0.5CH3CN, the CuI ion is coordinated by the N atoms of four acetonitrile ligands in a slightly distorted tetrahedral environment. The oxalic acid molecule lies across an inversion center. The acetonitrile solvent molecule is disordered across an inversion center and was refined with half occupancy. In the crystal, the hydrogen oxalate anions and oxalic acid molecules are linked via O—H...O hydrogen bonds, forming chains along [010]

B–N, B–O, and B–CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B‑Bromo-Carboranes

Carboranes are boron-rich molecules that can be functionalized through metal-catalyzed cross-coupling. Here, for the first time, we report the use of bromo-carboranes in palladium-catalyzed cross-coupling for efficient B–N, B–O, and unprecedented B–CN bond formation. In many cases bromo-carboranes outperform the traditionally utilized iodo-carborane species. This marked difference in reactivity is leveraged to circumvent multistep functionalization by directly coupling small nucleophiles (-OH, -NH₂, and -CN) and multiple functional groups onto the boron-rich clusters