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The structure of (R)‐rasagiline mesylate [(R)‐RasH+·Mes−], an active pharmaceutical ingredient used to treat Parkinson's disease, is presented. The structure was determined from laboratory and synchrotron powder diffraction data, refined using the Rietveld method, and validated and optimized using dispersion‐corrected DFT calculations. The unit‐cell parameters obtained in both experiments are in good agreement and the refinement with both datasets converged to good agreement factors. The final parameters obtained from laboratory data were a = 5.4905 (8), b = 6.536 (2), c = 38.953 (3) Å, V = 1398.0 (4) Å3 and from synchrotron powder data were a = 5.487530 (10) Å, b = 6.528939 (12) Å, c = 38.94313 (9) Å, V = 1395.245 (5) Å3 with Z = 4 and space group P212121. Preferred orientation was properly accounted for using the synchrotron radiation data, leading to a March–Dollase parameter of 1.140 (1) instead of the 0.642 (1) value obtained from laboratory data. In the structure, (R)‐RasH+ moieties form layers parallel to the ab plane connected by mesylate ions through N—H...O and C—H...O hydrogen bonds. These layers stack along the c axis and are further connected by C—H...π interactions. Hirshfeld surface analysis and fingerprint plot calculations indicate that the main interactions are: H...H (50.9%), H...C/C...H (27.1%) and H...O/O...H (21.1%). [ABSTRACT FROM AUTHOR]

Following Phase 2 of the upgrade of the ESRF in which the storage ring was replaced by a new low-emittance ring along with many other facility upgrades, the status of ID22, the high-resolution powder-diffraction beamline, is described. The beamline has an in-vacuum undulator as source providing X-rays in the range 6-75 keV. ID22's principle characteristics include very high angular resolution as a result of the highly collimated and monochromatic beam, coupled with a 13-channel Si 111 multi-analyser stage between the sample and a Dectris Eiger2 X 2M-W CdTe pixel detector. The detector's axial resolution allows recorded 2θ values to be automatically corrected for the effects of axial divergence, resulting in narrower and more-symmetric peaks compared with the previous fixed-axial-slit arrangement. The axial acceptance can also be increased with increasing diffraction angle, thus simultaneously improving the statistical quality of high-angle data. A complementary Perkin Elmer XRD1611 medical-imaging detector is available for faster, lower-resolution data, often used at photon energies of 60-70 keV for pair-distribution function analysis, although this is also possible in high-resolution mode by scanning up to 120° 2θ at 35 keV. There are various sample environments, allowing sample temperatures from 4 K to 1600°C, a capillary cell for non-corrosive gas atmospheres in the range 0-100 bar, and a sample-changing robot that can accommodate 75 capillary samples compatible with the temperature range 80 K to 950°C. [ABSTRACT FROM AUTHOR]

The ability to utilize a hybrid-photon-counting detector to its full potential can significantly influence data quality, data collection speed, as well as development of elaborate data acquisition schemes. This paper facilitates the optimal use of EIGER2 detectors by providing theory and practical advice on (i) the relation between detector design, technical specifications and operating modes, (ii) the use of corrections and calibrations, and (iii) new acquisition features: a doublegating mode, 8-bit readout mode for increasing temporal resolution, and lines region-of-interest readout mode for frame rates up to 98 kHz. Examples of the implementation and application of EIGER2 at several synchrotron sources (ESRF, PETRA III/DESY, ELETTRA, AS/ANSTO) are presented: high accuracy of high-throughput data in serial crystallography using hard X-rays; suppressing higher harmonics of undulator radiation, improving peak shapes, increasing data collection speed in powder X-ray diffraction; faster ptychography scans; and cleaner and faster pump-and-probe experiments. [ABSTRACT FROM AUTHOR]

Illustrated papyruses from Ancient Egypt have survived across millennia, depicting with vivid colors numerous stories and practices from a distant past. We have investigated a series of illustrated papyruses from Champollion's private collection showing scenes from the Book of the Dead, a document essential to prepare for the afterlife. The nature of the different pigments and their distribution are revealed by combining optical microscopy, Raman spectroscopy, and synchrotron X-ray powder diffraction and fluorescence. The standardized three-step process from the New Kingdom period was used, comprising a preparatory drawing made of red hematite, a coloring step using pigments from the Egyptian palette, and a final black contour drawn with a carbon-based ink. Interestingly, specific pigment mixes were deliberately chosen to obtain different shades. In some parts, the final contour significantly differs from the preliminary drawing, revealing the artist's creativity. These results enhance our knowledge of illustrative practices in Ancient Egypt. [ABSTRACT FROM AUTHOR]

The European Synchrotron Radiation Facility (ESRF) has recently commissioned the new Extremely Brilliant Source (EBS). The gain in brightness as well as the continuous development of beamline instruments boosts the beamline performances, in particular in terms of accelerated data acquisition. This has motivated the development of new access modes as an alternative to standard proposals for access to beamtime, in particular via the "block allocation group" (BAG) mode. Here, we present the recently implemented "historical materials BAG": a community proposal giving to 10 European institutes the opportunity for guaranteed beamtime at two X-ray powder diffraction (XRPD) beamlines—ID13, for 2D high lateral resolution XRPD mapping, and ID22 for high angular resolution XRPD bulk analyses—with a particular focus on applications to cultural heritage. The capabilities offered by these instruments, the specific hardware and software developments to facilitate and speed-up data acquisition and data processing are detailed, and the first results from this new access are illustrated with recent applications to pigments, paintings, ceramics and wood. [ABSTRACT FROM AUTHOR]

The use of organic additives presents the greatest versatility and control of zeolite synthesis in order to prepare novel architectures for desired applications. Despite this prospect, there is little clarity of how organic additives are involved in framework assembly and the range of behaviours that are available. To address this issue, we have considered zeolites RHO and ZK-5 which can both be prepared using 18-crown-6 ether as an additive. Previously, this additive has shown to employ different structure directing behaviours to assemble a variety of zeolites. We have used high resolution powder X-ray diffraction and Rietveld refinement to determine structural models for zeolites RHO and ZK-5 with 18-crown-6 ether occluded in the framework. In doing so, we can observe the identity, location and orientation of the occluded additive and reason the structure directing behaviour in synthesis. We report that the isolated 18-crown-6 ether molecule is involved in the assembly of zeolite RHO, and for zeolite ZK-5 it is the K+ coordinated macrocation. In both cases the relevant additive is disordered in the framework, suggesting that they behave as space-filling species that stabilise the formation of the α-cage. [ABSTRACT FROM AUTHOR]

The crystal structure of the stable form of vitamin B2 or riboflavin (C17H20N4O6) was solved using high‐resolution powder X‐ray diffraction (PXRD). The high‐resolution PXRD pattern of riboflavin was recorded at room temperature at the European Synchrotron Radiation Facility (Grenoble, France). The starting structural model was generated using a Monte Carlo simulated annealing method. The final structure was obtained through Rietveld refinement. The positions of the H atoms belonging to hydroxy groups were estimated from computational energy minimizations. The symmetry is orthorhombic with the space group P212121 and the following lattice parameters: a = 20.01308, b = 15.07337 and c = 5.31565 Å. [ABSTRACT FROM AUTHOR]

In a test experiment, a two‐dimensional pixel detector was mounted on the nine‐channel multi‐analyzer stage of the high‐resolution powder diffraction beamline ID22 at the ESRF. This detector replaces a bank of scintillation counters that detect the diffracted intensity passing via the analyzer crystals as the diffractometer arm is scanned. At each diffractometer detector arm angle 2Θ, a 2D image is recorded that displays nine distinct regions of interest corresponding to the diffraction signals transmitted by each of the analyzer crystals. Summing pixels from within each region of interest allows the diffracted intensity to be extracted for each channel. X‐rays are diffracted from the sample at various angles, 2gθ, into Debye–Scherrer cones. Depending on the azimuthal angle around the cone, diffracted photons satisfy the analyzer‐crystal Bragg condition at different diffractometer 2Θ values and arrive on the detector at different horizontal (axial) positions. The more the azimuthal angle deviates from diffraction in the vertical plane, the lower the 2Θ angle at which it is transmitted by an analyzer crystal, and the greater the distance of the detecting pixel from the centerline of the detector. This paper illustrates how the axial resolution afforded by the pixel detector can be used to correct the apparent diffraction angle, 2Θ, given by the diffractometer arm to its true diffraction angle, 2gθ. This allows a reduction in peak asymmetry at low angle, and even with a relatively small axial acceptance, the correction leads to narrower peaks than if no correction is applied. By varying axial acceptance with diffraction angle, it is possible to optimize angular resolution at low diffraction angles and counting statistics at high angles. In addition, there is an intrinsic peak broadening with increasing azimuthal angle, dependent on the axial beam and detector pixel sizes. This effect reduces with 2gθ, as the curvature of the Debye–Scherrer cones decreases. This broadening can be estimated and used to help choose the axial range to include as a function of diffraction angle. [ABSTRACT FROM AUTHOR]

The crystal structure of a new cocrystal of carbamazepine (systematic name: 5H‐dibenzo[b,f]azepine‐5‐carboxamide, C15H12N2O) and dl‐tartaric acid (C4H6O6), obtained by liquid‐assisted grinding, was solved by powder X‐ray diffraction (PXRD). The high‐resolution PXRD pattern of this new phase was recorded at room temperature thanks to synchrotron experiments at the European Synchrotron Radiation Facility (Grenoble, France). The starting structural model was generated by a Monte‐Carlo simulated annealing method. The final structure was obtained through Rietveld refinement and an energy minimization simulation was used to estimate the H‐atom positions. The stability of the proposed structure as a function of temperature was also assessed from molecular dynamics simulations. The symmetry is monoclinic (space group P21/c) and contains eight molecules per unit cell, namely, four dl‐tartaric acid and four carbamazepine molecules. [ABSTRACT FROM AUTHOR]

Lead–calcium phosphates are unusual compounds sometimes found in different kinds of cultural heritage objects. Structural and physicochemical properties of this family of materials, which fall into the hydroxypyromorphite–hydroxyapatite solid solution, or (Pb x Ca1− x )5(PO4)3OH, have received considerable attention during the last few decades for promising applications in different fields of environmental and material sciences, but their diagnostic implications in the cultural heritage context have been poorly explored. This paper aims to provide a clearer understanding of the relationship between compositional and structural properties of the peculiar series of (Pb x Ca1− x )5(PO4)3OH solid solutions and to determine key markers for their proper non-destructive and non-invasive identification in cultural heritage samples and objects. For this purpose, a systematic study of powders and paint mock-ups made up of commercial and in-house synthesized (Pb x Ca1− x )5(PO4)3OH compounds with a different Pb2+/Ca2+ ratio was carried out via a multi-technique approach based on scanning electron microscopy, synchrotron radiation-based X-ray techniques, i.e., X-ray powder diffraction and X-ray absorption near edge structure spectroscopy at the Ca K- and P K-edges, and vibrational spectroscopy methods, i.e., micro-Raman and Fourier transform infrared spectroscopy. The spectral modifications observed in the hydroxypyromorphite–hydroxyapatite solid solution series are discussed, by assessing the advantages and disadvantages of the proposed techniques and by providing reference data and optimized approaches for future non-destructive and non-invasive applications to study cultural heritage objects and samples. [ABSTRACT FROM AUTHOR]

Solid dispersions are important supersaturating formulations to orally deliver poorly water-soluble drugs. A most important process technique is hot melt extrusion but process requirements limit the choice of suitable polymers. One way around this limitation is to synthesize new polymers. However, their disadvantage is that they require toxicological qualification and present regulatory hurdles for their market authorization. Therefore, this study follows an alternative approach, where new polymeric matrices are created by combining a known polymer, small molecular additives, and an initial solvent-based process step. The polyelectrolyte, carboxymethylcellulose sodium (NaCMC), was tested in combination with different additives such as amino acids, meglumine, trometamol, and urea. It was possible to obtain a new polyelectrolyte matrix that was viable for manufacturing by hot melt extrusion. The amount of additives had to be carefully tuned to obtain an amorphous polymer matrix. This was achieved by probing the matrix using several analytical techniques, such as Fourier transform infrared spectroscopy, differential scanning calorimetry, hot stage microscopy, and X-ray powder diffraction. Next, the obtained matrices had to be examined to ensure the homogeneous distribution of the components and the possible residual crystallinity. As this analysis requires probing a sample on several points and relies on high quality data, X-ray diffraction and starring techniques at a synchrotron source had to be used. Particularly promising with NaCMC was the addition of lysine as well as meglumine. Further research is needed to harness the novel matrix with drugs in amorphous formulations. [ABSTRACT FROM AUTHOR]

During nuclear waste disposal process, radioactive iodine as a fission product can be released. The widespread implementation of sustainable nuclear energy thus requires the development of efficient iodine stores that have simultaneously high capacity, stability and more importantly, storage density (and hence minimized system volume). Here, we report high I2 adsorption in a series of robust porous metal-organic materials, MFM-300(M) (M = Al, Sc, Fe, In). MFM-300(Sc) exhibits fully reversible I2 uptake of 1.54 g g-1, and its structure remains completely unperturbed upon inclusion/removal of I2. Direct observation and quantification of the adsorption, binding domains and dynamics of guest I2 molecules within these hosts have been achieved using XPS, TGA-MS, high resolution synchrotron X-ray diffraction, pair distribution function analysis, Raman, terahertz and neutron spectroscopy, coupled with density functional theory modeling. These complementary techniques reveal a comprehensive understanding of the host-I2 and I2-I2 binding interactions at a molecular level. The initial binding site of I2 in MFM-300(Sc), …, is located near the bridging hydroxyl group of the [ScO[sub 4](OH)[sub 2]] moiety […⋯H-O = 2.263(9) Å] with an occupancy of 0.268. … is located interstitially between two phenyl rings of neighboring ligand molecules […⋯phenyl ring = 3.378(9) and 4.228(5) Å]. … is 4.565(2) Å from the hydroxyl group with an occupancy of 0.208. Significantly, at high I2 loading an unprecedented self-aggregation of I2 molecules into triple-helical chains within the confined nanovoids has been observed at crystallographic resolution, leading to a highly efficient packing of I2 molecules with an exceptional I2 storage density of 3.08 g cm-3 in MFM-300(Sc). [ABSTRACT FROM AUTHOR]

YNU-5 (YFI type) is the first zeolite reported with interconnected 12-, 12-, and 8-ring pores showing a remarkable catalytic potential towards the dimethyl ether (DME)-to-olefin reaction. In this work, the structures of the as-synthesized, calcined and dealuminated YNU-5 zeolites, were investigated by various techniques with special emphasis on advanced electron microscopy methods. The frameworks of the three materials were solely determined by three-dimension electron diffraction tomography, and the space group for the three of them was determined to be C mmm , which is of higher symmetry than the previous reported result. Rietveld refinement was performed against synchrotron Powder X-ray diffraction data in order to obtain precise information of the framework and to locate the organic species, cations and water. Additionally, spherical aberration-corrected scanning transmission electron microscopy was employed to study the local fine structure and to indicate surface reconstruction associated to the displacement of the vacancies through the dealumination process. Finally, a minor phase, whose structure was solved by electron microscopy was found to be MSE framework type, appeared in all the three YNU-5 materials. Overall, the electron microscopy analyses reported in the present work provide additional information regarding the YNU-5 structure in terms of space group determination, additional surface terminations and the identification of a minor phase. [Display omitted] • YNU-5 family of zeolites have been investigated by advanced electron microscopy methods. • The structures were solved by 3D-Electron diffraction tomography obtaining a higher symmetry that the one already reported. • Atomic resolution imaging of the surface revealed different terminations associated to the dealumination process. • An additional tetragonal minor phase, solved by electron diffraction as MSE framework type, was identified. [ABSTRACT FROM AUTHOR]